149 related articles for article (PubMed ID: 16621643)
21. Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stress.
Spiekerkoetter U; Tokunaga C; Wendel U; Mayatepek E; Exil V; Duran M; Wijburg FA; Wanders RJ; Strauss AW
Eur J Clin Invest; 2004 Mar; 34(3):191-6. PubMed ID: 15025677
[TBL] [Abstract][Full Text] [Related]
22. Identification of two novel mutations in the hypoglycemic phenotype of very long chain acyl-CoA dehydrogenase deficiency.
He G; Yang BZ; Roe DS; Teramoto R; Aleck K; Grebe TA; Roe CR; Ding JH
Biochem Biophys Res Commun; 1999 Oct; 264(2):483-7. PubMed ID: 10529389
[TBL] [Abstract][Full Text] [Related]
23. [Very-long-chain acyl-CoA dehydrogenase deficiency presenting with recurrent rhabdomyolysis in an adult].
Hamano H; Shinohara Y; Takizawa S; Tokuoka K; Kazahari S; Mandokoro H; Sato A
Rinsho Shinkeigaku; 2003 May; 43(5):253-7. PubMed ID: 12931630
[TBL] [Abstract][Full Text] [Related]
24. Expression and characterization of mutations in human very long-chain acyl-CoA dehydrogenase using a prokaryotic system.
Goetzman ES; Wang Y; He M; Mohsen AW; Ninness BK; Vockley J
Mol Genet Metab; 2007 Jun; 91(2):138-47. PubMed ID: 17374501
[TBL] [Abstract][Full Text] [Related]
25. Very-long-chain acyl-coenzyme a dehydrogenase deficiency in mice.
Exil VJ; Roberts RL; Sims H; McLaughlin JE; Malkin RA; Gardner CD; Ni G; Rottman JN; Strauss AW
Circ Res; 2003 Sep; 93(5):448-55. PubMed ID: 12893739
[TBL] [Abstract][Full Text] [Related]
26. Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset.
Smelt AH; Poorthuis BJ; Onkenhout W; Scholte HR; Andresen BS; van Duinen SG; Gregersen N; Wintzen AR
Ann Neurol; 1998 Apr; 43(4):540-4. PubMed ID: 9546340
[TBL] [Abstract][Full Text] [Related]
27. Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene.
Andresen BS; Bross P; Vianey-Saban C; Divry P; Zabot MT; Roe CR; Nada MA; Byskov A; Kruse TA; Neve S; Kristiansen K; Knudsen I; Corydon MJ; Gregersen N
Hum Mol Genet; 1996 Apr; 5(4):461-72. PubMed ID: 8845838
[TBL] [Abstract][Full Text] [Related]
28. A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase.
Aoyama T; Uchida Y; Kelley RI; Marble M; Hofman K; Tonsgard JH; Rhead WJ; Hashimoto T
Biochem Biophys Res Commun; 1993 Mar; 191(3):1369-72. PubMed ID: 8466512
[TBL] [Abstract][Full Text] [Related]
29. [A case of skeletal muscle type very-long-chain-acyl CoA dehydrogenase(VLCAD) deficiency with repeated rhabdomyolysis].
Aoyama T; Yazawa I; Sugie H; Shigematsu Y; Sakura N; Nakase H
No To Shinkei; 2004 Jan; 56(1):64-8. PubMed ID: 15024832
[TBL] [Abstract][Full Text] [Related]
30. Cloning and functional characterization of ACAD-9, a novel member of human acyl-CoA dehydrogenase family.
Zhang J; Zhang W; Zou D; Chen G; Wan T; Zhang M; Cao X
Biochem Biophys Res Commun; 2002 Oct; 297(4):1033-42. PubMed ID: 12359260
[TBL] [Abstract][Full Text] [Related]
31. Evidence for impaired gluconeogenesis in very long-chain acyl-CoA dehydrogenase-deficient mice.
Spiekerkoetter U; Ruiter J; Tokunaga C; Wendel U; Mayatepek E; Wijburg FA; Strauss AW; Wanders RJ
Horm Metab Res; 2006 Oct; 38(10):625-30. PubMed ID: 17075770
[TBL] [Abstract][Full Text] [Related]
32. Rat very-long-chain acyl-CoA dehydrogenase, a novel mitochondrial acyl-CoA dehydrogenase gene product, is a rate-limiting enzyme in long-chain fatty acid beta-oxidation system. cDNA and deduced amino acid sequence and distinct specificities of the cDNA-expressed protein.
Aoyama T; Ueno I; Kamijo T; Hashimoto T
J Biol Chem; 1994 Jul; 269(29):19088-94. PubMed ID: 8034667
[TBL] [Abstract][Full Text] [Related]
33. Novel mutation of early, perinatal-onset, myopathic-type very-long-chain acyl-CoA dehydrogenase deficiency.
Korematsu S; Kosugi Y; Kumamoto T; Yamaguchi S; Izumi T
Pediatr Neurol; 2009 Aug; 41(2):151-3. PubMed ID: 19589468
[TBL] [Abstract][Full Text] [Related]
34. Atypical presentation of VLCAD deficiency associated with a novel ACADVL splicing mutation.
Shchelochkov O; Wong LJ; Shaibani A; Shinawi M
Muscle Nerve; 2009 Mar; 39(3):374-82. PubMed ID: 19208414
[TBL] [Abstract][Full Text] [Related]
35. [A case of very-long-chain acyl-CoA dehydrogenase deficiency with adolescent onset being diagnosed by immunostain of biopsy muscle].
Sakata N; Kawai M; Morimatsu M; Oohashi Y; Nishino I; Hasegawa Y; Yamaguchi S
Rinsho Shinkeigaku; 2003 Sep; 43(9):568-70. PubMed ID: 14727566
[TBL] [Abstract][Full Text] [Related]
36. Cloning and expression of an acyl-CoA dehydrogenase from Mycobacterium tuberculosis.
Mahadevan U; Padmanaban G
Biochem Biophys Res Commun; 1998 Mar; 244(3):893-7. PubMed ID: 9535763
[TBL] [Abstract][Full Text] [Related]
37. Identification and characterization of temperature-sensitive mild mutations in three Japanese patients with nonsevere forms of very-long-chain acyl-CoA dehydrogenase deficiency.
Takusa Y; Fukao T; Kimura M; Uchiyama A; Abo W; Tsuboi Y; Hirose S; Fujioka H; Kondo N; Yamaguchi S
Mol Genet Metab; 2002 Mar; 75(3):227-34. PubMed ID: 11914034
[TBL] [Abstract][Full Text] [Related]
38. Development of a new enzymatic diagnosis method for very-long-chain Acyl-CoA dehydrogenase deficiency by detecting 2-hexadecenoyl-CoA production and its application in tandem mass spectrometry-based selective screening and newborn screening in Japan.
Tajima G; Sakura N; Shirao K; Okada S; Tsumura M; Nishimura Y; Ono H; Hasegawa Y; Hata I; Naito E; Yamaguchi S; Shigematsu Y; Kobayashi M
Pediatr Res; 2008 Dec; 64(6):667-72. PubMed ID: 18670371
[TBL] [Abstract][Full Text] [Related]
39. Medium-chain triglycerides impair lipid metabolism and induce hepatic steatosis in very long-chain acyl-CoA dehydrogenase (VLCAD)-deficient mice.
Tucci S; Primassin S; Ter Veld F; Spiekerkoetter U
Mol Genet Metab; 2010 Sep; 101(1):40-7. PubMed ID: 20580297
[TBL] [Abstract][Full Text] [Related]
40. The effect of dantrolene sodium in Very Long Chain Acyl-CoA Dehydrogenase Deficiency.
Voermans NC; Poels PJ; Kluijtmans LA; van Engelen BG
Neuromuscul Disord; 2005 Dec; 15(12):844-6. PubMed ID: 16288870
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
