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Tytuł :
Eighteenth-Century English Literature, 1660-1789. By CHARLOTTE SUSSMAN. Cambridge: Polity. 2012. 291 p. £16.99 (pb). ISBN 978-0-7456-2515-7. The Long 18th Century: Literature from 1660 to 1790. By PENNY PRITCHARD. Harlow: York Press. 2010. iv + 373 p. £10.99 (pb). ISBN 978-1-4082-0473-3. The Wiley-Blackwell Encyclopedia of Eighteenth-Century Writers and Writing, 1660-1789. Edited by PAUL BAINES , JULIAN FERRARO and PAT ROGERS . Oxford: Wiley-Blackwell. 2011. xxxiv + 397 p. £110 (hb). ISBN 978-1-4051-5669-1 [Review]
Index Terms :
PN0080 Criticism
PR English literature
Article
NonPeerReviewed
URL :
http://gala.gre.ac.uk/id/eprint/10458">http://gala.gre.ac.uk/id/eprint/10458
http://dx.doi.org/10.1111/1754-0208.12015">http://dx.doi.org/10.1111/1754-0208.12015
10.1111/1754-0208.12015
Zasób elektroniczny
Tytuł :
Eighteenth-Century English Literature, 1660-1789. By CHARLOTTE SUSSMAN. Cambridge: Polity. 2012. 291 p. £16.99 (pb). ISBN 978-0-7456-2515-7. The Long 18th Century: Literature from 1660 to 1790. By PENNY PRITCHARD. Harlow: York Press. 2010. iv + 373 p. £10.99 (pb). ISBN 978-1-4082-0473-3. The Wiley-Blackwell Encyclopedia of Eighteenth-Century Writers and Writing, 1660-1789. Edited by PAUL BAINES , JULIAN FERRARO and PAT ROGERS . Oxford: Wiley-Blackwell. 2011. xxxiv + 397 p. £110 (hb). ISBN 978-1-4051-5669-1 [Review]
Index Terms :
PN0080 Criticism
PR English literature
Article
NonPeerReviewed
URL :
http://gala.gre.ac.uk/id/eprint/10458">http://gala.gre.ac.uk/id/eprint/10458
http://dx.doi.org/10.1111/1754-0208.12015">http://dx.doi.org/10.1111/1754-0208.12015
10.1111/1754-0208.12015
Zasób elektroniczny
Tytuł :
Need for long-term follow-up in sinonasal inverted papilloma: A Single-institution experience.
Autorzy :
Binz GHA; Department of Otorhinolaryngology - Head and Neck Surgery, University Hospital Zurich, Zürich, Switzerland.; University of Zurich, Zurich, Switzerland.
Soyka MB; Department of Otorhinolaryngology - Head and Neck Surgery, University Hospital Zurich, Zürich, Switzerland.; University of Zurich, Zurich, Switzerland.
Holzmann D; Department of Otorhinolaryngology - Head and Neck Surgery, University Hospital Zurich, Zürich, Switzerland.; University of Zurich, Zurich, Switzerland.
Meerwein CM; Department of Otorhinolaryngology - Head and Neck Surgery, University Hospital Zurich, Zürich, Switzerland.; University of Zurich, Zurich, Switzerland.
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Źródło :
Head & neck [Head Neck] 2020 Oct 26. Date of Electronic Publication: 2020 Oct 26.
Typ publikacji :
Journal Article
Journal Info :
Publisher: John Wiley And Sons Country of Publication: United States NLM ID: 8902541 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0347 (Electronic) Linking ISSN: 10433074 NLM ISO Abbreviation: Head Neck Subsets: MEDLINE
Czasopismo naukowe
Tytuł :
Impact of early oral hydration on pharyngocutaneous fistula following total laryngectomy.
Autorzy :
Edafe O; Department of ENT, Sheffield Teaching Hospitals, Sheffield, UK.
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Źródło :
Head & neck [Head Neck] 2020 Oct 26. Date of Electronic Publication: 2020 Oct 26.
Typ publikacji :
Letter
Journal Info :
Publisher: John Wiley And Sons Country of Publication: United States NLM ID: 8902541 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0347 (Electronic) Linking ISSN: 10433074 NLM ISO Abbreviation: Head Neck Subsets: MEDLINE
Opinia redakcyjna
Tytuł :
Variants in NAA15 cause pediatric hypertrophic cardiomyopathy.
Autorzy :
Ritter A; Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Divison of Cardiology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Berger JH; Divison of Cardiology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Deardorff M; Department of Pathology and Laboratory Medicine and Pediatrics, Children's Hospital Los Angeles, Keck School of Medicine of the University of Southern California, Los Angeles, California, USA.
Izumi K; Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Lin KY; Divison of Cardiology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Medne L; Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Ahrens-Nicklas RC; Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Oct 26. Date of Electronic Publication: 2020 Oct 26.
Typ publikacji :
Case Reports
Journal Info :
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Raport
Tytuł :
Reply to the Letter to the Editor regarding "Early oral hydration protects against pharyngocutaneous fistula after total laryngectomy or total pharyngolaryngectomy".
Autorzy :
Le Flem M; Head and Neck Surgery, Universitary Hospital La Conception, Marseille, France.
Santini L; Head and Neck Surgery, Universitary Hospital La Conception, Marseille, France.
Boulze C; Head and Neck Surgery, Universitary Hospital La Conception, Marseille, France.
Alshukry A; Head and Neck Surgery, Universitary Hospital La Conception, Marseille, France.
Giovanni A; Head and Neck Surgery, Universitary Hospital La Conception, Marseille, France.
Dessi P; Head and Neck Surgery, Universitary Hospital La Conception, Marseille, France.
Fakhry N; Head and Neck Surgery, Universitary Hospital La Conception, Marseille, France.
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Źródło :
Head & neck [Head Neck] 2020 Oct 26. Date of Electronic Publication: 2020 Oct 26.
Typ publikacji :
Letter
Journal Info :
Publisher: John Wiley And Sons Country of Publication: United States NLM ID: 8902541 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0347 (Electronic) Linking ISSN: 10433074 NLM ISO Abbreviation: Head Neck Subsets: MEDLINE
Opinia redakcyjna
Tytuł :
Age-related changes in appendicular lean mass in males with Duchenne muscular dystrophy: a retrospective review.
Autorzy :
Summer SS; Center for Clinical and Translational Science and Training, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Wong BL; DMD Program, Department of Pediatrics and Neurology, University of Massachusetts Medical School, Worcester, MA.
Rutter MM; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.; Division of Endocrinology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Horn PS; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.; Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Tian C; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.; Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Rybalsky I; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.; Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Shellenbarger KC; DMD Program, Department of Pediatrics and Neurology, University of Massachusetts Medical School, Worcester, MA.
Kalkwarf HJ; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.; Division of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
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Źródło :
Muscle & nerve [Muscle Nerve] 2020 Oct 26. Date of Electronic Publication: 2020 Oct 26.
Typ publikacji :
Journal Article
Journal Info :
Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 7803146 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-4598 (Electronic) Linking ISSN: 0148639X NLM ISO Abbreviation: Muscle Nerve Subsets: MEDLINE
Czasopismo naukowe
Tytuł :
Disease aggressiveness signatures of amyotrophic lateral sclerosis in white matter tracts revealed by the D50 disease progression model.
Autorzy :
Steinbach R; Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.
Gaur N; Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.
Roediger A; Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.
Mayer TE; Department of Neuroradiology, Jena University Hospital, Jena, Germany.
Witte OW; Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.; Center for Healthy Ageing, Jena University Hospital, Jena, Germany.
Prell T; Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.; Center for Healthy Ageing, Jena University Hospital, Jena, Germany.
Grosskreutz J; Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.; Center for Healthy Ageing, Jena University Hospital, Jena, Germany.
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Źródło :
Human brain mapping [Hum Brain Mapp] 2020 Oct 26. Date of Electronic Publication: 2020 Oct 26.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Wiley Country of Publication: United States NLM ID: 9419065 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0193 (Electronic) Linking ISSN: 10659471 NLM ISO Abbreviation: Hum Brain Mapp Subsets: MEDLINE
Czasopismo naukowe
Tytuł :
Craniocervical junction issues after infancy in achondroplasia.
Autorzy :
Smid CJ; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.; The Midwest Regional Bone Dysplasia Clinic, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Legare JM; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.; Children's Wisconsin & Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Modaff P; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.; Children's Wisconsin & Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Pauli RM; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.; Children's Wisconsin & Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Oct 26. Date of Electronic Publication: 2020 Oct 26.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Czasopismo naukowe
Tytuł :
Patients with hepatocellular carcinoma from more rural and lower income households have more advanced tumor stage at diagnosis and significantly higher mortality.
Autorzy :
Wong RJ; Division of Gastroenterology and Hepatology, Veterans Affairs Palo Alto Health Care System, Palo Alto, California.; Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California.
Kim D; Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California.
Ahmed A; Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California.
Singal AK; Division of Gastroenterology and Hepatology, University of South Dakota, Sioux Falls, South Dakota.
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Źródło :
Cancer [Cancer] 2020 Oct 26. Date of Electronic Publication: 2020 Oct 26.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Wiley Country of Publication: United States NLM ID: 0374236 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0142 (Electronic) Linking ISSN: 0008543X NLM ISO Abbreviation: Cancer Subsets: Core Clinical (AIM); MEDLINE
Czasopismo naukowe
Tytuł :
Use of correlated scrambling variables in quantitative randomized response technique.
Autorzy :
Murtaza M; Department of Mathematics, COMSATS University Islamabad, Wah Campus, Pakistan.
Singh S; Department of Mathematics, Texas A&M University-Kingsville, Kingsville, TX, USA.
Hussain Z; Department of Social and Allied Sciences, Cholistan University of Veterinary and Animal Sciences, Bahawalpur, Pakistan.
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Źródło :
Biometrical journal. Biometrische Zeitschrift [Biom J] 2020 Oct 25. Date of Electronic Publication: 2020 Oct 25.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Wiley-VCH Verlag GmbH & Co. KGaA Country of Publication: Germany NLM ID: 7708048 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1521-4036 (Electronic) Linking ISSN: 03233847 NLM ISO Abbreviation: Biom J Subsets: MEDLINE
Czasopismo naukowe
Tytuł :
Multiple imputation methods for handling missing values in longitudinal studies with sampling weights: Comparison of methods implemented in Stata.
Autorzy :
De Silva AP; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.
De Livera AM; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.
Lee KJ; Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia.
Moreno-Betancur M; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.; Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia.
Simpson JA; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.
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Źródło :
Biometrical journal. Biometrische Zeitschrift [Biom J] 2020 Oct 25. Date of Electronic Publication: 2020 Oct 25.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Wiley-VCH Verlag GmbH & Co. KGaA Country of Publication: Germany NLM ID: 7708048 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1521-4036 (Electronic) Linking ISSN: 03233847 NLM ISO Abbreviation: Biom J Subsets: MEDLINE
Czasopismo naukowe
Tytuł :
Sensitivity and specificity of single and combined clouds analyses compared with quantitative motor unit potential analysis.
Autorzy :
Li C; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Jiang A; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Ding Q; Department of Neurology, Peking Union Medical College, Beijing, China.
Hu Y; Department of Neurology, Peking Union Medical College, Beijing, China.
Wang Y; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Tian G; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Wang H; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Pan S; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Cui L; Department of Neurology, Peking Union Medical College, Beijing, China.
Peng Y; Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
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Źródło :
Muscle & nerve [Muscle Nerve] 2020 Oct 24. Date of Electronic Publication: 2020 Oct 24.
Typ publikacji :
Journal Article
Journal Info :
Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 7803146 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-4598 (Electronic) Linking ISSN: 0148639X NLM ISO Abbreviation: Muscle Nerve Subsets: MEDLINE
Czasopismo naukowe
Tytuł :
Inherited intragenic PBX1 deletion: Expanding the phenotype.
Autorzy :
Fitzgerald KK; Nemours Cardiac Center, Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.; Division of Medical Genetics, Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.
Powell-Hamilton N; Division of Medical Genetics, Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.
Shillingford AJ; Nemours Cardiac Center, Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.
Robinson B; Nemours Cardiac Center, Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.
Gripp KW; Division of Medical Genetics, Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Oct 24. Date of Electronic Publication: 2020 Oct 24.
Typ publikacji :
Case Reports
Journal Info :
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Raport
Tytuł :
Early-onset severe spinocerebellar ataxia 42 with neurodevelopmental deficits (SCA42ND): Case report, pharmacological trial, and literature review.
Autorzy :
Casas-Alba D; Department of Pediatric Neurology and Early Stimulation Unit, Institut de Recerca, Hospital Sant Joan de Déu, Barcelona, Spain.; Department of Genetic and Molecular Medicine IPER, Institut de Recerca, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.
López-Sala L; Department of Pediatric Neurology and Early Stimulation Unit, Institut de Recerca, Hospital Sant Joan de Déu, Barcelona, Spain.
Pérez-Ordóñez M; Department of Pediatric Neurology and Early Stimulation Unit, Institut de Recerca, Hospital Sant Joan de Déu, Barcelona, Spain.
Mari-Vico R; Department of Pediatric Neurology and Early Stimulation Unit, Institut de Recerca, Hospital Sant Joan de Déu, Barcelona, Spain.
Bolasell M; Department of Genetic and Molecular Medicine IPER, Institut de Recerca, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.
Martínez-Monseny AF; Department of Genetic and Molecular Medicine IPER, Institut de Recerca, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.
Muchart J; Department of Radiology, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.
Fernández-Fernández JM; Department de Ciències Experimentals i de la Salut, Laboratori de Fisiologia Molecular, Universitat Pompeu Fabra, Barcelona, Spain.
Martorell L; Department of Genetic and Molecular Medicine IPER, Institut de Recerca, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Barcelona, Spain.
Serrano M; Department of Pediatric Neurology and Early Stimulation Unit, Institut de Recerca, Hospital Sant Joan de Déu, Barcelona, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Barcelona, Spain.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Oct 24. Date of Electronic Publication: 2020 Oct 24.
Typ publikacji :
Case Reports
Journal Info :
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Raport
Tytuł :
Multimodal imaging of brain reorganization in hearing late learners of sign language.
Autorzy :
Banaszkiewicz A; Laboratory of Brain Imaging, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Matuszewski J; Laboratory of Brain Imaging, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Bola Ł; Laboratory of Brain Imaging, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.; Institute of Psychology, Jagiellonian University, Kraków, Poland.; Department of Psychology, Harvard University, Boston, Massachusetts, USA.
Szczepanik M; Laboratory of Brain Imaging, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Kossowski B; Laboratory of Brain Imaging, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Rutkowski P; Section for Sign Linguistics, Faculty of Polish Studies, University of Warsaw, Warsaw, Poland.
Szwed M; Institute of Psychology, Jagiellonian University, Kraków, Poland.
Emmorey K; Laboratory for Language and Cognitive Neuroscience, San Diego State University, San Diego, California, USA.
Jednoróg K; Laboratory of Language Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Marchewka A; Laboratory of Brain Imaging, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
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Źródło :
Human brain mapping [Hum Brain Mapp] 2020 Oct 24. Date of Electronic Publication: 2020 Oct 24.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Wiley Country of Publication: United States NLM ID: 9419065 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0193 (Electronic) Linking ISSN: 10659471 NLM ISO Abbreviation: Hum Brain Mapp Subsets: MEDLINE
Czasopismo naukowe
Tytuł :
Growth hormone deficiency in a child with branchio-oto-renal spectrum disorder: Clinical evidence of EYA1 in pituitary development and a recommendation for pituitary function surveillance.
Autorzy :
Muthusamy K; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.
Hanna C; Division of Pediatric Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.
Johnson DR; Department of Diagnostic Radiology, Mayo Clinic, Rochester, Minnesota, USA.; Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Cramer CH; Division of Pediatric Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.
Tebben PJ; Divisions of Pediatric Endocrinology and Endocrinology, Diabetes and Metabolism and Nutrition, Mayo Clinic, Rochester, Minnesota, USA.
Libi SE; Department of Otorhinolaryngology-Head and Neck Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Poling GL; Department of Otorhinolaryngology-Head and Neck Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Lanpher BC; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.
Morava E; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.; Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, USA.
Schimmenti LA; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.; Department of Otorhinolaryngology-Head and Neck Surgery, Mayo Clinic, Rochester, Minnesota, USA.; Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, USA.; Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Oct 24. Date of Electronic Publication: 2020 Oct 24.
Typ publikacji :
Case Reports
Journal Info :
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Raport
Tytuł :
Mucopolysaccharidosis type I newborn screening: Importance of second tier testing for ethnically diverse populations.
Autorzy :
Bosfield K; Children's National Hospital, Washington, DC, USA.
Regier DS; Children's National Hospital, Washington, DC, USA.
Viall S; Children's National Hospital, Washington, DC, USA.
Hicks R; Children's National Hospital, Washington, DC, USA.
Shur N; Children's National Hospital, Washington, DC, USA.
Grant CL; Children's National Hospital, Washington, DC, USA.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Oct 24. Date of Electronic Publication: 2020 Oct 24.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Czasopismo naukowe
Tytuł :
Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome.
Autorzy :
Dyment DA; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
O'Donnell-Luria A; Broad Institute of MIT and Harvard, Broad Center for Mendelian Genomics, Cambridge, Massachusetts, USA.; Division of Genetics and Genomics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts, USA.
Agrawal PB; Division of Genetics and Genomics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts, USA.
Coban Akdemir Z; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Aleck KA; Department of Genetics and Metabolism, Phoenix Children's Medical Group, Phoenix, Arizona, USA.
Antaki D; Laboratory for Pediatric Brain Disease, Howard Hughes Medical Institute, University of California, San Diego, California, USA.; Rady Children's Institute for Genomic Medicine, Rady Children's Hospital, San Diego, California, USA.
Al Sharhan H; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Department of Pediatrics, Faculty of Medicine, Kuwait University, Kuwait City, Kuwait.
Au PB; Department of Medical Genetics and Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.
Aydin H; Centre of Genetics Diagnosis, Zeynep Kamil Maternity and Children's Training and Research Hospital, Istanbul, Turkey.
Beggs AH; Division of Genetics and Genomics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts, USA.
Bilguvar K; Department of Genetics, Yale School of Medicine, New Haven, Connecticut, USA.; Yale Center for Genome Analysis, Yale School of Medicine, New Haven, Connecticut, USA.
Boerwinkle E; Human Genome Sequencing Center, Baylor College of Medicine, Waco, Texas, USA.
Brand H; Broad Institute of MIT and Harvard, Broad Center for Mendelian Genomics, Cambridge, Massachusetts, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.; Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Brownstein CA; Division of Genetics and Genomics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts, USA.
Buyske S; Department of Statistics and Biostatistics, Rutgers University, Piscataway, New Jersey, USA.
Chodirker B; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada.
Choi J; Department of Genetics, Yale School of Medicine, New Haven, Connecticut, USA.; Department of Biomedical Sciences, Korea University College of Medicine, Seoul, South Korea.
Chudley AE; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada.
Clericuzio CL; Department of Pediatrics, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA.
Cox GF; Division of Genetics and Genomics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts, USA.
Curry C; University of California, San Francisco, California, USA.; Genetic Medicine, University Pediatric Specialists, Fresno, California, USA.
de Boer E; Department of Human Genetics, Raboud University Medical Centre, Nijmegen, Netherlands.
de Vries BBA; Department of Human Genetics, Raboud University Medical Centre, Nijmegen, Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Raboud University Medical Centre, Nijmegen, Netherlands.
Dunn K; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts, USA.
Dutmer CM; Children's Hospital Colorado and University of Colorado School of Medicine, Aurora, Colorado, USA.
England EM; Broad Institute of MIT and Harvard, Broad Center for Mendelian Genomics, Cambridge, Massachusetts, USA.
Fahrner JA; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Geckinli BB; Department of Medical Genetics, School of Medicine, Marmara University, Istanbul, Turkey.
Genetti CA; Division of Genetics and Genomics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts, USA.
Gezdirici A; Department of Medical Genetics, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
Gibson WT; Department of Medical Genetics and British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Gleeson JG; Laboratory for Pediatric Brain Disease, Howard Hughes Medical Institute, University of California, San Diego, California, USA.; Rady Children's Institute for Genomic Medicine, Rady Children's Hospital, San Diego, California, USA.
Greenberg CR; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada.
Hall A; Waisman Center Clinical Genetics, University of Wisconsin, Madison, Wisconsin, USA.
Hamosh A; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Hartley T; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
Jhangiani SN; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Karaca E; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Kernohan K; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
Lauzon JL; Department of Medical Genetics and Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.
Lewis MES; Department of Medical Genetics and British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Lowry RB; Department of Medical Genetics and Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.
López-Giráldez F; Department of Genetics, Yale School of Medicine, New Haven, Connecticut, USA.; Yale Center for Genome Analysis, Yale School of Medicine, New Haven, Connecticut, USA.
Matise TC; Department of Genetics, Human Genetics Institute of New Jersey, Rutgers University, Piscataway, New Jersey, USA.
McEvoy-Venneri J; Laboratory for Pediatric Brain Disease, Howard Hughes Medical Institute, University of California, San Diego, California, USA.; Rady Children's Institute for Genomic Medicine, Rady Children's Hospital, San Diego, California, USA.
McInnes B; Department of Medical Genetics and Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.
Mhanni A; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada.
Garcia Minaur S; Sección de Genética Clínica, INGEMM (Instituto de Genética Médica y Molecular), Madrid, Spain.
Moilanen J; Department of Clinical Genetics, Oulu University Hospital, Medical Research Center Oulu and PEDEGO Research Unit, University of Oulu, Oulu, Finland.
Nguyen A; Laboratory for Pediatric Brain Disease, Howard Hughes Medical Institute, University of California, San Diego, California, USA.; Rady Children's Institute for Genomic Medicine, Rady Children's Hospital, San Diego, California, USA.
Nowaczyk MJM; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
Posey JE; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Õunap K; United Laboratories, Department of Clinical Genetics, Tartu University Hospital, Tartu, Estonia.; Institute of Clinical Medicine, Department of Clinical Genetics, Tartu University Hospital, Tartu, Estonia.
Pehlivan D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Section of Pediatric Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Pajusalu S; Department of Genetics, Yale School of Medicine, New Haven, Connecticut, USA.; United Laboratories, Department of Clinical Genetics, Tartu University Hospital, Tartu, Estonia.; Institute of Clinical Medicine, Department of Clinical Genetics, Tartu University Hospital, Tartu, Estonia.
Penney LS; Department of Pediatrics, IWK Health Centre, Dalhousie University, Halifax, Nova Scotia, Canada.
Poterba T; Broad Institute of MIT and Harvard, Broad Center for Mendelian Genomics, Cambridge, Massachusetts, USA.; Analytical and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.
Prontera P; Medical Genetics Unit, Hospital Santa Maria della Misericordia and University of Perugia, Perugia, Italy.
Doriqui MJR; Complexo Hospitalar Materno Infantil do MA - Matern, Benedito Leite e Hospital Infantil Juvencio Mattos, Sao Luis, Brazil.
Sawyer SL; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
Sobreira N; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Stanley V; Laboratory for Pediatric Brain Disease, Howard Hughes Medical Institute, University of California, San Diego, California, USA.; Rady Children's Institute for Genomic Medicine, Rady Children's Hospital, San Diego, California, USA.
Torun D; Department of Medical Genetics, Gulhane Military Medical Academy, Ankara, Turkey.
Wargowski D; Division of Genetics, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Witmer PD; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Wong I; Broad Institute of MIT and Harvard, Broad Center for Mendelian Genomics, Cambridge, Massachusetts, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.; Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Xing J; Department of Genetics, Human Genetics Institute of New Jersey, Rutgers University, Piscataway, New Jersey, USA.
Zaki MS; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
Zhang Y; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
Boycott KM; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
Bamshad MJ; Department of Pediatrics, University of Washington, Seattle, Washington, USA.; Department of Genome Sciences, University of Washington, Seattle, Washington, USA.; Brotman-Baty Institute for Precision Medicine, Seattle, Washington, USA.
Nickerson DA; Brotman-Baty Institute for Precision Medicine, Seattle, Washington, USA.; Department of Genome Sciences, University of Washington, Seattle, Washington, USA.
Blue EE; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington, USA.
Innes AM; Department of Medical Genetics and Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.
Pokaż więcej
Corporate Authors :
Care4Rare Consortium; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
Centers for Mendelian Genomics
Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Oct 24. Date of Electronic Publication: 2020 Oct 24.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Czasopismo naukowe
Tytuł :
Evaluating brain structure traits as endophenotypes using polygenicity and discoverability.
Autorzy :
Matoba N; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.; UNC Neuroscience Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Love MI; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Stein JL; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.; UNC Neuroscience Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Pokaż więcej
Źródło :
Human brain mapping [Hum Brain Mapp] 2020 Oct 24. Date of Electronic Publication: 2020 Oct 24.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Wiley Country of Publication: United States NLM ID: 9419065 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0193 (Electronic) Linking ISSN: 10659471 NLM ISO Abbreviation: Hum Brain Mapp Subsets: MEDLINE
Czasopismo naukowe

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