144 related articles for article (PubMed ID: 8388688)
1. Fatal infantile mitochondrial encephalomyopathy with complex I and IV deficiencies.
Nagai T; Tuchiya Y; Taguchi Y; Sakuta R; Ichiki T; Nonaka I
Pediatr Neurol; 1993; 9(2):151-4. PubMed ID: 8388688
[TBL] [Abstract][Full Text] [Related]
2. Early-onset fatal encephalomyopathy associated with severe mtDNA depletion.
Paquis-Flucklinger V; Pellissier JF; Camboulives J; Chabrol B; Saunières A; Monfort MF; Giudicelli H; Desnuelle C
Eur J Pediatr; 1995 Jul; 154(7):557-62. PubMed ID: 7556323
[TBL] [Abstract][Full Text] [Related]
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]
8. Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.
Procaccio V; Mousson B; Beugnot R; Duborjal H; Feillet F; Putet G; Pignot-Paintrand I; Lombès A; De Coo R; Smeets H; Lunardi J; Issartel JP
J Clin Invest; 1999 Jul; 104(1):83-92. PubMed ID: 10393702
[TBL] [Abstract][Full Text] [Related]
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]
11. Ragged-red fibers and complex I deficiency in a neonate with arthrogryposis congenita.
Laubscher B; Janzer RC; Krähenbühl S; Hirt L; Deonna T
Pediatr Neurol; 1997 Oct; 17(3):249-51. PubMed ID: 9390702
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA.
Pancrudo J; Shanske S; Bonilla E; Daras M; Akman HO; Krishna S; Malkin E; DiMauro S
J Child Neurol; 2007 Jul; 22(7):858-62. PubMed ID: 17715279
[TBL] [Abstract][Full Text] [Related]
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]
15. Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.
Keightley JA; Anitori R; Burton MD; Quan F; Buist NR; Kennaway NG
Am J Hum Genet; 2000 Dec; 67(6):1400-10. PubMed ID: 11047755
[TBL] [Abstract][Full Text] [Related]
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]
17. Mitochondrial cytopathy with lactic acidosis, carnitine deficiency and DeToni-Fanconi-Debré syndrome.
Kitano A; Nishiyama S; Miike T; Hattori S; Ohtani Y; Matsuda I
Brain Dev; 1986; 8(3):289-95. PubMed ID: 3021012
[TBL] [Abstract][Full Text] [Related]
18. Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.
Leslie N; Wang X; Peng Y; Valencia CA; Khuchua Z; Hata J; Witte D; Huang T; Bove KE
Hum Pathol; 2016 Mar; 49():27-32. PubMed ID: 26826406
[TBL] [Abstract][Full Text] [Related]
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]