Bejaoui K - Search Results

1

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C, et al. Hentati A, et al. Among authors: bejaoui k. Nat Genet. 1994 Jul;7(3):425-8. doi: 10.1038/ng0794-425. Nat Genet. 1994. PMID: 7920663

2

Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33.

Hosler BA, Sapp PC, Berger R, O'Neill G, Bejaoui K, Hamida MB, Hentati F, Chin W, McKenna-Yasek D, Haines JL, Patterson D, Horvitz HR, Brown RH Jr, Day CB. Hosler BA, et al. Among authors: bejaoui k. Neurogenetics. 1998 Dec;2(1):34-42. doi: 10.1007/s100480050049. Neurogenetics. 1998. PMID: 9933298

3

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14.

Bejaoui K, Hirabayashi K, Hentati F, Haines JL, Ben Hamida C, Belal S, Miller RG, McKenna-Yasek D, Weissenbach J, Rowland LP, et al. Bejaoui K, et al. Neurology. 1995 Apr;45(4):768-72. doi: 10.1212/wnl.45.4.768. Neurology. 1995. PMID: 7723968

4

Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22.

Bejaoui K, McKenna-Yasek D, Hosler BA, Burns-Deater E, Deater LM, O'Neill G, Haines JL, Brown RH Jr. Bejaoui K, et al. Neurology. 1999 Feb;52(3):510-5. doi: 10.1212/wnl.52.3.510. Neurology. 1999. PMID: 10025779

5

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy.

Liu J, Aoki M, Illa I, Wu C, Fardeau M, Angelini C, Serrano C, Urtizberea JA, Hentati F, Hamida MB, Bohlega S, Culper EJ, Amato AA, Bossie K, Oeltjen J, Bejaoui K, McKenna-Yasek D, Hosler BA, Schurr E, Arahata K, de Jong PJ, Brown RH Jr. Liu J, et al. Among authors: bejaoui k. Nat Genet. 1998 Sep;20(1):31-6. doi: 10.1038/1682. Nat Genet. 1998. PMID: 9731526

6

Evolution of muscle specific proteins in Werdnig-Hoffman's disease.

Soussi-Yanicostas N, Ben Hamida C, Bejaoui K, Hentati F, Ben Hamida M, Butler-Browne GS. Soussi-Yanicostas N, et al. Among authors: bejaoui k. J Neurol Sci. 1992 May;109(1):111-20. doi: 10.1016/0022-510x(92)90103-r. J Neurol Sci. 1992. PMID: 1387678

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: bejaoui k. J Neurol Sci. 1991 Jul;104(1):64-73. doi: 10.1016/0022-510x(91)90217-u. J Neurol Sci. 1991. PMID: 1919599

8

Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy.

Ben Hamida C, Soussi-Yanicostas N, Butler-Browne GS, Bejaoui K, Hentati F, Ben Hamida M. Ben Hamida C, et al. Among authors: bejaoui k. Muscle Nerve. 1994 Apr;17(4):400-10. doi: 10.1002/mus.880170407. Muscle Nerve. 1994. PMID: 8170486

9

Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy.

Hamida CB, Soussi-Yanicostas N, Bejaoui K, Butler-Browne GS, Hentati F, Ben Hamida M. Hamida CB, et al. Among authors: bejaoui k. J Neurol Sci. 1994 May;123(1-2):114-21. doi: 10.1016/0022-510x(94)90212-7. J Neurol Sci. 1994. PMID: 8064303

10

Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13.

Liu J, Wu C, Bossie K, Bejaoui K, Hosler BA, Gingrich JC, Ben Hamida M, Hentati F, Schurr E, de Jong PJ, Brown RH Jr. Liu J, et al. Among authors: bejaoui k. Genomics. 1998 Apr 1;49(1):23-9. doi: 10.1006/geno.1998.5204. Genomics. 1998. PMID: 9570945

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