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Pachygyria
Known as:
Macrogyrias
, Cerebral pachygyria
, Broad Gyri of Cerebrum
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A congenital abnormality of the cerebral hemisphere chacterized by unusually thick gyrations (convolutions) of the cerebral cortex. [HPO:curators]
National Institutes of Health
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Related topics
Related topics
27 relations
Adams Oliver syndrome
Aicardi's syndrome
CK SYNDROME
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11
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Narrower (1)
Pachygyria, frontotemporal
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2001
Review
2001
Seckel's Syndrome and Malformations of Cortical Development: Report of Three New Cases and Review of the Literature
G. Capovilla
,
Maria Elena Lorenzetti
,
+5 authors
R. Caudana
Journal of Child Neurology
2001
Corpus ID: 27559606
Seckel's syndrome is a rare form of primordial dwarfism, characterized by peculiar facial appearance. In the past, this condition…
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Review
1999
Review
1999
Neuronal migration disorders in humans and in mouse models—an overview
A. Copp
,
B. Harding
Epilepsy Research
1999
Corpus ID: 13760408
1995
1995
Ocular findings in muscle-eye-brain (MEB) disease: a follow-up study
H. Pihko
,
M. Lappi
,
+4 authors
P. Santavuori
Brain & development (Tokyo. )
1995
Corpus ID: 33926340
1995
1995
Posterior agyria-pachygyria with polymicrogyria
C. Ferrie
,
G. Jackson
,
S. Giannakodimos
,
C. Panayiotopoulos
Neurology
1995
Corpus ID: 331130
Article abstract-We describe two brothers with mental retardation and refractory epilepsy. MRI revealed symmetrical agyria…
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1992
1992
Unilateral Opercular Macrogyria and Benign Childhood Epilepsy with Centrotemporal (Rolandic) Spikes: Report of a Case
G. Ambrosetto
Epilepsia
1992
Corpus ID: 21038724
Summary: An 18‐year‐old mentally normal epileptic boy had frequent left brachiofacial or unilateral motor seizures which started…
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1992
1992
Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal β-oxidation
L. Maldergem
,
M. Espeel
,
+6 authors
Y. Gillerot
Neuromuscular Disorders
1992
Corpus ID: 24985761
1992
1992
Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome.
J. F. Arena
,
C. Schwartz
,
+7 authors
J. Ott
American journal of medical genetics
1992
Corpus ID: 38101199
We report on a family with X-linked mental retardation (XLMR) and severe spastic paraplegia. Appearance is normal but there is…
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1992
1992
Clinical variation within sibships in Fukuyama-type congenital muscular dystrophy
M. Yoshioka
,
S. Kuroki
,
H. Nigami
,
T. Kawai
,
Hajime Nakamura
Brain & development (Tokyo. )
1992
Corpus ID: 4765888
1990
1990
Visual and auditory evoked potential correlates of cerebral malformations
S. Coupland
,
H. Sarnat
Brain & development (Tokyo. )
1990
Corpus ID: 4704794
1979
1979
Glycogen accumulation in the central nervous system in the cerebro-hepato-renal syndrome Report of a case with ultrastructural studies
D. Agamanolis
,
Subashini Patre
Journal of Neurological Sciences
1979
Corpus ID: 30729621
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