Mongi Ben Hamida

Affiliations: 
Neurology Institut National de Neurologie, Tunis, Tunis, Tunisia 
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"Mongi Hamida"
Mean distance: 18.03 (cluster 3)
 
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Publications

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Hamida MB, Wickleder MS. (2005) Selenious acid as a ligand: Molecular and crystal structure of [Co(H 2O)2Cl2(H2SeO3) 2] Zeitschrift Fur Anorganische Und Allgemeine Chemie. 631: 2306-2308
Kefi M, Amouri R, Driss A, et al. (2003) Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation. Neuromuscular Disorders : Nmd. 13: 779-87
Wickleder MS, Hamida MB. (2003) CoSm(SeO3)2Cl, CuGd(SeO3)2Cl, MnSm(SeO3)2Cl, CuGd2(SeO3)4, and CuSm2(SeO3)4: Transition metal containing selenites of samarium and gadolinum | CoSm(SeO3)2Cl, CuGd(SeO3)2Cl, MnSm(SeO3)2Cl, CuGd2(SeO3)4 und CuSm2(SeO3)4: Übergangsmetallhaltige selenite von samarium und gadolinum Zeitschrift Fur Anorganische Und Allgemeine Chemie. 629: 556-562
Baxter RV, Ben Othmane K, Rochelle JM, et al. (2002) Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21. Nature Genetics. 30: 21-2
Larnaout A, El-Euch G, Kchir N, et al. (2001) Wernicke's encephalopathy in a patient with Crohn's disease: a pathological study. Journal of Neurology. 248: 57-60
Hentati A, Deng HX, Zhai H, et al. (2000) Novel mutations in spastin gene and absence of correlation with age at onset of symptoms. Neurology. 55: 1388-90
Cavalier L, BenHamida C, Amouri R, et al. (2000) Giant axonal neuropathy locus refinement to a < 590 kb critical interval. European Journal of Human Genetics : Ejhg. 8: 527-34
Gouider-Khouja N, Belal S, Hamida MB, et al. (2000) Clinical and genetic study of familial Parkinson's disease in Tunisia. Neurology. 54: 1603-9
Mrissa N, Belal S, Hamida CB, et al. (2000) Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family. Neurology. 54: 1408-14
Othmane KB, Johnson E, Menold M, et al. (1999) Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15. Genomics. 62: 344-9
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