Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the …
AA Raymond, DR Fish, SM Sisodiya, N Alsanjari… - Brain, 1995 - academic.oup.com
Cerebral cortical dysgenesis (CD) is a heterogeneous disorder of cortical development and
organization commonly associated with epilepsy, with a variety of subtypes. We reviewed …
organization commonly associated with epilepsy, with a variety of subtypes. We reviewed …
Two distinct forms of minor neurological dysfunction: perspectives emerging from a review of data of the Groningen Perinatal Project
M Hadders-Algra - Developmental medicine and child neurology, 2002 - cambridge.org
In the past 40 years, children with minor developmental motor disorders have been studied
by professionals from various fields: paediatricians, neurologists, psychiatrists …
by professionals from various fields: paediatricians, neurologists, psychiatrists …
[BOOK][B] Pediatric neuroimaging
AJ Barkovich - 2005 - books.google.com
The thoroughly updated Fourth Edition of this acclaimed reference describes and illustrates
the full range of pediatric disorders diagnosable by modern neuroimaging. This edition …
the full range of pediatric disorders diagnosable by modern neuroimaging. This edition …
[BOOK][B] Cerebral palsies: epidemiology and causal pathways
FJ Stanley, E Blair, E Alberman, ED Alberman - 2000 - books.google.com
This is a clinical text about the commonest physical disability-the cerebral palsies. It follows
up on the authors' earlier work The Epidemiology of the Cerebral Palsies, and its focus is still …
up on the authors' earlier work The Epidemiology of the Cerebral Palsies, and its focus is still …
Classification system for malformations of cortical development: update 2001
The many recent discoveries concerning the molecular biologic bases of malformations of
cortical development and the discovery of new such malformations have rendered previous …
cortical development and the discovery of new such malformations have rendered previous …
[BOOK][B] Pediatric neuro-ophthalmology
MC Brodsky, RS Baker, LM Hamed, JT Flynn - 2010 - Springer
" Due to the generous representation of the afferent visual system within the brain,
neurological disease may disrupt vision as a presenting symptom or as a secondary effect of …
neurological disease may disrupt vision as a presenting symptom or as a secondary effect of …
Congenital cytomegalovirus infection of the brain: imaging analysis and embryologic considerations.
AJ Barkovich, CE Lindan - American journal of …, 1994 - Am Soc Neuroradiology
PURPOSE To analyze the cortical gyral patterns and myelination patterns in a series of
patients with congenital cytomegalovirus infections involving the central nervous system, to …
patients with congenital cytomegalovirus infections involving the central nervous system, to …
Cortical visual impairment in children
WV Good, JE Jan, L DeSa, AJ Barkovich… - Survey of …, 1994 - Elsevier
Cortical visual impairment (CVI) in children is most commonly caused by peri-or postnatal
hypoxia-ischemia, but may also occur following other insults, eg, trauma, epilepsy …
hypoxia-ischemia, but may also occur following other insults, eg, trauma, epilepsy …
Periventricular and subcortical nodular heterotopia A study of 33 patients
F Dubeau, D Tampieri, N Lee, E Andermann… - Brain, 1995 - academic.oup.com
Grey matter heterotopias, demonstrated by MRI, may present with a broad spectrum of
clinical severity. We have studied 33 patients with periventricular nodular heterotopias …
clinical severity. We have studied 33 patients with periventricular nodular heterotopias …
Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain
M Abitbol, C Menini, AL Delezoide, T Rhyner… - Nature …, 1993 - nature.com
The expression of the FMR–1 gene, which is implicated in fragile–X syndrome was
investigated in human fetuses by in situ hybridization. In 8 and 9 week–old fetuses, FMR–1 …
investigated in human fetuses by in situ hybridization. In 8 and 9 week–old fetuses, FMR–1 …