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Tytuł :
Prenatal sonographic diagnosis of X-linked hypohidrotic ectodermal dysplasia: An unusual case.
Autorzy :
Li TG; Department of Ultrasound Diagnosis, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, Gansu Province, China.
Ma B; Department of Ultrasound Diagnosis, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, Gansu Province, China.
Tie HX; Department of Ultrasound Diagnosis, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, Gansu Province, China.
Zhang QH; Department of Medical Genetics Center, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, Gansu Province, China.
Hao SJ; Department of Medical Genetics Center, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, Gansu Province, China.
Guan CL; Department of Gynecology, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, Gansu Province, China.
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Źródło :
Journal of clinical ultrasound : JCU [J Clin Ultrasound] 2021 Oct; Vol. 49 (8), pp. 838-840. Date of Electronic Publication: 2021 May 15.
Typ publikacji :
Case Reports
MeSH Terms :
Ectodermal Dysplasia*/diagnostic imaging
Ectodermal Dysplasia*/genetics
Ectodermal Dysplasia 1, Anhidrotic*/diagnostic imaging
Ectodermal Dysplasia 1, Anhidrotic*/genetics
Female ; Humans ; Mutation ; Pregnancy ; Sweat Glands ; Ultrasonography, Prenatal
Raport
Tytuł :
Hyperpolarized Xe magnetic resonance spectroscopy in a rat model of bronchopulmonary dysplasia.
Autorzy :
Fliss JD; Translational Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
Zanette B; Translational Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada.
Friedlander Y; Translational Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
Sadanand S; Department of Biomedical Physics, Ryerson University, Toronto, Ontario, Canada.
Lindenmaier AA; Translational Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
Stirrat E; Translational Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada.
Li D; Translational Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada.
Post M; Translational Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.; Department of Physiology, University of Toronto, Toronto, Ontario, Canada.; Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.
Jankov RP; Molecular Biomedicine Program, Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
Santyr G; Translational Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
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Źródło :
American journal of physiology. Lung cellular and molecular physiology [Am J Physiol Lung Cell Mol Physiol] 2021 Sep 01; Vol. 321 (3), pp. L507-L517. Date of Electronic Publication: 2021 Jun 30.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Magnetic Resonance Spectroscopy*
Pulmonary Gas Exchange*
Bronchopulmonary Dysplasia/*metabolism
Capillaries/*metabolism
Lung/*metabolism
Animals ; Animals, Newborn ; Bronchopulmonary Dysplasia/chemically induced ; Bronchopulmonary Dysplasia/pathology ; Capillaries/pathology ; Disease Models, Animal ; Female ; Humans ; Lung/blood supply ; Lung/pathology ; Male ; Rats ; Rats, Sprague-Dawley ; Xenon Isotopes
Czasopismo naukowe
Tytuł :
Denosumab for craniofacial fibrous dysplasia: duration of efficacy and post-treatment effects.
Autorzy :
Raborn LN; Skeletal Disorders and Mineral Homeostasis Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
Burke AB; Oral and Maxillofacial Surgery, University of Washington School of Dentistry, Seattle, WA, USA.
Ebb DH; Department of Pediatric Hematology Oncology, Massachusetts General Hospital, Boston, MA, USA.
Collins MT; Skeletal Disorders and Mineral Homeostasis Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
Kaban LB; Department of Oral & Maxillofacial Surgery, Massachusetts General Hospital, Harvard School of Dental Medicine, Boston, MA, USA.
Boyce AM; Skeletal Disorders and Mineral Homeostasis Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA. .; Metabolic Bone Disorders Unit, National Institute of Dental and Craniofacial Research, National Institutes of Health, 30 Convent Drive, Building 30, Room 228, MSC 4320, Bethesda, MD, 20892-4320, USA. .
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Źródło :
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA [Osteoporos Int] 2021 Sep; Vol. 32 (9), pp. 1889-1893. Date of Electronic Publication: 2021 Mar 27.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Craniofacial Fibrous Dysplasia*
Fibrous Dysplasia of Bone*/diagnostic imaging
Fibrous Dysplasia of Bone*/drug therapy
Hypercalcemia*
Adolescent ; Denosumab/therapeutic use ; Diphosphonates ; Female ; Humans
Czasopismo naukowe
Tytuł :
Nebulized curcumin protects neonatal lungs from antenatal insult in rats.
Autorzy :
Guillier C; Institut National de la Santé Et de la Recherche Médicale (INSERM) U1141, Paris, France.; Assistance Publique-Hôpitaux de Paris, Service de Médecine et Réanimation néonatales de Port-Royal, Paris, France.; Université Paris Descartes, Paris, France.
Carrière D; Institut National de la Santé Et de la Recherche Médicale (INSERM) U1141, Paris, France.; Assistance Publique-Hôpitaux de Paris, Service de Médecine et Réanimation néonatales de Port-Royal, Paris, France.; Université Paris Descartes, Paris, France.
Pansiot J; Institut National de la Santé Et de la Recherche Médicale (INSERM) U1141, Paris, France.; Université Paris Diderot, Paris, France.
Maroni A; Institut National de la Santé Et de la Recherche Médicale (INSERM) U1141, Paris, France.; Université Paris Descartes, Paris, France.
Billion E; Institut National de la Santé Et de la Recherche Médicale (INSERM) U1141, Paris, France.; Assistance Publique-Hôpitaux de Paris, Service de Médecine et Réanimation néonatales de Port-Royal, Paris, France.; Université Paris Descartes, Paris, France.
Ringot M; Institut National de la Santé Et de la Recherche Médicale (INSERM) U1141, Paris, France.; Université Paris Diderot, Paris, France.
Benoist JF; Assistance Publique-Hôpitaux de Paris, Service de Biochimie-Hormonologie, Hôpital Robert Debré, Paris, France.
Jacques S; Genom'ic. INSERM U1016, Centre National de la Recherche Scientifique (CNRS) Unite Mixte de Recherche (UMR) 8104, Paris, France.
Matrot B; Institut National de la Santé Et de la Recherche Médicale (INSERM) U1141, Paris, France.; Université Paris Diderot, Paris, France.
Jarreau PH; Assistance Publique-Hôpitaux de Paris, Service de Médecine et Réanimation néonatales de Port-Royal, Paris, France.; Université Paris Descartes, Paris, France.; Fondation PremUp, Paris, France.; Université de Paris, Epidemiology and Statistics Research Center (CRESS), INSERM, Institut national de la recherche agronomique (INRA), Paris, France.
Vaiman D; Institut Cochin, Inserm U1016-CNRS UMRS 104, Paris, France.
Baud O; Institut National de la Santé Et de la Recherche Médicale (INSERM) U1141, Paris, France.; Université Paris Diderot, Paris, France.; Assistance Publique-Hôpitaux de Paris, Service de Réanimation et Pédiatrie néonatales, Hôpital Robert Debré, Paris, France.; Division of Neonatology and Pediatric Intensive Care, Children's University Hospital of Geneva and University of Geneva, Geneva, Switzerland.
Zana-Taïeb E; Institut National de la Santé Et de la Recherche Médicale (INSERM) U1141, Paris, France.; Assistance Publique-Hôpitaux de Paris, Service de Médecine et Réanimation néonatales de Port-Royal, Paris, France.; Fondation PremUp, Paris, France.
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Źródło :
American journal of physiology. Lung cellular and molecular physiology [Am J Physiol Lung Cell Mol Physiol] 2021 Sep 01; Vol. 321 (3), pp. L545-L552. Date of Electronic Publication: 2021 Jun 23.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Bronchopulmonary Dysplasia/*prevention & control
Curcumin/*pharmacology
Diet, Protein-Restricted/*adverse effects
Pulmonary Alveoli/*metabolism
Animals ; Animals, Newborn ; Bronchopulmonary Dysplasia/etiology ; Bronchopulmonary Dysplasia/metabolism ; Bronchopulmonary Dysplasia/pathology ; Female ; Fetal Growth Retardation/drug therapy ; Fetal Growth Retardation/etiology ; Fetal Growth Retardation/metabolism ; Fetal Growth Retardation/pathology ; Male ; Nebulizers and Vaporizers ; PPAR gamma/agonists ; PPAR gamma/metabolism ; Pulmonary Alveoli/pathology ; Rats ; Rats, Sprague-Dawley
Czasopismo naukowe
Tytuł :
Chitin-Derived AVR-48 Prevents Experimental Bronchopulmonary Dysplasia (BPD) and BPD-Associated Pulmonary Hypertension in Newborn Mice.
Autorzy :
Das P; Department of Pediatrics, Division of Neonatology, Cooper University Hospital, Camden, NJ 08103, USA.; Department of Pediatrics, Division of Neonatology, Drexel University, Philadelphia, PA 19102, USA.
Acharya S; AyuVis Research, Inc., 1120 South Freeway, Fort Worth, TX 76104, USA.; Department of Pharmacology & Neuroscience, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.
Prahaladan VM; Department of Pediatrics, Division of Neonatology, Cooper University Hospital, Camden, NJ 08103, USA.; Department of Pediatrics, Division of Neonatology, Drexel University, Philadelphia, PA 19102, USA.
Kumova OK; Department of Microbiology & Immunology, Drexel University, Philadelphia, PA 19129, USA.
Malaeb S; Department of Pediatrics, Division of Neonatology, Drexel University, Philadelphia, PA 19102, USA.
Behera S; AyuVis Research, Inc., 1120 South Freeway, Fort Worth, TX 76104, USA.
Agarwal B; GenomeRxUS, Secane, PA 19018, USA.
Christensen DJ; Dale J. Christensen Consulting LLC, Cary, NC 27519, USA.; Department of Medicine, Division of Hematology, Duke University Medical Center, Durham, NC 27710, USA.
Carey AJ; Department of Pediatrics, Division of Neonatology, Drexel University, Philadelphia, PA 19102, USA.; Department of Microbiology & Immunology, Drexel University, Philadelphia, PA 19129, USA.
Bhandari V; Department of Pediatrics, Division of Neonatology, Cooper University Hospital, Camden, NJ 08103, USA.; Department of Pediatrics, Division of Neonatology, Drexel University, Philadelphia, PA 19102, USA.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2021 Aug 09; Vol. 22 (16). Date of Electronic Publication: 2021 Aug 09.
Typ publikacji :
Journal Article
MeSH Terms :
Bronchopulmonary Dysplasia*/drug therapy
Bronchopulmonary Dysplasia*/metabolism
Bronchopulmonary Dysplasia*/pathology
Chitin*/chemistry
Chitin*/pharmacology
Hypertension, Pulmonary*/drug therapy
Hypertension, Pulmonary*/metabolism
Hypertension, Pulmonary*/pathology
Pulmonary Alveoli*/metabolism
Pulmonary Alveoli*/pathology
Neovascularization, Physiologic/*drug effects
Animals ; Animals, Newborn ; Disease Models, Animal ; Drug Evaluation, Preclinical ; Mice ; Rats
Czasopismo naukowe
Tytuł :
Bronchopulmonary dysplasia: a predictive scoring system for very low birth weight infants. A diagnostic accuracy study with prospective data collection.
Autorzy :
El Faleh I; Clinic of Neonatology, Department Women-Mother-Child, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland. .; Department of Paediatrics, Hospital Neuchâtel, Neuchâtel, Switzerland. .
Faouzi M; Centre for Primary Care and Public Health (Unisanté), University of Lausanne, Lausanne, Switzerland.
Adams M; Department of Neonatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Gerull R; Department of Neonatology, University Children's Hospital Basel, Basel, Switzerland.
Chnayna J; Clinic of Neonatology, Department Women-Mother-Child, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.
Giannoni E; Clinic of Neonatology, Department Women-Mother-Child, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.
Roth-Kleiner M; Clinic of Neonatology, Department Women-Mother-Child, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.
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Corporate Authors :
Swiss Neonatal Network
Źródło :
European journal of pediatrics [Eur J Pediatr] 2021 Aug; Vol. 180 (8), pp. 2453-2461. Date of Electronic Publication: 2021 Apr 06.
Typ publikacji :
Journal Article
MeSH Terms :
Bronchopulmonary Dysplasia*/diagnosis
Bronchopulmonary Dysplasia*/epidemiology
Birth Weight ; Female ; Gestational Age ; Humans ; Incidence ; Infant ; Infant, Newborn ; Infant, Very Low Birth Weight ; Pregnancy ; Prospective Studies ; Risk Factors ; Switzerland/epidemiology
Czasopismo naukowe
Tytuł :
Baseline Characteristics of Patients with Symptomatic Carotid Webs: A Matched Case Control Study.
Autorzy :
Landzberg D; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
Nogueira RG; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
Al-Bayati AR; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
Kim SJ; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
Bouslama M; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
Pisani L; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
da Camara CP; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
Frankel M; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
Nahab FB; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
Bianchi N; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
Haussen DC; Department of Neurology, Emory University Hospital / Marcus Stroke and Neuroscience Center, Grady Memorial Hospital, Atlanta, USA. Electronic address: .
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Źródło :
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2021 Aug; Vol. 30 (8), pp. 105823. Date of Electronic Publication: 2021 May 23.
Typ publikacji :
Journal Article
MeSH Terms :
Carotid Artery Diseases/*complications
Fibromuscular Dysplasia/*complications
Ischemic Stroke/*etiology
Adult ; African Americans ; Carotid Artery Diseases/diagnostic imaging ; Carotid Artery Diseases/ethnology ; Carotid Artery Diseases/therapy ; Case-Control Studies ; Databases, Factual ; European Continental Ancestry Group ; Female ; Fibromuscular Dysplasia/diagnostic imaging ; Fibromuscular Dysplasia/ethnology ; Fibromuscular Dysplasia/therapy ; Humans ; Ischemic Stroke/diagnosis ; Ischemic Stroke/epidemiology ; Ischemic Stroke/therapy ; Male ; Middle Aged ; Prognosis ; Race Factors ; Risk Assessment ; Risk Factors ; Sex Factors
Czasopismo naukowe
Tytuł :
Endodontic treatment of dentin dysplasia type I D.
Autorzy :
Buchanan GD; Department of Odontology, School of Dentistry, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa.
Tredoux S; Department of Odontology, School of Dentistry, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa.
Nel C; Department of Oral Biology and Oral Pathology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa.
Gamieldien MY; Department of Maxillofacial and Oral Surgery, School of Dentistry, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa.
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Źródło :
Australian endodontic journal : the journal of the Australian Society of Endodontology Inc [Aust Endod J] 2021 Aug; Vol. 47 (2), pp. 343-349. Date of Electronic Publication: 2020 Sep 22.
Typ publikacji :
Case Reports
MeSH Terms :
Dentin Dysplasia*/diagnostic imaging
Dentin Dysplasia*/genetics
Dentin Dysplasia*/therapy
Pulpitis*/therapy
Dental Pulp Necrosis ; Humans ; Incisor
Raport
Tytuł :
Short- and Long-Term Complications of Bronchopulmonary Dysplasia.
Autorzy :
Homan TD; Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri.
Nayak RP; Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, Missouri. .
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Źródło :
Respiratory care [Respir Care] 2021 Oct; Vol. 66 (10), pp. 1618-1629.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Bronchopulmonary Dysplasia*/complications
Adult ; Humans ; Infant ; Infant, Low Birth Weight ; Infant, Newborn ; Infant, Premature ; Lung ; Quality of Life
Czasopismo naukowe
Tytuł :
Molecular Genetics of Cleidocranial Dysplasia.
Autorzy :
Motaei J; Department of Medical Genetics, Medical Genetics Research Center, Student Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Salmaninejad A; Department of Medical Genetics, Medical Genetics Research Center, Student Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.; Halal Research Center of IRI, FDA, Tehran, Iran.
Jamali E; Department of Biology, Tonekabon Branch, Islamic Azad University, Tonekabon, Iran.
Khorsand I; Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Ahmadvand M; Hematology-Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Shabani S; Department of Optometry, School of Para Medical Sciences, Mashhad University of Medical Sciences, Mashhad, Iran.
Karimi F; Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Nazari MS; Postgraduate Student, Department of Orthodontics, School of Dentistry, Mashhad University of Medical Science, Mashhad, Iran.
Ketabchi G; Postgraduate Student, Department of Oral and Maxillofacial Radiology, School of Dentistry, Mashhad University of Medical Science, Mashhad, Iran.
Naqipour F; Postgraduate Student, Department of Oral and Maxillofacial Radiology, School of Dentistry, Mashhad University of Medical Science, Mashhad, Iran.
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Źródło :
Fetal and pediatric pathology [Fetal Pediatr Pathol] 2021 Oct; Vol. 40 (5), pp. 442-454. Date of Electronic Publication: 2020 Jan 26.
Typ publikacji :
Journal Article
MeSH Terms :
Cleidocranial Dysplasia*/genetics
Core Binding Factor Alpha 1 Subunit/*genetics
DNA Copy Number Variations ; Humans ; Mutation ; Transcription Factors/genetics
Czasopismo naukowe
Tytuł :
Characterization of EDARADD gene mutations responsible for hypohidrotic ectodermal dysplasia.
Autorzy :
Asano N; Department of Dermatology, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Yasuno S; Department of Dermatology, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Hayashi R; Division of Dermatology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Shimomura Y; Department of Dermatology, Yamaguchi University Graduate School of Medicine, Ube, Japan.
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Źródło :
The Journal of dermatology [J Dermatol] 2021 Oct; Vol. 48 (10), pp. 1533-1541. Date of Electronic Publication: 2021 Jul 04.
Typ publikacji :
Journal Article
MeSH Terms :
Anodontia*
Ectodermal Dysplasia 1, Anhidrotic*
Edar-Associated Death Domain Protein*/genetics
Hypohidrosis*
Limb Deformities, Congenital*
Ectodysplasins ; Humans ; Mutation
Czasopismo naukowe
Tytuł :
Integrative analysis of lncRNAs, miRNAs, and mRNAs-associated ceRNA network in a neonatal mouse model of bronchopulmonary dysplasia.
Autorzy :
Dong Y; Department of Pediatrics, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, China.
Zhang X; Department of Pediatrics, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, China.
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Źródło :
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians [J Matern Fetal Neonatal Med] 2021 Oct; Vol. 34 (19), pp. 3234-3245. Date of Electronic Publication: 2020 Sep 13.
Typ publikacji :
Journal Article
MeSH Terms :
Bronchopulmonary Dysplasia*/genetics
MicroRNAs*/genetics
RNA, Long Noncoding*
Animals ; Animals, Newborn ; Cell Cycle Proteins ; Gene Expression Profiling ; Gene Regulatory Networks ; Humans ; Infant, Newborn ; Mice ; Nerve Tissue Proteins ; RNA, Messenger/genetics ; Receptors, Immunologic
Czasopismo naukowe
Tytuł :
First Experience of ARTip Cruise VITOM-assisted OPF Removal of Frontal Fibro-osseous Lesion: Operative Video.
Autorzy :
Bignami M; Department of Otorhinolaryngology Head and Neck Surgery, University of Insubria, Varese, Italy.; Head and Neck Surgery and Forensic Dissection Research Center (HNS&FDRc), Department of Biotechnology and Life Sciences, University of Insubria, Varese, Italy.
Arosio AD; Department of Otorhinolaryngology Head and Neck Surgery, University of Insubria, Varese, Italy.
Dalfino G; Department of Otorhinolaryngology Head and Neck Surgery, University of Insubria, Varese, Italy.
Sileo G; Department of Otorhinolaryngology Head and Neck Surgery, University of Insubria, Varese, Italy.
Czaczkes C; Department of Otorhinolaryngology Head and Neck Surgery, University of Insubria, Varese, Italy.
Valenzise V; Department of Otorhinolaryngology Head and Neck Surgery, University of Insubria, Varese, Italy.
Zannella S; Department of Pathology, Ospedale Sant'Anna, Como, Italy.
Demelas L; Department of Radiology, Ospedale Sant'Anna, Como, Italy.
Castelnuovo P; Department of Otorhinolaryngology Head and Neck Surgery, University of Insubria, Varese, Italy.; Head and Neck Surgery and Forensic Dissection Research Center (HNS&FDRc), Department of Biotechnology and Life Sciences, University of Insubria, Varese, Italy.
Volpi L; Department of Otorhinolaryngology Head and Neck Surgery, University of Insubria, Varese, Italy.
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Źródło :
The Laryngoscope [Laryngoscope] 2021 Oct; Vol. 131 (10), pp. 2219-2223. Date of Electronic Publication: 2021 Mar 31.
Typ publikacji :
Case Reports; Journal Article; Video-Audio Media
MeSH Terms :
Fibrous Dysplasia of Bone/*surgery
Frontal Sinus/*surgery
Video-Assisted Surgery/*instrumentation
Adult ; Fibrous Dysplasia of Bone/diagnosis ; Fibrous Dysplasia of Bone/pathology ; Frontal Sinus/diagnostic imaging ; Frontal Sinus/pathology ; Humans ; Magnetic Resonance Imaging ; Male ; Tomography, X-Ray Computed ; Treatment Outcome
Czasopismo naukowe
Tytuł :
Determinants of the lung microbiome in intubated premature infants at risk for bronchopulmonary dysplasia.
Autorzy :
Brewer MR; Neonatal-Perinatal Medicine, Cohen Children's Medical Center, Lilling Family Neonatal Research Laboratory, Feinstein Institutes for Medical Research, Northwell Health, New Hyde Park, NY, USA.
Maffei D; Neonatal-Perinatal Medicine, Cohen Children's Medical Center, Lilling Family Neonatal Research Laboratory, Feinstein Institutes for Medical Research, Northwell Health, New Hyde Park, NY, USA.
Cerise J; Biostatistics Unit, Feinstein Institutes for Medical Research, Northwell Health, Great Neck, NY, USA.
Ahn S; Biostatistics Unit, Feinstein Institutes for Medical Research, Northwell Health, Great Neck, NY, USA.
DeVoti J; Immunology and Inflammation, Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY, USA.
Codipilly C; Neonatal-Perinatal Medicine, Cohen Children's Medical Center, Lilling Family Neonatal Research Laboratory, Feinstein Institutes for Medical Research, Northwell Health, New Hyde Park, NY, USA.
Lee A; Translational Genetics, Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY, USA.
Weinberger B; Neonatal-Perinatal Medicine, Cohen Children's Medical Center, Lilling Family Neonatal Research Laboratory, Feinstein Institutes for Medical Research, Northwell Health, New Hyde Park, NY, USA.
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Źródło :
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians [J Matern Fetal Neonatal Med] 2021 Oct; Vol. 34 (19), pp. 3220-3226. Date of Electronic Publication: 2019 Nov 17.
Typ publikacji :
Journal Article
MeSH Terms :
Bronchopulmonary Dysplasia*
Microbiota*
Dysbiosis ; Humans ; Infant ; Infant, Newborn ; Infant, Premature ; Lung
Czasopismo naukowe
Tytuł :
Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease.
Autorzy :
Getwan M; Institute of Anatomy, University of Zurich, 8057 Zurich, Switzerland.; Swiss National Centre of Competence in Research Kidney Control of Homeostasis, University of Zurich, 8057 Zurich, Switzerland.; Renal Division, Department of Medicine, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
Hoppmann A; Institute of Genetic Epidemiology, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
Schlosser P; Institute of Genetic Epidemiology, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
Grand K; Institute of Anatomy, University of Zurich, 8057 Zurich, Switzerland.; Swiss National Centre of Competence in Research Kidney Control of Homeostasis, University of Zurich, 8057 Zurich, Switzerland.; Renal Division, Department of Medicine, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
Song W; Renal Division, Department of Medicine, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
Diehl R; Renal Division, Department of Medicine, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
Schroda S; Renal Division, Department of Medicine, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
Heeg F; Renal Division, Department of Medicine, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
Deutsch K; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
Hildebrandt F; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
Lausch E; Department of Pediatrics, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
Köttgen A; Institute of Genetic Epidemiology, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
Lienkamp SS; Institute of Anatomy, University of Zurich, 8057 Zurich, Switzerland; .; Swiss National Centre of Competence in Research Kidney Control of Homeostasis, University of Zurich, 8057 Zurich, Switzerland.; Renal Division, Department of Medicine, Faculty of Medicine, Medical Center - University of Freiburg, 79110 Freiburg, Germany.
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Źródło :
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2021 Sep 28; Vol. 118 (39).
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Bone and Bones/*abnormalities
Ciliopathies/*pathology
Craniosynostoses/*pathology
Cytoskeletal Proteins/*metabolism
Ectodermal Dysplasia/*pathology
Embryo, Nonmammalian/*pathology
Musculoskeletal Abnormalities/*pathology
Polycystic Kidney Diseases/*pathology
Tubulin/*chemistry
Animals ; Bone and Bones/metabolism ; Bone and Bones/pathology ; Ciliopathies/genetics ; Ciliopathies/metabolism ; Craniosynostoses/genetics ; Craniosynostoses/metabolism ; Cytoskeletal Proteins/genetics ; Disease Models, Animal ; Ectodermal Dysplasia/genetics ; Ectodermal Dysplasia/metabolism ; Embryo, Nonmammalian/metabolism ; Musculoskeletal Abnormalities/genetics ; Musculoskeletal Abnormalities/metabolism ; Phenotype ; Polycystic Kidney Diseases/genetics ; Polycystic Kidney Diseases/metabolism ; Tubulin/metabolism ; Xenopus laevis
SCR Disease Name :
Cranioectodermal Dysplasia
Czasopismo naukowe
Tytuł :
Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia.
Autorzy :
Hennig V; Department of Pediatrics, University Hospital Erlangen, University of Erlangen-Nürnberg, Loschgestr. 15, 91054, Erlangen, Germany.; Center for Ectodermal Dysplasias, University Hospital Erlangen, University of Erlangen-Nürnberg, Erlangen, Germany.
Schuh W; Division of Molecular Immunology, University Hospital Erlangen, University of Erlangen-Nürnberg, Erlangen, Germany.
Neubert A; Department of Pediatrics, University Hospital Erlangen, University of Erlangen-Nürnberg, Loschgestr. 15, 91054, Erlangen, Germany.
Mielenz D; Division of Molecular Immunology, University Hospital Erlangen, University of Erlangen-Nürnberg, Erlangen, Germany.
Jäck HM; Division of Molecular Immunology, University Hospital Erlangen, University of Erlangen-Nürnberg, Erlangen, Germany.
Schneider H; Department of Pediatrics, University Hospital Erlangen, University of Erlangen-Nürnberg, Loschgestr. 15, 91054, Erlangen, Germany. .; Center for Ectodermal Dysplasias, University Hospital Erlangen, University of Erlangen-Nürnberg, Erlangen, Germany. .
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Źródło :
Orphanet journal of rare diseases [Orphanet J Rare Dis] 2021 Sep 03; Vol. 16 (1), pp. 373. Date of Electronic Publication: 2021 Sep 03.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
COVID-19*
Ectodermal Dysplasia 1, Anhidrotic*
Fatigue Syndrome, Chronic*
Adolescent ; Adult ; Alopecia ; Child ; Humans ; Longitudinal Studies ; Middle Aged ; SARS-CoV-2 ; Spike Glycoprotein, Coronavirus ; Young Adult
Czasopismo naukowe
Tytuł :
Three-dimensional surgical contouring of craniofacial fibrous dysplasia via patient-specific cutting guides and depth screws.
Autorzy :
Rengarajoo J; Department of Oral and Maxillofacial Clinical Sciences, Faculty of Dentistry, University of Malaya, W. Persekutuan Kuala Lumpur, Malaysia; Department of Oral and Maxillofacial Surgery, Sungai Buloh Hospital, Selangor, Malaysia. Electronic address: .
Syed Husman SI; Department of Oral and Maxillofacial Surgery, Sungai Buloh Hospital, Selangor, Malaysia.
Hariri F; Department of Oral and Maxillofacial Clinical Sciences, Faculty of Dentistry, University of Malaya, W. Persekutuan Kuala Lumpur, Malaysia.
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Źródło :
The British journal of oral & maxillofacial surgery [Br J Oral Maxillofac Surg] 2021 Sep; Vol. 59 (7), pp. 843-844. Date of Electronic Publication: 2020 Sep 28.
Typ publikacji :
Journal Article
MeSH Terms :
Craniofacial Fibrous Dysplasia*
Surgery, Computer-Assisted*
Bone Screws ; Facial Bones/diagnostic imaging ; Facial Bones/surgery ; Humans ; Imaging, Three-Dimensional ; Printing, Three-Dimensional ; Skull/diagnostic imaging ; Skull/surgery
Czasopismo naukowe
Tytuł :
Risk stratification in patients with arrhythmogenic cardiomyopathy.
Autorzy :
Hauer RNW; Department of Cardiology, University Medical Center Utrecht, Netherlands Heart Institute, Utrecht, the Netherlands. Electronic address: .
Velthuis BK; Department of Radiology, University Medical Center Utrecht, Utrecht, the Netherlands.
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Źródło :
International journal of cardiology [Int J Cardiol] 2021 Sep 01; Vol. 338, pp. 143-144. Date of Electronic Publication: 2021 Jun 03.
Typ publikacji :
Editorial; Comment
MeSH Terms :
Arrhythmogenic Right Ventricular Dysplasia*/diagnostic imaging
Arrhythmogenic Right Ventricular Dysplasia*/epidemiology
Death, Sudden, Cardiac ; Humans ; Risk Assessment
Opinia redakcyjna
Tytuł :
Role of the SENP1-SIRT1 pathway in hyperoxia-induced alveolar epithelial cell injury.
Autorzy :
Dong W; Department of Neonatology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China; Division of Neonatology, Department of Pediatrics, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, China.
Zhu X; Division of Neonatology, Department of Pediatrics, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, China.
Liu X; Division of Neonatology, Department of Pediatrics, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, China.
Zhao X; Division of Neonatology, Department of Pediatrics, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, China.
Lei X; Division of Neonatology, Department of Pediatrics, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, China.
Kang L; Division of Neonatology, Department of Pediatrics, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, China.
Liu L; Department of Neonatology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China. Electronic address: .
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Źródło :
Free radical biology & medicine [Free Radic Biol Med] 2021 Sep; Vol. 173, pp. 142-150. Date of Electronic Publication: 2021 Jul 24.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Bronchopulmonary Dysplasia*/genetics
Hyperoxia*/genetics
Alveolar Epithelial Cells ; Animals ; Animals, Newborn ; Cysteine Endopeptidases ; Humans ; Infant, Newborn ; Infant, Premature ; Leukocytes, Mononuclear ; Lung ; Peptide Hydrolases ; Sirtuin 1/genetics
Czasopismo naukowe
Tytuł :
Right atrial thrombus complicating a right-sided arrhythmogenic cardiomyopathy.
Autorzy :
Li XD; Department of Echocardiography, The First Hospital of Jilin University, Changchun, Jilin, China.
Kong BY; Department of Radiology, The First Hospital of Jilin University, Changchun, Jilin, China.
Bai Y; Department of Cardiac Surgery, The First Hospital of Jilin University, Changchun, Jilin, China.
Xu H; Department of Echocardiography, The First Hospital of Jilin University, Changchun, Jilin, China.
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Źródło :
Journal of clinical ultrasound : JCU [J Clin Ultrasound] 2021 Sep; Vol. 49 (7), pp. 674-677. Date of Electronic Publication: 2020 Dec 29.
Typ publikacji :
Case Reports
MeSH Terms :
Arrhythmogenic Right Ventricular Dysplasia*/complications
Arrhythmogenic Right Ventricular Dysplasia*/diagnostic imaging
Heart Diseases*/complications
Heart Diseases*/diagnostic imaging
Thrombosis*/complications
Thrombosis*/diagnostic imaging
Echocardiography ; Electrocardiography ; Humans ; Magnetic Resonance Imaging
Raport

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