| Year |
Citation |
Score |
| 2002 |
Feki M, Belal S, Feki H, Souissi M, Frih-Ayed M, Kaabachi N, Hentati F, Hamida MB, Mebazaa A. Serum Vitamin E and Lipid-adjusted Vitamin E Assessment in Friedreich Ataxia Phenotype Patients and Unaffected Family Members Clinical Chemistry. 48: 577-579. DOI: 10.1093/Clinchem/48.3.577 |
0.497 |
|
| 2001 |
Larnaout A, El-Euch G, Kchir N, Filali A, Hamida MB, Hentati F. Wernicke's encephalopathy in a patient with Crohn's disease: a pathological study. Journal of Neurology. 248: 57-60. PMID 11266021 DOI: 10.1007/s004150170270 |
0.414 |
|
| 2000 |
Cavalier L, BenHamida C, Amouri R, Belal S, Bomont P, Lagarde N, Gressin L, Callen D, Demir E, Topaloglu H, Landrieu P, Ioos C, Hamida MB, Koenig M, Hentati F. Giant axonal neuropathy locus refinement to a < 590 kb critical interval. European Journal of Human Genetics : Ejhg. 8: 527-34. PMID 10909853 DOI: 10.1038/sj.ejhg.5200476 |
0.582 |
|
| 2000 |
Gouider-Khouja N, Belal S, Hamida MB, Hentati F. Clinical and genetic study of familial Parkinson's disease in Tunisia. Neurology. 54: 1603-9. PMID 10762501 DOI: 10.1212/Wnl.54.8.1603 |
0.553 |
|
| 2000 |
Mrissa N, Belal S, Hamida CB, Amouri R, Turki I, Mrissa R, Hamida MB, Hentati F. Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family. Neurology. 54: 1408-14. PMID 10751248 DOI: 10.1212/Wnl.54.7.1408 |
0.676 |
|
| 1999 |
Othmane KB, Johnson E, Menold M, Graham FL, Hamida MB, Hasegawa O, Rogala AD, Ohnishi A, Pericak-Vance M, Hentati F, Vance JM. Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15. Genomics. 62: 344-9. PMID 10644431 DOI: 10.1006/Geno.1999.6028 |
0.64 |
|
| 1998 |
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, Day CB. Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33. Neurogenetics. 2: 34-42. PMID 9933298 DOI: 10.1007/S100480050049 |
0.639 |
|
| 1998 |
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, et al. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nature Genetics. 20: 31-6. PMID 9731526 DOI: 10.1038/1682 |
0.592 |
|
| 1998 |
Bönnemann CG, Wong J, Ben Hamida C, Hamida MB, Hentati F, Kunkel LM. LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3. Neuromuscular Disorders : Nmd. 8: 193-7. PMID 9631401 DOI: 10.1016/S0960-8966(98)00014-5 |
0.511 |
|
| 1997 |
Othmane KB, Rochelle JM, Johnson E, Hamida MB, Pericak-Vance MA, Hentati F, Vance JM. Clinical and genetic aspects of autosomal recessive CMT Neuromuscular Disorders. 7: 464-465. DOI: 10.1016/S0960-8966(97)87315-4 |
0.537 |
|
| 1995 |
Nicole S, Hamida CB, Beighton P, Bakouri S, Belal S, Romero N, Viljoen D, Ponsot G, Sammoud A, Weissenbach J, Fardeau M, Hamida MB, Fontaine B, Hentati F. Localization of the schwartz-jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping Human Molecular Genetics. 4: 1633-1636. PMID 8541852 DOI: 10.1093/Hmg/4.9.1633 |
0.624 |
|
| 1993 |
Hamida CB, Doerflinger N, Belal S, Linder C, Reutenauer L, Dib C, Gyapay G, Vignal A, Le Paslier D, Cohen D, Pandolfo M, Mokini V, Novelli G, Hentati F, Hamida MB, et al. Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping Nature Genetics. 5: 195-200. PMID 8252047 DOI: 10.1038/ng1093-195 |
0.606 |
|
| 1992 |
Hamida MB, Miladi N, Turki I, Zaiem H. Duchenne muscular dystrophy in Tunisia: A clinical and morphological study of 77 cases Journal of the Neurological Sciences. 107: 60-64. DOI: 10.1016/0022-510X(92)90209-4 |
0.399 |
|
| 1990 |
Jelloun-Dellagi SB, Chaffey P, Hentati F, Hamida CB, Tome F, Colin H, Dellagi K, Kaplan JC, Fardeau M, Hamida MB. Presence of normal dystrophin in tunisian severe childhood autosomal recessive muscular dystrophy Neurology. 40: 1903. |
0.485 |
|
| 1983 |
Hamida MB, Fardeau M, Attia N. Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia Muscle and Nerve. 6: 469-480. PMID 6633560 DOI: 10.1002/Mus.880060702 |
0.377 |
|
| 1981 |
Hamida MB, Letaief F, Hamida CB, Samoud S. Les atrophies péronières en Tunisie. Étude de 70 observations pures ou associées à d'autres affections hérédodégénératives Journal of the Neurological Sciences. 50: 335-356. PMID 7264702 DOI: 10.1016/0022-510X(81)90147-7 |
0.416 |
|
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