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 |
|
Low-probability matches (unlikely to be authored by this person) |
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 DOI: 10.1177/088307389200700103 |
0.268 |
|
1980 |
Hamida MB, Marakchi D. [Genetic study of myopathies in Tunisia]. L'Uniã³N Mã©Dicale Du Canada. 109: 1609-28. PMID 7210305 |
0.239 |
|
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 |
0.22 |
|
1971 |
Sieben RL, Hamida MB, Shulman K. Multiple cranial nerve deficits associated with the Arnold-Chiari malformation. Neurology. 21: 673-81. PMID 4934956 DOI: 10.1212/Wnl.21.7.673 |
0.211 |
|
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 |
0.172 |
|
2011 |
Khaled A, Hamida MB, Goucha S, Zermani R, Rameh S, Taazayet SB, Kamoun MR, Fazaa B. Bullous darier's disease mimicking hailey-hailey disease Dermatology and Therapy. 2: 31-35. DOI: 10.1007/s13555-011-0007-x |
0.139 |
|
1972 |
Hamida MB, Rondot P. [Fahr's diseases. Biological and anatomical study. Absence of biological signs for hypoparathyroidism]. Annales De Mã©Decine Interne. 123: 909-21. PMID 4659556 |
0.139 |
|
1977 |
Hamida MB. [Multiple sclerosis in Tunisia. Clinical study of 100 cases]. Revue Neurologique. 133: 109-17. PMID 301285 |
0.133 |
|
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 |
0.118 |
|
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. |
0.105 |
|
1977 |
Belkahia A, Hamida MB, Bouzouita H. [Multiple sclerosis in Tunisia: cochleo-vestibular study (author's transl)]. Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Sociã©Tã© D'Oto-Laryngologie Des Hã´Pitaux De Paris. 94: 617-22. PMID 303492 |
0.088 |
|
1982 |
Hamida MB. Epidemiological study of multiple sclerosis in Tunisia African Journal of Neurological Sciences. 1: 45-47. |
0.084 |
|
2012 |
Khaled A, Hamida MB, Zeglaoui F, Kharfi M, Ezzine N, Fazaa B. [Not Available]. ThéRapie. 67: 49-52. PMID 27393658 DOI: 10.2515/therapie/2012004 |
0.08 |
|
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 |
0.079 |
|
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 |
0.076 |
|
1993 |
Hamida MB, Bedrossian J, Duboust A, Pruna A, Fouqueray B, Metivier F, Idatte JM. Renal transplantation and autosomal dominant polycystic kidney disease: 20 Years' experience Transplantation Proceedings. 25: 2162-2163. PMID 8516852 |
0.069 |
|
1987 |
Zakraoui L, Cheour I, Mrabet A, Jeridi T, Hamza M, Hamza R, Hila A, Hamida MB, Haddad S. Diagnosis of fluor osteosis: Unusual neurological aspects | ASPECTS INHABITUELS DE LA FLUOROSE OSSEUSE Rhumatologie - Revue International De Rhumatologie. 17: 101-105. |
0.059 |
|
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. |
0.053 |
|
2012 |
Khaled A, Kharfi M, Hamida MB, El Fekih N, El Aidli S, Zeglaoui F, Ezzine N, Fazaa B, Kamoun MR. Cutaneous adverse drug reactions in children. A series of 90 cases | Les toxidermies chez l'enfant. Une série de 90 cas Tunisie Medicale. 90: 45-50. PMID 22311448 |
0.047 |
|
1977 |
Hamida MB, Younsi E. [Electrophoresis of the cerebrospinal fluid in spinal and spino-cerebellar degeneration]. Revue Neurologique. 133: 727-9. PMID 614683 |
0.032 |
|
1992 |
Mrabet A, Maalej M, Hammouda IM, Khouja-Gouider N, Besbes M, Hamida MB. [Post radiation myelopathies: six case reports]. La Tunisie Mã©Dicale. 70: 25-8. PMID 1570648 |
0.03 |
|
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 |
0.029 |
|
2012 |
Mlika RB, Hamida MB, Hammami H, Jannet SB, Badri T, Fenniche S, Mokhtar I. Should we continue to indicate meglumine antimoniate as first-line treatment for cutaneous leishmaniasis in Tunisia. Dermatologic Therapy. 25: 615-8. PMID 23210761 DOI: 10.1111/j.1529-8019.2012.01522.x |
0.025 |
|
1993 |
Hamida MB, Bedrossian J, Pruna A, Fouqueray B, Metivier F, Idatte JM. Wilms tumor and renal transplantation: A case report and literature review Transplantation Proceedings. 25: 2346-2347. PMID 7685951 |
0.018 |
|
1993 |
Hamida MB, Bedrossian J, Pruna A, Fouqueray B, Metivier F, Idatte JM. Fungal mycotic aneurysms and visceral infection due to Scedosporium apiospermum in a kidney transplant patient Transplantation Proceedings. 25: 2290-2291. PMID 8516902 |
0.017 |
|
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 |
0.016 |
|
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 |
0.014 |
|
2012 |
Hamida MB, Baccouche D, El Fekih N, Fazaa B, Kamoun R. Lymphangiectasia of the vulva, treatment with CO₂ laser. Indian Journal of Dermatology, Venereology and Leprology. 78: 122. PMID 22199085 DOI: 10.4103/0378-6323.90973 |
0.01 |
|
2010 |
Hamouda C, Hamida MB, Benzarti N, Zouari B, Chébil M. Tunisian survey about organ donation, attitude and opinion? | Don d'organes et population tunisienne, attitude et opinion ? Presse Medicale. 39: e11-e16. PMID 19740622 DOI: 10.1016/j.lpm.2009.05.019 |
0.01 |
|
2006 |
Hamida MB, Wickleder MS. Nd5(AsO3)4Cl3: The first oxo-arsenate(III)-chloride of the lanthanides Zeitschrift Fur Anorganische Und Allgemeine Chemie. 632: 2195-2197. DOI: 10.1002/zaac.200600173 |
0.01 |
|
2005 |
Hamida MB, Warns C, Wickleder MS. Syntheses and crystal structures of RE2As4O 9 (RE = Nd, Sm): Oxo-arsenates(III) according to RE 4(As2O5)2(As4O 8) exhibiting the cyclic As4O8 4- anion Zeitschrift Fur Naturforschung - Section B Journal of Chemical Sciences. 60: 1219-1223. |
0.01 |
|
2003 |
Bahloul H, Kammoun K, Kharrat M, Jarraya F, Charffedine K, Hamida MB, Hachicha J. Pregnancy in chronic hemodialysis women: outcome of multicentric study. Saudi Journal of Kidney Diseases and Transplantation : An Official Publication of the Saudi Center For Organ Transplantation, Saudi Arabia. 14: 530-1. PMID 17657128 |
0.01 |
|
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 |
|
1978 |
Hamida MB. [The concept of inhibition in psychiatry. Welcoming address]. L'Encã©Phale. 4: 399-401. PMID 38101 |
0.01 |
|
1962 |
RYCKEWAERT A, HAMIDA MB, FRENEAUX R. [Ischemic neuritis in rheumatoid polyarthritis]. Concours Mã©Dical. 84: 6833-8. PMID 13975792 |
0.01 |
|
Hide low-probability matches. |