Slassi I - Search Results

1

Novel mutations in the amyloid precursor protein gene within Moroccan patients with Alzheimer's disease.

El Kadmiri N, Zaid N, Hachem A, Zaid Y, Dubé MP, Hamzi K, El Moutawakil B, Slassi I, Nadifi S. El Kadmiri N, et al. Among authors: slassi i. J Mol Neurosci. 2014 Jun;53(2):189-95. doi: 10.1007/s12031-014-0278-7. Epub 2014 Mar 14. J Mol Neurosci. 2014. PMID: 24627227

2

[Crohn's disease presenting with recurrent acute polyradiculoneuropathy].

El Moutawakil B, Rafai MA, Gam I, Tahiri JM, Rhimou A, Slassi I. El Moutawakil B, et al. Among authors: slassi i. Rev Neurol (Paris). 2007 Feb;163(2):244-6. doi: 10.1016/s0035-3787(07)90398-7. Rev Neurol (Paris). 2007. PMID: 17351546 French.

3

[Postoperative dementia: toxicity of nitrous oxide].

El Otmani H, El Moutawakil B, Moutaouakil F, Gam I, Rafai MA, Slassi I. El Otmani H, et al. Among authors: slassi i. Encephale. 2007 Jan-Feb;33(1):95-7. doi: 10.1016/s0013-7006(07)91563-8. Encephale. 2007. PMID: 17457299 French.

4

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

Nadifi S, Slassi I, Hachimi KM, Gazzaz B, Bellayou H, Raddaoui K, Laplanche JL. Nadifi S, et al. Among authors: slassi i. Pathol Biol (Paris). 2008 May;56(3):133-6. doi: 10.1016/j.patbio.2007.08.011. Epub 2008 Jan 9. Pathol Biol (Paris). 2008. PMID: 18191917

5

[Phenotype-genotype correspondence in spinal muscular atrophy in a Moroccan family].

They-They TP, Nadifi S, Dehbi H, Bellayou H, Brik H, Slassi I, Itri M. They-They TP, et al. Among authors: slassi i. Arch Pediatr. 2008 Jul;15(7):1201-5. doi: 10.1016/j.arcped.2008.04.015. Epub 2008 Jun 5. Arch Pediatr. 2008. PMID: 18538551 French.

6

[Granulocytic sarcoma of the brain revealed on vascular mode].

Moudden M, El Moutawakil B, Boulajaj FZ, Slassi I, Azhari A. Moudden M, et al. Among authors: slassi i. Rev Neurol (Paris). 2008 Jun-Jul;164(6-7):620-3. doi: 10.1016/j.neurol.2007.12.006. Epub 2008 May 23. Rev Neurol (Paris). 2008. PMID: 18565363 French.

7

[Neurological manifestations of chronic inflammatory bowel disease].

Sibai M, El Moutawakil B, Chourkani N, Bourezgui M, Rafai MA, Slassi I. Sibai M, et al. Among authors: slassi i. Rev Neurol (Paris). 2008 Oct;164(10):859-65. doi: 10.1016/j.neurol.2008.03.001. Epub 2008 May 2. Rev Neurol (Paris). 2008. PMID: 18926245 French.

8

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

Bellayou H, Dehbi H, Bourezgui M, Slassi I, Nadifi S. Bellayou H, et al. Among authors: slassi i. Pathol Biol (Paris). 2009 Jul;57(5):425-6. doi: 10.1016/j.patbio.2008.09.014. Epub 2008 Nov 26. Pathol Biol (Paris). 2009. PMID: 19038506 No abstract available.

9

Duchenne and Becker muscular dystrophy: contribution of a molecular and immunohistochemical analysis in diagnosis in Morocco.

Bellayou H, Hamzi K, Rafai MA, Karkouri M, Slassi I, Azeddoug H, Nadifi S. Bellayou H, et al. Among authors: slassi i. J Biomed Biotechnol. 2009;2009:325210. doi: 10.1155/2009/325210. Epub 2009 May 19. J Biomed Biotechnol. 2009. PMID: 19461958 Free PMC article.

10

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

Hamzi K, Bellayou H, Slassi I, Nadifi S. Hamzi K, et al. Among authors: slassi i. Neurol India. 2010 Jan-Feb;58(1):99-102. doi: 10.4103/0028-3886.60411. Neurol India. 2010. PMID: 20228473 Free article.

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