Diabète de type MODY (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Diabète de type MODY" in French language version.

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books.google.com

doi.org

dx.doi.org

  • Yorifuji, Kurokawa, K, Mamada, M et Imai, T, « Neonatal diabetes mellitus and neonatal polycystic, dysplastic kidneys: Phenotypically discordant recurrence of a mutation in the hepatocyte nuclear factor-1beta gene due to germline mosaicism. », The Journal of Clinical Endocrinology and Metabolism, vol. 89, no 6,‎ , p. 2905–8 (PMID 15181075, DOI 10.1210/jc.2003-031828)
  • Edghill, Bingham, C, Slingerland, AS et Minton, JA, « Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF-1beta in human pancreatic development », Diabetic Medicine, vol. 23, no 12,‎ , p. 1301–6 (PMID 17116179, DOI 10.1111/j.1464-5491.2006.01999.x)
  • Steele AM, Shields BM, Wensley KJ, Colclough K, Ellard S, Hattersley AT., « Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia. », JAMA, vol. 311, no 3,‎ , p. 279–86 (PMID 24430320, DOI 10.1001/jama.2013.283980)
  • Dickens LT, Letourneau LR, Sanyoura M, Greeley SAW, Philipson LH, Naylor RN., « Management and pregnancy outcomes of women with GCK-MODY enrolled in the US Monogenic Diabetes Registry. », Acta Diabetologica, vol. 56, no 3,‎ , p. 405–411 (PMID 30535721, PMCID 6468988, DOI 10.1007/s00592-018-1267-z)
  • Frayling, Evans, Bulman et Pearson, « beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors », Diabetes, vol. 50 Suppl, no 1,‎ , S94-100 (PMID 11272211, DOI 10.2337/diabetes.50.2007.S94)
  • « Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function », Proc. Natl. Acad. Sci. U.S.A., vol. 102, no 13,‎ , p. 4807–12 (PMID 15774581, PMCID 554843, DOI 10.1073/pnas.0409177102)
  • « Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction », Nat. Genet., vol. 38, no 1,‎ , p. 54–62 (PMID 16369531, DOI 10.1038/ng1708)
  • « Maturity-onset diabetes of the young (MODY): current perspectives on diagnosis and treatment », Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy, Diabetes Metabolic Syndrome & Obesity, vol. 12,‎ , p. 1047–1056 (PMID 31360071, PMCID 6625604, DOI 10.2147/DMSO.S179793)
  • « Positivity for islet cell autoantibodies in patients with monogenic diabetes is associated with later diabetes onset and higher HbA1c level », Diabetic Medicine, vol. 31, no 4,‎ , p. 466–71 (PMID 24102923, DOI 10.1111/dme.12314)
  • Lerario, Brito, Mariani et Fragoso, « A missense TCF1 mutation in a patient with MODY-3 and liver adenomatosis », Clinics, vol. 65, no 10,‎ , p. 1059–1060 (PMID 21120312, PMCID 2972616, DOI 10.1590/S1807-59322010001000024)
  • Galler, Stange, Müller et Näke, « Incidence of Childhood Diabetes in Children Aged Less than 15 Years and Its Clinical and Metabolic Characteristics at the Time of Diagnosis: Data from the Childhood Diabetes Registry of Saxony, Germany », Hormone Research in Paediatrics, vol. 74, no 4,‎ , p. 285–91 (PMID 20516654, DOI 10.1159/000303141, lire en ligne)
  • Tattersall, « Maturity-onset diabetes of the young: A clinical history », Diabetic Medicine, vol. 15, no 1,‎ , p. 11–4 (PMID 9472858, DOI 10.1002/(SICI)1096-9136(199801)15:1<11::AID-DIA561>3.0.CO;2-0)
  • American Diabetes, « Diagnosis and Classification of Diabetes Mellitus », Diabetes Care, vol. 32, no Suppl 1,‎ , S62–S67 (PMID 19118289, PMCID 2613584, DOI 10.2337/dc09-S062)

drmohans.com

nih.gov

ncbi.nlm.nih.gov

  • Yorifuji, Kurokawa, K, Mamada, M et Imai, T, « Neonatal diabetes mellitus and neonatal polycystic, dysplastic kidneys: Phenotypically discordant recurrence of a mutation in the hepatocyte nuclear factor-1beta gene due to germline mosaicism. », The Journal of Clinical Endocrinology and Metabolism, vol. 89, no 6,‎ , p. 2905–8 (PMID 15181075, DOI 10.1210/jc.2003-031828)
  • Edghill, Bingham, C, Slingerland, AS et Minton, JA, « Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF-1beta in human pancreatic development », Diabetic Medicine, vol. 23, no 12,‎ , p. 1301–6 (PMID 17116179, DOI 10.1111/j.1464-5491.2006.01999.x)
  • Steele AM, Shields BM, Wensley KJ, Colclough K, Ellard S, Hattersley AT., « Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia. », JAMA, vol. 311, no 3,‎ , p. 279–86 (PMID 24430320, DOI 10.1001/jama.2013.283980)
  • Dickens LT, Letourneau LR, Sanyoura M, Greeley SAW, Philipson LH, Naylor RN., « Management and pregnancy outcomes of women with GCK-MODY enrolled in the US Monogenic Diabetes Registry. », Acta Diabetologica, vol. 56, no 3,‎ , p. 405–411 (PMID 30535721, PMCID 6468988, DOI 10.1007/s00592-018-1267-z)
  • Frayling, Evans, Bulman et Pearson, « beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors », Diabetes, vol. 50 Suppl, no 1,‎ , S94-100 (PMID 11272211, DOI 10.2337/diabetes.50.2007.S94)
  • « Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function », Proc. Natl. Acad. Sci. U.S.A., vol. 102, no 13,‎ , p. 4807–12 (PMID 15774581, PMCID 554843, DOI 10.1073/pnas.0409177102)
  • « Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction », Nat. Genet., vol. 38, no 1,‎ , p. 54–62 (PMID 16369531, DOI 10.1038/ng1708)
  • « Maturity-onset diabetes of the young (MODY): current perspectives on diagnosis and treatment », Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy, Diabetes Metabolic Syndrome & Obesity, vol. 12,‎ , p. 1047–1056 (PMID 31360071, PMCID 6625604, DOI 10.2147/DMSO.S179793)
  • « Positivity for islet cell autoantibodies in patients with monogenic diabetes is associated with later diabetes onset and higher HbA1c level », Diabetic Medicine, vol. 31, no 4,‎ , p. 466–71 (PMID 24102923, DOI 10.1111/dme.12314)
  • Lerario, Brito, Mariani et Fragoso, « A missense TCF1 mutation in a patient with MODY-3 and liver adenomatosis », Clinics, vol. 65, no 10,‎ , p. 1059–1060 (PMID 21120312, PMCID 2972616, DOI 10.1590/S1807-59322010001000024)
  • Galler, Stange, Müller et Näke, « Incidence of Childhood Diabetes in Children Aged Less than 15 Years and Its Clinical and Metabolic Characteristics at the Time of Diagnosis: Data from the Childhood Diabetes Registry of Saxony, Germany », Hormone Research in Paediatrics, vol. 74, no 4,‎ , p. 285–91 (PMID 20516654, DOI 10.1159/000303141, lire en ligne)
  • Tattersall RB, « Mild familial diabetes with dominant inheritance », Q J Med, vol. 43, no 170,‎ , p. 339–357 (PMID 4212169)
  • Tattersall, « Maturity-onset diabetes of the young: A clinical history », Diabetic Medicine, vol. 15, no 1,‎ , p. 11–4 (PMID 9472858, DOI 10.1002/(SICI)1096-9136(199801)15:1<11::AID-DIA561>3.0.CO;2-0)
  • American Diabetes, « Diagnosis and Classification of Diabetes Mellitus », Diabetes Care, vol. 32, no Suppl 1,‎ , S62–S67 (PMID 19118289, PMCID 2613584, DOI 10.2337/dc09-S062)

niddk.nih.gov

omim.org

qucosa.de

tud.qucosa.de

  • Galler, Stange, Müller et Näke, « Incidence of Childhood Diabetes in Children Aged Less than 15 Years and Its Clinical and Metabolic Characteristics at the Time of Diagnosis: Data from the Childhood Diabetes Registry of Saxony, Germany », Hormone Research in Paediatrics, vol. 74, no 4,‎ , p. 285–91 (PMID 20516654, DOI 10.1159/000303141, lire en ligne)