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[DOI] [PMC free article] [PubMed] [Google Scholar] 118.Liang WS, Reiman EM, Valla J, Dunckley T, Beach TG, Grover A, et al

These pathways might illuminate causal pathways that are similar or different in diet-associated versus primary (genetic) DCM

Cell 89 , 331340 (1997)

Possible association of CAG repeat polymorphism in KCNN3 encoding the potassium channel SK3 with oxaliplatin-induced neurotoxicity

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Back to Journals Therapeutics and Clinical Risk Management Volume 12 Guidelines for acute management of hyperammonemia in the Middle East region Authors Alfadhel M , Al Mutairi F, Makhseed N, Al Jasmi F, Al-Thihli K, Al-Jishi E, Al-Sayed M, Al-Hassnan ZN, Al Murshedi F, Hberle J, Ben-Omran T Received 26 July 2015 Accepted for publication 23 December 2015 Published 31 March 2016 Volume 2016:12 Pages 479487 DOI Checked for plagiarism Yes Review by Single anonymous peer review Peer reviewer comments 2 Editor who approved publication: Professor Garry Walsh Majid Alfadhel, 1,2 Fuad Al Mutairi, 1,2 Nawal Makhseed, 3 Fatma Al Jasmi, 4 Khalid Al-Thihli, 5 Emtithal Al-Jishi, 6 Moeenaldeen AlSayed, 7 Zuhair N Al-Hassnan, 7,8 Fathiya Al-Murshedi, 5 Johannes Hberle, 9 Tawfeg Ben-Omran 10 Middle East Hyperammonemia and Urea Cycle Disorders Scientific Group (MHUSG) 1 Department of Pediatrics, Division of Genetics, 2 King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia
