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Wolfram Syndrome
Known as:
DIDMOAD
, WFS
, Syndrome, Wolfram
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A hereditary condition characterized by multiple symptoms including those of DIABETES INSIPIDUS; DIABETES MELLITUS; OPTIC ATROPHY; and DEAFNESS. This…
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National Institutes of Health
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Related topics
Related topics
33 relations
Ataxia
Autosomal recessive inheritance
Blepharoptosis
Cardiomyopathies
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Narrower (1)
Wolfram-Like Syndrome, Autosomal Dominant
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
A replication study of 19 GWAS-validated type 2 diabetes at-risk variants in the Lebanese population.
W. Almawi
,
Rita Nemr
,
+4 authors
Eddie Racoubian
Diabetes Research and Clinical Practice
2013
Corpus ID: 25920249
2003
2003
Cladistic analysis of the Neotropical butterfly genus Adelpha (Lepidoptera: Nymphalidae), with comments on the subtribal classification of Limenitidini
K. Willmott
2003
Corpus ID: 13579210
Abstract. A two‐stage cladistic analysis of 114 characters from adult and immature stage morphology provided phylogenetic…
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Highly Cited
2001
Highly Cited
2001
WFS 1 ( Wolfram syndrome 1 ) gene product : predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain
K. Takeda
,
H. Inoue
,
+5 authors
Y. Oka
2001
Corpus ID: 91176647
Wolfram (DIDMOAD) syndrome is an autosomal recessive neurodegenerative disorder accompanied by insulin-dependent diabetes…
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1999
1999
MRI of Wolfram syndrome (DIDMOAD)
P. Galluzzi
,
G. Filosomi
,
I. Vallone
,
A. Bardelli
,
C. Venturi
Neuroradiology
1999
Corpus ID: 42414970
Abstract Wolfram syndrome (DIDMOAD) is a rare diffuse neurodegenerative disorder characterised by diabetes insipidus, diabetes…
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1998
1998
Evidence of an increased risk of hearing loss in heterozygous carriers in a Wolfram syndrome family
T. Ohata
,
A. Koizumi
,
+8 authors
G. Takada
Human Genetics
1998
Corpus ID: 1032048
Wolfram syndrome (MIM 222300) is characterized by juvenile-onset diabetes mellitus and optic atrophy. Previous linkage analyses…
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Highly Cited
1996
Highly Cited
1996
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.
D. A. Collier
,
T. Barrett
,
+4 authors
S. Bundey
American Journal of Human Genetics
1996
Corpus ID: 6947241
Wolfram syndrome (DIDMOAD syndrome; MIM 222300) is an autosomal recessive neurodegenerative disorder characterized by juvenile…
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Review
1995
Review
1995
Differentials in infertility in Cameroon and Nigeria.
U. Larsen
1995
Corpus ID: 72418568
Data from the 1978 World Fertility Survey (WFS) and the 1991 Demographic and Health Survey (DHS) in Cameroon as well as data from…
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Highly Cited
1992
Highly Cited
1992
Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia.
J. V. D. van den Ouweland
,
G. Bruining
,
D. Lindhout
,
J. Wit
,
B. Veldhuyzen
,
J. Maassen
Nucleic Acids Research
1992
Corpus ID: 31277743
We have recently identified a point mutation in the mitochondrially encoded tRNA(Leu(UUR)) gene which associates with a…
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Review
1989
Review
1989
Maternal age, gravidity, and pregnancy spacing effects on spontaneous fetal mortality.
John B Casterline
Social Biology
1989
Corpus ID: 37972995
Differentials in the probability of pregnancy loss are examined using pregnancy history data from eight WFS surveys in developing…
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Highly Cited
1964
Highly Cited
1964
Die Reaktionsweise und das Reaktionsspektrum von Riechzellen bei Antheraea pernyi (Lepidoptera, Saturniidae)
D. Schneider
,
V. Lacher
,
K. Kaissling
Zeitschrift für Vergleichende Physiologie
1964
Corpus ID: 34114978
Zusammenfassung1.Extrazelluläre Impulse einzelner olfaktorischer Sinnesnervenzellen lassen sich mit Wolfram-Mikroelektroden von…
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