Resultados da busca - Mutaz Sultan

Case Report: DGAT1 deficiency in three infants including a novel missense variant: structural insights and comparison with reported cases por Elie G. Malki, Ahmad Adawi, Mayar Idkedek, Yaqoub Ashhab, Nadirah Damseh, Nadirah Damseh, Mutaz Sultan, Mutaz Sultan

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Mutations in the kinesin KIF12 promote MASH in humans and mice by disrupting lipogenic enzyme turnover por Asieh Etemad, Yosuke Tanaka, Shuo Wang, Mordechai Slae, Mutaz Sultan, Orly Elpeleg, Nobutaka Hirokawa

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Pediatric Ménétrier’s Disease Triggered by Cytomegalovirus Infection: A Rare Case of Severe Hypoalbuminemia and Edema por Issa Snoubar, Tariq Alhendi, Dalia Batanji, Noor Nabresi, Mutaz Sultan, Sami Bannoura, Kamaledein Einar

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Pancrelipase as Adjunctive Therapy in Severe SCOT Deficiency: A Case of a Novel OXCT1 Gene Deletion por Mo'ath Abu Hamdeh, Lema Jaber, Jamal Abdullah, Anas Manhal, Mahmoud M. Qouqas, Mohammed Aldwaik, Sarah Abu Rmeilah, Mutaz Sultan, Shaher Shweiki, Nadirah Damseh

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RIPK1 mutations causing infantile-onset IBD with inflammatory and fistulizing features por Mutaz Sultan, Mohammad Adawi, Nitzan Kol, Nitzan Kol, Nitzan Kol, Blake McCourt, Blake McCourt, Ihda Adawi, Liran Baram, Liran Baram, Noa Tal, Noa Tal, Lael Werner, Lael Werner, Atar Lev, Atar Lev, Atar Lev, Atar Lev, Scott B. Snapper, Scott B. Snapper, Ortal Barel, Ortal Barel, Ortal Barel, Liza Konnikova, Liza Konnikova, Raz Somech, Raz Somech, Raz Somech, Raz Somech, Dror S. Shouval, Dror S. Shouval

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