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3. Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene. Debray FG; Seneca S; Gonce M; Vancampenhaut K; Bianchi E; Boemer F; Weekers L; Smet J; Van Coster R Mitochondrion; 2014 Jul; 17():101-5. PubMed ID: 24956508 [TBL] [Abstract][Full Text] [Related]
4. Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency. Romero NB; Marsac C; Paturneau-Jouas M; Ogier H; Magnier S; Fardeau M Neuromuscul Disord; 1993 Jan; 3(1):31-42. PubMed ID: 8392409 [TBL] [Abstract][Full Text] [Related]
5. Mitochondrial respiratory-chain defects presenting as nonspecific features in children. Tsao CY; Mendell JR; Lo WD; Luquette M; Rusin J J Child Neurol; 2000 Jul; 15(7):445-8. PubMed ID: 10921514 [TBL] [Abstract][Full Text] [Related]
6. Defects of the mitochondrial respiratory chain complexes in three pediatric cases with hypotonia and cardiac involvement. Figarella-Branger D; Pellissier JF; Scheiner C; Wernert F; Desnuelle C J Neurol Sci; 1992 Mar; 108(1):105-13. PubMed ID: 1320661 [TBL] [Abstract][Full Text] [Related]
7. [Delayed manifestation of mitochondrial myopathy--complex I and IV deficiency of the mitochondrial respiratory chain with progressive paresis]. Beyenburg S; von Wersebe O; Zierz S Nervenarzt; 1991 Aug; 62(8):506-11. PubMed ID: 1658669 [TBL] [Abstract][Full Text] [Related]
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9. Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle. Bentlage HA; Wendel U; Schägger H; ter Laak HJ; Janssen AJ; Trijbels JM Neurology; 1996 Jul; 47(1):243-8. PubMed ID: 8710086 [TBL] [Abstract][Full Text] [Related]
10. Infantile mitochondria encephalomyopathies: report on 4 cases. Pastoris O; Dossena M; Scelsi R; Savasta S; Bianchi E Eur Neurol; 1993; 33(1):54-61. PubMed ID: 8440289 [TBL] [Abstract][Full Text] [Related]
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13. Cytochrome C oxidase-deficient mitochondria in mitochondrial myopathy. Haginoya K; Miyabayashi S; Iinuma K; Okino E; Maesaka H; Tada K Pediatr Neurol; 1992; 8(1):13-8. PubMed ID: 1313674 [TBL] [Abstract][Full Text] [Related]
14. A novel mutation in the mitochondrial tRNA Asn gene associated with a lethal disease. Coulbault L; Herlicoviez D; Chapon F; Read MH; Penniello MJ; Reynier P; Fayet G; Lombès A; Jauzac P; Allouche S Biochem Biophys Res Commun; 2005 Apr; 329(3):1152-4. PubMed ID: 15752774 [TBL] [Abstract][Full Text] [Related]
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16. [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]
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19. Fatal neonatal lactic acidosis with respiratory insufficiency due to complex I and IV deficiency. von Döbeln U; Wibom R; Ahlman H; Nennesmo I; Nyctelius H; Hultman E; Hagenfeldt L Acta Paediatr; 1993 Dec; 82(12):1079-81. PubMed ID: 8155932 [TBL] [Abstract][Full Text] [Related]
20. [A case of mitochondrial encephalomyopathy with cardiomyopathy due to decreased complex I and IV activities]. Kajiyama M; Kawamura I; Fujita A; Hamamoto K; Nishi Y; Kitano A; Matsuda I; Ohtani Y; Miike T No To Hattatsu; 1989 Jul; 21(4):369-73. PubMed ID: 2551357 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]