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M Ben Hamida

Showing results (61-70 of 112) with videos related to

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Neuromuscular Disorders : NMD|January 1, 1992
Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosumF Hentati, C Ben Hamida, M Zeghal, et al.
Brain Research|March 20, 1999
Localization of alpha-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disordersR P Copp, T Wisniewski, F Hentati, et al.
European Journal of Cancer & Clinical Oncology|October 1, 1987
Pyrimidine pathways enzymes in human tumors of brain and associated tissues: potentialities for the therapeutic use of N-(phosphonacetyl-L-aspartate and 1-beta-D-arabinofuranosylcytosineS Madani, J Baillon, J Fries, et al.
Archives Francaises De Pediatrie|December 1, 1992
[Antenatal bilateral sylvian infarction and congenital syphilis]A Larnaout, M A Mongalgi, H Ben Ameur, et al.
Clinical and Experimental Rheumatology|September 1, 1994
CD11/CD18 bearing lymphocytes in cerebrospinal fluid from patients with active Behçet's diseaseK Hamzaoui, F Hentati, A Hamzaoui, et al.
La Tunisie Medicale|January 1, 1987
[Polymyositis with polyradiculoneuritis]F Zouiten, F Letaief, M Hamza, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|July 28, 2007
Pregnancy in chronic hemodialysis women: outcome of multicentric studyH Bahloul, K Kammoun, M Kharrat, et al.
Transplantation Proceedings|June 1, 1993
Renal transplantation and autosomal dominant polycystic kidney disease: 20 years' experienceM Ben Hamida, J Bedrossian, A Duboust, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3C Barhoumi, R Amouri, C Ben Hamida, et al.
La Tunisie Medicale|April 1, 1985
[The motor handicapped]M Ben Hamida, N Attia-Romdhane, A Mrabet-Bahri, et al.
Pageof 12

Showing results (61-70 of 112) with videos related to

Sort By:
Pageof 12
Neuromuscular Disorders : NMD|January 1, 1992
Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosumF Hentati, C Ben Hamida, M Zeghal, et al.
Brain Research|March 20, 1999
Localization of alpha-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disordersR P Copp, T Wisniewski, F Hentati, et al.
European Journal of Cancer & Clinical Oncology|October 1, 1987
Pyrimidine pathways enzymes in human tumors of brain and associated tissues: potentialities for the therapeutic use of N-(phosphonacetyl-L-aspartate and 1-beta-D-arabinofuranosylcytosineS Madani, J Baillon, J Fries, et al.
Archives Francaises De Pediatrie|December 1, 1992
[Antenatal bilateral sylvian infarction and congenital syphilis]A Larnaout, M A Mongalgi, H Ben Ameur, et al.
Clinical and Experimental Rheumatology|September 1, 1994
CD11/CD18 bearing lymphocytes in cerebrospinal fluid from patients with active Behçet's diseaseK Hamzaoui, F Hentati, A Hamzaoui, et al.
La Tunisie Medicale|January 1, 1987
[Polymyositis with polyradiculoneuritis]F Zouiten, F Letaief, M Hamza, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|July 28, 2007
Pregnancy in chronic hemodialysis women: outcome of multicentric studyH Bahloul, K Kammoun, M Kharrat, et al.
Transplantation Proceedings|June 1, 1993
Renal transplantation and autosomal dominant polycystic kidney disease: 20 years' experienceM Ben Hamida, J Bedrossian, A Duboust, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3C Barhoumi, R Amouri, C Ben Hamida, et al.
La Tunisie Medicale|April 1, 1985
[The motor handicapped]M Ben Hamida, N Attia-Romdhane, A Mrabet-Bahri, et al.
Pageof 12