Nadifi S - Search Results

1

Genetic Aspects of Myoclonus-Dystonia Syndrome (MDS).

Rachad L, El Kadmiri N, Slassi I, El Otmani H, Nadifi S. Rachad L, et al. Among authors: nadifi s. Mol Neurobiol. 2017 Mar;54(2):939-942. doi: 10.1007/s12035-016-9712-x. Epub 2016 Jan 20. Mol Neurobiol. 2017. PMID: 26790671 Review.

2

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. 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

3

[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: nadifi s. 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.

4

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: nadifi s. 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.

5

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: nadifi s. J Biomed Biotechnol. 2009;2009:325210. doi: 10.1155/2009/325210. Epub 2009 May 19. J Biomed Biotechnol. 2009. PMID: 19461958 Free PMC article.

6

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: nadifi s. Neurol India. 2010 Jan-Feb;58(1):99-102. doi: 10.4103/0028-3886.60411. Neurol India. 2010. PMID: 20228473 Free article.

7

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

They-They TP, Nadifi S, Rafai MA, Battas O, Slassi I. They-They TP, et al. Among authors: nadifi s. Acta Neurol Scand. 2011 Feb;123(2):105-10. doi: 10.1111/j.1600-0404.2010.01348.x. Acta Neurol Scand. 2011. PMID: 20637011

8

Prothrombin G20210A and factor V Leiden polymorphisms in stroke.

They-They TP, Battas O, Slassi I, Rafai MA, Katumbay DT, Nadifi S. They-They TP, et al. Among authors: nadifi s. J Mol Neurosci. 2012 Jan;46(1):210-6. doi: 10.1007/s12031-011-9580-9. Epub 2011 Jun 24. J Mol Neurosci. 2012. PMID: 21701789

9

Sickle cell disease with double stroke in a Moroccan family.

Hamzi K, Itto AB, Jouhadi Z, Slassi I, Nadifi S. Hamzi K, et al. Among authors: nadifi s. J Mol Neurosci. 2013 Jun;50(2):311-3. doi: 10.1007/s12031-013-9967-x. Epub 2013 Jan 23. J Mol Neurosci. 2013. PMID: 23340961

10

Evolution of molecular diagnosis of Duchenne muscular dystrophy.

Itto AB, Hamzi K, Bellayou H, Itri M, Slassi I, Nadifi S. Itto AB, et al. Among authors: nadifi s. J Mol Neurosci. 2013 Jun;50(2):314-6. doi: 10.1007/s12031-013-9971-1. Epub 2013 Feb 5. J Mol Neurosci. 2013. PMID: 23381834

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