Search Results - "Ben Farhat, M H"

Fh-Souassi: a founder frameshift mutation in exon 10 of the LDL-receptor gene, associated with a mild phenotype in Tunisian families by Slimane, M.N., Lestavel, S., Sun, X.-M., Maatouk, F., Soutar, A.K., Ben Farhat, M.H., Clavey, V., Benlian, P., Hammami, M.

“…Familial hypercholesterolemia (FH) has a higher prevalence in central Tunisia together with a milder clinical expression than in western countries. The…”
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Phenotypic expression of familial hypercholesterolaemia in central and southern Tunisia by Slimane, M N, Pousse, H, Maatoug, F, Hammami, M, Ben Farhat, M H

“…We studied 14 families with familial hypercholesterolaemia (FH) from Central and Southern Tunisia. Twenty-six living homozygotes were identified in these areas…”
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Cardiac involvement in Steinert's myotonic dystrophy by Chebel, S, Ben Hamda, K, Boughammoura, A, Frih Ayed, M, Ben Farhat, M H

“…Cardiac involvement is described as one of the most frequent multisystemic manifestations of Steinert myotonic dystrophy (DM1). This study was performed to…”
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Fh-Souassi: a founder frameshift mutation in exon 10 of the LDL-receptor gene, associated with a mild phenotype in Tunisian families: Genetics and atherosclerosis: broadening the horizon by SLIMANE, M. N, LESTAVEL, S, SUN, X.-M, MAATOUK, F, SOUTAR, A. K, BEN FARHAT, M. H, CLAVEY, V, BENLIAN, P, HAMMAMI, M

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Anomalies cardiaques au cours de la dystrophie myotonique de Steinert by Chebel, S., Ben Hamda, K., Boughammoura, A., Frih Ayed, M., Ben Farhat, M.H.

“…L’atteinte cardiaque est l’une des plus fréquentes des manifestations systémiques de la dystrophie myotonique de Steinert (DM1). Ce travail a pour objectif de…”
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Lipids--lipoproteins--apolipoproteins--risk markers in atherosclerosis by Slimane, M N, Bouslama, A, Maatoug, F, Hammami, M, Ben Farhat, M H

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Distal tubular acidosis and renal lithiasis by el-May, M, Tabka, H, Radhouane, M, Mahjoub, S, Kharrat, T H, Brigui, M, el-Matri, A, Ben Farhat, M H

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