لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Harmon JL, Barroso J, Pence BW, Leserman J, Salahuddin N

المصدر: JANAC: Journal of the Association of Nurses in AIDS Care; Mar2008, Vol. 19 Issue 2, p90-97, 8p

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Guzman H; Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia, Philadelphia, PA, United States.; Division of Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, United States., Yazdani S; Division of General Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, United States., Harmon JL; Rare Disease Institute, Children's National Hospital, Washington, DC, United States., Chapman KA; Rare Disease Institute, Children's National Hospital, Washington, DC, United States., Vitola B; Division of Gastroenterology, Hepatology and Nutrition, Children's National Hospital, Washington, DC, United States.; Transplant Institute, MedStar Georgetown University Hospital, Washington, DC, United States., Pyle L; Rare Disease Institute, Children's National Hospital, Washington, DC, United States., McKnight H; Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia, Philadelphia, PA, United States., Sigal W; Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia, Philadelphia, PA, United States.; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States., Lord K; Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia, Philadelphia, PA, United States.; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States., De Leon DD; Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia, Philadelphia, PA, United States.; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States., Merchant N; Rare Disease Institute, Children's National Hospital, Washington, DC, United States.; Division of Endocrinology and Diabetes, Children's National Hospital, Washington, DC, United States., Ganetzky R; Division of Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, United States.; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States.

المصدر: Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2023 Nov 01; Vol. 14, pp. 1268135. Date of Electronic Publication: 2023 Nov 01 (Print Publication: 2023).

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2392 (Print) Linking ISSN: 16642392 NLM ISO Abbreviation: Front Endocrinol (Lausanne) Subsets: MEDLINE

مواضيع طبية MeSH: Cholestasis* , Hyperinsulinism* , Hypoglycemia*/complications , Hypoglycemia*/diagnosis , Hypoglycemia*/genetics , Liver Failure*/genetics, Humans ; Infant, Newborn ; DNA, Mitochondrial/genetics ; Mutation

SCR Disease Name: Deoxyguanosine Kinase Deficiency