Mariam Arabi

Homozygous familial hypercholesterolemia in Lebanon: A genotype/phenotype correlation

Akl C. Fahed, Raya Safa, F. Haddad et al. · Molecular Genetics and Metabolism · 2010 · 58 citations

Life Sciences, Genetics, Molecular Genetics +14

Serum paraoxonase 1 activity is decreased in thyroid dysfunction

Fereidoun Azizi, Farbod Raiszadeh, Mehrdad Solati et al. · Journal of Endocrinological Investigation · 2003 · 56 citations

Medicine, Biochemistry, Endocrinology +2

Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype

Kamel Shibbani, Akl C. Fahed, Laila Al‐Shaar et al. · Clinical Genetics · 2013 · 47 citations

Medicine, Biochemistry, Cardiology +11

NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity

Ossama Abou Hassan, Akl C. Fahed, Manal Batrawi et al. · Scientific Reports · 2015 · 45 citations · Full text

Medicine, Cardiology, Genetics +16

Pulmonary hypertension in children and young adults with sickle cell disease: Evidence for familial clustering

Hanane A. Dahoui, Munya N. Hayek, Paul J. Nietert et al. · Pediatric Blood & Cancer · 2009 · 25 citations

Medicine, Child Health, Pediatrics +14