Hentati F - Search Results

1

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 interval.

Fontaine B, Nicole S, Topaloglu H, Ben Hamida C, Beighton P, Spaans F, Cantu JM, Bakouri S, Romero N, Ricker K, Barros-Nunez P, Ponsot G, Ben Hamida M, Weissenbach J, Hentati F, Lehmann-Horn F. Fontaine B, et al. Among authors: hentati f. Hum Genet. 1996 Sep;98(3):380-5. doi: 10.1007/s004390050225. Hum Genet. 1996. PMID: 8707312

2

Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus.

Belal S, Panayides K, Sirugo G, Ben Hamida C, Ioannou P, Hentati F, Beckmann J, Koenig M, Mandel JL, Ben Hamida M, et al. Belal S, et al. Among authors: hentati f. Am J Hum Genet. 1992 Dec;51(6):1372-6. Am J Hum Genet. 1992. PMID: 1463017 Free PMC article.

3

Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus.

Belal S, Hentati F, Ben Hamida C, Ben Hamida M. Belal S, et al. Among authors: hentati f. Clin Neurosci. 1995;3(1):39-42. Clin Neurosci. 1995. PMID: 7614093

4

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families.

Doerflinger N, Linder C, Ouahchi K, Gyapay G, Weissenbach J, Le Paslier D, Rigault P, Belal S, Ben Hamida C, Hentati F, et al. Doerflinger N, et al. Among authors: hentati f. Am J Hum Genet. 1995 May;56(5):1116-24. Am J Hum Genet. 1995. PMID: 7726167 Free PMC article.

5

The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate gene.

Nicole S, White PS, Topaloglu H, Beigthon P, Salih M, Hentati F, Fontaine B. Nicole S, et al. Among authors: hentati f. Hum Genet. 1999 Jul-Aug;105(1-2):98-103. doi: 10.1007/s004399900065. Hum Genet. 1999. PMID: 10480361

6

Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia).

Nicole S, Davoine CS, Topaloglu H, Cattolico L, Barral D, Beighton P, Hamida CB, Hammouda H, Cruaud C, White PS, Samson D, Urtizberea JA, Lehmann-Horn F, Weissenbach J, Hentati F, Fontaine B. Nicole S, et al. Among authors: hentati f. Nat Genet. 2000 Dec;26(4):480-3. doi: 10.1038/82638. Nat Genet. 2000. PMID: 11101850

7

Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome.

Soussi-Yanicostas N, Ben Hamida C, Butler-Browne GS, Hentati F, Bejaoui K, Ben Hamida M. Soussi-Yanicostas N, et al. Among authors: hentati f. J Neurol Sci. 1991 Jul;104(1):64-73. doi: 10.1016/0022-510x(91)90217-u. J Neurol Sci. 1991. PMID: 1919599

8

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T. Hentati A, et al. Among authors: hentati f. Hum Mol Genet. 1994 Aug;3(8):1263-7. doi: 10.1093/hmg/3.8.1263. Hum Mol Genet. 1994. PMID: 7987300

9

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: hentati f. Neurology. 1994 Aug;44(8):1423-6. doi: 10.1212/wnl.44.8.1423. Neurology. 1994. PMID: 8058142

10

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

Ben Othmane K, Hentati F, Lennon F, Ben Hamida C, Blel S, Roses AD, Pericak-Vance MA, Ben Hamida M, Vance JM. Ben Othmane K, et al. Among authors: hentati f. Hum Mol Genet. 1993 Oct;2(10):1625-8. doi: 10.1093/hmg/2.10.1625. Hum Mol Genet. 1993. PMID: 8268915

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