Diagnostic and Therapeutic Challenges of Hereditary Tyrosinemia Type 1 in Lebanon: A 12-Year Retrospective Review

por Daou, Karim N., Barhoumi, Abir, Bassyouni, Amina, Karam, Pascale E.
Publicado 2021

Pamidronate Rescue Therapy for Hypercalcemia in a Child With Williams Syndrome

por Sanjad, Sami A., Aoun, Bilal, Yammine, Halim, Bassyouni, Amina, Karam, Pascale E.
Publicado 2018

Kidney and Metabolic Phenotypes in Glycogen Storage Disease Type-I Patients

por Aoun, Bilal, Sanjad, Sami, Degheili, Jad A., Barhoumi, Abir, Bassyouni, Amina, Karam, Pascale E.
Publicado 2020