Works matching Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

Results: 21

Topical Review: Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Strokelike Episodes (MELAS): Current Concepts.

Published in:

Journal of Child Neurology, 1994, v. 9, n. 1, p. 4, doi. 10.1177/088307389400900102

By:

Hirano, Michio;
Pavlakis, Steven G.

Publication type:

Article

The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).

Published in:

1996

By:

Nishino, Ichizo;
Komatsu, Mikio;
Kodama, Soichi;
Horai, Satoshi;
Nonaka, Ikuya;
Goto, Yu-Ichi;
Nishino, I;
Komatsu, M;
Kodama, S;
Horai, S;
Nonaka, I;
Goto, Y

Publication type:

journal article

Novel Mitochondrial DNA Transversion Mutation in Transfer Ribonucleic Acid for Leucine 2 (CUN) in a Patient With the Clinical Features of MELAS.

Published in:

Journal of Child Neurology, 2006, v. 21, n. 11, p. 971, doi. 10.1177/08830738060210110601

By:

Abu-Amero, Khaled K.;
Ozand, Pinar T.;
Al-Dhalaan, Hesham

Publication type:

Article

G M1 Gangliosidosis Type 2 in Two Siblings.

Published in:

Journal of Child Neurology, 1992, v. 7, n. 1S, p. S41, doi. 10.1177/088307389200700107

By:

Gascon, Generoso G.;
Ozand, Pinar T.;
Erwin, Robert E.

Publication type:

Article

Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system.

Published in:

2008

By:

Janssen AJM;
Schuelke M;
Smeitink JAM;
Trijbels FJM;
Sengers RCA;
Lucke B;
Wintjes LTM;
Morava E;
van Engelen BGM;
Smits BW;
Hol FA;
Siers MH;
Ter Laak H;
van der Knaap MS;
van Spronsen FJ;
Rodenburg RJT;
van den Heuvel LP

Publication type:

Journal Article

Muscle 3243A→G mutation load and capacity of the mitochondrial energy-generating system.

Published in:

Annals of Neurology, 2008, v. 63, n. 4, p. 473, doi. 10.1002/ana.21328

By:

Janssen, Antoon J. M.;
Schuelke, Markus;
Smeitink, Jan A. M.;
Trijbels, Frans J. M.;
Sengers, Rob C. A.;
Lucke, Barbara;
Wintjes, Liesbeth T. M.;
Morava, Eva;
van Engelen, Baziel G. M.;
Smits, Bart W.;
Hol, Frans A.;
Siers, Marloes H.;
Ter Laak, Henk;
van der Knaap, Marjo S.;
Van Spronsen, Francjan J.;
Rodenburg, Richard J. T.;
van den Heuvel, Lambert P.

Publication type:

Article

MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.

Published in:

Annals of Neurology, 1996, v. 40, n. 3, p. 459, doi. 10.1002/ana.410400318

By:

Taylor, R. W.;
Chinnery, P. F.;
Haldane, F.;
Morris, A. A. M.;
Bindoff, L. A.;
Turnbull, D. M.;
Wilson, J.

Publication type:

Article

MELAS- and kearns-sayre-type with myopathy and autoimmune polyendocrinopahy.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 761, doi. 10.1002/ana.410390612

By:

Ohno, Kinji;
Yamamoto, Masahiko;
Engel, Andrew G.;
Michel, C. Michel;
Roberts, Lewis R.;
Tan, Gerry H.;
Fatourechi, Vahab

Publication type:

Article

Mitochondrial myopathy with progressive decrease in mitochondrial tRNALeu(UUR) mutant genomes.

Published in:

Annals of Neurology, 1994, v. 35, n. 3, p. 370, doi. 10.1002/ana.410350322

By:

Kawakami, Yasuhiko;
Sakuta, Ryoichi;
Hashimoto, Kiyoshi;
Fujino, Osamu;
Fujita, Takehisa;
Hida, Masatoshi;
Horai, Satoshi;
Goto, Yu-ichi;
Nonaka, Ikuya

Publication type:

Article

Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency.

Published in:

Annals of Neurology, 1988, v. 24, n. 6, p. 749, doi. 10.1002/ana.410240609

By:

Koga, Yasutoshi;
Nonaka, Ikuya;
Kobayashi, Masanori;
Tojyo, Megumu;
Nihei, Kenji

Publication type:

Article

Early Onset of Diabetes Mellitus Accelerates Cognitive Decline in Japanese Patients with Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes.

Published in:

Tohoku Journal of Experimental Medicine, 2016, v. 238, n. 4, p. 311, doi. 10.1620/tjem.238.311

By:

Takaaki Murakami;
Yuya Shinoto;
Shin Yonemitsu;
Seiji Muro;
Shogo Oki;
Yasutoshi Koga;
Yu-ichi Goto;
Daita Kaneda

Publication type:

Article

Clinical, physiological, and histological features in a kindred with the T3271C melas mutation.

Published in:

1998

By:

Tarnopolsky, M.A.;
Maguire, J.;
Myint, T.;
Applegarth, D.;
Robinson, B.H.

Publication type:

journal article

Quantitation of heteroplasmy of mitochondrial trnaLeu(UUR) gene using PCR-SSCP.

Published in:

Muscle & Nerve, 1995, v. 18, n. 12, p. 1390, doi. 10.1002/mus.880181208

By:

Tanno, Yoshinori;
Yoneda, Makoto;
Tanaka, Keiko;
Tanaka, Hajime;
Yamazaki, Motoyoshi;
Nishiawa, Masatoyo;
Wakabayashi, Koichi;
Ohama, Eisaku;
Tsuji, Shoji

Publication type:

Article

Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.

Published in:

Muscle & Nerve, 1995, v. 18, n. S14, p. S113, doi. 10.1002/mus.880181423

By:

Mita, Shuji;
Tokunaga, Makoto;
Kumamoto, Toshihide;
Uchino, Makoto;
Nonaka, Ikuya;
Ando, Masayuki

Publication type:

Article

Clinical features of melas and mitochondrial DNA mutations.

Published in:

Muscle & Nerve, 1995, v. 18, n. S14, p. S107, doi. 10.1002/mus.880181422

By:

Goto, Yu-Ichi

Publication type:

Article

Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNALeu(UUR) gene.

Published in:

Muscle & Nerve, 1995, v. 18, n. S14, p. S119, doi. 10.1002/mus.880181424

By:

Koga, Yasutoshi;
Davidson, Mercy;
Schon, Eric A.;
King, Michael P.

Publication type:

Article

Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes.

Published in:

Annals of the New York Academy of Sciences, 2008, v. 1142, p. 133, doi. 10.1196/annals.1444.011

By:

Sproule, Douglas M.;
Kaufmann, Petra

Publication type:

Article

Application of NMR spectroscopy to monitoring MELAS treatment: a case report.

Published in:

2002

By:

Möller, Harald E.;
Wiedermann, Dirk;
Kurlemann, Gerhard;
Hilbich, Thorsten;
Schuierer, Gerhard;
Möller, Harald E

Publication type:

journal article

Childhood mitochondrial encephalomyopathies: clinical course, diagnosis, neuroimaging findings, mtDNA mutations and outcome in six children.

Published in:

Italian Journal of Pediatrics, 2013, v. 39, n. 1, p. 60, doi. 10.1186/1824-7288-39-60

By:

Jun Lu;
Yuanyuan Huang

Publication type:

Article

MELAS syndrome diagnosed in ICU in a 56-year-old patient presenting with status epilepticus.

Published in:

2013

By:

Vrettou, Charikleia;
Zervakis, Dimitrios;
Priovolos, Andreas;
Koskina, Sofia;
Tsamouri, Magdalini;
Routsi, Christina

Publication type:

Letter

Deficiency of subunits of Complex I and mitochondrial encephalomyopathy.

Published in:

1988

By:

Ichiki, Takashi;
Tanaka, Masashi;
Nishikimi, Morimitsu;
Suzuki, Hiroshi;
Ozawa, Takayuki;
Kobayashi, Masanori;
Wada, Yoshiro;
Ichiki, T;
Tanaka, M;
Nishikimi, M;
Suzuki, H;
Ozawa, T;
Kobayashi, M;
Wada, Y

Publication type:

journal article

Works matching Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

Topical Review: Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Strokelike Episodes (MELAS): Current Concepts.

The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).

Novel Mitochondrial DNA Transversion Mutation in Transfer Ribonucleic Acid for Leucine 2 (CUN) in a Patient With the Clinical Features of MELAS.

G M1 Gangliosidosis Type 2 in Two Siblings.

Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system.

Muscle 3243A→G mutation load and capacity of the mitochondrial energy-generating system.

MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.

MELAS- and kearns-sayre-type with myopathy and autoimmune polyendocrinopahy.

Mitochondrial myopathy with progressive decrease in mitochondrial tRNA<sup>Leu(UUR)</sup> mutant genomes.

Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency.

Early Onset of Diabetes Mellitus Accelerates Cognitive Decline in Japanese Patients with Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes.

Clinical, physiological, and histological features in a kindred with the T3271C melas mutation.

Quantitation of heteroplasmy of mitochondrial trna<sup>Leu(UUR)</sup> gene using PCR-SSCP.

Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.

Clinical features of melas and mitochondrial DNA mutations.

Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNA<sup>Leu(UUR)</sup> gene.

Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes.

Application of NMR spectroscopy to monitoring MELAS treatment: a case report.

Childhood mitochondrial encephalomyopathies: clinical course, diagnosis, neuroimaging findings, mtDNA mutations and outcome in six children.

MELAS syndrome diagnosed in ICU in a 56-year-old patient presenting with status epilepticus.

Deficiency of subunits of Complex I and mitochondrial encephalomyopathy.