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C Khati

Showing results (1-10 of 7) with videos related to

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Indian Journal of Dermatology, Venereology and Leprology|July 24, 2007
Scrub typhus: a case reportR Rajagopal, C Khati, V Vasdev, et al.
Medical Journal, Armed Forces India|August 4, 2017
CARBOHYDRATE METABOLIC DISTURBANCES IN HYPERTHYROIDISMJ S Saini, A S Narula, C Khati, et al.
Brain : a Journal of Neurology|December 1, 1993
Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneityA Dürr, H Chneiweiss, C Khati, et al.
Human Molecular Genetics|September 1, 1993
Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1G Cancel, C Khati, G Stevanin, et al.
Neurology|June 1, 1993
Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French familiesC Khati, G Stevanin, A Durr, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's diseaseA Brice, A L Boch, G Stevanin, 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.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Indian Journal of Dermatology, Venereology and Leprology|July 24, 2007
Scrub typhus: a case reportR Rajagopal, C Khati, V Vasdev, et al.
Medical Journal, Armed Forces India|August 4, 2017
CARBOHYDRATE METABOLIC DISTURBANCES IN HYPERTHYROIDISMJ S Saini, A S Narula, C Khati, et al.
Brain : a Journal of Neurology|December 1, 1993
Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneityA Dürr, H Chneiweiss, C Khati, et al.
Human Molecular Genetics|September 1, 1993
Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1G Cancel, C Khati, G Stevanin, et al.
Neurology|June 1, 1993
Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French familiesC Khati, G Stevanin, A Durr, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's diseaseA Brice, A L Boch, G Stevanin, 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.
Pageof 1