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M Ben Hamida

Showing results (101-110 of 112) with videos related to

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Neurogenetics|March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1C Ben Hamida, L Cavalier, S Belal, et al.
Journal Francais D'Ophtalmologie|November 23, 2006
[Ocular manifestations associated with nephronophthisis and genetic study in three Tunisian families]D Sellami, K Makni, H Chaker, et al.
Genomics|May 8, 1998
Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13J Liu, C Wu, K Bossie, et al.
Nature Genetics|December 1, 1992
Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13qK Ben Othmane, M Ben Hamida, M A Pericak-Vance, et al.
Neurogenetics|May 18, 1999
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markersA Hentati, K Ouahchi, M A Pericak-Vance, et al.
Human Genetics|September 1, 1996
Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM intervalB Fontaine, S Nicole, H Topaloglu, et al.
Nature Genetics|October 5, 2001
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisY Yang, A Hentati, H X Deng, et al.
Neurology|November 23, 2000
Novel mutations in spastin gene and absence of correlation with age at onset of symptomsA Hentati, H X Deng, H Zhai, et al.
Science (New York, N.Y.)|November 3, 1995
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophyS Noguchi, E M McNally, K Ben Othmane, et al.
Journal of the Neurological Sciences|February 12, 1997
International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the World Federation of NeurologyP Trouillas, T Takayanagi, M Hallett, et al.
Pageof 12

Showing results (101-110 of 112) with videos related to

Sort By:
Pageof 12
Neurogenetics|March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1C Ben Hamida, L Cavalier, S Belal, et al.
Journal Francais D'Ophtalmologie|November 23, 2006
[Ocular manifestations associated with nephronophthisis and genetic study in three Tunisian families]D Sellami, K Makni, H Chaker, et al.
Genomics|May 8, 1998
Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13J Liu, C Wu, K Bossie, et al.
Nature Genetics|December 1, 1992
Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13qK Ben Othmane, M Ben Hamida, M A Pericak-Vance, et al.
Neurogenetics|May 18, 1999
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markersA Hentati, K Ouahchi, M A Pericak-Vance, et al.
Human Genetics|September 1, 1996
Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM intervalB Fontaine, S Nicole, H Topaloglu, et al.
Nature Genetics|October 5, 2001
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisY Yang, A Hentati, H X Deng, et al.
Neurology|November 23, 2000
Novel mutations in spastin gene and absence of correlation with age at onset of symptomsA Hentati, H X Deng, H Zhai, et al.
Science (New York, N.Y.)|November 3, 1995
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophyS Noguchi, E M McNally, K Ben Othmane, et al.
Journal of the Neurological Sciences|February 12, 1997
International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the World Federation of NeurologyP Trouillas, T Takayanagi, M Hallett, et al.
Pageof 12