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Showing articles 0 to 13 of 13 Filter Applied: mitochondrial disease (Click to remove) Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy NEJM 381:164-172, Case 21-2019, 2019 A 31-Year-Old Man with Sequential Vision Loss Neurol 98:163-169, Fortes, B.,et al, 2022 A Young Man with Progressive Vision and Hearing Loss JAMA Neurol 73:880-883, Kung, N.H.,et al, 2016 MELAS MedLink.com, August, Klopstock, T., 2012 Mitochondrial Optic Neuropathies JNNP 72:423-425, Sadun,A.A., 2002 Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998 NEJM 339:1914-1923, , 1998 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Mitochondrial DNA mutations in an Outbreak of Optic Neuropathy in Cuba Neurol 44:843-845, Hirano,M.,et al, 1994 Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993 Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation Brain 115:979-989, Harding,A.E.,et al, 1992 Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy NEJM 323:1488-1489, Johns,D.R., 1990 Mitochondrial DNA and Genetic Disease Editorial, Lancet 1:250-2511989., , 1989 A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy NEJM 320:1300-1305, Singh,G.,et al, 1989 Showing articles 0 to 13 of 13