Zobrazeno 1 - 10
of 244
pro vyhledávání: '"T, Chkili"'
Autor:
Reda Ouazzani, Stéphane Lehéricy, Simon Heath, Merle Ruberg, Mohamed Jiddane, Ahmed Bouhouche, Naima Khalili, T. Chkili, Fatiha Lahjouji, Philippe Couarch, Wafae Regragui, Stéphanie Baulac, Ali Benomar, Bouchra Ouled Amar Ben Cheikh, Mohamed Yahyaoui, Eric LeGuern
Publikováno v:
neurogenetics. 10:35-42
We describe the clinical, radiographic, and genetic features of a large consanguineous Moroccan family in which bilateral occipital polymicrogyria segregated as an autosomal recessive trait. Six affected members of the family had partial complex seiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eab04852268bfd699cda039f22715684
https://doi.org/10.1007/s10048-008-0143-3
https://doi.org/10.1007/s10048-008-0143-3
Publikováno v:
Scopus-Elsevier
Background:The gene encoding the ganglioside-induced-differentiation-associated protein 1 (GDAP1) has been associated with both axonal and demyelinating neuropathy. Up to date, 25 mutations in the GDAP1 gene have been reported in patients from differ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::276bc2dadd815a0d55bad9c3c789f180
https://doi.org/10.1017/s0317167100007290
https://doi.org/10.1017/s0317167100007290
Autor:
Saadia Aidi, T. Chkili, Mohamed Jiddane, M. El Alaoui Faris, M. Bennani, M. Benabdeljlil, M. Rahmani
Publikováno v:
Revue Neurologique. 162:1240-1247
Resume Introduction L’intoxication oxycarbonee est a l’origine de sequelles cognitives severes peu etudiees dans la litterature. Methodes Nous en rapportons 5 cas avec etude neuropsychologique et neuroradiologique par imagerie par resonance magne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3ec8fb0ad5faf868d8758fa470ca5ed
https://doi.org/10.1016/s0035-3787(06)75137-2
https://doi.org/10.1016/s0035-3787(06)75137-2
Publikováno v:
European Journal of Human Genetics. 14:249-252
Autosomal recessive ulcero-mutilating neuropathy with spastic paraplegia is a very rare disease since only few cases were described up to date. We report in this study a consanguineous Moroccan family with four affected males with this syndrome. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26ab8f2cc7a715fc685988b5a104b763
https://doi.org/10.1038/sj.ejhg.5201537
https://doi.org/10.1038/sj.ejhg.5201537
Autor:
T. Chkili, Leila Errguig, Mohammed Yahyaoui, O. Mouti, Wafaa Regragui, S. Serragui, A. Benomar
Publikováno v:
Eastern Mediterranean Health Journal. 11:470-477
Neurosyphilis accounts for 56%-70% of all visceral syphilis and is a complication in 5%-10% of cases of untreated syphilis. The aim of this study was to evaluate the epidemiological aspects and clinical presentations of neurosyphilis in Morocco throu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43910c4300c135ed98d0ac27017b2b8c
https://doi.org/10.26719/2005.11.3.470
https://doi.org/10.26719/2005.11.3.470
Autor:
Elhachmia Aitbenhaddou, B. Benaaboud, T. Chkili, Wafaa Regragui, Leila Errguig, Mohammed Yahyaoui, O. Mouti, Ali Benomar
Publikováno v:
Revue Neurologique. 160:1187-1190
Resume Introduction L’hypertension intracrânienne benigne (HTICB) est une urgence medicale et therapeutique dont le diagnostic repose sur les criteres modifies de Dandy. Les auteurs se proposent d’etudier le profil clinique et evolutif d’une s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b54462c78311ca3cdf64417a71769c58
https://doi.org/10.1016/s0035-3787(04)71164-9
https://doi.org/10.1016/s0035-3787(04)71164-9
Autor:
Reda Ouazzani, Ali Benomar, Ahmed Bouhouche, Naima Bouslam, T. Chkili, Mohammed Yahyaoui, N. Birouk
Publikováno v:
Journal of Neurology. 250:1209-1213
Spinal muscular atrophy (SMA) is an autosomal recessive motor neuropathy characterized by selective degeneration of anterior horn cells of the spinal cord. Childhood SMA is divided into three types (I-III) on the basis of age of onset and severity. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb2278f4c955fdb08b5f5dbb9889d442
https://doi.org/10.1007/s00415-003-0186-1
https://doi.org/10.1007/s00415-003-0186-1
Autor:
Eric LeGuern, T. Taïeb, N. Birouk, Hamid Azzedine, Alexis Brice, Ahmed Bouhouche, T. Chkili, M. Di Duca, T. Hammadouche, Jocelyn Laporte, Alessandra Bolino, S. Benamou, Roberto Ravazzolo, R. Gouider, Amel Mrabet
Publikováno v:
The American Journal of Human Genetics. 72(5):1141-1153
Charcot-Marie-Tooth disease (CMT) with autosomal recessive (AR) inheritance is a heterogeneous group of inherited motor and sensory neuropathies. In some families from Japan and Brazil, a demyelinating CMT, mainly characterized by the presence of mye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47bc2a38f7373620e55bbcf1f8fa75b6
Autor:
Ali Benomar, Saadia Aidi, T. Chkili, M. El Alaoui-Faris, O. Moutie, W. Bono, Mohamed Yahyaoui
Publikováno v:
La Revue de Médecine Interne. 23:419-431
Resume Propos. – La maladie de Wilson est caracterisee par des manifestations neuropsychiatriques dominees par l’atteinte extrapyramidale et intellectuelle. Elles sont d’evolution insidieuse, ce qui rend compte du retard diagnostique et du mauv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c173f9721a5fd631dcc20b9d69bded76
https://doi.org/10.1016/s0248-8663(02)00589-1
https://doi.org/10.1016/s0248-8663(02)00589-1
Publikováno v:
Neurophysiologie Clinique/Clinical Neurophysiology. 31:398-405
Resume La panencephalite sclerosante subaigue (PESS) est une affection de moins en moins observee au Maroc, du fait de la generalisation de la vaccination antirougeoleuse depuis 1982. Parmi les manifestations neurologiques de la PESS, l’epilepsie n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::898e278aa7596127d81130934f2f8bae
https://doi.org/10.1016/s0987-7053(01)00278-7
https://doi.org/10.1016/s0987-7053(01)00278-7