Results 61 to 70 of about 1,298,739 (158)
Visual Function in Wolfram Syndrome
, 2018 To characterize the visual function in Wolfram syndrome and literature ...
An-Guor Wang; Hui-Chen Cheng
core
Bilateral Optic Nerve Atrophy Case Report
Majalah Kedokteran BandungWolfram syndrome, also known as DIDMOAD or juvenile onset diabetes mellitus, optic nerve atrophy, diabetes insipidus, and deafness, is a genetic neurological condition.
Mohammed R. Naqeeb, Dina M Abdulmannan
doaj +1 more source
Radiotherapy‐Induced Side Effects: Epidemiology, Pathogenesis, Prevention and Treatments
MedComm, Volume 7, Issue 10, October 2026.Radiotherapy for malignancies frequently injures the organs’ systems through oxidative stress, fibrosis, inflammation, and vascular damage. This review systematically maps the epidemiology, pathogenesis, and emerging therapies to propose a mechanism‑network‑targeted framework for integrated, personalized care in radiation oncology.
Xiaowen Ma +9 more
wiley +1 more source
Summary of clinical features associated with Wolfram-like syndrome from previous studies.
, 2018 Summary of clinical features associated with Wolfram-like syndrome from previous studies.
Ikuyo Miyanohara (4952176) +20 more
core +1 more source
Genetic predisposition for type 1 diabetes mellitus: The role of endoplasmic reticulum stress in human disease etiopathogenesis [PDF]
Journal of Medical Biochemistry, 2010 The increasing incidence of diabetes mellitus worldwide has prompted a rapid growth in the pace of scientific discovery of the mechanisms involved in the etiopathogenesis of this multifactorial disease.
Stankov Karmen
doaj
A young diabetic with suicidal risk: Rare disease with a rarer presentation
Indian Journal of Endocrinology and Metabolism, 2013 Rare genetic or inherited forms of diabetes can mimic immune mediated type 1 diabetes. Early age of onset and associated features help to differentiate these diseases from type 1 diabetes.
Rajeev Philip +3 more
doaj +1 more source
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Suzan Al‐Gburi +17 more
wiley +1 more source
Urological manifestations of the Wolfram syndrome: Observations in 14 patients
, 1999 Purpose: Since the initial description of the Wolfram syndrome, various anomalies have been associated with this rare entity. Urinary tract dilatation and bladder dysfunction, usually in the form of a large, atonic bladder, are coexisting features of ...
Tekgul, S +4 more
core +1 more source
BILATERAL ATROPHIC MACULOPATHY IN TWO SIBLINGS OF WOLFRAM SYNDROM
Pakistan Armed Forces Medical Journal, 2018 Wolfram disease is a rare genetic disease which mainly presents as diabetes mellitus and optic atrophy. Presence of maculopathy in a case of wolfram disease is rarely reported in literature. We present here two cases/siblings with age of 12 and 14 years.
Tayyab Azeem Janjua +4 more
doaj +4 more sources