Mongi Ben Hamida - Publications

Neurology Institut National de Neurologie, Tunis, Tunis, Tunisia 

55 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2005 Hamida MB, Wickleder MS. 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. DOI: 10.1002/zaac.200500241  0.01
2003 Kefi M, Amouri R, Driss A, Ben Hamida C, Ben Hamida M, Kunkel LM, Hentati F. Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation. Neuromuscular Disorders : Nmd. 13: 779-87. PMID 14678800 DOI: 10.1016/S0960-8966(03)00136-6  0.68
2003 Wickleder MS, Hamida MB. 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. DOI: 10.1002/zaac.200390090  0.01
2002 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. Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21. Nature Genetics. 30: 21-2. PMID 11743579 DOI: 10.1038/ng796  0.68
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  0.68
2000 Hentati A, Deng HX, Zhai H, Chen W, Yang Y, Hung WY, Azim AC, Bohlega S, Tandan R, Warner C, Laing NG, Cambi F, Mitsumoto H, Roos RP, Boustany RM, et al. Novel mutations in spastin gene and absence of correlation with age at onset of symptoms. Neurology. 55: 1388-90. PMID 11087788  0.68
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  0.68
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  0.68
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  0.68
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  0.68
1999 Gouider-Khouja N, Turki I, Ben Hamida M, Hentati F. [Hemifacial spasm and its treatment with botulinum toxin]. La Tunisie MéDicale. 77: 41-4. PMID 10333697  0.68
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  0.68
1998 Ben Othmane K, Rochelle JM, Ben Hamida M, Slotterbeck B, Rao N, Hentati F, Pericak-Vance MA, Vance JM. Fine localization of the CMT4A locus using a PAC contig and haplotype analysis. Neurogenetics. 2: 18-23. PMID 9933296 DOI: 10.1007/s100480050047  0.68
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  0.68
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  0.68
1998 Liu J, Wu C, Bossie K, Bejaoui K, Hosler BA, Gingrich JC, Ben Hamida M, Hentati F, Schurr E, de Jong PJ, Brown RH. Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13. Genomics. 49: 23-9. PMID 9570945 DOI: 10.1006/geno.1998.5204  0.68
1997 Trouillas P, Takayanagi T, Hallett M, Currier RD, Subramony SH, Wessel K, Bryer A, Diener HC, Massaquoi S, Gomez CM, Coutinho P, Hamida MB, Campanella G, Filla A, Schut L, et al. International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome Journal of the Neurological Sciences. 145: 205-211. PMID 9094050 DOI: 10.1016/S0022-510X(96)00231-6  0.68
1996 Ben Hamida M, Ben Hamida C, Zouari M, Belal S, Hentati F. Limb-girdle muscular dystrophy 2C: clinical aspects. Neuromuscular Disorders : Nmd. 6: 493-4. PMID 9027861 DOI: 10.1016/S0960-8966(96)00395-1  0.68
1996 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, et al. 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. Human Genetics. 98: 380-5. PMID 8707312 DOI: 10.1007/s004390050225  0.68
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  0.68
1995 Othmane KB, Loeb D, Hayworth-Hodgte R, Hentati F, Rao N, Roses AD, Ben Hamida M, Pericak-Vance MA, Vance JM. Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A. Genomics. 28: 286-90. PMID 8530038 DOI: 10.1006/geno.1995.1143  0.68
1995 Doerflinger N, Linder C, Ouahchi K, Gyapay G, Weissenbach J, Le Paslier D, Rigault P, Belal S, Ben Hamida C, Hentati F. Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families. American Journal of Human Genetics. 56: 1116-24. PMID 7726167  0.68
1995 Bejaoui K, Hirabayashi K, Hentati F, Haines JL, Ben Hamida C, Belal S, Miller RG, McKenna-Yasek D, Weissenbach J, Rowland LP. Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14. Neurology. 45: 768-72. PMID 7723968  0.68
1995 Ouahchi K, Arita M, Kayden H, Hentati F, Ben Hamida M, Sokol R, Arai H, Inoue K, Mandel JL, Koenig M. Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein. Nature Genetics. 9: 141-5. PMID 7719340 DOI: 10.1038/ng0295-141  0.68
1995 Ben Othmane K, Speer MC, Stauffer J, Blel S, Middleton L, Ben Hamida C, Etribi A, Loeb D, Hentati F, Roses AD. Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C) American Journal of Human Genetics. 57: 732-4. PMID 7668303  0.68
1994 Belal S, Cancel G, Stevanin G, Hentati F, Khati C, Ben Hamida C, Auburger G, Agid Y, Ben Hamida M, Brice A. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus. Neurology. 44: 1423-6. PMID 8058142  0.68
1994 Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung WY, Boustany RM, Bohlega S. Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers. Human Molecular Genetics. 3: 1867-71. PMID 7849714  0.68
1994 Hamzaoui K, Hamzaoui A, Hentati F, Kahan A, Ayed K, Chabbou A, Ben Hamida M, Hamza M. Phenotype and functional profile of T cells expressing gamma delta receptor from patients with active Behçet's disease. The Journal of Rheumatology. 21: 2301-6. PMID 7699633  0.68
1993 Romdhane NA, Hamida MB, Mrabet A, Larnaout A, Samoud S, Hamda AB, Hamda MB, Oueslati S. Prevalence study of neurologic disorders in Kelibia (Tunisia) Neuroepidemiology. 12: 285-299. PMID 8309504  0.56
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  0.68
1993 Attia-Romdhane N, Mrabet A, Hamida MB, Genton P, Portera-Sanchez A. Prevalence of epilepsy in Kelibia, Tunisia Epilepsia. 34: 1028-1032. PMID 8243352 DOI: 10.1111/j.1528-1157.1993.tb02129.x  0.68
1992 Miladi N, Larnaout A, Kaabachi N, Helayem M, Hamida MB. Phenylketonuria: An underlying etiology of autistic syndrome. A case report Journal of Child Neurology. 7: 22-23. PMID 1552146  0.68
1992 Belal S, Panayides K, Sirugo G, Ben Hamida C, Ioannou P, Hentati F, Beckmann J, Koenig M, Mandel JL, Ben Hamida M. Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus. American Journal of Human Genetics. 51: 1372-6. PMID 1463017  0.68
1992 Soussi-Yanicostas N, Ben Hamida C, Bejaoui K, Hentati F, Ben Hamida M, Butler-Browne GS. Evolution of muscle specific proteins in Werdnig-Hoffman's disease. Journal of the Neurological Sciences. 109: 111-20. PMID 1387678 DOI: 10.1016/0022-510X(92)90103-R  0.68
1992 Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nature Genetics. 2: 315-7. PMID 1303286 DOI: 10.1038/ng1292-315  0.68
1992 Hentati F, Ben Hamida C, Zeghal M, Kamoun M, Fezaa B, Ben Hamida M. Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum. Neuromuscular Disorders : Nmd. 2: 361-9. PMID 1300184 DOI: 10.1016/S0960-8966(06)80007-6  0.68
1992 Ben Jelloun-Dellagi S, Dellagi K, Burger D, Ben Younes-Chennoufi A, Hentati FF, Steck A, Ben Hamida M. Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein P0. Annals of Neurology. 32: 700-2. PMID 1280408 DOI: 10.1002/ana.410320515  0.68
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  0.68
1991 Hamida MB, Chabbi N, Hamida CB, Mhiri C, Kallel R. Peripheral neuropathy in an anecdotic case of cerebrotendinous xanthomatosis | NEUROPATHIE PERIPHERIQUE DANS UN CAS SPORADIQUE DE XANTHOMATOSE CEREBROTENDINEUSE Revue Neurologique. 147: 385-388.  0.68
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.  0.68
1990 Mrabet A, Attia-Romdhane N, Hamida MB, Gharbi N, Le Noan H, Hentati R, Mansour JB, Srairi I. Epidemiological features of cetebrovascualr disease in Tunisia | ASPECTS EPIDEMIOLOGIQUES DES ACCIDENTS VASCULAIRES CEREBRAUX EN TUNISIE Revue Neurologique. 146: 297-301.  0.68
1987 Ben Hamida M, Letaief F, Hentati F, Ben Hamida C. Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 78: 313-29. PMID 3585405 DOI: 10.1016/0022-510X(87)90045-1  0.68
1987 Madani S, Baillon J, Fries J, Belhadj O, Bettaieb A, Hamida MB, Hervé G. Pyrimidine pathways enzymes in human tumors of brain and associated tissues: Potentialities for the therapeutic use of N-(Phosphonacetyl-l-aspartate and 1-β-d-arabinofuranosylcytosine European Journal of Cancer and Clinical Oncology. 23: 1485-1490. PMID 2824206 DOI: 10.1016/0277-5379(87)90090-3  0.68
1984 Chami I, Miladi N, Hamida MB, Zmerli S. Disturbances of continence in hereditary spino cerebellar degeneration. Confrontation of clinical and urodynamics considerations | LES TROUBLES DE LA CONTINENCE DANS LES HEREDO-DEGENERESCENCES SPINO-CEREBELLEUSES. CONFRONTATIONS DES DONNEES CLINIQUES ET URODYNAMIQUES DANS 55 CAS Acta Neurologica Belgica. 84: 194-203. PMID 6496033  0.68
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  0.68
1982 Hamida MB. Epidemiological study of multiple sclerosis in Tunisia African Journal of Neurological Sciences. 1: 45-47.  0.68
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  0.68
1980 Hamida MB, Madani S, Zmerli S, Chami I. Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders | LES HEREDODEGENERESCENCES SPINO-CEREBELLEUSES EN TUNISIE AVEC ETUDE CYSTOMANOMETRIQUE DES TROUBLES SPHINCTERIENS. 204 CAS DE MALADIES DE FRIEDRIECH, DE PIERRE MARIE ET DE STRUMPELL-LORRAIN Revue Neurologique. 136: 495-508. PMID 7221327  0.68
1980 Hamida MB, Marakchi D. [Genetic study of myopathies in Tunisia]. L'UnióN MéDicale Du Canada. 109: 1609-28. PMID 7210305  0.68
1978 Hamida MB. [The concept of inhibition in psychiatry. Welcoming address]. L'EncéPhale. 4: 399-401. PMID 38101  0.68
1977 Hamida MB, Younsi E. [Electrophoresis of the cerebrospinal fluid in spinal and spino-cerebellar degeneration]. Revue Neurologique. 133: 727-9. PMID 614683  0.68
1972 Hamida MB, Rondot P. [Fahr's diseases. Biological and anatomical study. Absence of biological signs for hypoparathyroidism]. Annales De MéDecine Interne. 123: 909-21. PMID 4659556  0.68
1971 Sieben RL, Hamida MB, Shulman K. Multiple cranial nerve deficits associated with the Arnold-Chiari malformation. Neurology. 21: 673-81. PMID 4934956  0.68
1970 Lapresle J, Hamida MB. The dentato-olivary pathway. Somatotopic relationship between the dentate nucleus and the contralateral inferior olive. Archives of Neurology. 22: 135-43. PMID 4188259 DOI: 10.1001/archneur.1970.00480200041004  0.68
1962 RYCKEWAERT A, HAMIDA MB, FRENEAUX R. [Ischemic neuritis in rheumatoid polyarthritis]. Concours MéDical. 84: 6833-8. PMID 13975792  0.68
Show low-probability matches.