C Ben Hamida - JoVE Visualize

Showing results (31-40 of 51) with videos related to

Pageof 6

Sort By:

Journal Des Maladies Vasculaires|November 18, 2005

[Celiac disease, cerebral venous thrombosis and protein S deficiency, a fortuitous association?]M Bahloul, A Chaari, N Khlaf-Bouaziz, et al.

Journal Des Maladies Vasculaires|January 5, 2007

[Traumatic unilateral renal artery thrombosis and protein C deficiency. A case report]M Bahloul, D Abid, H Ketata, et al.

Intensive Care Medicine|May 29, 2007

Safety and efficacy of colistin compared with imipenem in the treatment of ventilator-associated pneumonia: a matched case-control studyH Kallel, L Hergafi, M Bahloul, et al.

Human Molecular Genetics|September 1, 1995

Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mappingS Nicole, C Ben Hamida, P Beighton, et al.

American Journal of Human Genetics|May 1, 1995

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 familiesN Doerflinger, C Linder, K Ouahchi, et al.

Nephrologie|May 4, 2004

[Hemolytic-uremic syndrome secondary to scorpion envenomation (apropos of 2 cases)]M Bahloul, M Ben Hmida, W Belhoul, et al.

Neurology|August 1, 1994

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locusS Belal, G Cancel, G Stevanin, et al.

Nature Genetics|October 1, 1993

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mappingC Ben Hamida, N Doerflinger, S Belal, et al.

American Journal of Human Genetics|December 1, 1992

Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locusS Belal, K Panayides, G Sirugo, et al.

Neurology|November 1, 1993

Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian familiesM Ben Hamida, S Belal, G Sirugo, et al.

Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:

Pageof 6

Journal Des Maladies Vasculaires|November 18, 2005

[Celiac disease, cerebral venous thrombosis and protein S deficiency, a fortuitous association?]M Bahloul, A Chaari, N Khlaf-Bouaziz, et al.

Journal Des Maladies Vasculaires|January 5, 2007

[Traumatic unilateral renal artery thrombosis and protein C deficiency. A case report]M Bahloul, D Abid, H Ketata, et al.

Intensive Care Medicine|May 29, 2007

Safety and efficacy of colistin compared with imipenem in the treatment of ventilator-associated pneumonia: a matched case-control studyH Kallel, L Hergafi, M Bahloul, et al.

Human Molecular Genetics|September 1, 1995

Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mappingS Nicole, C Ben Hamida, P Beighton, et al.

American Journal of Human Genetics|May 1, 1995

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 familiesN Doerflinger, C Linder, K Ouahchi, et al.

Nephrologie|May 4, 2004

[Hemolytic-uremic syndrome secondary to scorpion envenomation (apropos of 2 cases)]M Bahloul, M Ben Hmida, W Belhoul, et al.

Neurology|August 1, 1994

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locusS Belal, G Cancel, G Stevanin, et al.

Nature Genetics|October 1, 1993

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mappingC Ben Hamida, N Doerflinger, S Belal, et al.

American Journal of Human Genetics|December 1, 1992

Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locusS Belal, K Panayides, G Sirugo, et al.

Neurology|November 1, 1993

Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian familiesM Ben Hamida, S Belal, G Sirugo, et al.

Pageof 6