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A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Abu-Amero, Khaled ; Al-Dhalaan, Hesham ; Bohlega, Saeed ; Hellani, Ali ; Taylor, Robert

Journal of Medical Case Reports, 2009, Vol.3(1), p.77 [Periódico revisado por pares]

BioMed Central

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A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Abu-Amero, Khaled K ; Al-Dhalaan, Hesham ; Bohlega, Saeed ; Hellani, Ali ; Taylor, Robert W

Journal of Medical Case Reports, 2009, Vol.3, p.77-77 [Periódico revisado por pares]

U.S. National Library of Medicine (NIH/NLM)

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A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Abu-Amero, Khaled K ; Al-Dhalaan, Hesham ; Bohlega, Saeed ; Hellani, Ali ; Taylor, Robert W

Journal of medical case reports, 15 October 2009, Vol.3, pp.77 [Periódico revisado por pares]

MEDLINE/PubMed (U.S. National Library of Medicine)

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A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Abu-Amero Khaled K ; Al-Dhalaan Hesham ; Bohlega Saeed ; Hellani Ali ; Taylor Robert W

Journal of Medical Case Reports, 01 October 2009, Vol.3(1), p.77 [Periódico revisado por pares]

Directory of Open Access Journals (DOAJ)

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