172 related articles for article (PubMed ID: 7651935)
1. 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]
2. Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorder.
Van Hove JL; Shanske S; Ciacci F; Ballinger S; Shoffner JS; Wallace DC; Hanioka T; Folkers K; Bossen EH; Kussin PS
Am J Med Genet; 1994 Jun; 51(2):114-20. PubMed ID: 8092186
[TBL] [Abstract][Full Text] [Related]
3. An autopsy case of mitochondrial encephalomyopathy (MELAS) with special reference to extra-neuromuscular abnormalities.
Ban S; Mori N; Saito K; Mizukami K; Suzuki T; Shiraishi H
Acta Pathol Jpn; 1992 Nov; 42(11):818-25. PubMed ID: 1471529
[TBL] [Abstract][Full Text] [Related]
4. Anesthetic considerations in mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome: a case series.
Gurrieri C; Kivela JE; Bojanić K; Gavrilova RH; Flick RP; Sprung J; Weingarten TN
Can J Anaesth; 2011 Aug; 58(8):751-63. PubMed ID: 21656321
[TBL] [Abstract][Full Text] [Related]
5. An autopsy case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) with intestinal bleeding in chronic renal failure.
Mima A; Shiota F; Matsubara T; Iehara N; Akagi T; Abe H; Nagai K; Matsuura M; Murakami T; Kishi S; Araoka T; Kishi F; Kondo N; Shigeta R; Yoshikawa K; Kita T; Doi T; Fukatsu A
Ren Fail; 2011; 33(6):622-5. PubMed ID: 21631236
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Cardiac involvement in mitochondrial disease: a clinical study of 38 patients].
Anan R
Igaku Kenkyu; 1991 Sep; 61(2):49-61. PubMed ID: 1823506
[TBL] [Abstract][Full Text] [Related]
8. [A case of mitochondrial encephalomyopathy (MELAS)].
Suzuki T; Fujino T; Sugiyama M; Ishida M
Nihon Jinzo Gakkai Shi; 1996 Feb; 38(2):109-14. PubMed ID: 8717314
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Heart diseases in mitochondrial encephalomyopathy, lactic acidosis, and stroke syndrome.
Fayssoil A
Congest Heart Fail; 2009; 15(6):284-7. PubMed ID: 19925507
[TBL] [Abstract][Full Text] [Related]
11. MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation.
Connolly BS; Feigenbaum AS; Robinson BH; Dipchand AI; Simon DK; Tarnopolsky MA
Biochem Biophys Res Commun; 2010 Nov; 402(2):443-7. PubMed ID: 20965148
[TBL] [Abstract][Full Text] [Related]
12. [MELAS syndrome (mitochondrial encephalopathy with lactic acidosis and stroke-like episodes].
Carmi E; Defossez C; Morin G; Fraitag S; Lok C; Westeel PF; Canaple S; Denoeux JP
Ann Dermatol Venereol; 2001 Oct; 128(10 Pt 1):1031-5. PubMed ID: 11907964
[TBL] [Abstract][Full Text] [Related]
13. MELAS Syndrome and Kidney Disease Without Fanconi Syndrome or Proteinuria: A Case Report.
Rudnicki M; Mayr JA; Zschocke J; Antretter H; Regele H; Feichtinger RG; Windpessl M; Mayer G; Pölzl G
Am J Kidney Dis; 2016 Dec; 68(6):949-953. PubMed ID: 27683045
[TBL] [Abstract][Full Text] [Related]
14. [Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy].
Márquez C; Bautista J; Arenas J; Segura D; Chinchón I; Rafel E; Campos Y; Huerta R
Neurologia; 1991 May; 6(5):185-7. PubMed ID: 1908255
[TBL] [Abstract][Full Text] [Related]
15. Heart transplantation for progressive cardiomyopathy as a manifestation of MELAS syndrome.
Bhati RS; Sheridan BC; Mill MR; Selzman CH
J Heart Lung Transplant; 2005 Dec; 24(12):2286-9. PubMed ID: 16364883
[TBL] [Abstract][Full Text] [Related]
16. An autopsy case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with chronic renal failure.
Yanagihara C; Oyama A; Tanaka M; Nakaji K; Nishimura Y
Intern Med; 2001 Jul; 40(7):662-5. PubMed ID: 11506313
[TBL] [Abstract][Full Text] [Related]
17. High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families.
Cevoli S; Pallotti F; La Morgia C; Valentino ML; Pierangeli G; Cortelli P; Baruzzi A; Montagna P; Carelli V
Cephalalgia; 2010 Aug; 30(8):919-27. PubMed ID: 20656703
[TBL] [Abstract][Full Text] [Related]
18. Neonatal mitochondrial cardiomyopathy.
Taylor GP
Pediatr Dev Pathol; 2004; 7(6):620-4. PubMed ID: 15630531
[No Abstract] [Full Text] [Related]
19. Mitochondrial encephalomyopathy with lactic acidosis and stroke (MELAS).
Matsumoto J; Saver JL; Brennan KC; Ringman JM
Rev Neurol Dis; 2005; 2(1):30-4. PubMed ID: 16400302
[TBL] [Abstract][Full Text] [Related]
20. MR OEF imaging in MELAS.
Xie S
Methods Enzymol; 2014; 547():433-44. PubMed ID: 25416369
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]