Maturity-onset diabetes of the young (English Wikipedia)

Dhavendra Kumar; D. J. Weatherall (2008). Genomics and clinical medicine. Oxford University Press US. pp. 184–. ISBN 978-0-19-518813-4. Retrieved 12 June 2010.

doi.org

Urakami T (2019). "Maturity-onset diabetes of the young (MODY): current perspectives on diagnosis and treatment". Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. 12. Diabetes Metabolic Syndrome & Obesity: 1047–1056. doi:10.2147/DMSO.S179793. PMC 6625604. PMID 31360071.
Urbanova J, Rypackova B, Prochazkova Z, Kucera P, Cerna M, Andel M, Heneberg P (2014). "Positivity for islet cell autoantibodies in patients with monogenic diabetes is associated with later diabetes onset and higher HbA1c level". Diabetic Medicine. 31 (4): 466–71. doi:10.1111/dme.12314. PMID 24102923. S2CID 1867195.
Lerario, A. M.; Brito, L. P.; Mariani, B. M.; Fragoso, M. C.; Machado, M. A.; Teixeira, R. (2010). "A missense TCF1 mutation in a patient with MODY-3 and liver adenomatosis". Clinics. 65 (10): 1059–1060. doi:10.1590/S1807-59322010001000024. PMC 2972616. PMID 21120312.
Steele AM, Shields BM, Wensley KJ, Colclough K, Ellard S, Hattersley AT (2014). "Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia". JAMA. 311 (3): 279–86. doi:10.1001/jama.2013.283980. hdl:10871/15378. PMID 24430320.
Dickens LT, Letourneau LR, Sanyoura M, Greeley SA, Philipson LH, Naylor RN (2019). "Management and pregnancy outcomes of women with GCK-MODY enrolled in the US Monogenic Diabetes Registry". Acta Diabetologica. 56 (3): 405–411. doi:10.1007/s00592-018-1267-z. PMC 6468988. PMID 30535721.
Frayling, TM; Evans, JC; Bulman, MP; Pearson, E (February 2001). "beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors". Diabetes. 50 Suppl (1): S94-100. doi:10.2337/diabetes.50.2007.S94. PMID 11272211.
Neve B, Fernandez-Zapico ME, Ashkenazi-Katalan V, et al. (March 2005). "Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function". Proc. Natl. Acad. Sci. U.S.A. 102 (13): 4807–12. doi:10.1073/pnas.0409177102. PMC 554843. PMID 15774581.
Raeder H, Johansson S, Holm PI, et al. (January 2006). "Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction". Nat. Genet. 38 (1): 54–62. doi:10.1038/ng1708. PMID 16369531. S2CID 8338877.
Bansal, V; Winkelmann, BR; Dietrich, JW; Boehm, BO (2024). "Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene". Frontiers in Endocrinology. 15: 1258982. doi:10.3389/fendo.2024.1258982. hdl:10356/178608. PMID 38444585.
Urbanova, J.; et al. (2015). "Half-Life of Sulfonylureas in HNF1A and HNF4A Human MODY Patients is not Prolonged as Suggested by the Mouse Hnf1a-/- Model". Current Pharmaceutical Design. 21 (39): 5736–5748. doi:10.2174/1381612821666151008124036. PMID 26446475.
Galler, Angela; Stange, Thoralf; Müller, Gabriele; Näke, Andrea; Vogel, Christian; Kapellen, Thomas; Bartelt, Heike; Kunath, Hildebrand; Koch, Rainer; Kiess, Wieland; Rothe, Ulrike (2010). "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. 74 (4): 285–91. doi:10.1159/000303141. PMID 20516654. S2CID 1313999.
Tattersall, R (1998). "Maturity-onset diabetes of the young: A clinical history". Diabetic Medicine. 15 (1): 11–4. doi:10.1002/(SICI)1096-9136(199801)15:1<11::AID-DIA561>3.0.CO;2-0. PMID 9472858. S2CID 31690226.
American Diabetes, Association (2009). "Diagnosis and Classification of Diabetes Mellitus". Diabetes Care. 32 (Suppl 1): S62–S67. doi:10.2337/dc09-S062. PMC 2613584. PMID 19118289.

drmohans.com

Chennai, India, Dr. V Mohan (2020-07-15). "'Maturity Onset Diabetes of the Young (MODY) | Dr Mohans". Dr Mohan's Diabetes Center in Chennai.

handle.net

hdl.handle.net

Steele AM, Shields BM, Wensley KJ, Colclough K, Ellard S, Hattersley AT (2014). "Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia". JAMA. 311 (3): 279–86. doi:10.1001/jama.2013.283980. hdl:10871/15378. PMID 24430320.
Bansal, V; Winkelmann, BR; Dietrich, JW; Boehm, BO (2024). "Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene". Frontiers in Endocrinology. 15: 1258982. doi:10.3389/fendo.2024.1258982. hdl:10356/178608. PMID 38444585.

nih.gov

pubmed.ncbi.nlm.nih.gov

Urakami T (2019). "Maturity-onset diabetes of the young (MODY): current perspectives on diagnosis and treatment". Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. 12. Diabetes Metabolic Syndrome & Obesity: 1047–1056. doi:10.2147/DMSO.S179793. PMC 6625604. PMID 31360071.
Urbanova J, Rypackova B, Prochazkova Z, Kucera P, Cerna M, Andel M, Heneberg P (2014). "Positivity for islet cell autoantibodies in patients with monogenic diabetes is associated with later diabetes onset and higher HbA1c level". Diabetic Medicine. 31 (4): 466–71. doi:10.1111/dme.12314. PMID 24102923. S2CID 1867195.
Lerario, A. M.; Brito, L. P.; Mariani, B. M.; Fragoso, M. C.; Machado, M. A.; Teixeira, R. (2010). "A missense TCF1 mutation in a patient with MODY-3 and liver adenomatosis". Clinics. 65 (10): 1059–1060. doi:10.1590/S1807-59322010001000024. PMC 2972616. PMID 21120312.
Steele AM, Shields BM, Wensley KJ, Colclough K, Ellard S, Hattersley AT (2014). "Prevalence of vascular complications among patients with glucokinase mutations and prolonged, mild hyperglycemia". JAMA. 311 (3): 279–86. doi:10.1001/jama.2013.283980. hdl:10871/15378. PMID 24430320.
Dickens LT, Letourneau LR, Sanyoura M, Greeley SA, Philipson LH, Naylor RN (2019). "Management and pregnancy outcomes of women with GCK-MODY enrolled in the US Monogenic Diabetes Registry". Acta Diabetologica. 56 (3): 405–411. doi:10.1007/s00592-018-1267-z. PMC 6468988. PMID 30535721.
Frayling, TM; Evans, JC; Bulman, MP; Pearson, E (February 2001). "beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors". Diabetes. 50 Suppl (1): S94-100. doi:10.2337/diabetes.50.2007.S94. PMID 11272211.
Neve B, Fernandez-Zapico ME, Ashkenazi-Katalan V, et al. (March 2005). "Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function". Proc. Natl. Acad. Sci. U.S.A. 102 (13): 4807–12. doi:10.1073/pnas.0409177102. PMC 554843. PMID 15774581.
Raeder H, Johansson S, Holm PI, et al. (January 2006). "Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction". Nat. Genet. 38 (1): 54–62. doi:10.1038/ng1708. PMID 16369531. S2CID 8338877.
Bansal, V; Winkelmann, BR; Dietrich, JW; Boehm, BO (2024). "Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene". Frontiers in Endocrinology. 15: 1258982. doi:10.3389/fendo.2024.1258982. hdl:10356/178608. PMID 38444585.
Urbanova, J.; et al. (2015). "Half-Life of Sulfonylureas in HNF1A and HNF4A Human MODY Patients is not Prolonged as Suggested by the Mouse Hnf1a-/- Model". Current Pharmaceutical Design. 21 (39): 5736–5748. doi:10.2174/1381612821666151008124036. PMID 26446475.
Galler, Angela; Stange, Thoralf; Müller, Gabriele; Näke, Andrea; Vogel, Christian; Kapellen, Thomas; Bartelt, Heike; Kunath, Hildebrand; Koch, Rainer; Kiess, Wieland; Rothe, Ulrike (2010). "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. 74 (4): 285–91. doi:10.1159/000303141. PMID 20516654. S2CID 1313999.
Tattersall RB (1974). "Mild familial diabetes with dominant inheritance". Q J Med. 43 (170): 339–357. PMID 4212169.
Tattersall, R (1998). "Maturity-onset diabetes of the young: A clinical history". Diabetic Medicine. 15 (1): 11–4. doi:10.1002/(SICI)1096-9136(199801)15:1<11::AID-DIA561>3.0.CO;2-0. PMID 9472858. S2CID 31690226.
American Diabetes, Association (2009). "Diagnosis and Classification of Diabetes Mellitus". Diabetes Care. 32 (Suppl 1): S62–S67. doi:10.2337/dc09-S062. PMC 2613584. PMID 19118289.

ncbi.nlm.nih.gov

Urakami T (2019). "Maturity-onset diabetes of the young (MODY): current perspectives on diagnosis and treatment". Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. 12. Diabetes Metabolic Syndrome & Obesity: 1047–1056. doi:10.2147/DMSO.S179793. PMC 6625604. PMID 31360071.
Lerario, A. M.; Brito, L. P.; Mariani, B. M.; Fragoso, M. C.; Machado, M. A.; Teixeira, R. (2010). "A missense TCF1 mutation in a patient with MODY-3 and liver adenomatosis". Clinics. 65 (10): 1059–1060. doi:10.1590/S1807-59322010001000024. PMC 2972616. PMID 21120312.
Dickens LT, Letourneau LR, Sanyoura M, Greeley SA, Philipson LH, Naylor RN (2019). "Management and pregnancy outcomes of women with GCK-MODY enrolled in the US Monogenic Diabetes Registry". Acta Diabetologica. 56 (3): 405–411. doi:10.1007/s00592-018-1267-z. PMC 6468988. PMID 30535721.
Neve B, Fernandez-Zapico ME, Ashkenazi-Katalan V, et al. (March 2005). "Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function". Proc. Natl. Acad. Sci. U.S.A. 102 (13): 4807–12. doi:10.1073/pnas.0409177102. PMC 554843. PMID 15774581.
American Diabetes, Association (2009). "Diagnosis and Classification of Diabetes Mellitus". Diabetes Care. 32 (Suppl 1): S62–S67. doi:10.2337/dc09-S062. PMC 2613584. PMID 19118289.

niddk.nih.gov

"Monogenic Diabetes (Neonatal Diabetes Mellitus & MODY)". National Institute of Diabetes and Digestive and Kidney Diseases. Retrieved 2023-02-01.
"Monogenic Diabetes (Neonatal Diabetes Mellitus & MODY)". National Institute of Diabetes and Digestive and Kidney Diseases. Retrieved 2023-02-10.

omim.org

Renal Cysts and Diabetes Syndrome (Report). Retrieved May 19, 2011.
Online Mendelian Inheritance in Man (OMIM): MATURITY-ONSET DIABETES OF THE YOUNG, TYPE VII; MODY7 - 610508
Online Mendelian Inheritance in Man (OMIM): MATURITY-ONSET DIABETES OF THE YOUNG, TYPE VIII, WITH EXOCRINE DYSFUNCTION; MODY8 - 609812

phlaunt.com

MODY (Report). Retrieved Jan 25, 2010.

qucosa.de

tud.qucosa.de

Galler, Angela; Stange, Thoralf; Müller, Gabriele; Näke, Andrea; Vogel, Christian; Kapellen, Thomas; Bartelt, Heike; Kunath, Hildebrand; Koch, Rainer; Kiess, Wieland; Rothe, Ulrike (2010). "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. 74 (4): 285–91. doi:10.1159/000303141. PMID 20516654. S2CID 1313999.

semanticscholar.org

api.semanticscholar.org

Urbanova J, Rypackova B, Prochazkova Z, Kucera P, Cerna M, Andel M, Heneberg P (2014). "Positivity for islet cell autoantibodies in patients with monogenic diabetes is associated with later diabetes onset and higher HbA1c level". Diabetic Medicine. 31 (4): 466–71. doi:10.1111/dme.12314. PMID 24102923. S2CID 1867195.
Raeder H, Johansson S, Holm PI, et al. (January 2006). "Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction". Nat. Genet. 38 (1): 54–62. doi:10.1038/ng1708. PMID 16369531. S2CID 8338877.
Galler, Angela; Stange, Thoralf; Müller, Gabriele; Näke, Andrea; Vogel, Christian; Kapellen, Thomas; Bartelt, Heike; Kunath, Hildebrand; Koch, Rainer; Kiess, Wieland; Rothe, Ulrike (2010). "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. 74 (4): 285–91. doi:10.1159/000303141. PMID 20516654. S2CID 1313999.
Tattersall, R (1998). "Maturity-onset diabetes of the young: A clinical history". Diabetic Medicine. 15 (1): 11–4. doi:10.1002/(SICI)1096-9136(199801)15:1<11::AID-DIA561>3.0.CO;2-0. PMID 9472858. S2CID 31690226.

Maturity-onset diabetes of the young (English Wikipedia)

books.google.com

doi.org

drmohans.com

handle.net

hdl.handle.net

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

niddk.nih.gov

omim.org

phlaunt.com

qucosa.de

tud.qucosa.de

semanticscholar.org

api.semanticscholar.org

sparkpeople.com

staywellsolutionsonline.com

harvardatoz.demo.staywellsolutionsonline.com