139 related articles for article (PubMed ID: 8469836)
1. [A study of myocardial disorders in an autopsy case of mitochondrial encephalomyopathy].
Hiruta Y; Muto M; Ichihara T; Uruga K; Mochizuki M; Wachi E; Miyabayashi S; Mayumi F; Adachi K; Toshima H
Kokyu To Junkan; 1993 Mar; 41(3):281-6. PubMed ID: 8469836
[TBL] [Abstract][Full Text] [Related]
2. [A case of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) with progressive cytochrome c oxidase deficiency].
Sumi K; Nagaura T; Itagaki Y; Inui K; Abe J
Rinsho Shinkeigaku; 1989 Jul; 29(7):901-8. PubMed ID: 2553313
[TBL] [Abstract][Full Text] [Related]
3. Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency.
Müller-Höcker J; Hübner G; Bise K; Förster C; Hauck S; Paetzke I; Pongratz D; Kadenbach B
Arch Pathol Lab Med; 1993 Feb; 117(2):202-10. PubMed ID: 8381271
[TBL] [Abstract][Full Text] [Related]
4. [Cardiac changes in a case of mitochondrial encephalomyopathy].
Reis F; Gonçalo L; Machado I; Coelho I; Almeida J
Rev Port Cardiol; 1993 Mar; 12(3):255-60. PubMed ID: 8512718
[TBL] [Abstract][Full Text] [Related]
5. [Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) associated with hypothalamo-pituitary hypofunction--a case report].
Ishii A; Watanabe S; Ohkoshi N; Mizusawa H; Kanazawa I
Rinsho Shinkeigaku; 1991 Feb; 31(2):179-83. PubMed ID: 2060243
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Report of an autopsy.
Hamazaki S; Okada S; Kusaka H; Fujii T; Okuno T; Kashu I; Midorikawa O
Acta Pathol Jpn; 1989 Sep; 39(9):599-606. PubMed ID: 2596299
[TBL] [Abstract][Full Text] [Related]
7. [A case of mitochondrial encephalomyopathy characterized by repeated stroke-like episodes].
Mizuno Y; Ishiguro K; Okamoto K; Morimatsu M; Hirai S
Rinsho Shinkeigaku; 1989 Mar; 29(3):360-6. PubMed ID: 2502353
[TBL] [Abstract][Full Text] [Related]
8. [Mitochondrial DNA deletion in hereditary cardio-encephalo-myopathy].
Melegh B; Seress L; Sümegi B; Trombitás K; Bock I; Kispál G; Oláh E; Méhes K
Orv Hetil; 1995 Jun; 136(24):1275-9. PubMed ID: 7596586
[TBL] [Abstract][Full Text] [Related]
9. [A patient with mitochondrial encephalomyopathy presenting gynecomastia with elevation of serum estriol level].
Yamasaki R; Ohyagi Y; Kawajiri M; Shigeto H; Ikezoe K; Furuya H; Kira J
Rinsho Shinkeigaku; 2004; 44(4-5):291-5. PubMed ID: 15287512
[TBL] [Abstract][Full Text] [Related]
10. Acute hearing loss in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
Chen JC; Tsai TC; Liu CS; Lu CT
Acta Neurol Taiwan; 2007 Sep; 16(3):168-72. PubMed ID: 17966957
[TBL] [Abstract][Full Text] [Related]
11. [MELAS-like episodes in an adult case with cytochrome c oxidase deficiency].
Kihira T; Kohmoto J; Yoshida S; Hironishi M; Kondo T; Nakao N; Goto Y; Nishino K; Nonaka I
Rinsho Shinkeigaku; 2004 Mar; 44(3):187-92. PubMed ID: 15233272
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial encephalomyopathy with A to G transition of mitochondrial transfer RNA(Leu(UUR)) 3,243 presenting hypertrophic cardiomyopathy.
Hiruta Y; Chin K; Shitomi K; Ichihara T; Mochizuki M; Adachi K; Obayashi T; Tanaka M; Ozawa T
Intern Med; 1995 Jul; 34(7):670-3. PubMed ID: 7496082
[TBL] [Abstract][Full Text] [Related]
13. Severe mitochondrial cardiomyopathy and extra-neuromuscular abnormalities in mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode (MELAS).
Ishikawa Y; Asuwa N; Ishii T; Masuda S; Kiguchi H; Hirai S; Akashi N; Yonenami K; Fujisawa Y
Pathol Res Pract; 1995 Feb; 191(1):64-9; discussion 70-5. PubMed ID: 7651935
[TBL] [Abstract][Full Text] [Related]
14. [Mitochondrial encephalomyopathy: clinical aspects, CT morphology and neuropathology].
Wessel K; Poremba M; Pfeiffer J; Roggendorf W
Fortschr Neurol Psychiatr; 1988 May; 56(5):154-62. PubMed ID: 3397029
[TBL] [Abstract][Full Text] [Related]
15. [A mitochondrial encephalomyopathy due to partial cytochrome c oxidase deficiency with giant evoked potentials--a case report].
Higashi Y; Higashi S; Terao A; Yasuda T; Shirabe T
Rinsho Shinkeigaku; 1990 Oct; 30(10):1084-9. PubMed ID: 2177689
[TBL] [Abstract][Full Text] [Related]
16. CMR gives clue to "ragged red fibers" in the heart in a patient with mitochondrial myopathy.
Jose T; Gdynia HJ; Mahrholdt H; Vöhringer M; Klingel K; Kandolf R; Bornemann A; Yilmaz A
Int J Cardiol; 2011 May; 149(1):e24-7. PubMed ID: 19344965
[TBL] [Abstract][Full Text] [Related]
17. Point mutations of muscle mitochondrial DNA from patients with mitochondrial encephalomyopathies.
Song D; Zhang Y; Shi J; Lü Q; Chen J; Zhang H; Zhang W; Wang H; Cai Q
Chin Med J (Engl); 2001 Dec; 114(12):1273-5. PubMed ID: 11793851
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
Prayson RA; Wang N
Arch Pathol Lab Med; 1998 Nov; 122(11):978-81. PubMed ID: 9822126
[TBL] [Abstract][Full Text] [Related]
19. [A case of mitochondrial encephalomyopathy with peripheral neuropathy and autonomic symptoms].
Sasaki I; Tsukaguchi M; Takeuchi H; Yamada A; Touge T; Deguchi K; Nishioka M
No To Shinkei; 1995 Jun; 47(6):563-7. PubMed ID: 7605684
[TBL] [Abstract][Full Text] [Related]
20. [Enzymatic activities of the mitochondrial respiratory chain in child cardiomyopathies. 34 cases prospectively studied by endomyocardial biopsy].
Sidi D; Le Bidois J; Piéchaud JF; Da Cruz E; Marchal C; Gournay V; Kachaner J; Rustin P; Chrétien D; Munnich A
Arch Mal Coeur Vaiss; 1992 May; 85(5):541-6. PubMed ID: 1530392
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
