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authFullName_s : Ridha M'Rad
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Heterogeneous clinical features in Cockayne syndrome-A patients with the same mutation and in siblings

Asma Chikhaoui , Ichraf Kraoua , Nadège Calmels , Sami Bouchoucha , Cathy Obringer , et al.
Preprints, Working Papers, ... pasteur-03548783v1

Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndrome

Lilia Kraoua , Hager Jaouadi , Mohamed Allouche , Ahlem Achour , Hakim Kaouther , et al.
MOLECULAR GENETICS & GENOMIC MEDICINE, 2022, 10 (7), ⟨10.1002/mgg3.1954⟩
Journal articles hal-03780229v1

Importance comparative respective de l'analyse infra rouge et de l'analyse chimique classique dans le diagnostique étiologique de la lithiase urinaire

S. Ben Ammar , Hayet Fellah , Ridha M'Rad , A. Zghal , D Khiari , et al.
Tunisie Medicale, 1998, 76 (2), pp.1056-1060
Journal articles pasteur-01985701v1