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Wyszukujesz frazę ""Neurodevelopmental disorders"" wg kryterium: Temat


Tytuł :
Increased RNA editing in maternal immune activation model of neurodevelopmental disease.
Autorzy :
Tsivion-Visbord H; Sackler Faculty of Medicine, Human Molecular Genetics & Biochemistry, Felsenstein Medical Research Center, Tel-Aviv University, Tel Aviv, Israel.
Kopel E; The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, Israel.
Feiglin A; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Sofer T; Departments of Medicine and of Biostatistics, Harvard University, Boston, MA, USA.
Barzilay R; Lifespan Brain Institute Children's Hospital of Philadelphia and Penn Medicine; the Department of Child and Adolescent Psychiatry and Behavioral Sciences, CHOP, Philadelphia, PA, USA.
Ben-Zur T; Sackler Faculty of Medicine, Human Molecular Genetics & Biochemistry, Felsenstein Medical Research Center, Tel-Aviv University, Tel Aviv, Israel.
Yaron O; The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, Israel.
Offen D; Sackler Faculty of Medicine, Human Molecular Genetics & Biochemistry, Felsenstein Medical Research Center, Tel-Aviv University, Tel Aviv, Israel. .
Levanon EY; The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, Israel. .
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Źródło :
Nature communications [Nat Commun] 2020 Oct 16; Vol. 11 (1), pp. 5236. Date of Electronic Publication: 2020 Oct 16.
Typ publikacji :
Journal Article
MeSH Terms :
RNA Editing*
Neurodevelopmental Disorders/*etiology
Neurodevelopmental Disorders/*genetics
Pregnancy/*immunology
Pregnancy Complications/*immunology
Prenatal Exposure Delayed Effects/*genetics
Animals ; Behavior, Animal ; Brain/growth & development ; Brain/immunology ; Brain/metabolism ; Disease Models, Animal ; Female ; Immunity, Maternally-Acquired ; Mice ; Mice, Inbred C57BL ; Neurodevelopmental Disorders/immunology ; Neurodevelopmental Disorders/psychology ; Poly I-C/adverse effects ; Poly I-C/immunology ; Pregnancy Complications/etiology ; Pregnancy Complications/genetics ; Prenatal Exposure Delayed Effects/immunology ; Prenatal Exposure Delayed Effects/psychology
Czasopismo naukowe
Tytuł :
Childhood and Adolescent Neurodevelopmental Disorders.
Autorzy :
Kalin NH; Department of Psychiatry, University of Wisconsin School of Medicine and Public Health, Madison.
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Źródło :
The American journal of psychiatry [Am J Psychiatry] 2020 Sep 01; Vol. 177 (9), pp. 792-794.
Typ publikacji :
Editorial
MeSH Terms :
Mental Health*
Neurodevelopmental Disorders*/classification
Neurodevelopmental Disorders*/psychology
Neurodevelopmental Disorders*/therapy
Social Problems*/prevention & control
Social Problems*/psychology
Substance-Related Disorders*/prevention & control
Substance-Related Disorders*/psychology
Mental Health Services/*standards
Problem Behavior/*psychology
Adolescent ; Behavioral Research ; Child ; Humans ; Psychopathology ; Quality Improvement
Opinia redakcyjna
Tytuł :
Pediatric neuropsychological evaluation via telehealth: Novel models of care.
Autorzy :
Pritchard AE; Department of Neuropsychology, Kennedy Krieger Institute, Baltimore, MD, USA.; Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Sweeney K; Department of Neuropsychology, Kennedy Krieger Institute, Baltimore, MD, USA.
Salorio CF; Department of Neuropsychology, Kennedy Krieger Institute, Baltimore, MD, USA.; Department of Physical Medicine & Rehabilitation, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Jacobson LA; Department of Neuropsychology, Kennedy Krieger Institute, Baltimore, MD, USA.; Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, USA.
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Źródło :
The Clinical neuropsychologist [Clin Neuropsychol] 2020 Oct - Nov; Vol. 34 (7-8), pp. 1367-1379. Date of Electronic Publication: 2020 Aug 13.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Neuropsychological Tests*
Coronavirus Infections/*therapy
Neurodevelopmental Disorders/*therapy
Neuropsychology/*trends
Telemedicine/*trends
Child ; Coronavirus Infections/epidemiology ; Humans ; Neurodevelopmental Disorders/epidemiology ; Neurodevelopmental Disorders/psychology ; Neuropsychology/methods ; Parents/psychology ; Telemedicine/methods
Czasopismo naukowe
Tytuł :
COVID-19 issues related to pediatric neuropsychology and inpatient rehabilitation - challenges to usual care and solutions during the pandemic.
Autorzy :
Koterba CH; Pediatric Psychology and Neuropsychology, Nationwide Children's Hospital, Columbus, Ohio, USA.; Department of Pediatrics, The Ohio State University, Columbus, Ohio, USA.
Baum KT; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Hamner T; Department of Psychology, Drexel University, Philadelphia, Pennsylvania, USA.; Neuropsychology Department, Kennedy Krieger Institute, Baltimore, Maryland, USA.; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Busch TA; Pediatric Psychology and Neuropsychology, Nationwide Children's Hospital, Columbus, Ohio, USA.
Davis KC; Department of Psychology, Texas Children's Hospital, Houston, Texas, USA.; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Tlustos-Carter S; Department of Rehabilitation, Children's Hospital Colorado, Aurora, Colorado, USA.; Department of Physical Medicine and Rehabilitation, University of Colorado, Denver, Colorado, USA.
Howarth R; Department of Neuropsychology, Children's Healthcare Atlanta, Atlanta, Georgia, USA.
Fournier-Goodnight A; Department of Neuropsychology, Children's Healthcare Atlanta, Atlanta, Georgia, USA.
Kramer M; Neuropsychology Department, Kennedy Krieger Institute, Baltimore, Maryland, USA.; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Landry A; Pediatric Psychology and Neuropsychology, Nationwide Children's Hospital, Columbus, Ohio, USA.; Department of Pediatrics, The Ohio State University, Columbus, Ohio, USA.
O'Neill J; Pediatric Psychology and Neuropsychology, Nationwide Children's Hospital, Columbus, Ohio, USA.; Department of Pediatrics, The Ohio State University, Columbus, Ohio, USA.
Cass J; Pediatric Psychology and Neuropsychology, Nationwide Children's Hospital, Columbus, Ohio, USA.; Department of Pediatrics, The Ohio State University, Columbus, Ohio, USA.
Wilson C; Pediatric Psychology and Neuropsychology, Nationwide Children's Hospital, Columbus, Ohio, USA.; Department of Pediatrics, The Ohio State University, Columbus, Ohio, USA.
Slomine BS; Neuropsychology Department, Kennedy Krieger Institute, Baltimore, Maryland, USA.; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
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Źródło :
The Clinical neuropsychologist [Clin Neuropsychol] 2020 Oct - Nov; Vol. 34 (7-8), pp. 1380-1394. Date of Electronic Publication: 2020 Aug 26.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Betacoronavirus*
Pandemics*
Coronavirus Infections/*therapy
Neurodevelopmental Disorders/*rehabilitation
Neuropsychology/*trends
Pneumonia, Viral/*therapy
Telemedicine/*trends
Child ; Coronavirus Infections/epidemiology ; Female ; Humans ; Inpatients/psychology ; Male ; Neurodevelopmental Disorders/epidemiology ; Neurodevelopmental Disorders/psychology ; Neuropsychological Tests ; Neuropsychology/methods ; Pneumonia, Viral/epidemiology ; Telemedicine/methods
SCR Disease Name :
COVID-19
Czasopismo naukowe
Tytuł :
Resolving Neurodevelopmental and Vision Disorders Using Organoid Single-Cell Multi-omics.
Autorzy :
Brancati G; Institute of Molecular and Clinical Ophthalmology, 4031 Basel, Switzerland; Department of Biosystems Science and Engineering, ETH Zürich, 4058 Basel, Switzerland.
Treutlein B; Department of Biosystems Science and Engineering, ETH Zürich, 4058 Basel, Switzerland. Electronic address: .
Camp JG; Institute of Molecular and Clinical Ophthalmology, 4031 Basel, Switzerland; Department of Ophthalmology, University of Basel, 4031 Basel, Switzerland. Electronic address: .
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Źródło :
Neuron [Neuron] 2020 Sep 23; Vol. 107 (6), pp. 1000-1013.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Genomics/*methods
Neurodevelopmental Disorders/*metabolism
Organoids/*metabolism
Primary Cell Culture/*methods
Single-Cell Analysis/*methods
Vision Disorders/*metabolism
Humans ; Neurodevelopmental Disorders/genetics ; Neurodevelopmental Disorders/pathology ; Organoids/growth & development ; Organoids/pathology ; Vision Disorders/genetics ; Vision Disorders/pathology
Czasopismo naukowe
Tytuł :
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype.
Autorzy :
Breen MS; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Garg P; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Tang L; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Mendonca D; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Levy T; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Barbosa M; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Arnett AB; Department of Psychiatry & Behavioral Sciences, University of Washington, Seattle, WA 98195, USA.
Kurtz-Nelson E; Department of Psychiatry & Behavioral Sciences, University of Washington, Seattle, WA 98195, USA.
Agolini E; Laboratory of Medical Genetics Unit, Bambino Gesù Children's Hospital, 00145 Rome, Italy.
Battaglia A; Department of Developmental Neuroscience, IRCCS 'Stella Maris Foundation,' 56128 Pisa, Italy.
Chiocchetti AG; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Autism Research and Intervention Center of Excellence, University Hospital Frankfurt Goethe University, Deutschordenstr. 50, 60528 Frankfurt am Main, Germany.
Freitag CM; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Autism Research and Intervention Center of Excellence, University Hospital Frankfurt Goethe University, Deutschordenstr. 50, 60528 Frankfurt am Main, Germany.
Garcia-Alcon A; Child and Adolescent Psychiatry Department, Hospital General Universitario Gregorio Marañón, School of Medicine, Universidad Complutense, IiSGM, CIBERSAM, Madrid 28007, Spain.
Grammatico P; Medical Genetics, Department of Molecular Medicine, Sapienza University, San Camillo-Forlanini Hospital, 00152 Rome, Italy.
Hertz-Picciotto I; MIND Institute, School of Medicine, University of California, Davis, Davis, CA 95817, USA; Department of Public Health Sciences, School of Medicine, University of California, Davis, Davis, CA 95616, USA.
Ludena-Rodriguez Y; Department of Public Health Sciences, School of Medicine, University of California, Davis, Davis, CA 95616, USA.
Moreno C; Child and Adolescent Psychiatry Department, Hospital General Universitario Gregorio Marañón, School of Medicine, Universidad Complutense, IiSGM, CIBERSAM, Madrid 28007, Spain.
Novelli A; Laboratory of Medical Genetics Unit, Bambino Gesù Children's Hospital, 00145 Rome, Italy.
Parellada M; Child and Adolescent Psychiatry Department, Hospital General Universitario Gregorio Marañón, School of Medicine, Universidad Complutense, IiSGM, CIBERSAM, Madrid 28007, Spain.
Pascolini G; Medical Genetics, Department of Molecular Medicine, Sapienza University, San Camillo-Forlanini Hospital, 00152 Rome, Italy.
Tassone F; MIND Institute, School of Medicine, University of California, Davis, Davis, CA 95817, USA; Department of Biochemistry and Molecular Medicine, University of California, Davis, Davis, CA 95817, USA.
Grice DE; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Di Marino D; Department of Life and Environmental Sciences, New York-Marche Structural Biology Center (NY-MaSBiC), Polytechnic University of Marche, 60131 Ancona, Italy.
Bernier RA; Department of Psychiatry & Behavioral Sciences, University of Washington, Seattle, WA 98195, USA.
Kolevzon A; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Sharp AJ; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Buxbaum JD; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Siper PM; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address: .
De Rubeis S; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address: .
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Źródło :
American journal of human genetics [Am J Hum Genet] 2020 Sep 03; Vol. 107 (3), pp. 555-563. Date of Electronic Publication: 2020 Aug 05.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Autism Spectrum Disorder/*genetics
Homeodomain Proteins/*genetics
Intellectual Disability/*genetics
Nerve Tissue Proteins/*genetics
Neurodevelopmental Disorders/*genetics
Autism Spectrum Disorder/pathology ; Child ; DNA Methylation/genetics ; Developmental Disabilities/genetics ; Developmental Disabilities/pathology ; Epigenesis, Genetic/genetics ; Female ; Humans ; Intellectual Disability/pathology ; Male ; Mutation/genetics ; Neurodevelopmental Disorders/pathology ; Phenotype ; Transcriptome/genetics
Czasopismo naukowe
Tytuł :
Impact of Social Isolation due to the COVID-19 Pandemic in Patients With Pediatric Disorders: Rehabilitation Perspectives From a Developing Country.
Autorzy :
Meireles ALF; Centro de Ciências da Saúde e do Esporte (CEFID), Universidade do Estado de Santa Catarina (UDESC), Av. Pascoal Simone 358, Florianópolis, Santa Catarina, Brazil.
de Meireles LCF; Health Science Center, Universidade Regional do Alto Uruguai e das Missões, Erechim, Rio Grande do Sul, Brazil.
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Źródło :
Physical therapy [Phys Ther] 2020 Oct 30; Vol. 100 (11), pp. 1910-1912.
Typ publikacji :
Journal Article
MeSH Terms :
Betacoronavirus*
Developing Countries*
Pandemics*/prevention & control
Coronavirus Infections/*epidemiology
Neurodevelopmental Disorders/*rehabilitation
Pneumonia, Viral/*epidemiology
Quarantine/*psychology
Telerehabilitation/*methods
Brazil ; Child ; Comorbidity ; Coronavirus Infections/prevention & control ; Coronavirus Infections/psychology ; Humans ; Neurodevelopmental Disorders/psychology ; Pneumonia, Viral/prevention & control ; Pneumonia, Viral/psychology ; Social Isolation/psychology ; Vulnerable Populations
SCR Disease Name :
COVID-19
Czasopismo naukowe
Tytuł :
Performance of the German version of the PARCA-R questionnaire as a developmental screening tool in two-year-old very preterm infants.
Autorzy :
Picotti E; Department of Neonatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Bechtel N; Division of Neuropaediatrics and Developmental Medicine, University Children's Hospital Basel, Basel, Switzerland.
Latal B; Child Development Centre, University Children's Hospital Zurich, Zurich, Switzerland.
Borradori-Tolsa C; Department of Woman, Child and Adolescent, Geneva University Hospital, Geneva, Switzerland.
Bickle-Graz M; Department Woman-Mother-Child, University Hospital Lausanne, Lausanne, Switzerland.
Grunt S; Division of Neuropaediatrics, Development and Rehabilitation, University Children's Hospital, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Johnson S; Department of Health Sciences, University of Leicester, Leicester, United Kingdom.
Wolke D; Department of Psychology, University of Warwick, Coventry, United Kingdom.
Natalucci G; Department of Neonatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.; Child Development Centre, University Children's Hospital Zurich, Zurich, Switzerland.; Larson-Rosenquist Family Foundation Centre for Neurodevelopment, Growth and Nutrition of the Newborn, University of Zurich, Zurich Switzerland.
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Corporate Authors :
Swiss Neonatal Network & Follow-Up Group
Źródło :
PloS one [PLoS One] 2020 Sep 03; Vol. 15 (9), pp. e0236289. Date of Electronic Publication: 2020 Sep 03 (Print Publication: 2020).
Typ publikacji :
Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
MeSH Terms :
Child Development*
Infant, Premature*/physiology
Neurodevelopmental Disorders/*diagnosis
Child, Preschool ; Cross-Sectional Studies ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Neurodevelopmental Disorders/epidemiology ; Surveys and Questionnaires ; Switzerland/epidemiology
Czasopismo naukowe
Tytuł :
Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing.
Autorzy :
Fliedner A; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
Kirchner P; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
Wiesener A; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
van de Beek I; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, the Netherlands.
Waisfisz Q; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, the Netherlands.
van Haelst M; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, the Netherlands.
Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030, USA.
Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Baylor Genetics Laboratories, Houston, TX 77021, USA.
Azamian MS; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Xia F; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Baylor Genetics Laboratories, Houston, TX 77021, USA.
Dutra-Clarke M; Division of Medical Genetics, Department of Pediatrics, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA.
Martinez-Agosto JA; Division of Medical Genetics, Department of Pediatrics, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA; Department of Human Genetics, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA.
Lee H; Department of Human Genetics, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA.
Noh GJ; Department of Genetics, Southern California Permanente Medical Group, Fontana, CA 92335, USA.
Lippa N; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY 10019, USA.
Alkelai A; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, NY 10019, USA.
Aggarwal V; Institute for Genomic Medicine and Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10019, USA.
Agre KE; Department of Clinical Genomics, Mayo Clinic, Rochester, MN 55905, USA.
Gavrilova R; Department of Clinical Genomics, Mayo Clinic, Rochester, MN 55905, USA; Department of Neurology, Mayo Clinic, Rochester, MN 55905, USA.
Mirzaa GM; Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA 98195, USA; Department of Pediatrics, University of Washington, Seattle, WA 98195, USA; Brotman Baty Institute for Precision Medicine, Seattle, WA 98195, USA.
Straussberg R; Neurogenetics Clinic, Neurology Unit, Schneider Children's Medical Center, Petah Tikva 49202, Israel; Sackler School of Medicine, Tel Aviv University, Ramat Aviv, Tel Aviv 69978, Israel.
Cohen R; Sackler School of Medicine, Tel Aviv University, Ramat Aviv, Tel Aviv 69978, Israel; Neurology Institute and Epilepsy Center, Schneider Children's Medical Center, Petah Tikva 49202, Israel.
Horist B; Pediatrics and Genetics, Alpharetta, GA 30005, USA.
Krishnamurthy V; Pediatrics and Genetics, Alpharetta, GA 30005, USA.
McWalter K; Clinical Genomics, GeneDx, Gaithersburg, MD 20877, USA.
Juusola J; Clinical Genomics, GeneDx, Gaithersburg, MD 20877, USA.
Davis-Keppen L; University of South Dakota, Sanford School of Medicine, Sioux Falls, SD 57105, USA.
Ohden L; University of South Dakota, Sanford School of Medicine, Sioux Falls, SD 57105, USA.
van Slegtenhorst M; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, the Netherlands.
de Man SA; Department of Pediatrics, Amphia Hospital, 4818 CK Breda, the Netherlands.
Ekici AB; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
Gregor A; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
van de Laar I; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, the Netherlands.
Zweier C; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany. Electronic address: .
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Corporate Authors :
UCLA Clinical Genomics Center
Źródło :
American journal of human genetics [Am J Hum Genet] 2020 Sep 03; Vol. 107 (3), pp. 544-554. Date of Electronic Publication: 2020 Jul 29.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Intellectual Disability/*genetics
Neurodevelopmental Disorders/*genetics
Seizures/*genetics
Serine-Arginine Splicing Factors/*genetics
Animals ; Child ; Drosophila melanogaster/genetics ; Female ; Gene Knockdown Techniques ; Genetic Variation/genetics ; Heterozygote ; Humans ; Intellectual Disability/physiopathology ; Locomotion/genetics ; Male ; Mutation/genetics ; Neurodevelopmental Disorders/physiopathology ; RNA Polymerase II/genetics ; RNA Processing, Post-Transcriptional/genetics ; RNA, Messenger/genetics ; Seizures/physiopathology ; Whole Exome Sequencing
Czasopismo naukowe
Tytuł :
Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum.
Autorzy :
Motta M; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Pannone L; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Pantaleoni F; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Bocchinfuso G; Department of Chemical Science and Technologies, University of Rome Tor Vergata, 00133, Rome, Italy.
Radio FC; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Cecchetti S; Microscopy Area, Core Facilities, Istituto Superiore di Sanità, 00161 Rome, Italy.
Ciolfi A; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Di Rocco M; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy; Department of Biochemical Science 'A. Rossi Fanelli,' Sapienza University of Rome, 00185 Rome, Italy.
Elting MW; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit, 1117 Amsterdam, the Netherlands.
Brilstra EH; Department of Genetics, University Medical Center Utrecht, 3584 CX Utrecht, the Netherlands.
Boni S; Medical Genetics Unit, S. Martino Hospital, 32100 Belluno, Italy.
Mazzanti L; Department of Medical and Surgical Sciences, Policlinico S. Orsola-Malpighi Hospital, University of Bologna, 40138 Bologna, Italy.
Tamburrino F; Department of Medical and Surgical Sciences, Policlinico S. Orsola-Malpighi Hospital, University of Bologna, 40138 Bologna, Italy.
Walsh L; Indiana University Health at Riley Hospital for Children, Indianapolis, IN 46202, USA.
Payne K; Indiana University Health at Riley Hospital for Children, Indianapolis, IN 46202, USA.
Fernández-Jaén A; Department of Pediatrics Neurology, Hospital Universitario Quirón de Madrid, Universidad Europea de Madrid, 28223 Madrid, Spain.
Ganapathi M; Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA.
Chung WK; Departments of Pediatrics and Medicine, Columbia University Medical Center, New York, NY 10032, USA.
Grange DK; Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Dave-Wala A; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH 43215, USA.
Reshmi SC; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH 43215, USA; Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH 43215, USA.
Bartholomew DW; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH 43215, USA.
Mouhlas D; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH 43215, USA.
Carpentieri G; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Bruselles A; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Pizzi S; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Bellacchio E; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Piceci-Sparascio F; Medical Genetics Division, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.
Lißewski C; Institute of Human Genetics, University Hospital Magdeburg, 39120 Magdeburg, Germany.
Brinkmann J; Institute of Human Genetics, University Hospital Magdeburg, 39120 Magdeburg, Germany.
Waclaw RR; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.
Waisfisz Q; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit, 1117 Amsterdam, the Netherlands.
van Gassen K; Department of Genetics, University Medical Center Utrecht, 3584 CX Utrecht, the Netherlands.
Wentzensen IM; GeneDx, Gaithersburg, 20877 MD, USA.
Morrow MM; GeneDx, Gaithersburg, 20877 MD, USA.
Álvarez S; Medical Department, NimGenetics, 28049 Madrid, Spain.
Martínez-García M; Medical Department, NimGenetics, 28049 Madrid, Spain.
De Luca A; Medical Genetics Division, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.
Memo L; Ambulatorio Genetica Clinica, Ospedale San Bortolo, 36100 Vicenza, Italy.
Zampino G; Center for Rare Disease and Congenital Defects, Fondazione Policlinico Universitario Gemelli, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Rossi C; Medical Genetics Unit, Policlinico S. Orsola-Malpighi, University of Bologna, 40138 Bologna, Italy.
Seri M; Medical Genetics Unit, Policlinico S. Orsola-Malpighi, University of Bologna, 40138 Bologna, Italy.
Gelb BD; Mindich Child Health and Development Institute and Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Zenker M; Institute of Human Genetics, University Hospital Magdeburg, 39120 Magdeburg, Germany.
Dallapiccola B; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy.
Stella L; Department of Chemical Science and Technologies, University of Rome Tor Vergata, 00133, Rome, Italy.
Prada CE; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Martinelli S; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Flex E; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Tartaglia M; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy. Electronic address: .
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Źródło :
American journal of human genetics [Am J Hum Genet] 2020 Sep 03; Vol. 107 (3), pp. 499-513. Date of Electronic Publication: 2020 Jul 27.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Carcinogenesis/*genetics
Mitogen-Activated Protein Kinase 1/*genetics
Neurodevelopmental Disorders/*genetics
Noonan Syndrome/*genetics
Child, Preschool ; Female ; Humans ; MAP Kinase Signaling System/genetics ; Male ; Mutation, Missense/genetics ; Neurodevelopmental Disorders/pathology ; Noonan Syndrome/physiopathology ; Phenotype ; Protein Tyrosine Phosphatase, Non-Receptor Type 11/genetics ; Signal Transduction ; Whole Exome Sequencing ; ras Proteins/genetics
Czasopismo naukowe
Tytuł :
Provider-Level Caseload of Psychosocial Services for Medicaid-Insured Children.
Autorzy :
Harati PM; 1372122529 H. Milton Stewart School of Industrial and Systems Engineering, Georgia Institute of Technology, Atlanta, GA, USA.
Cummings JR; 1371 Department of Health Policy and Management, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
Serban N; 1372122529 H. Milton Stewart School of Industrial and Systems Engineering, Georgia Institute of Technology, Atlanta, GA, USA.
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Źródło :
Public health reports (Washington, D.C. : 1974) [Public Health Rep] 2020 Sep/Oct; Vol. 135 (5), pp. 599-610. Date of Electronic Publication: 2020 Jul 09.
Typ publikacji :
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Health Services Accessibility/*statistics & numerical data
Hospitals, Pediatric/*statistics & numerical data
Hospitals, Psychiatric/*statistics & numerical data
Medicaid/*statistics & numerical data
Neurodevelopmental Disorders/*therapy
Primary Health Care/*statistics & numerical data
Psychiatric Rehabilitation/*statistics & numerical data
Adolescent ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Neurodevelopmental Disorders/epidemiology ; United States/epidemiology
Czasopismo naukowe
Tytuł :
Duration of Resuscitation at Birth, Mortality, and Neurodevelopment: A Systematic Review.
Autorzy :
Foglia EE; Division of Neonatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; .
Weiner G; Division of Neonatal-Perinatal Medicine, C.S. Mott Children's Hospital and University of Michigan, Ann Arbor, Michigan.
de Almeida MFB; Division of Neonatal Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
Wyllie J; Departments of Paediatrics and Neonatology, The James Cook University Hospital, South Tees Hospitals National Health Services Foundation Trust, Middlesbrough, United Kingdom.
Wyckoff MH; Division of Neonatal-Perinatal Medicine, Department of Pediatrics, The University of Texas Southwestern Medical Center, Dallas, Texas; and.
Rabi Y; Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada.
Guinsburg R; Division of Neonatal Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
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Corporate Authors :
INTERNATIONAL LIAISON COMMITTEE ON RESUSCITATION NEONATAL LIFE SUPPORT TASK FORCE
Źródło :
Pediatrics [Pediatrics] 2020 Sep; Vol. 146 (3). Date of Electronic Publication: 2020 Aug 12.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Systematic Review
MeSH Terms :
Child Development*
Bradycardia/*therapy
Cardiopulmonary Resuscitation/*statistics & numerical data
Heart Arrest/*therapy
Neurodevelopmental Disorders/*epidemiology
Advisory Committees ; Bias ; Heart Rate ; Humans ; Infant, Newborn ; Neurodevelopmental Disorders/mortality ; Survivors/statistics & numerical data ; Time Factors
Czasopismo naukowe
Tytuł :
The COVID-19 pandemic, psychological stress during pregnancy, and risk of neurodevelopmental disorders in offspring: a neglected consequence.
Autorzy :
Abdoli A; Department of Parasitology and Mycology, School of Medicine, Jahrom University of Medical Sciences, Jahrom, Iran.; Zoonoses Research Center, Jahrom University of Medical Sciences, Jahrom, Iran.
Falahi S; Zoonotic Diseases Research Center, Ilam University of Medical Sciences, Ilam, Iran.
Kenarkoohi A; Department of Microbiology, Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran.
Shams M; Zoonotic Diseases Research Center, Ilam University of Medical Sciences, Ilam, Iran.
Mir H; Nutrition and Metabolic Diseases Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.; Research Center for Noncommunicable Diseases, School of Medicine, Jahrom University of Medical Sciences, Jahrom, Iran.
Jahromi MAM; Research Center for Noncommunicable Diseases, School of Medicine, Jahrom University of Medical Sciences, Jahrom, Iran.; Department of Advanced Medical Sciences and Technologies, School of Medicine, Jahrom University of Medical Sciences, Jahrom, Iran.; Department of Laboratory Sciences, School of Medicine, Jahrom University of Medical Sciences, Jahrom, Iran.
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Źródło :
Journal of psychosomatic obstetrics and gynaecology [J Psychosom Obstet Gynaecol] 2020 Sep; Vol. 41 (3), pp. 247-248. Date of Electronic Publication: 2020 May 08.
Typ publikacji :
Letter; Comment
MeSH Terms :
Coronavirus*
Coronavirus Infections*
Neurodevelopmental Disorders*
Pandemics*
Pneumonia, Viral*
Betacoronavirus ; China ; Female ; Humans ; Pregnancy ; Stress, Psychological
SCR Disease Name :
COVID-19
Opinia redakcyjna
Tytuł :
Social isolation and exclusion: the parents' experience of caring for children with rare neurodevelopmental disorders.
Autorzy :
Currie G; School of Nursing and Midwifery, Faculty of Health, Community and Education, Mount Royal University, Calgary, Alberta, Canada.
Szabo J; School of Nursing and Midwifery, Faculty of Health, Community and Education, Mount Royal University, Calgary, Alberta, Canada.
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Źródło :
International journal of qualitative studies on health and well-being [Int J Qual Stud Health Well-being] 2020 Dec; Vol. 15 (1), pp. 1725362.
Typ publikacji :
Journal Article
MeSH Terms :
Neurodevelopmental Disorders*
Rare Diseases*
Caregivers/*psychology
Parents/*psychology
Social Isolation/*psychology
Adult ; Canada/epidemiology ; Child ; Child Health Services/standards ; Delivery of Health Care/standards ; Female ; Humans ; Male ; Middle Aged ; Parent-Child Relations ; Social Stigma ; Social Support ; Stress, Psychological
Czasopismo naukowe
Tytuł :
Supporting Students with Neurodevelopment Disorders in School Health Care-School Nurses' Experiences.
Autorzy :
Berglund Melendez A; Faculty of Health Sciences, Kristianstad University, 291 88 Kristianstad, Sweden.
Malmsten M; Faculty of Health Sciences, Kristianstad University, 291 88 Kristianstad, Sweden.
Einberg EL; Faculty of Health Sciences, Kristianstad University, 291 88 Kristianstad, Sweden.
Clausson EK; Faculty of Health Sciences, Kristianstad University, 291 88 Kristianstad, Sweden.
Garmy P; Faculty of Health Sciences, Kristianstad University, 291 88 Kristianstad, Sweden.; Clinical Health Promoting Centre, Lund University, 221 00 Lund, Sweden.
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Źródło :
International journal of environmental research and public health [Int J Environ Res Public Health] 2020 Aug 09; Vol. 17 (16). Date of Electronic Publication: 2020 Aug 09.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Neurodevelopmental Disorders*/nursing
School Nursing*
Adolescent ; Attitude of Health Personnel ; Child ; Humans ; Qualitative Research ; Schools ; Students ; Sweden
Czasopismo naukowe
Tytuł :
The prevalence and comorbidity rates of specific learning disorder among primary school children in Turkey.
Autorzy :
Büber A; Department of Child and Adolescent Psychiatry, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Başay Ö; Department of Child and Adolescent Psychiatry, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Şenol H; Department of Biostatistics, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
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Źródło :
Nordic journal of psychiatry [Nord J Psychiatry] 2020 Aug; Vol. 74 (6), pp. 453-460. Date of Electronic Publication: 2020 Mar 18.
Typ publikacji :
Journal Article
MeSH Terms :
Neurodevelopmental Disorders/*epidemiology
Neurodevelopmental Disorders/*psychology
Schools/*trends
Specific Learning Disorder/*epidemiology
Specific Learning Disorder/*psychology
Attention Deficit Disorder with Hyperactivity/diagnosis ; Child ; Child Behavior Disorders/diagnosis ; Child Behavior Disorders/epidemiology ; Child Behavior Disorders/psychology ; Comorbidity ; Diagnostic and Statistical Manual of Mental Disorders ; Female ; Humans ; Male ; Neurodevelopmental Disorders/diagnosis ; Prevalence ; Specific Learning Disorder/diagnosis ; Turkey/epidemiology
Czasopismo naukowe
Tytuł :
Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders.
Autorzy :
Seidlitz J; Developmental Neurogenomics Unit, National Institute of Mental Health, Bethesda, MD, USA. .; Department of Psychiatry, University of Cambridge, Cambridge, UK. .
Nadig A; Developmental Neurogenomics Unit, National Institute of Mental Health, Bethesda, MD, USA.
Liu S; Developmental Neurogenomics Unit, National Institute of Mental Health, Bethesda, MD, USA.
Bethlehem RAI; Department of Psychiatry, University of Cambridge, Cambridge, UK.
Vértes PE; Department of Psychiatry, University of Cambridge, Cambridge, UK.; School of Mathematical Sciences, Queen Mary University of London, London, UK.; The Alan Turing Institute, London, UK.
Morgan SE; Department of Psychiatry, University of Cambridge, Cambridge, UK.
Váša F; Department of Psychiatry, University of Cambridge, Cambridge, UK.
Romero-Garcia R; Department of Psychiatry, University of Cambridge, Cambridge, UK.
Lalonde FM; Developmental Neurogenomics Unit, National Institute of Mental Health, Bethesda, MD, USA.
Clasen LS; Developmental Neurogenomics Unit, National Institute of Mental Health, Bethesda, MD, USA.
Blumenthal JD; Developmental Neurogenomics Unit, National Institute of Mental Health, Bethesda, MD, USA.
Paquola C; McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, Montreal, QC, Canada.
Bernhardt B; McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, Montreal, QC, Canada.
Wagstyl K; Department of Psychiatry, University of Cambridge, Cambridge, UK.; McGill Centre for Integrative Neuroscience, McGill University, Montreal, QC, Canada.
Polioudakis D; Department of Neurology, Center for Autism Research and Treatment, Semel Institute, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.
de la Torre-Ubieta L; Department of Neurology, Center for Autism Research and Treatment, Semel Institute, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.; Department of Psychiatry and Biobehavioral Sciences, Semel Institute, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.
Geschwind DH; Department of Neurology, Center for Autism Research and Treatment, Semel Institute, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.; Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.
Han JC; Departments of Pediatrics and Physiology, University of Tennessee Health Science Center and Le Bonheur Children's Foundation Research Institute, Memphis, TN, USA.; Pediatrics and Developmental Neuropsychiatry Branch, National Institute of Mental Health, NIH, Bethesda, MD, USA.; Unit on Metabolism and Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD, USA.
Lee NR; Department of Psychology, Drexel University, Philadelphia, PA, USA.
Murphy DG; Institute of Psychiatry, King's College London, London, UK.
Bullmore ET; Department of Psychiatry, University of Cambridge, Cambridge, UK.; Cambridgeshire and Peterborough NHS Foundation Trust, Huntingdon, UK.
Raznahan A; Developmental Neurogenomics Unit, National Institute of Mental Health, Bethesda, MD, USA. .
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Źródło :
Nature communications [Nat Commun] 2020 Jul 03; Vol. 11 (1), pp. 3358. Date of Electronic Publication: 2020 Jul 03.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
MeSH Terms :
DNA Copy Number Variations*
Genetic Predisposition to Disease*
Cerebral Cortex/*pathology
Neurodevelopmental Disorders/*genetics
Adolescent ; Adult ; Brain Mapping ; Cerebral Cortex/cytology ; Cerebral Cortex/diagnostic imaging ; Cerebral Cortex/growth & development ; Child ; Cohort Studies ; Female ; Gene Expression Profiling ; Genome, Human ; Humans ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Neurodevelopmental Disorders/diagnosis ; Neurodevelopmental Disorders/pathology ; Neuroimaging ; Neurons/metabolism ; Neurons/pathology ; Oligodendroglia/metabolism ; Oligodendroglia/pathology ; Spatial Analysis ; Young Adult
Czasopismo naukowe
Tytuł :
Neurocognitive and Neurobehavioral Phenotype of Youth with Schaaf-Yang Syndrome.
Autorzy :
Thomason MM; Baylor College of Medicine, Houston, TX, USA. .; Clinical Care Center - Psychology Service, Texas Children's Hospital, 6701 Fannin Street, Suite 1630, Houston, TX, 77030-2608, USA. .
McCarthy J; Baylor College of Medicine, Houston, TX, USA.; Clinical Care Center - Psychology Service, Texas Children's Hospital, 6701 Fannin Street, Suite 1630, Houston, TX, 77030-2608, USA.; John P. and Kathrine G. McGovern Medical School, University of Texas Health Science Center, Houston, TX, USA.
Goin-Kochel RP; Baylor College of Medicine, Houston, TX, USA.; Clinical Care Center - Psychology Service, Texas Children's Hospital, 6701 Fannin Street, Suite 1630, Houston, TX, 77030-2608, USA.; Institute of Human Genetics, University Hospital Cologne, Cologne, Nordrhein-Westfalen, Germany.
Dowell LR; Baylor College of Medicine, Houston, TX, USA.; Clinical Care Center - Psychology Service, Texas Children's Hospital, 6701 Fannin Street, Suite 1630, Houston, TX, 77030-2608, USA.
Schaaf CP; Baylor College of Medicine, Houston, TX, USA.; Clinical Care Center - Psychology Service, Texas Children's Hospital, 6701 Fannin Street, Suite 1630, Houston, TX, 77030-2608, USA.; Institute of Human Genetics, University Hospital Cologne, Cologne, Nordrhein-Westfalen, Germany.; University of Cologne, Cologne, Germany.
Berry LN; Baylor College of Medicine, Houston, TX, USA.; Clinical Care Center - Psychology Service, Texas Children's Hospital, 6701 Fannin Street, Suite 1630, Houston, TX, 77030-2608, USA.
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Źródło :
Journal of autism and developmental disorders [J Autism Dev Disord] 2020 Jul; Vol. 50 (7), pp. 2491-2500.
Typ publikacji :
Journal Article
MeSH Terms :
Mental Status and Dementia Tests*
Phenotype*
Proteins*/genetics
Abnormalities, Multiple/*diagnosis
Autism Spectrum Disorder/*diagnosis
Neurodevelopmental Disorders/*diagnosis
Abnormalities, Multiple/genetics ; Abnormalities, Multiple/psychology ; Adolescent ; Autism Spectrum Disorder/genetics ; Autism Spectrum Disorder/psychology ; Child ; Female ; Humans ; Male ; Neurodevelopmental Disorders/genetics ; Neurodevelopmental Disorders/psychology ; Syndrome
Czasopismo naukowe
Tytuł :
Neurodevelopmental impairment in necrotising enterocolitis survivors: systematic review and meta-analysis.
Autorzy :
Matei A; Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, Ontario, Canada.
Montalva L; Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, Ontario, Canada.
Goodbaum A; Division of General and Thoracic Surgery, Department of Surgery, Hospital for Sick Children, Toronto, Ontario, Canada.
Lauriti G; Department of Pediatric Surgery, Spirito Santo Hospital, Pescara, Italy.; G. d'Annunzio University, Chieti-Pescara, Italy.
Zani A; Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, Ontario, Canada .
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Źródło :
Archives of disease in childhood. Fetal and neonatal edition [Arch Dis Child Fetal Neonatal Ed] 2020 Jul; Vol. 105 (4), pp. 432-439. Date of Electronic Publication: 2019 Dec 04.
Typ publikacji :
Journal Article; Meta-Analysis; Systematic Review
MeSH Terms :
Enterocolitis, Necrotizing/*complications
Neurodevelopmental Disorders/*epidemiology
Cerebellum/pathology ; Humans ; Incidence ; Infant, Newborn ; Neurodevelopmental Disorders/etiology ; Neurodevelopmental Disorders/pathology
Czasopismo naukowe
Tytuł :
Children's Mental Health Emergency Department Visits: 2007-2016.
Autorzy :
Lo CB; Division of Emergency Medicine, Nationwide Children's Hospital, Columbus, Ohio.
Bridge JA; Centers for Suicide Prevention and Research.; Departments of Pediatrics.; Psychiatry, and Behavioral Health, College of Medicine, The Ohio State University, Columbus, Ohio; and.
Shi J; Pediatric Trauma Research, and.; Injury Research and Policy, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Ludwig L; Emergency Medical Services for Children, Division of Child, Adolescent, and Family Health, Maternal and Child Health Bureau, Health Resources and Services Administration, Rockville, Maryland.
Stanley RM; Division of Emergency Medicine, Nationwide Children's Hospital, Columbus, Ohio; .; Departments of Pediatrics.
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Źródło :
Pediatrics [Pediatrics] 2020 Jun; Vol. 145 (6). Date of Electronic Publication: 2020 May 11.
Typ publikacji :
Journal Article
MeSH Terms :
Emergency Medical Services/*trends
Emergency Service, Hospital/*trends
Mental Health/*trends
Neurodevelopmental Disorders/*therapy
Pediatric Emergency Medicine/*trends
Adolescent ; Child ; Child, Preschool ; Databases, Factual/trends ; Emergency Medical Services/methods ; Female ; Humans ; Male ; Neurodevelopmental Disorders/diagnosis ; Neurodevelopmental Disorders/epidemiology ; Pediatric Emergency Medicine/methods ; United States/epidemiology
Czasopismo naukowe

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