CONTRIBUTION A L'ETUDE QUANTITATIVE STRUCTURALE ET ULTRA-STRUCTURALE DE BIOPSIES CUTANEES ET NERVEUSES DANS LE DIAGNOSTIC DE L'INDIFFERENCE CONGENITALE A LA DOULEURBEN HAMIDA C; SAMOUDA F.1980; J. NEUROL. SCI.; NLD; DA. 1980; VOL. 45; NO 2-3; PP. 379-389; ABS. ENG; BIBL. 21 REF.Article

LE PHEOCHROMOCYTOME: ATTITUDE DIAGNOSTIQUE ET THERAPEUTIQUE: A PROPOS DE DEUX CASBEN AYED H; HAMIDA C; ZMERLI S et al.1978; TUNISIE MED.; TUN; DA. 1978; VOL. 56; NO 3; PP. 295-305; BIBL. 8 REF.Article

L'INSUFFISANCE RENALE PAR OBSTACLE CERVICO-PROSTATIQUE: A PROPOS DE 56 OBSERVATIONSHAMIDA C; BEN AYED H; AYED M et al.1979; TUNISIE MED.; TUN; DA. 1979; VOL. 57; NO 1; PP. 32-37; ABS. ENG; BIBL. 8 REF.Article

LE CANCER DE LA PROSTATE: ETUDE DIAGNOSTIQUE ET ATTITUDE THERAPEUTIQUE A PROPOS DE 89 CAS (1974-1978)HAMIDA C; AYED A; HORCHANI A et al.1979; TUNISIE MED.; TUN; DA. 1979; VOL. 57; NO 4-5; PP. 264-268; ABS. ARA/ENG; BIBL. 23 REF.Article

LE TRAITEMENT DU RETRECISSEMENT SCLERO-INFLAMMATOIRE DE L'URETHRE: A PROPOS DE 148 CASSMIDA L; CHAMI I; HAMIDA C et al.1979; TUNISIE MED.; TUN; DA. 1979; VOL. 57; NO 4-5; PP. 260-262; ABS. ARA/ENG; BIBL. 20 REF.Article

TUMEURS UROTHELIALES DES VOIES EXCRETRICES HAUTES: A PROPOS DE 12 OBSERVATIONSAYED M; SLIM R; HORCHANI A et al.1979; TUNISIE MED.; TUN; DA. 1979; VOL. 57; NO 4-5; PP. 270-275; ABS. ARA/ENG; BIBL. 14 REF.Article

PLACE DE L'URETHROTOMIE EXTERNE COMPLETEE D'UN GREFFON DANS LE TRAITEMENT D'UN RETRECISSEMENT SCLERO-INFLAMMATOIRE DE L'URETHRESMIDA L; CHAMI I; HAMIDA C et al.1980; TUNISIE MED.; ISSN 0041-4131; HUN; DA. 1980; VOL. 58; NO 1-2; PP. 416-417; ABS. ARA/ENG; BIBL. 8 REF.Article

Syndrome de Schwartz-Jampel : étude clinique et histopathologique de 4 cas = Schwartz Jampel syndrome clinical and histopathological study of 4 casesBEN HAMIDA, M; MILADI, N; BEN HAMIDA, C et al.Revue neurologique (Paris). 1991, Vol 147, Num 4, pp 279-284, issn 0035-3787, 6 p.Article

Les valves de l'uretère. A propos d'un cas = Ureteral valves. One caseMOSBAH, A; JEMNI, M; HAMIDA, C et al.Journal d'urologie. 1988, Vol 94, Num 1, pp 45-48, issn 0248-0018Article

Maladie à multiminicores au cours d'un syndrome de la colonne raide = Rigid spine syndrome associated with multiminicore diseaseBEN HAMIDA, M; HENTATI, F; BEN HAMIDA, C et al.Revue neurologique (Paris). 1987, Vol 143, Num 4, pp 284-289, issn 0035-3787Article

Histomorphometric study of the superficial peroneal nerve in leprosyMONGI BEN HAMIDA; FETHI LETAIEF; BEN HAMIDA, C et al.Acta leprologica. 1987, Vol 5, Num 2, pp 101-114, issn 0001-5938Article

Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindredBEN HAMIDA, M; HENTATI, F; BEN HAMIDA, C et al.Neurology. 1990, Vol 40, Num 2, pp 245-250, issn 0028-3878Article

Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophyMONGI BEN HAMIDA; FAYCAL HENTATI; BEN HAMIDA, C et al.Brain. 1990, Vol 113, Num 2, pp 347-363, issn 0006-8950, 17 p.Article

Postnatal maturation of the vascularisation of the suprasylvian gyrus of the catBEN HAMIDA, C; BISCONTE, J. C; MARGULES, S et al.Journal of anatomy (Print). 1983, Vol 137, Num 2, pp 371-385, issn 0021-8782Article

Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosisMONGI BEN HAMIDA; FETHI LETAIEF; FAYCAL HENTATI et al.Journal of the neurological sciences. 1987, Vol 78, Num 3, pp 313-329, issn 0022-510XArticle

Hypertrophic neuropathy in spinocerebellar degeneration: morphological study of the superficial peroneal nerve in fourteen casesBEN HAMIDA, M; LETAIEF, F; HENTATI, F et al.Acta neuropathologica. 1987, Vol 75, Num 1, pp 51-61, issn 0001-6322Article

Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduriaLARNAOUT, A; HENTATI, F; BELAL, S et al.Acta neuropathologica. 1994, Vol 88, Num 4, pp 367-370, issn 0001-6322Article

Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration : a clinicopathological observation in three siblingsLARNAOUT, A; BELAL, S; BEN HAMIDA, C et al.Journal of neurology. 1998, Vol 245, Num 4, pp 231-235, issn 0340-5354Article

MALADIE DE NIEMANN-PICK TYPE B. RAPPORT D'UN CAS, ETUDE HISTOCHIMIQUE, ENZYMATIQUE ET ULTRASTRUCTURALEKHODJET EL KHIL A; ENNOURI A; KHODJET EL KHIL R et al.1982; ARCH. ANAT. CYTOL. PATHOL.; ISSN 0395-501X; FRA; DA. 1982; VOL. 30; NO 2; PP. 69-76; ABS. ENG; BIBL. 57 REF.Article

Neuropathie périphérique dans un cas sporadique de xanthomatose cérébrotendineuse = Peripheral neuropathy in an anecdotic case of cerebrotendinous xanthomatosisBAN HAMIDA, M; CHABBI, N; BEN HAMIDA, C et al.Revue neurologique (Paris). 1991, Vol 147, Num 5, pp 385-388, issn 0035-3787, 4 p.Article

Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophyBEN HAMIDA, C; SOUSSI-YANICOSTAS, N; BEJAOUI, K et al.Journal of the neurological sciences. 1994, Vol 123, Num 1-2, pp 114-121, issn 0022-510XArticle

Evolution of muscle specific proteins in Werdig-Hoffman's diseaseSOUSSI-YANICOSTA, N; BEN HAMIDA, C; BEJAOUI, K et al.Journal of the neurological sciences. 1992, Vol 109, Num 1, pp 111-120, issn 0022-510XArticle

Maladie coeliaque, thrombose veineuse cérébrale et déficit en protéine s, une association fortuite ? = Celiac disease, cerebral venous thrombosis and protein s deficiency, a fortuitous association?BAHLOUL, M; CHAARI, A; KHLAF-BOUAZIZ, N et al.Journal des maladies vasculaires. 2005, Vol 30, Num 4, pp 228-230, issn 0398-0499, 3 p., CAH1Article

Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian familyMRISSA, N; BELAL, S; BEN HAMIDA, C et al.Neurology. 2000, Vol 54, Num 7, pp 1408-1414, issn 0028-3878Article

Fibrolipome congénitale de la région mésencéphaloprotubérantielle = Congenital fibrolipoma of the mesencephalo-protuberantial areaLARNAOUT, A; HENTATI, F; BEN HAMIDA, C et al.Archives de pédiatrie (Paris). 1994, Vol 1, Num 10, pp 913-915, issn 0929-693XConference Paper