Wolfram syndrome 1 and Wolfram syndrome 2
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pediatrics, Perinatology and Child Health
Reference48 articles.
1. Diabetes mellitus and optic atrophy among siblings: report of four cases.;Wolfram;Mayo Clin Proc,1938
2. Decreased beta-cell mass in diabetes: significance, mechanisms and therapeutic implications.;Donath;Diabetologia,2004
3. Beta-cell deficit and increased beta-cell apoptosis in humans with type 2 diabetes.;Butler;Diabetes,2003
4. A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome).;Inoue;Nat Genet,1998
5. Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein.;Strom;Hum Mol Genet,1998
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1. Wolfram Syndrome: A Rare Genetic disorder affecting Multiple Organ Systems;Research Journal of Pharmacology and Pharmacodynamics;2023-11-09
2. ER Calcium Depletion as a Key Driver for Impaired ER-to-Mitochondria Calcium Transfer and Mitochondrial Dysfunction in Wolfram Syndrome;2023-10-13
3. AMPK–FOXO–IP3R signaling pathway mediates neurological and developmental defects caused by mitochondrial DNA mutations;Proceedings of the National Academy of Sciences;2023-08-28
4. Wolfram Syndrome-2, a Cause of Severe Gastrointestinal Bleeding: A Case Series and a Literature Review;JPGN Reports;2023-07-17
5. Paediatric Wolfram syndrome Type 1: should gonadal dysfunction be part of the diagnostic criteria?;Frontiers in Endocrinology;2023-06-13
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