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MELAS a clinically and genetically heterogeneous syndrome.
Clin Biochem. 2023 Feb;112:75-76. doi: 10.1016/j.clinbiochem.2022.11.007. Epub 2022 Nov 17.
Clin Biochem. 2023.
PMID: 36402172
No abstract available.
Independent origin for m.3243A>G mitochondrial mutation in three Venezuelan cases of MELAS syndrome.
Florez I, Pirrone I, Casique L, Domínguez CL, Mahfoud A, Rodríguez T, Rodríguez D, De Lucca M, Ramírez JL.
Florez I, et al. Among authors: mahfoud a.
Clin Biochem. 2022 Nov-Dec;109-110:98-101. doi: 10.1016/j.clinbiochem.2022.09.007. Epub 2022 Sep 18.
Clin Biochem. 2022.
PMID: 36130631
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Current Practices and Challenges in the Diagnosis and Management of PKU in Latin America: A Multicenter Survey.
Poloni S, Dos Santos BB, Chiesa A, Specola N, Pereyra M, Saborío-Rocafort M, Salazar MF, Leal-Witt MJ, Castro G, Peñaloza F, Wong SP, Porras RB, Paranza LO, Sanabria MC, Amieva MV, Morales M, Naranjo ARC, Mahfoud A, Colmenares AR, Lemes A, Sotillo-Lindo JF, Perez C, Rey LM, Torriente GMZ, Refosco LF, Schwartz IVD, Cornejo V.
Poloni S, et al. Among authors: mahfoud a.
Nutrients. 2021 Jul 27;13(8):2566. doi: 10.3390/nu13082566.
Nutrients. 2021.
PMID: 34444728
Free PMC article.
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[Diagnosis and treatment of methylmalonic aciduria: a case report].
Mahfoud A, Domínguez CL, Pérez A, Rizzo C, Merinero B, Pérez B.
Mahfoud A, et al.
Invest Clin. 2007 Mar;48(1):99-105.
Invest Clin. 2007.
PMID: 17432548
Spanish.
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