Abderrezak Reghis

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Fédérica Piccolo, Steven L. Roberds, Marc Jeanpierre et al. · Nature Genetics · 1995 · 191 citations

Medicine, Neurology, Neuromuscular Disorders +3

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12

Kemal Azlbi, L Bachner, J. Beckmann et al. · Human Molecular Genetics · 1993 · 101 citations

Life Sciences, Genetics, Molecular Genetics +9

Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis

Keren Borensztajn, Ouerdia Chafa, Martine Alhenc‐Gelas et al. · British Journal of Haematology · 2002 · 79 citations

Life Sciences, Genetics, Molecular Genetics +17

At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria

Khédoudja Nafa, Abderrezak Reghis, Naima Osmani et al. · Human Genetics · 1994 · 53 citations

Life Sciences, Genetics, Molecular Genetics +8

Severe hypofibrinogenemia associated with bilateral ischemic necrosis of toes and fingers

Ouerdia Chafa, T. Chellali, C. Sternberg et al. · Blood Coagulation & Fibrinolysis · 1995 · 45 citations

Medicine, Hematology, Pathology +16