130 related articles for article (PubMed ID: 10518284)
21. Clinical heterogeneity in respiratory chain complex III deficiency in childhood.
Mourmans J; Wendel U; Bentlage HA; Trijbels JM; Smeitink JA; de Coo IF; Gabreëls FJ; Sengers RC; Ruitenbeek W
J Neurol Sci; 1997 Jul; 149(1):111-7. PubMed ID: 9168175
[TBL] [Abstract][Full Text] [Related]
22. Apoptosis is suspended in muscle of mitochondrial encephalomyopathies.
Ikezoe K; Nakagawa M; Yan C; Kira J; Goto Y; Nonaka I
Acta Neuropathol; 2002 Jun; 103(6):531-40. PubMed ID: 12012084
[TBL] [Abstract][Full Text] [Related]
23. Familial carnitine deficiency. A fatal case and subclinical state in a sister.
Scholte HR; Meijer AE; van Wijngaarden GK; Leenders KL
J Neurol Sci; 1979 Jun; 42(1):87-101. PubMed ID: 156248
[TBL] [Abstract][Full Text] [Related]
24. Ultrastructural localisation of carnitine acetyltransferase activity in mitochondria of rat myocardium.
Bakker A; Biermans W; Van Belle H; De Bie M; Bernaert I; Jacob W
Biochim Biophys Acta; 1994 Mar; 1185(1):97-102. PubMed ID: 8142416
[TBL] [Abstract][Full Text] [Related]
25. [Carnitine deficiency: a treatable cardiomyopathy].
Hirata K; Yoshioka F; Eto Y; Suzuki K; Yokochi K; Kato H; Ohta K; Terasawa M
J Cardiogr; 1986 Mar; 16(1):217-25. PubMed ID: 3782884
[TBL] [Abstract][Full Text] [Related]
26. Fumarase deficiency: a new cause of mitochondrial encephalomyopathy.
Zinn AB; Kerr DS; Hoppel CL
N Engl J Med; 1986 Aug; 315(8):469-75. PubMed ID: 3736629
[TBL] [Abstract][Full Text] [Related]
27. Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses.
Carrozzo R; Hirano M; Fromenty B; Casali C; Santorelli FM; Bonilla E; DiMauro S; Schon EA; Miranda AF
Neurology; 1998 Jan; 50(1):99-106. PubMed ID: 9443465
[TBL] [Abstract][Full Text] [Related]
28. [Mitochondrial neurogastrointestinal encephalomyopathy presenting with protein-losing gastroenteropathy and serum copper deficiency: a case report].
Hamano H; Ohta T; Takekawa Y; Kouda K; Shinohara Y
Rinsho Shinkeigaku; 1997 Oct; 37(10):917-22. PubMed ID: 9490904
[TBL] [Abstract][Full Text] [Related]
29. Carnitine acetyltransferase activity in the human brain and its microvessels is decreased in Alzheimer's disease.
Kalaria RN; Harik SI
Ann Neurol; 1992 Oct; 32(4):583-6. PubMed ID: 1456745
[TBL] [Abstract][Full Text] [Related]
30. Does the patient have a mitochondrial encephalomyopathy?
DiMauro S; Bonilla E; De Vivo DC
J Child Neurol; 1999 Nov; 14 Suppl 1():S23-35. PubMed ID: 10593563
[TBL] [Abstract][Full Text] [Related]
31. Fatal systemic carnitine deficiency with lipid storage in skeletal muscle, heart, liver and kidney.
Boudin G; Mikol J; Guillard A; Engel AG
J Neurol Sci; 1976 Dec; 30(2-3):313-25. PubMed ID: 187738
[TBL] [Abstract][Full Text] [Related]
32. Mitochondrial DNA deletion in a child with mitochondrial encephalomyopathy, growth hormone deficiency, and hypoparathyroidism.
Cassandrini D; Savasta S; Bozzola M; Tessa A; Pedemonte M; Assereto S; Stringara S; Minetti C; Santorelli FM; Bruno C
J Child Neurol; 2006 Nov; 21(11):983-5. PubMed ID: 17092469
[TBL] [Abstract][Full Text] [Related]
33. Isolation and characterization of carnitine acetyltransferase from S. cerevisiae.
Kispal G; Cseko J; Alkonyi I; Sandor A
Biochim Biophys Acta; 1991 Sep; 1085(2):217-22. PubMed ID: 1892891
[TBL] [Abstract][Full Text] [Related]
34. Psychosis and progressing dementia: presenting features of a mitochondriopathy.
Amemiya S; Hamamoto M; Goto Y; Komaki H; Nishino I; Nonaka I; Katayama Y
Neurology; 2000 Aug; 55(4):600-1. PubMed ID: 10953207
[No Abstract] [Full Text] [Related]
35. Quantitative evaluation of electron transport system proteins in mitochondrial encephalomyopathy.
Haginoya K; Miyabayashi S; Iinuma K; Tada K
Acta Neuropathol; 1993; 85(4):370-7. PubMed ID: 8386896
[TBL] [Abstract][Full Text] [Related]
36. Induction of carnitine acetyltransferase by clofibrate in rat liver.
Mittal B; Kurup CK
Biochem J; 1981 Jan; 194(1):249-55. PubMed ID: 6796058
[TBL] [Abstract][Full Text] [Related]
37. A case of lipid storage myopathy with carnitine deficiency. Biochemical and electromyographic correlations.
Scarlato G; Albizzati MG; Bassi S; Cerri C; Frattola L
Eur Neurol; 1977; 16(1-6):222-9. PubMed ID: 615713
[TBL] [Abstract][Full Text] [Related]
38. Carnitine supplementation and depletion: tissue carnitines and enzymes in fatty acid oxidation.
Negrao CE; Ji LL; Schauer JE; Nagle FJ; Lardy HA
J Appl Physiol (1985); 1987 Jul; 63(1):315-21. PubMed ID: 3624133
[TBL] [Abstract][Full Text] [Related]
39. Multiple mtDNA deletions with features of MNGIE.
Vissing J; Ravn K; Danielsen ER; Dunø M; Wibrand F; Wevers RA; Schwartz M
Neurology; 2002 Sep; 59(6):926-9. PubMed ID: 12297582
[TBL] [Abstract][Full Text] [Related]
40. Multiple muscle cell alterations in a case of encephalomyopathy.
Fujioka H; Tandler B; Rosca M; McCandless SE; Katirji B; Cohen ML; Rapisuwon S; Hoppel CL
Ultrastruct Pathol; 2014 Feb; 38(1):13-25. PubMed ID: 24134831
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]