المؤلفون: Margolis MG; The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petach Tikva, Israel., Weizman S; The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petach Tikva, Israel., Lazar L; The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel., Yakobovich-Gavan M; The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel., Tenenbaum A; The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel., Phillip M; The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel., Oron T; The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

المصدر: Diabetic medicine : a journal of the British Diabetic Association [Diabet Med] 2024 May; Vol. 41 (5), pp. e15250. Date of Electronic Publication: 2023 Nov 14.

نوع المنشور: Observational Study; Journal Article

بيانات الدورية: Publisher: Blackwell Science Country of Publication: England NLM ID: 8500858 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1464-5491 (Electronic) Linking ISSN: 07423071 NLM ISO Abbreviation: Diabet Med Subsets: MEDLINE

مواضيع طبية MeSH: Diabetes Mellitus, Type 1*/epidemiology , COVID-19*/epidemiology , Diabetic Ketoacidosis*, Child ; Humans ; Pandemics ; Retrospective Studies ; SARS-CoV-2

المؤلفون: Vogel GF; Department of Paediatrics I, Medical University of Innsbruck, Innsbruck, Austria; Institute of Cell Biology, Biocenter, Medical University of Innsbruck, Innsbruck, Austria. Electronic address: georg.vogel@i-med.ac.at., Mozer-Glassberg Y; Institute for Gastroenterology, Nutrition and Liver diseases, Schneider Children's Medical Center of Israel, Petah Tiqwa, Israel., Landau YE; Metabolism Service, Schneider Children's Medical Center of Israel, Petah Tiqwa, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel., Schlieben LD; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany; Institute of Neurogenomics, Computational Health Center, Helmholtz Zentrum München, Neuherberg, Germany., Prokisch H; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany; Institute of Neurogenomics, Computational Health Center, Helmholtz Zentrum München, Neuherberg, Germany., Feichtinger RG; University Children's Hospital, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, Austria., Mayr JA; University Children's Hospital, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, Austria., Brennenstuhl H; Division of Neuropaediatrics and Metabolic Medicine, Center for Paediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany., Schröter J; Division of Paediatric Epileptology, Center for Paediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany., Pechlaner A; Department of Paediatrics I, Medical University of Innsbruck, Innsbruck, Austria., Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia., Baker JJ; Division of Genetics, Birth Defects and Metabolism, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL., Barcia G; Department of Medical Genetics and Reference Center for Mitochondrial Diseases (CARAMMEL), Necker Hospital, Université Paris Cité, Paris, France; Institut Imagine, INSERM UMR 1163, Paris, France., Baric I; Department of Pediatrics, School of Medicine, University Hospital Center Zagreb and University of Zagreb, Zagreb, Croatia., Braverman N; Division of Medical Genetics, Department of Pediatrics and Human Genetics, McGill University, Montreal, Quebec, Canada., Burnyte B; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Christodoulou J; Brain and Mitochondrial Research Group, Murdoch Children's Research Institute, Melbourne, Victoria, Australia; Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia., Ciara E; Department of Medical Genetics, The Children's Memorial Health Institute, Warsaw, Poland., Coman D; Faculty of Medicine, Queensland Children's Hospital, University of Queensland, Herston, Brisbane, Queensland, Australia., Das AM; Department of Paediatrics, Paediatric Metabolic Medicine, Hannover Medical School, Hannover, Germany., Darin N; Department of Pediatrics, Institute of Clinical Sciences, University of Gothenburg, Gothenburg, Sweden., Della Marina A; Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- und Behavioral Sciences, University Duisburg-Essen, Essen, Germany., Distelmaier F; Department of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich-Heine-University Dusseldorf, Dusseldorf, Germany., Eklund EA; Section for Pediatrics, Department of Clinical Sciences, Lund University, Lund, Sweden., Ersoy M; Department of Pediatrics, Division of Pediatric Metabolism, University of Health Sciences, Bakırkoy Dr. Sadi Konuk Training and Research, Istanbul, Turkey., Fang W; The Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China., Gaignard P; Department of Biochemistry, Reference Center for Mitochondrial Disease, FILNEMUS, Bicêtre University Hospital, University of Paris-Saclay, Assistance Publique-Hôpitaux de Paris, Le Kremlin-Bicêtre, Paris, France., Ganetzky RD; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA., Gonzales E; Pediatric Hepatology and Pediatric Liver Transplantation Unit, Reference Center for Mitochondrial Disease, FILNEMUS, Bicêtre University Hospital, University of Paris-Saclay, Assistance Publique-Hôpitaux de Paris, Le Kremlin-Bicêtre, Paris, France; Inserm U1193, Hepatinov, University Paris-Saclay, Orsay, Paris, France., Howard C; Children's Health Ireland, Temple Street Hospital, Dublin, Ireland., Hughes J; Children's Health Ireland, Temple Street Hospital, Dublin, Ireland., Konstantopoulou V; Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria., Kose M; Division of Inborn Errors of Metabolism, Department of Pediatrics, İzmir Katip Çelebi University, Izmir, Turkey; Division of Genetics, Department of Pediatrics, Ege University, Izmir, Turkey., Kerr M; Discovery DNA, Metabolics and Genetics in Canada (M.A.G.I.C.) Clinic Ltd, Department of Pediatrics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada., Khan A; Discovery DNA, Metabolics and Genetics in Canada (M.A.G.I.C.) Clinic Ltd, Department of Pediatrics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada., Lenz D; Division of Neuropaediatrics and Metabolic Medicine, Center for Paediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany., McFarland R; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom., Margolis MG; Institute of Endocrinology and Diabetes, National Center of Childhood Diabetes Schneider Children's Medical Center of Israel, Petah Tiqwa, Israel., Morrison K; Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL., Müller T; Department of Paediatrics I, Medical University of Innsbruck, Innsbruck, Austria., Murayama K; Department of Metabolism, Chiba Children's Hospital, Midori-ku, Chiba, Japan., Nicastro E; Pediatric Hepatology, Gastroenterology and Transplantation, Hospital Papa Giovanni XXIII, Bergamo, Italy., Pennisi A; Department of Medical Genetics and Reference Center for Mitochondrial Diseases (CARAMMEL), Necker Hospital, Université Paris Cité, Paris, France; Institut Imagine, INSERM UMR 1163, Paris, France., Peters H; Department of Metabolic Medicine, Royal Children's Hospital, Melbourne, Victoria, Australia., Piekutowska-Abramczuk D; Department of Medical Genetics, The Children's Memorial Health Institute, Warsaw, Poland., Rötig A; Institut Imagine, INSERM UMR 1163, Paris, France., Santer R; Department of Pediatrics, University Medical Center Hamburg Eppendorf, Hamburg, Germany., Scaglia F; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX; Texas Children's Hospital, Houston, TX; Joint BCM-CUHK Center of Medical Genetics, Prince of Wales Hospital, Shatin, Hong Kong SAR., Schiff M; Department of Medical Genetics and Reference Center for Mitochondrial Diseases (CARAMMEL), Necker Hospital, Université Paris Cité, Paris, France; Institut Imagine, INSERM UMR 1163, Paris, France; Reference Center of Inherited Metabolic Disorders, Necker Hospital, Université Paris Cité, Paris, France., Shagrani M; Department of Liver & Small Bowel Health Centre King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia., Sharrard M; Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom., Soler-Alfonso C; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX., Staufner C; Division of Neuropaediatrics and Metabolic Medicine, Center for Paediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany., Storey I; University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom., Stormon M; Department of Gastroenterology, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Taylor RW; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom., Thorburn DR; Brain and Mitochondrial Research Group, Murdoch Children's Research Institute, Melbourne, Victoria, Australia; Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia., Teles EL; Inherited Metabolic Diseases Reference Centre, São João Hospital University Centre, EPE, Porto, Portugal., Wang JS; The Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China., Weghuber D; University Children's Hospital, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, Austria., Wortmann S; University Children's Hospital, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, Austria; Amalia Children's Hospital, Radboudumc, Nijmegen, The Netherlands.

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2023 Jun; Vol. 25 (6), pp. 100314. Date of Electronic Publication: 2022 Oct 29.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

مواضيع طبية MeSH: Liver Failure*/drug therapy , Liver Failure*/genetics , Liver Failure, Acute*/drug therapy , Liver Failure, Acute*/genetics, Adolescent ; Child ; Child, Preschool ; Humans ; Infant ; Young Adult ; Acetylcysteine/therapeutic use ; Mitochondrial Proteins/genetics ; Mutation ; Retrospective Studies ; tRNA Methyltransferases/genetics

المؤلفون: Vogel GF, Mozer-Glassberg Y, Landau YE, Schlieben LD, Prokisch H, Feichtinger RG, Mayr JA, Brennenstuhl H, Schröter J, Pechlaner A, Alkuraya FS, Baker JJ, Barcia G, Baric I, Braverman N, Burnyte B, Christodoulou J, Ciara E, Coman D, Das AM, Darin N, Della Marina A, Distelmaier F, Eklund EA, Ersoy M, Fang W, Gaignard P, Ganetzky RD, Gonzales E, Howard C, Hughes J, Konstantopoulou V, Kose M, Kerr M, Khan A, Lenz D, McFarland R, Margolis MG, Morrison K, Müller T, Murayama K, Nicastro E, Pennisi A, Peters H, Piekutowska-Abramczuk D, Rötig A, Santer R, Scaglia F, Schiff M, Shagrani M, Sharrard M, Soler-Alfonso C, Staufner C, Storey I, Stormon M, Taylor RW, Thorburn DR, Teles EL, Wang JS, Weghuber D, Wortmannd S

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2023 Jun; Vol. 25 (6), pp. 100828. Date of Electronic Publication: 2023 Apr 13.

نوع المنشور: Published Erratum

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: PubMed not MEDLINE; MEDLINE

عنوان ترانسليتريتد: O pogreshnostiakh izlozheniia v meditsinskoĭ literature.

المؤلفون: Margolis MG

المصدر: Klinicheskaia meditsina [Klin Med (Mosk)] 1978 Dec; Vol. 56 (12), pp. 115-6.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Med. informat︠s︡ionnoe agentstvo Country of Publication: Russia (Federation) NLM ID: 2985204R Publication Model: Print Cited Medium: Print ISSN: 0023-2149 (Print) Linking ISSN: 00232149 NLM ISO Abbreviation: Klin Med (Mosk) Subsets: MEDLINE

مواضيع طبية MeSH: Terminology as Topic*, Reference Standards ; Semantics

عنوان ترانسليتريتد: Diabeticheskaia retinopatiia

المؤلفون: Margolis MG

المصدر: Oftalmologicheskii zhurnal [Oftalmol Zh] 1974; Vol. 29 (2), pp. 150-8.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Zdorovia Country of Publication: Ukraine NLM ID: 0401105 Publication Model: Print Cited Medium: Print ISSN: 0030-0675 (Print) Linking ISSN: 00300675 NLM ISO Abbreviation: Oftalmol Zh Subsets: MEDLINE

مواضيع طبية MeSH: Diabetic Retinopathy*/blood , Diabetic Retinopathy*/diagnosis , Diabetic Retinopathy*/drug therapy , Diabetic Retinopathy*/epidemiology , Diabetic Retinopathy*/etiology , Diabetic Retinopathy*/metabolism , Diabetic Retinopathy*/physiopathology , Diabetic Retinopathy*/prevention & control , Diabetic Retinopathy*/surgery, Anabolic Agents/therapeutic use ; Anticoagulants/therapeutic use ; Capillary Permeability ; Carbohydrate Metabolism ; Galactosamine/blood ; Gonadal Steroid Hormones/therapeutic use ; Humans ; Light Coagulation ; Lipid Metabolism ; Retinal Vessels/physiopathology ; Thiamine Pyrophosphate/therapeutic use ; Venous Pressure ; Vitamins/therapeutic use

عنوان ترانسليتريتد: O zapozdaloĭ diagnostike nekotorykh glaznykh zabolevaniĭ

المؤلفون: Margolis MG

المصدر: Meditsinskaia sestra [Med Sestra] 1975 Aug; Vol. 34 (8), pp. 13-5.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Ministerstvo Zdravookhraneniia Rsfsr Country of Publication: Russia (Federation) NLM ID: 18620490R Publication Model: Print Cited Medium: Print ISSN: 0025-8342 (Print) Linking ISSN: 00258342 NLM ISO Abbreviation: Med Sestra

مواضيع طبية MeSH: Eye Diseases/*diagnosis, Humans ; Time Factors

عنوان ترانسليتريتد: Tonografiia glaza.

المؤلفون: Margolis MG

المصدر: Meditsinskaia sestra [Med Sestra] 1977 Mar; Vol. 36 (3), pp. 36-7.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Ministerstvo Zdravookhraneniia Rsfsr Country of Publication: Russia (Federation) NLM ID: 18620490R Publication Model: Print Cited Medium: Print ISSN: 0025-8342 (Print) Linking ISSN: 00258342 NLM ISO Abbreviation: Med Sestra

مواضيع طبية MeSH: Tonometry, Ocular*, Humans

عنوان ترانسليتريتد: Diffuznye zabolevaniia soedinitel'noĭ tkani i rol' glaznykh simptomov v ikh diagnostike (obzor literatury).

المؤلفون: Margolis MG, Evtushenko VI, Istomin MG

المصدر: Voprosy revmatizma [Vopr Revm] 1980 Apr-Jun (2), pp. 54-7.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Izdatelstvo Meditsina Country of Publication: Russia (Federation) NLM ID: 0064753 Publication Model: Print Cited Medium: Print ISSN: 0042-885X (Print) Linking ISSN: 0042885X NLM ISO Abbreviation: Vopr Revm Subsets: MEDLINE

مواضيع طبية MeSH: Eye Manifestations*, Connective Tissue Diseases/*diagnosis, Arthritis, Rheumatoid/diagnosis ; Dermatomyositis/diagnosis ; Giant Cell Arteritis/diagnosis ; Humans ; Lupus Erythematosus, Systemic/diagnosis ; Polyarteritis Nodosa/diagnosis ; Spondylitis, Ankylosing/diagnosis ; Stevens-Johnson Syndrome/diagnosis

عنوان ترانسليتريتد: Gormonal'naia terapiia.

المؤلفون: Margolis MG, Mal'kovich VK

المصدر: Meditsinskaia sestra [Med Sestra] 1979 Mar; Vol. 38 (3), pp. 12-5.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Ministerstvo Zdravookhraneniia Rsfsr Country of Publication: Russia (Federation) NLM ID: 18620490R Publication Model: Print Cited Medium: Print ISSN: 0025-8342 (Print) Linking ISSN: 00258342 NLM ISO Abbreviation: Med Sestra

مواضيع طبية MeSH: Endocrine System Diseases/*drug therapy , Hormones/*therapeutic use, Humans

عنوان ترانسليتريتد: Uspekhi otechestvennoĭ oftal'moéndokrinologii.

المؤلفون: Krasnov ML, Margolis MG

المصدر: Vestnik oftalmologii [Vestn Oftalmol] 1977 Sep-Oct (5), pp. 91-5.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Media Sfera Country of Publication: Russia (Federation) NLM ID: 0415216 Publication Model: Print Cited Medium: Print ISSN: 0042-465X (Print) Linking ISSN: 0042465X NLM ISO Abbreviation: Vestn Oftalmol Subsets: MEDLINE

مواضيع طبية MeSH: Endocrinology* , Ophthalmology*, Adrenal Cortex Hormones/therapeutic use ; Adrenal Glands/physiopathology ; Diabetic Retinopathy/diagnosis ; Diabetic Retinopathy/drug therapy ; Exophthalmos/diagnosis ; Eye Burns/drug therapy ; Eye Diseases/physiopathology ; Fluorescein Angiography ; Glaucoma/diagnosis ; Gonadal Steroid Hormones/physiology ; Humans ; Hypothalamus/physiopathology ; Insulin/therapeutic use ; Intraocular Pressure ; Pituitary Gland/physiopathology ; Time Factors ; Tonometry, Ocular ; USSR