Khati C - Search Results

1

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus.

Belal S, Cancel G, Stevanin G, Hentati F, Khati C, Ben Hamida C, Auburger G, Agid Y, Ben Hamida M, Brice A. Belal S, et al. Among authors: khati c. Neurology. 1994 Aug;44(8):1423-6. doi: 10.1212/wnl.44.8.1423. Neurology. 1994. PMID: 8058142

2

Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French families.

Khati C, Stevanin G, Durr A, Chneiweiss H, Belal S, Seck A, Cann H, Brice A, Agid Y. Khati C, et al. Neurology. 1993 Jun;43(6):1131-7. doi: 10.1212/wnl.43.6.1131. Neurology. 1993. PMID: 8170557

3

Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity.

Dürr A, Chneiweiss H, Khati C, Stevanin G, Cancel G, Feingold J, Agid Y, Brice A. Dürr A, et al. Among authors: khati c. Brain. 1993 Dec;116 ( Pt 6):1497-508. doi: 10.1093/brain/116.6.1497. Brain. 1993. PMID: 8293283

4

Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1.

Cancel G, Khati C, Stevanin G, Pages JC, Agid Y, Brice A, Cann HM. Cancel G, et al. Among authors: khati c. Hum Mol Genet. 1993 Sep;2(9):1477-9. doi: 10.1093/hmg/2.9.1477. Hum Mol Genet. 1993. PMID: 8242075 No abstract available.

5

Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's disease.

Brice A, Boch AL, Stevanin G, Khati C, Dubois B, Agid Y, Campion D, Clerget F, Mallet J, Bellis M, et al. Brice A, et al. Among authors: khati c. J Neurol Neurosurg Psychiatry. 1993 Jan;56(1):112-3. doi: 10.1136/jnnp.56.1.112-a. J Neurol Neurosurg Psychiatry. 1993. PMID: 8429314 Free PMC article. No abstract available.

6

Scrub typhus: a case report.

Rajagopal R, Khati C, Vasdev V, Trehan A. Rajagopal R, et al. Among authors: khati c. Indian J Dermatol Venereol Leprol. 2003 Nov-Dec;69(6):413-5. Indian J Dermatol Venereol Leprol. 2003. PMID: 17642955

7

CARBOHYDRATE METABOLIC DISTURBANCES IN HYPERTHYROIDISM.

Saini JS, Narula AS, Khati C, Uberoi HS. Saini JS, et al. Among authors: khati c. Med J Armed Forces India. 1996 Jul;52(3):149-152. doi: 10.1016/S0377-1237(17)30789-X. Epub 2017 Jun 26. Med J Armed Forces India. 1996. PMID: 28769373 Free PMC article.

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