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Global brain atrophy
Known as:
Generalized brain atrophy
, Generalized cerebral atrophy
, Diffuse brain atrophy
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Unlocalized atrophy of the brain with decreased total brain matter volume and increased ventricular size. [HPO:sdoelken]
National Institutes of Health
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Related topics
Related topics
11 relations
Narrower (1)
Alzheimer's Disease
Amish Infantile Epilepsy Syndrome
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2
Cerebral atrophy
Combined Oxidative Phosphorylation Deficiency 1
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Brain atrophy and white matter hyperintensities in early Parkinson's disease
Turi O. Dalaker
,
J. Larsen
,
+8 authors
R. Zivadinov
Movement Disorders
2009
Corpus ID: 27631592
The purpose of this research was to examine the extent of global brain atrophy and white matter hyperintensities (WMH) in early…
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2009
2009
“Hot Cross Bun” Sign in Variant Creutzfeldt-Jakob Disease
J. Soares-Fernandes
,
M. Ribeiro
,
Á. Machado
American Journal of Neuroradiology
2009
Corpus ID: 30850623
The “hot cross bun” sign refers to pontine cruciform hyperintensity on long TR sequences, which can be observed in multiple…
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2008
2008
Acute encephalitis with refractory, repetitive partial seizures
Ching-Shan Shyu
,
Hsiu-Fen Lee
,
C. Chi
,
Chao-Huei Chen
Brain & development (Tokyo. )
2008
Corpus ID: 8735917
2005
2005
CDG‐IL: An infant with a novel mutation in the ALG9 gene and additional phenotypic features
M. Weinstein
,
E. Schollen
,
+9 authors
N. Poplawski
American Journal of Medical Genetics. Part A
2005
Corpus ID: 28069253
We describe the second case of congenital disorder of glycosylation type IL (CDG‐IL) caused by deficiency of the ALG9 a1,2…
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Review
2004
Review
2004
Pathogenesis of Brain and Spinal Cord Atrophy in Multiple Sclerosis
A. Minagar
,
E. G. Toledo
,
J. S. Alexander
,
R. Kelley
Journal of Neuroimaging
2004
Corpus ID: 24605664
For more than a century, multiple sclerosis was viewed as a disease process characterized by oligodendrocyte and myelin loss, and…
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2001
2001
Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA
L. Lien
,
H. Lee
,
K-L. Wang
,
J.‐C. Chiu
,
Hui-Ching Chiu
,
Y. Wei
Acta Neurologica Scandinavica
2001
Corpus ID: 3230019
Objectives – The A3243G mutation of mitochondrial DNA (mtDNA) has been associated with maternally inherited diabetes and deafness…
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Review
1997
Review
1997
RETT SYNDROME: NEUROBIOLOGICAL CHANGES UNDERLYING SPECIFIC SYMPTOMS
G. Wenk
Progress in neurobiology
1997
Corpus ID: 25083805
1994
1994
Familial progressive subcortical gliosis
D. Lanska
,
R. Currier
,
+6 authors
W. Markesbery
Neurology
1994
Corpus ID: 10311605
We report clinical and pathologic findings from two kindreds afflicted with a familial form of progressive subcortical gliosis…
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1993
1993
Neuropsychiatric and brain CT findings in polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
H. Hakola
,
M. Puranen
Acta Neurologica Scandinavica
1993
Corpus ID: 37099380
Seven patients with polycystic lipomembranous osteodysplasia and sclerosing leukoencephalopathy (PLO‐SL or membranous…
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Review
1992
Review
1992
Neurodevelopmental outcome in neonates after extracorporeal membrane oxygenation: cranial magnetic resonance imaging and ultrasonography correlation.
M. P. Griffin
,
P. Minifee
,
S. Landry
,
P. L. Allison
,
L. Swischuk
,
J. Zwischenberger
Journal of Pediatric Surgery
1992
Corpus ID: 25100580
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