Ben Hamida M - Search Results

1

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD, et al. Ben Othmane K, et al. Among authors: ben hamida m, ben hamida c. Nat Genet. 1992 Dec;2(4):315-7. doi: 10.1038/ng1292-315. Nat Genet. 1992. PMID: 1303286

2

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.

Baxter RV, Ben Othmane K, Rochelle JM, Stajich JE, Hulette C, Dew-Knight S, Hentati F, Ben Hamida M, Bel S, Stenger JE, Gilbert JR, Pericak-Vance MA, Vance JM. Baxter RV, et al. Among authors: ben hamida m, ben othmane k. Nat Genet. 2002 Jan;30(1):21-2. doi: 10.1038/ng796. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743579

3

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: ben hamida m, ben hamida c. Hum Mol Genet. 1993 Oct;2(10):1625-8. doi: 10.1093/hmg/2.10.1625. Hum Mol Genet. 1993. PMID: 8268915

4

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: ben hamida m. Hum Mol Genet. 1994 Aug;3(8):1263-7. doi: 10.1093/hmg/3.8.1263. Hum Mol Genet. 1994. PMID: 7987300

5

Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.

Othmane KB, Loeb D, Hayworth-Hodgte R, Hentati F, Rao N, Roses AD, Ben Hamida M, Pericak-Vance MA, Vance JM. Othmane KB, et al. Among authors: ben hamida m. Genomics. 1995 Jul 20;28(2):286-90. doi: 10.1006/geno.1995.1143. Genomics. 1995. PMID: 8530038

6

Fine localization of the CMT4A locus using a PAC contig and haplotype analysis.

Ben Othmane K, Rochelle JM, Ben Hamida M, Slotterbeck B, Rao N, Hentati F, Pericak-Vance MA, Vance JM. Ben Othmane K, et al. Among authors: ben hamida m. Neurogenetics. 1998 Dec;2(1):18-23. doi: 10.1007/s100480050047. Neurogenetics. 1998. PMID: 9933296

7

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: ben hamida m, ben hamida c. Hum Genet. 1996 Sep;98(3):380-5. doi: 10.1007/s004390050225. Hum Genet. 1996. PMID: 8707312

8

Limb-girdle muscular dystrophy 2C: clinical aspects.

Ben Hamida M, Ben Hamida C, Zouari M, Belal S, Hentati F. Ben Hamida M, et al. Among authors: ben hamida c. Neuromuscul Disord. 1996 Dec;6(6):493-4. doi: 10.1016/s0960-8966(96)00395-1. Neuromuscul Disord. 1996. PMID: 9027861

9

A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3.

Driss A, Amouri R, Ben Hamida C, Souilem S, Gouider-Khouja N, Ben Hamida M, Hentati F. Driss A, et al. Among authors: ben hamida m, ben hamida c. Neuromuscul Disord. 2000 Jun;10(4-5):240-6. doi: 10.1016/s0960-8966(00)00099-7. Neuromuscul Disord. 2000. PMID: 10838249

10

Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3.

Barhoumi C, Amouri R, Ben Hamida C, Ben Hamida M, Machghoul S, Gueddiche M, Hentati F. Barhoumi C, et al. Among authors: ben hamida m, ben hamida c. Neuromuscul Disord. 2001 Jan;11(1):27-34. doi: 10.1016/s0960-8966(00)00162-0. Neuromuscul Disord. 2001. PMID: 11166163

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