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F Hentati

Showing results (101-110 of 120) with videos related to

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Regenerative capacity of human satellite cells: the mitotic clock in cell transplantationS Di Donna, V Renault, C Forestier, 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.
Journal of the Neurological Sciences|April 30, 1998
A gliotoxic factor and multiple sclerosisA Ménard, R Amouri, T Dobránsky, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Giant axonal neuropathy locus refinement to a < 590 kb critical intervalL Cavalier, C BenHamida, R Amouri, et al.
International Journal of Stroke : Official Journal of the International Stroke Society|October 10, 2019
Stroke in the Middle-East and North Africa: A 2-year prospective observational study of intravenous thrombolysis treatment in the region. Results from the SITS-MENA RegistryS Al-Rukn, M Mazya, N Akhtar, et al.
Human Molecular Genetics|March 21, 1998
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)G David, A Dürr, G Stevanin, et al.
Neurogenetics|May 18, 1999
Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33B A Hosler, P C Sapp, R Berger, et al.
Nature Genetics|December 2, 2000
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)S Nicole, C S Davoine, H Topaloglu, 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.
Pageof 12

Showing results (101-110 of 120) with videos related to

Sort By:
Pageof 12
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Regenerative capacity of human satellite cells: the mitotic clock in cell transplantationS Di Donna, V Renault, C Forestier, 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.
Journal of the Neurological Sciences|April 30, 1998
A gliotoxic factor and multiple sclerosisA Ménard, R Amouri, T Dobránsky, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Giant axonal neuropathy locus refinement to a < 590 kb critical intervalL Cavalier, C BenHamida, R Amouri, et al.
International Journal of Stroke : Official Journal of the International Stroke Society|October 10, 2019
Stroke in the Middle-East and North Africa: A 2-year prospective observational study of intravenous thrombolysis treatment in the region. Results from the SITS-MENA RegistryS Al-Rukn, M Mazya, N Akhtar, et al.
Human Molecular Genetics|March 21, 1998
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)G David, A Dürr, G Stevanin, et al.
Neurogenetics|May 18, 1999
Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33B A Hosler, P C Sapp, R Berger, et al.
Nature Genetics|December 2, 2000
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)S Nicole, C S Davoine, H Topaloglu, 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.
Pageof 12