The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
Koenig, Michel, Belal, Samir, Hentati, Fayçal, Bomont, Pascale, Cavalier, Laurent, Demir, Ercan, Korinthenberg, Rudolf, Tüysüz, Beyhan, Hamida, Christiane Ben, Blondeau, François, Topaloglu, Haluk, Landrieu, Pierre, Tazir, Meriem
Published in Nature genetics (01.11.2000)
Published in Nature genetics (01.11.2000)
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Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)
Hammouda, Hadi, Nicole, Sophie, Topaloglu, Haluk, Weissenbach, Jean, Lehmann-Horn, Franck, Samson, Delphine, Cruaud, Corinne, Hentati, Faycal, Davoine, Claire-Sophie, Beighton, Peter, Barral, Duarte, Fontaine, Bertrand, Urtizberea, J. Andoni, White, Peter S, Cattolico, Laurence, Hamida, Christiane Ben
Published in Nature genetics (01.12.2000)
Published in Nature genetics (01.12.2000)
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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35
Bejaoui, Khemissa, Pericak-Vance, Margaret A, Hentati, Afif, Brown, Robert H, Hung, Wu-Yen, Siddique, Teepu, Speer, Marcy C, Ben Hamida, Christiane, Ben Hamida, Mongi, Hentati, Faycal, Figlewicz, Denise A, Haines, Jonathan, Rimmler, Jackie
Published in Nature genetics (01.07.1994)
Published in Nature genetics (01.07.1994)
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Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q
Ben Othmane, Kamel, Ben Hamida, Mongi, Pericak-Vance, Margaret A, Ben Hamida, Christiane, Blel, Samir, Carter, Susan C, Bowcock, Anne M, Petruhkin, Konstantin, Conrad Gilliam, T, Roses, Allen D, Hentati, Faycal, Vance, Jeffery M
Published in Nature genetics (01.12.1992)
Published in Nature genetics (01.12.1992)
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Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study
Gouider-Khouja, Neziha, Larnaout, Abdelmajid, Amouri, Rim, Sfar, Sana, Belal, Samir, Ben Hamida, Christiane, Ben Hamida, Mongi, Hattori, Nobutaka, Mizuno, Yoshikuni, Hentati, Fayçal
Published in Parkinsonism & related disorders (01.06.2003)
Published in Parkinsonism & related disorders (01.06.2003)
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Ataxia with vitamin E deficiency : refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families
DOERFLINGER, N, LINDER, C, MONGI BEN HAMIDA, PANDOLFO, M, DIDONATO, S, SOKOL, R, KAYDEN, H, LANDRIEU, P, DURR, A, BRICE, A, GOUTIERES, F, KOHLSCHÜTTER, A, OUAHCHI, K, SABOURAUD, P, ALI BENOMAR, MOHAMED YAHYAOUI, MANDEL, J.-L, KOENIG, M, GYAPAY, G, WEISSENBACH, J, LE PASLIER, D, RIGAULT, P, SAMIR BELAL, BEN HAMIDA, C, HENTATI, F
Published in American journal of human genetics (01.05.1995)
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Published in American journal of human genetics (01.05.1995)
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Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy
Ben Hamida, C, Soussi-Yanicostas, N, Butler-Browne, G S, Bejaoui, K, Hentati, F, Ben Hamida, M
Published in Muscle & nerve (01.04.1994)
Published in Muscle & nerve (01.04.1994)
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Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping
Nicole, S, Ben Hamida, C, Beighton, P, Bakouri, S, Belal, S, Romero, N, Viljoen, D, Ponsot, G, Sammoud, A, Weissenbach, J
Published in Human molecular genetics (01.09.1995)
Published in Human molecular genetics (01.09.1995)
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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
Fontaine, B, Nicole, S, Topaloglu, H, Ben Hamida, C, Beighton, P, Spaans, F, Cantu, J M, Bakouri, S, Romero, N, Ricker, K, Barros-Nunez, P, Ponsot, G, Ben Hamida, M, Weissenbach, J, Hentati, F, Lehmann-Horn, F
Published in Human genetics (01.09.1996)
Published in Human genetics (01.09.1996)
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Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus
BELAL, S, PANAYIDES, K, MIDDLETON, L. T, SIRUGO, G, BEN HAMIDA, C, IOANNOU, P, HENTATI, F, BECKMANN, J, KOENIG, M, MANDEL, J.-L, MONGI BEN HAMIDA
Published in American journal of human genetics (01.12.1992)
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Published in American journal of human genetics (01.12.1992)
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Les atrophies péronières en Tunisie
Hamida, Mongi Ben, Letaief, Fethi, Hamida, Christiane Ben, Samoud, Slaheddine
Published in Journal of the neurological sciences (01.06.1981)
Published in Journal of the neurological sciences (01.06.1981)
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