Challenges of genetic diagnosis of inborn errors of metabolism in a major tertiary care center in Lebanon by Doaa O. Salman, Rami Mahfouz, Elio R. Bitar, Jinane Samaha, Jinane Samaha, Pascale E. Karam, Pascale E. Karam

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Pamidronate Rescue Therapy for Hypercalcemia in a Child With Williams Syndrome by Sami A. Sanjad, Bilal Aoun, Halim Yammine, Amina Bassyouni, Pascale E. Karam

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Mitochondrial depletion syndrome type 3: the Lebanese variant by Marianne Majdalani, Nadine Yazbeck, Lamis El Harake, Jinane Samaha, Pascale E. Karam

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Kidney and Metabolic Phenotypes in Glycogen Storage Disease Type-I Patients by Bilal Aoun, Sami Sanjad, Jad A. Degheili, Abir Barhoumi, Amina Bassyouni, Pascale E. Karam

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Genetic literacy among primary care physicians in a resource-constrained setting by Pascale E. Karam, Lina Hamad, Mohamed Elsherif, Khalil Kreidieh, Ghunwa Nakouzi, Khalil El Asmar, Tamar Kabakian-Khasholian, Dany Assaf Curi, Soha N. Yazbek

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