Search Results - "Slassi I"

Methylenehydrofolate reductase (C677T) polymorphism and large artery ischemic stroke subtypes.

Authors: They-They, T. P. Nadifi, S. Rafai, M. A. et al.

Source: Acta Neurologica Scandinavica. Feb2011, Vol. 123 Issue 2, p105-110. 6p.

Subjects: Genetic polymorphisms, Arterial diseases, Cerebrovascular disease risk factors, Case-control method, Gene frequency

Geographic Terms: Casablanca (Morocco), Morocco

Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and Alzheimer's disease.

Authors: El Kadmiri, N. Slassi, I. El Moutawakil, B. et al.

Source: Pathologie Biologie. Dec2014, Vol. 62 Issue 6, p333-336. 4p.

The normal distribution of PRNP codon 129 polymorphism in the Moroccan population (Arabs and Casablanca residents)

Alternate Title: Génotypage et distribution du polymorphisme du codon 129 du gène du prion (PRNP) dans un échantillon de la population marocaine (Arabe, Casablancais et Berbère)

Authors: Nadifi, S. Slassi, I. Hachimi, K.M. El et al.

Source: Pathologie Biologie. May2008, Vol. 56 Issue 3, p133-136. 4p.

A rapid polymerase chain reaction-based test for screening Steinert's disease (DM1)

Authors: Hamzi K Bellayou H Slassi I et al.

Source: Neurology India. Jan2010, Vol. 58 Issue 1, p99-102. 4p.

Clinical and genetic aspects of Moroccan patients with Alzheimer's disease.

Authors: El Kadmiri, N. El Moutawakil, B. Slassi, I. et al.

Source: Journal of the Neurological Sciences. Oct2013, Vol. 333, pe323-e323. 1p.

Novel presenilin mutations within Moroccan patients with Early-Onset Alzheimer’s Disease.

Authors: El Kadmiri, N. Zaid, N. Zaid, Y. et al.

Source: Neuroscience. Jun2014, Vol. 269, p215-222. 8p.

Les aspects génétiques de la maladie d’Alzheimer (Revue).

Alternate Title: Genetic aspects of Alzheimer's disease (Review)

Authors: El Kadmiri, N. Hamzi, K. El Moutawakil, B. et al.

Source: Pathologie Biologie. Dec2013, Vol. 61 Issue 6, p228-238. 11p.

Place des bolus de méthylprednisolone dans le traitement des polyradiculonévrites chroniques de l’enfant

Alternate Title: Methylprednisolone pulse in treatment of childhood chronic inflammatory demyelinating polyneuropathy

Authors: Rafai, M.A. Boulaajaj, F.Z. Sekkat, Z. et al.

Source: Archives de Pédiatrie. Sep2010, Vol. 17 Issue 9, p1293-1299. 7p.

Neurological manifestations revealing primitive Gougerot-Sjogren syndrome: 9 cases.

Authors: Rafai MA Boulaajaj FZ Moutawakil F et al.

Source: Joint Bone Spine. Mar2009, Vol. 76 Issue 2, p139-145. 7p.

Syndrome de Sjögren-Larsson en rapport avec une nouvelle mutation chez un enfant marocain

Alternate Title: Sjögren-larsson syndrome: A novel mutation in a Moroccan child

Authors: Rafai, M.A. Boulaajaj, F.Z. Seito, A. et al.

Source: Archives de Pédiatrie. Nov2008, Vol. 15 Issue 11, p1648-1651. 4p.

Étude de la corrélation génotype–phénotype dans l’amyotrophie spinale infantile (ASI) dans une famille marocaine

Alternate Title: Phenotype–genotype correspondance in spinal muscular atrophy in a moroccan family

Authors: They-They, T.P. Nadifi, S. Dehbi, H. et al.

Source: Archives de Pédiatrie. Jul2008, Vol. 15 Issue 7, p1201-1205. 5p.

Botulisme alimentaire chez l'enfant au Maroc: à propos de 5 cas

Alternate Title: Food-born botulism in infants in Morocco: apropos of 5 cases

Authors: Kissani, N. Najib, J. Amine, M. et al.

Source: Archives de Pédiatrie. Nov2007, Vol. 14 Issue 11, p1324-1327. 4p.

Aspects cliniques et électrophysiologiques de l’intoxication aiguë aux organophosphorés

Alternate Title: Clinical and electrophysiological aspects of acute organophosphate intoxication

Authors: Rafai, M.A. Boulaajaj, F.Z. Bourezgui, M. et al.

Source: Clinical Neurophysiology / Neurophysiologie Clinique. Jan2007, Vol. 37 Issue 1, p35-39. 5p.

Syncopes gélastiques récurrentes

Alternate Title: Recurrent gelastic syncopes

Authors: El Otmani, H. Moutaouakil, F. Fadel, H. et al.

Source: Revue de Médecine Interne. Sep2012, Vol. 33 Issue 9, p522-524. 3p.

Ataxia with vitamin E deficiency (AVED); an example of the contribution of research in molecular genetic to counselling in Morocco

Alternate Title: L’ataxie par hypovitaminose E ; un exemple de recherche moléculaire dans le conseil génétique

Authors: Bellayou, H. Dehbi, H. Bourezgui, M. et al.

Source: Pathologie Biologie. Jul2009, Vol. 57 Issue 5, p425-426. 2p.

Fatal paraneoplasic encephalo-myelo-neuropathy associated with anti-Hu antibodies: a case report.

Authors: Habtany, Y. Rafaii, M.A. Mouni, F.Z. et al.

Source: Journal of the Neurological Sciences. Oct2015 Supplement 1, Vol. 357, pe199-e200. 1p.

Characteristics of the posterior reversible encephalopathy syndome in a cohort of 1130 eclamptic patients.

Authors: Bennis, A. El Otmani, H. Moussaid, I. et al.

Source: Journal of the Neurological Sciences. Oct2015 Supplement 1, Vol. 357, pe324-e325. 1p.

Stroke risk factors in a Moroccan population: a multicentric prospective study.

Authors: Benkirane, N. Bennis, A. Bellakhdar, S. et al.

Source: Journal of the Neurological Sciences. Oct2015 Supplement 1, Vol. 357, pe367-e367. 1p.

How to use verbal autopsy to study stroke incidence in developing countries.

Authors: Aidi, S. Bellamine, S. Yahyaoui, M. et al.

Source: Journal of the Neurological Sciences. Oct2013, Vol. 333, pe190-e191. 0p.

Syndrome de Goujerot-Sjögren primitif et neuromyélite optique de Devic

Alternate Title: Primary Sjögren's syndrome and neuromyelitis optica

Authors: Chourkani, N. El Moutawakil, B. Sibai, M. et al.

Source: Revue de Médecine Interne. Sep2010, Vol. 31 Issue 9, pe13-e15. 0p.