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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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M F Ben Dridi

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La Revue De Medecine Interne|January 28, 2004

[Gaucher's disease in Tunisia (multicenter study)]M Chaabouni, H Aoulou, N Tebib, et al.

Archives De L'Institut Pasteur De Tunis|April 25, 2009

[Mutation spectrum of Gaucher disease in Tunisia: high frequency of N370S/Rec NciI compound heterozygous]W Cherif, H Ben Turkia, N Tebib, et al.

Pathologie-Biologie|May 1, 2012

[Molecular diagnosis of Gaucher disease in Tunisia]W Cherif, H Ben Turkia, F Ben Rhouma, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 14, 2011

[Rosai-Dorfman disease: therapeutic issues in 2 cases]H Ben Turkia, M Ben Romdhane, H Azzouz, et al.

Journal of Inherited Metabolic Disease|November 17, 2007

Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosisE Barkaoui, W Cherif, N Tebib, et al.

Molecular Genetics and Metabolism|April 1, 2006

Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutationsC Charfeddine, K Monastiri, M Mokni, et al.

Pageof 3

Search research articles

Showing results (21-30 of 26) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 26 results.

La Revue De Medecine Interne|January 28, 2004

[Gaucher's disease in Tunisia (multicenter study)]M Chaabouni, H Aoulou, N Tebib, et al.

Archives De L'Institut Pasteur De Tunis|April 25, 2009

[Mutation spectrum of Gaucher disease in Tunisia: high frequency of N370S/Rec NciI compound heterozygous]W Cherif, H Ben Turkia, N Tebib, et al.

Pathologie-Biologie|May 1, 2012

[Molecular diagnosis of Gaucher disease in Tunisia]W Cherif, H Ben Turkia, F Ben Rhouma, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 14, 2011

[Rosai-Dorfman disease: therapeutic issues in 2 cases]H Ben Turkia, M Ben Romdhane, H Azzouz, et al.

Journal of Inherited Metabolic Disease|November 17, 2007

Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosisE Barkaoui, W Cherif, N Tebib, et al.

Molecular Genetics and Metabolism|April 1, 2006

Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutationsC Charfeddine, K Monastiri, M Mokni, et al.

Pageof 3