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Page 1
Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients.
Bouchard L, Robert MF, Vinarov D, Stanley CA, Thompson GN, Morris A, Leonard JV, Quant P, Hsu BY, Boneh A, Boukaftane Y, Ashmarina L, Wang S, Miziorko H, Mitchell GA. Bouchard L, et al. Among authors: boukaftane y. Pediatr Res. 2001 Mar;49(3):326-31. doi: 10.1203/00006450-200103000-00005. Pediatr Res. 2001. PMID: 11228257
Medical aspects of ketone body metabolism.
Mitchell GA, Kassovska-Bratinova S, Boukaftane Y, Robert MF, Wang SP, Ashmarina L, Lambert M, Lapierre P, Potier E. Mitchell GA, et al. Among authors: boukaftane y. Clin Invest Med. 1995 Jun;18(3):193-216. Clin Invest Med. 1995. PMID: 7554586 Review.
Inborn errors of ketogenesis.
Mitchell GA, Wang SP, Ashmarina L, Robert MF, Bouchard G, Laurin N, Kassovska-Bratinova S, Boukaftane Y. Mitchell GA, et al. Among authors: boukaftane y. Biochem Soc Trans. 1998 May;26(2):136-40. doi: 10.1042/bst0260136. Biochem Soc Trans. 1998. PMID: 9649735 Review. No abstract available.