Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency
Gabsi, S., Gouider-Khouja, N., Belal, S., Fki, M., Kefi, M., Turki, I., Hamida, M. Ben, Kayden, H., Mebazaa, R., Hentati, F.
Published in European journal of neurology (01.09.2001)
Published in European journal of neurology (01.09.2001)
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Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family
Mrissa, N, Belal, S, Hamida, C B, Amouri, R, Turki, I, Mrissa, R, Hamida, M B, Hentati, F
Published in Neurology (11.04.2000)
Published in Neurology (11.04.2000)
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Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping
Dib, C, Belal, S, Cohen, D, Novelli, G, Reutenauer, L, Ben Hamida, C, Mandel, J.-L, Linder, C, Vignal, A, Gyapay, G, Doerflinger, N, Hentati, F, Mokini, V, Kœnig, M, Le Paslier, D, Ben Hamida, M, Pandolfo, M
Published in Nature genetics (01.10.1993)
Published in Nature genetics (01.10.1993)
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Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation
Kefi, M, Amouri, R, Driss, A, Ben Hamida, C, Ben Hamida a, M, Kunkel, L.M, Hentati, F
Published in Neuromuscular disorders : NMD (01.12.2003)
Published in Neuromuscular disorders : NMD (01.12.2003)
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Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14
Bejaoui, K, Hirabayashi, K, Hentati, F, Haines, J L, Ben Hamida, C, Belal, S, Miller, R G, McKenna-Yasek, D, Weissenbach, J, Rowland, L P
Published in Neurology (01.04.1995)
Published in Neurology (01.04.1995)
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POS-647 A RARE CAUSE OF PERITONEAL DIALYSIS RELATED PERITONITIS : ACTINOMYCES ODONTOLYTICUS
DAHMANE, R., Chaker, H., Toumi, S., Ben Brahim, R., Kammoun, K., Mseddi, F., Koubaa, M., Yaich, S., Ben hamida, M.
Published in Kidney international reports (01.04.2021)
Published in Kidney international reports (01.04.2021)
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PB2017: YOUNG PATIENTS WITH NEWLY DIAGNOSED MULTIPLE MYELOMA AND RENAL IMPAIRMENT: A TUNISIAN SINGLE‐CENTER EXPERIENCE
Kallel, F., Mezghani, K., Siala, N., Fakhfekh, Y., Khalifa, L., Hadiji, S., Kassar, O., Frikha, I., Ben Amor, I., Charfi, M., Balloumi, D., Torjmen, L., Kammoun, K., Ben Hamida, M., Ben Othmen, T., Medhaffar, M., Elloumi, M.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families
Ben Hamida, M, Belal, S, Sirugo, G, Ben Hamida, C, Panayides, K, Ionannou, P, Beckmann, J, Mandel, J L, Hentati, F, Koenig, M
Published in Neurology (01.11.1993)
Published in Neurology (01.11.1993)
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POS-015 BIOPSY PROVEN ACUTE TUBULAR NECROSIS: SPECTRUM AND PROGNOSIS
EL HENI, W., Toumi, S., Turki, O., Agrebi, I., Dammak, N., Chaker, H., Masmoudi, M., Yaich, S., Boudawara, T., Kammoun, K., Ben Hamida, M.
Published in Kidney international reports (01.04.2021)
Published in Kidney international reports (01.04.2021)
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POS-648 PRURITUS AND QUALITY OF LIFE IN PERITONEAL DIALYSIS PATIENTS
DAHMANE, R., Chaker, H., Toumi, S., Mseddi, F., Ghorbali, H., Souissi, H., Aguerbi, I., Masmoudi, M., Yaich, S., Kammoun, K., Ben hamida, M., Masmoudi, A.
Published in Kidney international reports (01.04.2021)
Published in Kidney international reports (01.04.2021)
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Friedreich's ataxia with isolated vitamin E deficiency : a neuropathological study of a Tunisian patient
LARNAOUT, A, BELAL, S, ZOUARI, M, FKI, M, HAMIDA, C. B, GOEBEL, H. H, BEN HAMIDA, M, HENTATI, F
Published in Acta neuropathologica (01.06.1997)
Published in Acta neuropathologica (01.06.1997)
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Sequence and structural analyses of NSP4 proteins from human group A rotavirus strains detected in Tunisia
Ben Hadj Fredj, M., Ben Hamida-Rebaï, M., Zeller, M., Heylen, E., Van Ranst, M., Matthijnssens, J., Trabelsi, A.
Published in Pathologie biologie (Paris) (01.06.2014)
Published in Pathologie biologie (Paris) (01.06.2014)
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Limb-girdle muscular dystrophy 2C: Clinical aspects
Ben Hamida, M., Ben Hamida, Ch, Zouari, M., Belal, S., Hentati, F.
Published in Neuromuscular disorders : NMD (01.12.1996)
Published in Neuromuscular disorders : NMD (01.12.1996)
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Relationship between MDM2 and p53 alterations in colorectal cancer and their involvement and prognostic value in the Tunisian population
Chaar, Ines, Amara, Sameh, Khiari, Mariem, Ounissi, Donia, Dhraif, Monia, Ben Hamida, Abd E M, Gharbi, Lassad, Mzabi, Sabeh, Bouraoui, Saadia
Published in Applied immunohistochemistry & molecular morphology (01.05.2013)
Published in Applied immunohistochemistry & molecular morphology (01.05.2013)
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A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
Driss, A., Amouri, R., Ben Hamida, C., Souilem, S., Gouider-Khouja, N., Ben Hamida, M., Hentati, F.
Published in Neuromuscular disorders : NMD (01.06.2000)
Published in Neuromuscular disorders : NMD (01.06.2000)
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Congenital anomalies in Tunisia: Frequency and risk factors
Aloui, M., Nasri, K., Ben Jemaa, N., Ben Hamida, A.M., Masmoudi, A., Gaïgi, S.S., Marrakchi, R.
Published in Journal of gynecology obstetrics and human reproduction (01.10.2017)
Published in Journal of gynecology obstetrics and human reproduction (01.10.2017)
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