Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Olivier Robain"'
Autor:
Francoise Fouquet, Jia Min Zhou, Evelyn Ralston, Kerren Murray, Frédéric Troalen, Ella Magal, Olivier Robain, M. Dubois-Dalcq, Patrick Aubourg
Publikováno v:
Neurobiology of Disease, Vol 3, Iss 4, Pp 271-285 (1997)
The gene mutated in X-linked adrenoleukodystrophy (ALD), a progressive demyelinating disease, codes for a protein (ALDP) involved in very-long-chain fatty acid (VLCFA) transport. The expression of ALDP and of two peroxisomal enzymes involved in β-ox
Externí odkaz:
https://doaj.org/article/86226d97e6cb4bc894b6577f32e9a5fe
Publikováno v:
Developmental Medicine & Child Neurology. 17:787-792
SUMMARY An isolated peripheral nerve palsy is reported in three members of the same family. In the two children, aged eight years and four years, a lesion of the lateral popliteal nerve resulted in foot-drop. In both cases there was progressive recov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15567df16aacaa8b5f82388c15136cb7
https://doi.org/10.1111/j.1469-8749.1975.tb04704.x
https://doi.org/10.1111/j.1469-8749.1975.tb04704.x
Autor:
Alessandra Battaglia, Marie-Odile Livet, Danielle Gambarelli, Charles Raybaud, Renzo Guerrini, Joseph Roger, Michelle Bureau, Olivier Robain, Charlotte Dravet
Publikováno v:
Developmental Medicine & Child Neurology. 34:706-718
The authors studied 10 patients (mean age 15 years 6 months) with localized developmental gyral disorder detected by MRI. There were two groups of major malformations. Seven patients (group 1) had unilateral 'macrogyric-like' insulo-opercular changes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fd2338e0b937fe5e822a377a97eabac
https://doi.org/10.1111/j.1469-8749.1992.tb11506.x
https://doi.org/10.1111/j.1469-8749.1992.tb11506.x
Publikováno v:
Pediatric neurosurgery. 27(5)
We report a case with hemimegalencephaly and catastrophic epilepsy treated early at 4 months by functional hemispherectomy. The boy had intractable continuous epilepsy, with seizures every 10 min, hemiparesis and absence of psychomotor acquisition. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d5803076d390321577be9f968fa720d
https://pubmed.ncbi.nlm.nih.gov/9620005
https://pubmed.ncbi.nlm.nih.gov/9620005
Autor:
Olivier Robain, Joseph Roger, Marie-Odile Livet, Gabriella Colicchio, Michelle Bureau, Renzo Guerrini, Charles Raybaud, Agatino Battaglia, Charlotte Dravet
Publikováno v:
Developmental medicine and child neurology. 34(8)
SUMMARY The authors studied 10 patients aged between six and 23 years (mean age 14 years 5 months) with magnetic resonance imaging, which detected bilateral ‘macrogyric-like’ maldevelopment of the insulo-opercular regions. The data confirm that b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc275b56a422926b1d51c6f5b813dd7c
https://pubmed.ncbi.nlm.nih.gov/1644232
https://pubmed.ncbi.nlm.nih.gov/1644232
Publikováno v:
The Japanese journal of psychiatry and neurology. 40(2)
Several cases of human herpes simplex encephalitis treated with Vidarabin have been investigated with the histological and immunocytochemical techniques. Cases with a subacute evolution revealed areas of focal perivascular myelin destruction in the w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daae1c7acb4990f142c0e1b7a298de11
https://pubmed.ncbi.nlm.nih.gov/3023729
https://pubmed.ncbi.nlm.nih.gov/3023729