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F Hentati

Showing results (81-90 of 120) with videos related to

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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.
European Journal of Neurology|September 14, 2001
Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiencyS Gabsi, N Gouider-Khouja, S Belal, 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.
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.
Human Molecular Genetics|August 1, 1994
Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneityA Hentati, M A Pericak-Vance, W Y Hung, 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.
American Journal of Human Genetics|September 1, 1995
Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)K Ben Othmane, M C Speer, J Stauffer, et al.
Neurology|April 1, 1995
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14K Bejaoui, K Hirabayashi, F Hentati, et al.
Genomics|July 20, 1995
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4AK B Othmane, D Loeb, R Hayworth-Hodgte, et al.
Human Molecular Genetics|October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8qK Ben Othmane, F Hentati, F Lennon, et al.
Pageof 12

Showing results (81-90 of 120) with videos related to

Sort By:
Pageof 12
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.
European Journal of Neurology|September 14, 2001
Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiencyS Gabsi, N Gouider-Khouja, S Belal, 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.
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.
Human Molecular Genetics|August 1, 1994
Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneityA Hentati, M A Pericak-Vance, W Y Hung, 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.
American Journal of Human Genetics|September 1, 1995
Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)K Ben Othmane, M C Speer, J Stauffer, et al.
Neurology|April 1, 1995
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14K Bejaoui, K Hirabayashi, F Hentati, et al.
Genomics|July 20, 1995
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4AK B Othmane, D Loeb, R Hayworth-Hodgte, et al.
Human Molecular Genetics|October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8qK Ben Othmane, F Hentati, F Lennon, et al.
Pageof 12