M.S. Abdelmoula

Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia

Reyhan El Kares, Mohamed‐Ridha Barbouche, Houda Elloumi‐Zghal et al. · Journal of Human Genetics · 2006 · 52 citations · Full text

Mendelian Disorder, Autoimmune Disease, Genetic Disorder +8

Pediatric Systemic Lupus Erythematosus with C1q Deficiency

M. Kallel‐Sellami, LILIA BAILI‐KLILA, Y. Zerzeri et al. · Annals of the New York Academy of Sciences · 2007 · 32 citations

Phenotypic spectrum of fucosidosis in Tunisia

Hadhami Ben Turkia, Néji Tebib, Hatem Azzouz et al. · Journal of Inherited Metabolic Disease · 2008 · 25 citations

Phenotypic continuum of type 2 Gaucher's disease: an intermediate phenotype between perinatal-lethal and classic type 2 Gaucher's disease

Hadhami Ben Turkia, Néji Tebib, Hatem Azzouz et al. · Journal of Perinatology · 2009 · 16 citations

Classic Type 2, Intermediate Phenotype, Genetics +4

Mutation spectrum of glycogen storage disease type Ia in Tunisia: Implication for molecular diagnosis

E. Barkaoui, Wafa Cherif, Néji Tebib et al. · Journal of Inherited Metabolic Disease · 2007 · 15 citations