Zobrazeno 1 - 10
of 432
pro vyhledávání: '"I. Rapin"'
Publikováno v:
European Journal of Neurology. 9:663-670
Pigmentary type of orthochromatic leukodystrophy (POLD) is an adult-onset leukodystrophy, characterized pathologically by the presence of glial and microglial cytoplasmic pigment inclusions. The complete phenotype, genotype and pathogenetic mechanism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af16d2979113a338edfd890a4050cacc
https://doi.org/10.1046/j.1468-1331.2002.00469.x
https://doi.org/10.1046/j.1468-1331.2002.00469.x
Autor:
I, Rapin
Publikováno v:
New England Journal of Medicine. 337:97-104
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97fcc2cad948383712f46558d32898f1
https://doi.org/10.1056/nejm199707103370206
https://doi.org/10.1056/nejm199707103370206
Autor:
I Rapin
Publikováno v:
Archives de Pédiatrie. 3:S57-S60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::852a33547dbee6811b98fd15bcd9b2bd
https://doi.org/10.1016/0929-693x(96)85994-x
https://doi.org/10.1016/0929-693x(96)85994-x
Publikováno v:
European Journal of Neurology. 2:151-162
Autism is a behaviorally defined developmental disorder of the brain almost always presenting in infancy or the preschool years. Its symptoms persist life-long, although partial compensation is possible through targeted special education that address
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f746eff38bc1b2e8f4b3d2e2ea8e804
https://doi.org/10.1111/j.1468-1331.1995.tb00110.x
https://doi.org/10.1111/j.1468-1331.1995.tb00110.x
Autor:
I, Rapin
Publikováno v:
Pediatrics in Review. 14:43-49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cc317de9834ca10d08993c03e59ff3d
https://doi.org/10.1542/pir.14-2-43
https://doi.org/10.1542/pir.14-2-43
Publikováno v:
Pediatrics. 88:1211-1218
Autism and dysphasia are behaviorally defined disorders of higher cerebral function which in preschool children share the common core symptom of impairment of language. In this study we describe the clinical characteristics of 314 autistic and 237 dy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38eaf5f9056c3e73df45788ba3661a68
https://doi.org/10.1542/peds.88.6.1211
https://doi.org/10.1542/peds.88.6.1211
Autor:
I. Rapin
Publikováno v:
Neuropediatrics. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32ef4f7eed184fb5c087d22657811fd2
https://doi.org/10.1055/s-2006-946006
https://doi.org/10.1055/s-2006-946006
Publikováno v:
Revista de neurologia. 40
Neurodevelopmental disorders and the epilepsies share common etiologies and pathologies. The severity of impairment and the variety of symptoms associated with neurodevelopmental disorders or with particular epilepsy syndromes reflect focal or global
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b71b97106371942cbc3b4e597ae82fd8
https://pubmed.ncbi.nlm.nih.gov/15736089
https://pubmed.ncbi.nlm.nih.gov/15736089
Autor:
I, Rapin
Publikováno v:
Advances in neurology. 85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::309da7e9965d0fd65e1a411e21055db9
https://pubmed.ncbi.nlm.nih.gov/11530449
https://pubmed.ncbi.nlm.nih.gov/11530449