Found: 14
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Human islets expressing HNF1A variant have defective β cell transcriptional regulatory networks.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Management and pregnancy outcomes of women with GCK-MODY enrolled in the US Monogenic Diabetes Registry.
- Published in:
- Acta Diabetologica, 2019, v. 56, n. 4, p. 405, doi. 10.1007/s00592-018-1267-z
- By:
- Publication type:
- Article
WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 24, p. 4012, doi. 10.1093/hmg/ddn304
- By:
- Publication type:
- Article
A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 1, p. 140, doi. 10.1038/ejhg.2013.87
- By:
- Publication type:
- Article
178-LB: Insights from the University of Chicago Monogenic Diabetes Registry on Diagnosis and Management of Monogenic Diabetes.
- Published in:
- Diabetes, 2020, v. 69, p. N.PAG, doi. 10.2337/db20-178-LB
- By:
- Publication type:
- Article
Geographical Structure of the Y-chromosomal Genetic Landscape of the Levant: A coastal-inland contrast.
- Published in:
- Annals of Human Genetics, 2009, v. 73, n. 6, p. 568, doi. 10.1111/j.1469-1809.2009.00538.x
- By:
- Publication type:
- Article
Relaxin polymorphisms associated with metabolic disturbance in patients treated with antipsychotics.
- Published in:
- Journal of Psychopharmacology, 2012, v. 26, n. 3, p. 374, doi. 10.1177/0269881111408965
- By:
- Publication type:
- Article
Pancreatic Histopathology of Human Monogenic Diabetes Due to Causal Variants in KCNJ11, HNF1A, GATA6, and LMNA.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Monogenic Diabetes in Children and Adolescents: Recognition and Treatment Options.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Integrated Analysis of the Pancreas and Islets Reveals Unexpected Findings in Human Male With Type 1 Diabetes.
- Published in:
- Journal of the Endocrine Society, 2021, v. 5, n. 12, p. 1, doi. 10.1210/jendso/bvab162
- By:
- Publication type:
- Article
<italic>FOXP3</italic> mutations causing early‐onset insulin‐requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X‐linked syndrome.
- Published in:
- Pediatric Diabetes, 2018, v. 19, n. 3, p. 388, doi. 10.1111/pedi.12612
- By:
- Publication type:
- Article
Prenatal and neonatal Group B Streptococcus screening and serotyping in Lebanon: incidence and implications.
- Published in:
- Acta Obstetricia et Gynecologica Scandinavica, 2010, v. 89, n. 3, p. 399, doi. 10.3109/00016340903560008
- By:
- Publication type:
- Article
Update of variants identified in the pancreatic β‐cell K<sub>ATP</sub> channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes.
- Published in:
- Human Mutation, 2020, v. 41, n. 5, p. 884, doi. 10.1002/humu.23995
- By:
- Publication type:
- Article
Diabetes Presentation in Infancy: High Risk of Diabetic Ketoacidosis.
- Published in:
- 2017
- By:
- Publication type:
- letter