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Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
Charcot-Marie-Tooth disease is a genetically heterogeneous group of hereditary motor and sensory neuropathies. Three loci for the axonal autosomal recessive subgroup (ARCMT2) have been reported inExpand
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[Cobalamin deficiency: neurological aspects in 27 cases].
INTRODUCTION Combined medullar sclerosis, together with peripheral sensory neuropathies, is the most common neurological manifestation observed in cobalamin deficiency. Biermer's disease is theExpand
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[Postoperative dementia: toxicity of nitrous oxide].
INTRODUCTION Post-operative neuropsychiatric manifestations represent a frequent situation and may be due to several aetiologies. The responsibility of vitamin B12 deficiency must be evoked,Expand
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A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report
BackgroundX-linked adrenoleukodystrophy (X-ALD; OMIM: 300100) is the most common peroxisomal disease caused by mutations in the ATP-binding cassette, sub-family D member 1 gene or ABCD1 (geneID:Expand
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Les aspects génétiques de la maladie d’Alzheimer (Revue)
Resume La maladie d’Alzheimer est une affection degenerative du cerveau qui associe des troubles de la memoire, troubles cognitifs et ou des troubles comportementales. Cette demence dont l’etiologieExpand
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Biomarkers for Alzheimer Disease: Classical and Novel Candidates’ Review
The biomarkers may be useful for predictive diagnosis of Alzheimer's disease (AD). The current challenge is to diagnose it in its preclinical phase. The combination of cerebrospinal fluid (CSF)Expand
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Neurological manifestations revealing primitive Gougerot-Sjogren syndrome: 9 cases.
INTRODUCTION Neurological manifestations in Gougerot-Sjogren syndrome (GSS) are valued differently. This is essentially the achievement of the peripheral nervous system. METHODS We report 9 casesExpand
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Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and Alzheimer's disease.
Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a ubiquitous enzyme that catalyzes the sixth step of glycolysis and thus, serves to break down glucose for energy production. Beyond theExpand
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Genetic Aspects of Myoclonus–Dystonia Syndrome (MDS)
Myoclonus–dystonia (M–D) is an autosomal-dominant movement disorder with onset in the first two decades of life. Mutations in the epsilon-sarcoglycan gene (SGCE, DYT11) on chromosome 7q21–q31Expand
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Methylenehydrofolate reductase (C677T) polymorphism and large artery ischemic stroke subtypes
They‐They TP, Nadifi S, Rafai MA, Battas O, Slassi I. Methylenehydrofolate reductase (C677T) polymorphism and large artery ischemic stroke subtypes.
Acta Neurol Scand: 2011: 123: 105–110.
© 2010 JohnExpand
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