. These authors contributed equally to this work. Wolfram syndrome (WFS) is inherited as an autosomal recessive disease with main clinical features of diabetes mellitus, optic atrophy, diabetes insipidus and deafness. However, various neurological defects may also be detected. The aim of this study was to evaluate aspects of brain structure and function using PET-CT (positron emission tomography and computed tomography) and MRI (magnetic resonance imaging) in pediatric patients with WFS. Regional changes in brain glucose metabolism were measured using standardized uptake values (SUVs) based on images of (18F) fluorodeoxyglucose (FDG) uptake in 7 WFS patients aged 10.1–16.0 years (mean 12.9¡2.4) and in 20 healthy children aged 3–17.9 years (...
is a progressive neurodegenerative disorder characterised by the association of juvenile, non-autoim...
Wolfram syndrome (WS) is a rare genetic disorder typically characterized by juvenile onset diabetes ...
BACKGROUND: Wolfram Syndrome (WS) is an autosomal recessive neurodegenerative disorder characterized...
Wolfram syndrome (WFS) is inherited as an autosomal recessive disease with main clinical features of...
<div><p>Wolfram syndrome (WFS) is inherited as an autosomal recessive disease with main clinical fea...
Wolfram Syndrome (WFS) is a rare autosomal recessive disease characterized by insulin-dependent diab...
Wolfram Syndrome (WFS) is a rare autosomal recessive disease characterized by insulin-dependent diab...
Neurofibromatosis-1 is an autosomal dominant genetic disorder commonly associated with neuropsycholo...
Abstract Wolfram syndrome is a rare disease caused by mutations in the WFS1 gene leading to symptoms...
SUMMARY: Wolfram syndrome is a rare autosomal recessive disorder featuring diabetes insipidus, diabe...
In this study, we examined whether topologic network analysis, using resting state functional magnet...
Wolfram Syndrome (WS) is a rare hereditary disease with autosomal recessive inheritance with incompl...
This article is freely available via Open Access. Click on the Publisher URL to access it via the pu...
MRI of brain findings of Wolfram (DIDMOAD) syndrome A 31-year-old woman was diagnosed with type 1 di...
Diabetes insipidus, diabetes mellitus, and optic atrophy (DIDMOAD) or Wolfram syndrome (WFS) is asso...
is a progressive neurodegenerative disorder characterised by the association of juvenile, non-autoim...
Wolfram syndrome (WS) is a rare genetic disorder typically characterized by juvenile onset diabetes ...
BACKGROUND: Wolfram Syndrome (WS) is an autosomal recessive neurodegenerative disorder characterized...
Wolfram syndrome (WFS) is inherited as an autosomal recessive disease with main clinical features of...
<div><p>Wolfram syndrome (WFS) is inherited as an autosomal recessive disease with main clinical fea...
Wolfram Syndrome (WFS) is a rare autosomal recessive disease characterized by insulin-dependent diab...
Wolfram Syndrome (WFS) is a rare autosomal recessive disease characterized by insulin-dependent diab...
Neurofibromatosis-1 is an autosomal dominant genetic disorder commonly associated with neuropsycholo...
Abstract Wolfram syndrome is a rare disease caused by mutations in the WFS1 gene leading to symptoms...
SUMMARY: Wolfram syndrome is a rare autosomal recessive disorder featuring diabetes insipidus, diabe...
In this study, we examined whether topologic network analysis, using resting state functional magnet...
Wolfram Syndrome (WS) is a rare hereditary disease with autosomal recessive inheritance with incompl...
This article is freely available via Open Access. Click on the Publisher URL to access it via the pu...
MRI of brain findings of Wolfram (DIDMOAD) syndrome A 31-year-old woman was diagnosed with type 1 di...
Diabetes insipidus, diabetes mellitus, and optic atrophy (DIDMOAD) or Wolfram syndrome (WFS) is asso...
is a progressive neurodegenerative disorder characterised by the association of juvenile, non-autoim...
Wolfram syndrome (WS) is a rare genetic disorder typically characterized by juvenile onset diabetes ...
BACKGROUND: Wolfram Syndrome (WS) is an autosomal recessive neurodegenerative disorder characterized...
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