102 related articles for article (PubMed ID: 11933462)
1. Mitochondrial cardiomyopathy--case report.
Steiner I; Zeman J; Spacek J; Hansíková H; Wenchich L
Cesk Patol; 2002 Jan; 38(1):41-5. PubMed ID: 11933462
[TBL] [Abstract][Full Text] [Related]
2. A case of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation.
Vallance HD; Jeven G; Wallace DC; Brown MD
Pediatr Cardiol; 2004; 25(5):538-40. PubMed ID: 15164143
[TBL] [Abstract][Full Text] [Related]
3. [An autopsy case of neonatal lactic acidosis].
Giordano G; Corradi D; D'Adda T; Melissari M
Pathologica; 2001 Feb; 93(1):39-43. PubMed ID: 11294018
[TBL] [Abstract][Full Text] [Related]
4. A case of fatal mitochondrial cardiomyopathy.
Yokoyama U; Shibata T; Yasui K; Iwamoto M; Takigiku K; Yokota S
Jpn Heart J; 2002 Jan; 43(1):61-7. PubMed ID: 12041891
[TBL] [Abstract][Full Text] [Related]
5. Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunction.
Raha S; Merante F; Shoubridge E; Myint AT; Tein I; Benson L; Johns T; Robinson BH
Hum Mutat; 1999; 13(3):245-54. PubMed ID: 10090480
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Increased reactive oxygen species and anti-oxidative response in mitochondrial cardiomyopathy.
Ishikawa K; Kimura S; Kobayashi A; Sato T; Matsumoto H; Ujiie Y; Nakazato K; Mitsugi M; Maruyama Y
Circ J; 2005 May; 69(5):617-20. PubMed ID: 15849452
[TBL] [Abstract][Full Text] [Related]
8. Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G).
Pastores GM; Santorelli FM; Shanske S; Gelb BD; Fyfe B; Wolfe D; Willner JP
Am J Med Genet; 1994 Apr; 50(3):265-71. PubMed ID: 8042671
[TBL] [Abstract][Full Text] [Related]
9. Clinical presentations of mitochondrial cardiomyopathies.
Lev D; Nissenkorn A; Leshinsky-Silver E; Sadeh M; Zeharia A; Garty BZ; Blieden L; Barash V; Lerman-Sagie T
Pediatr Cardiol; 2004; 25(5):443-50. PubMed ID: 15185043
[TBL] [Abstract][Full Text] [Related]
10. Cardiomyopathy in respiratory chain disorders.
Guenthard J; Wyler F; Fowler B; Baumgartner R
Arch Dis Child; 1995 Mar; 72(3):223-6. PubMed ID: 7741568
[TBL] [Abstract][Full Text] [Related]
11. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
Auré K; Fayet G; Leroy JP; Lacène E; Romero NB; Lombès A
Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
[TBL] [Abstract][Full Text] [Related]
12. [Diagnosis of mitochondrial cardiomyopathies: the need for a multidisciplinary approach].
Santorelli FM; Bertini E
G Ital Cardiol; 1999 Oct; 29(10):1181-3. PubMed ID: 10546130
[No Abstract] [Full Text] [Related]
13. Rapid progression of cardiomyopathy in mitochondrial diabetes.
Momiyama Y; Atsumi Y; Ohsuzu F; Ui S; Morinaga S; Matsuoka K; Kimura M
Jpn Circ J; 1999 Feb; 63(2):130-2. PubMed ID: 10084376
[TBL] [Abstract][Full Text] [Related]
14. Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy.
Marin-Garcia J; Ananthakrishnan R; Goldenthal MJ; Filiano JJ; Perez-Atayde A
J Inherit Metab Dis; 1997 Sep; 20(5):674-80. PubMed ID: 9323562
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Is age a contributory factor of mitochondrial bioenergetic decline and DNA defects in idiopathic dilated cardiomyopathy?
Marin-Garcia J; Goldenthal MJ; Pierpont EM; Ananthakrishnan R; Perez-Atayde A
Cardiovasc Pathol; 1999; 8(4):217-22. PubMed ID: 10724526
[TBL] [Abstract][Full Text] [Related]
17. Mitochondrial creatine kinase activity in patients with disturbed energy generation in muscle mitochondria.
Smeitink J; Ruitenbeek W; Sengers R; Wevers R; van Lith T; Trijbels F
J Inherit Metab Dis; 1994; 17(1):67-73. PubMed ID: 8051938
[TBL] [Abstract][Full Text] [Related]
18. Hereditary mitochondrial hypertrophic cardiomyopathy with mitochondrial myopathy of skeletal muscle, congenital cataract and lactic acidosis.
van Ekeren GJ; Stadhouders AM; Egberink GJ; Sengers RC; Daniëls O; Kubat K
Virchows Arch A Pathol Anat Histopathol; 1987; 412(1):47-52. PubMed ID: 3120403
[TBL] [Abstract][Full Text] [Related]
19. Defects in the mitochondrial energy metabolism outside the respiratory chain and the pyruvate dehydrogenase complex.
Trijbels FJ; Ruitenbeek W; Huizing M; Wendel U; Smeitink JA; Sengers RC
Mol Cell Biochem; 1997 Sep; 174(1-2):243-7. PubMed ID: 9309695
[TBL] [Abstract][Full Text] [Related]
20. Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects.
De Paepe B; Smet J; Lammens M; Seneca S; Martin JJ; De Bleecker J; De Meirleir L; Lissens W; Van Coster R
J Clin Pathol; 2009 Feb; 62(2):172-6. PubMed ID: 19181635
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
