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Wyświetlanie 1-2 z 2
Tytuł:
Can untreated PKU patients escape from intellectual disability? A systematic review.
Autorzy:
van Vliet D; University of Groningen, University Medical Center Groningen, Beatrix Children's Hospital, 9700, RB, Groningen, The Netherlands.
van Wegberg AMJ; University of Groningen, University Medical Center Groningen, Beatrix Children's Hospital, 9700, RB, Groningen, The Netherlands.; Department of Gastroenterology, Radboud University Medical Center, Nijmegen, The Netherlands.
Ahring K; Department of PKU, Kennedy Center, Copenhagen University Hospital, Glostrup, Denmark.
Bik-Multanowski M; University Children's Hospital, Jagiellonian University, Krakow, Poland.
Blau N; Dietmar-Hopp Metabolic Center, University Children's Hospital, Heidelberg, Germany.
Bulut FD; Department of Pediatrics, Cukurova University Faculty of Medicine, Adana, Turkey.
Casas K; Medical Genetics, Sanford Health, Fargo, ND, USA.
Didycz B; University Children's Hospital, Jagiellonian University, Krakow, Poland.
Djordjevic M; Mother and Child Health Care Institute of Serbia Dr Vukan Cupic, School of Medicine, University of Belgrade, Belgrade, Serbia.
Federico A; Department of Medical, Surgical and Neurological Sciences, Medical School, University of Siena, Policlinico Santa Maria Alle Scotte, Siena, Italy.
Feillet F; Department of Pediatrics, Hôpital d'Enfants Brabois, CHU Nancy, Vandoeuvre les Nancy, France.
Gizewska M; Department of Pediatrics, Endocrinology, Diabetology, Metabolic Diseases and Cardiology of the Developmental Age, Pomeranian Medical University, Szczecin, Poland.
Gramer G; Department of General Pediatrics, Division of Neuropediatrics and Metabolic Medicine, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
Hertecant JL; Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab Emirates.
Hollak CEM; Department of Internal Medicine, Division of Endocrinology and Metabolism, Academic Medical Center, Amsterdam, Netherlands.
Jørgensen JV; Department of Pediatrics, Oslo University Hospital, Oslo, Norway.
Karall D; Clinic for Pediatrics, Inherited Metabolic Disorders, Medical University of Innsbruck, Innsbruck, Austria.
Landau Y; Metabolic Disease Unit, Sheba Medical Center, Edmond and Lily Safra Children's Hospital, Tel Aviv, Israel.
Leuzzi V; Department of Pediatrics, Child Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy.
Mathisen P; Department of Internal Medicine, Oslo University Hospital, Oslo, Norway.
Moseley K; Genetics Division, Department of Pediatrics, Keck School of Medicine, University of Southern California, California, Los Angeles, USA.
Mungan NÖ; Department of Pediatrics, Cukurova University Faculty of Medicine, Adana, Turkey.
Nardecchia F; Department of Pediatrics, Child Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy.
Õunap K; Department of Clinical Genetics, United Laboratories, Tartu University Hospital and Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
Powell KK; Department of Genetics and Metabolism, Chapel Hill hospital, University of North Carolina, Chapel Hill, USA.
Ramachandran R; Department of Chemical Pathology and Metabolic Medicine, Guys and St Thomas' Hospitals NHS foundation trust, London, UK.
Rutsch F; Department of General Pediatrics, Muenster University Children's Hospital, Muenster, Germany.
Setoodeh A; Department of Pediatrics, Tehran University of Medical Sciences, Tehran, Iran.
Stojiljkovic M; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
Trefz FK; Dietmar-Hopp Metabolic Center, University Children's Hospital, Heidelberg, Germany.
Usurelu N; Institute of Mother and Child, Centre of Reproductive Health and Medical Genetics, Chisinau, Moldova.
Wilson C; Newborn Metabolic Screening Unit, LabPlus, Auckland City Hospital, Auckland, New Zealand.
van Karnebeek CD; Departments of Pediatrics and Clinical Genetics, Academic Medical Centre, Emma Children's Hospital, Amsterdam, The Netherlands.; Department of Pediatrics, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, Canada.
Hanley WB; Clinical and Biochemical Genetics, Department of Pediatrics, The Hospital for Sick Children and the University of Toronto, Toronto, Canada.
van Spronsen FJ; University of Groningen, University Medical Center Groningen, Beatrix Children's Hospital, 9700, RB, Groningen, The Netherlands. .
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Źródło:
Orphanet journal of rare diseases [Orphanet J Rare Dis] 2018 Aug 29; Vol. 13 (1), pp. 149. Date of Electronic Publication: 2018 Aug 29.
Typ publikacji:
Journal Article; Systematic Review
MeSH Terms:
Intellectual Disability/*blood
Intellectual Disability/*etiology
Phenylketonurias/*blood
Phenylketonurias/*complications
Female ; Humans ; Male ; Phenylalanine/blood
Czasopismo naukowe
Tytuł:
Do Parents and Clinicians Agree on Ratings of Autism-Related Behaviors at 12 Months of Age? A Study of Infants at High and Low Risk for ASD.
Autorzy:
Macari SL; Child Study Center, Yale University School of Medicine, New Haven, CT, USA. .
Wu GC; Child Study Center, Yale University School of Medicine, New Haven, CT, USA.; Stanford University, Stanford, CA, USA.
Powell KK; Child Study Center, Yale University School of Medicine, New Haven, CT, USA.
Fontenelle S 4th; Child Study Center, Yale University School of Medicine, New Haven, CT, USA.
Macris DM; Child Study Center, Yale University School of Medicine, New Haven, CT, USA.
Chawarska K; Child Study Center, Yale University School of Medicine, New Haven, CT, USA.
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Źródło:
Journal of autism and developmental disorders [J Autism Dev Disord] 2018 Apr; Vol. 48 (4), pp. 1069-1080.
Typ publikacji:
Comparative Study; Journal Article
MeSH Terms:
Dissent and Disputes*
Early Diagnosis*
Parents*
Physicians*/psychology
Autism Spectrum Disorder/*diagnosis
Autism Spectrum Disorder/*psychology
Autism Spectrum Disorder/nursing ; Female ; Humans ; Infant ; Male ; Social Behavior
Czasopismo naukowe
    Wyświetlanie 1-2 z 2

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