Results 121 to 130 of about 1,384 (167)

Consensus Recommendations for the Clinical Management of Wolfram syndrome Using a Delphi Method

open access: yes
Elliott J   +8 more
europepmc   +1 more source

Mitochondrial abnormalities in the DIDMOAD syndrome

open access: yesJournal of Inherited Metabolic Disease, 1992
DIDMOAD syndrome, or Wolfram syndrome (McKusick 222300), refers to the combination of diabetes inspidus, diabetes mellitus, optic atrophy and deafness. Diabetes mellitus is an invariable finding; the diabetes insipidus, optic atrophy and deafness can all be attributed to neuronal degeneration (Cremers et al 1911; Mtanda et al 1986), as can the less ...
S, Bundey   +5 more
exaly   +4 more sources
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MRI of Wolfram syndrome (DIDMOAD)

Neuroradiology, 1999
Wolfram syndrome (DIDMOAD) is a rare diffuse neurodegenerative disorder characterised by diabetes insipidus, diabetes mellitus, optic atrophy, deafness, and a wide variety of abnormalities of the central nervous system, urinary tract and endocrine glands. It may be familial or sporadic.
A M Bardelli
exaly   +3 more sources

The challenge of pregnancy in the DIDMOAD syndrome

Practical Diabetes International: the International Journal for Diabetes Care Teams Worldwide, 2001
AbstractDIDMOAD syndrome includes diabetes insipidus, diabetes mellitus, optic atrophy and deafness.Pregnancies in the DIDMOAD syndrome are rare, and successful pregnancies are extremely rare. Despite the full DIDMOAD syndrome including diabetes mellitus for 30 years, our patient had a successful pregnancy, delivering an infant weighing 1740 g at 32 ...
Gallagher A, Hutchison RS, Kelly WF
exaly   +3 more sources

Mitochondrial DNA studies in Wolfram (DIDMOAD) syndrome

Lancet, The, 1996
The power of the overlap formalism is illustrated by regularizing theoriesbased on Majorana-Weyl fermions.
Halûk Topaloğlu   +2 more
exaly   +4 more sources

Wolfram (DIDMOAD) Syndrome: Report of Two Patients

Journal of Pediatric Endocrinology and Metabolism, 2004
We report a girl with Wolfram syndrome who presented with juvenile-onset diabetes mellitus when she was 4 3/12 years old. Optic atrophy and high frequency sensorineural hearing loss were found at 7 and 9 5/12 years of age, respectively. Her younger brother also developed Wolfram syndrome when he was 3 2/12 years old.
Chaohsu Lin, Chi-Yu Huang
exaly   +3 more sources

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