These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
240 related articles for article (PubMed ID: 23868323)
41. Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts. Roe DS; Yang BZ; Vianey-Saban C; Struys E; Sweetman L; Roe CR Mol Genet Metab; 2006 Jan; 87(1):40-7. PubMed ID: 16297647 [TBL] [Abstract][Full Text] [Related]
42. [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]
43. Isolated mitochondrial long-chain ketoacyl-CoA thiolase deficiency resulting from mutations in the HADHB gene. Das AM; Illsinger S; Lücke T; Hartmann H; Ruiter JP; Steuerwald U; Waterham HR; Duran M; Wanders RJ Clin Chem; 2006 Mar; 52(3):530-4. PubMed ID: 16423905 [TBL] [Abstract][Full Text] [Related]
44. [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]
45. Genetic, biochemical, and clinical spectrum of patients with mitochondrial trifunctional protein deficiency identified after the introduction of newborn screening in the Netherlands. Schwantje M; Fuchs SA; de Boer L; Bosch AM; Cuppen I; Dekkers E; Derks TGJ; Ferdinandusse S; Ijlst L; Houtkooper RH; Maase R; van der Pol WL; de Vries MC; Verschoof-Puite RK; Wanders RJA; Williams M; Wijburg F; Visser G J Inherit Metab Dis; 2022 Jul; 45(4):804-818. PubMed ID: 35383965 [TBL] [Abstract][Full Text] [Related]
46. Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein. Spiekerkoetter U; Bennett MJ; Ben-Zeev B; Strauss AW; Tein I Muscle Nerve; 2004 Jan; 29(1):66-72. PubMed ID: 14694500 [TBL] [Abstract][Full Text] [Related]
47. Disturbance of mitochondrial functions provoked by the major long-chain 3-hydroxylated fatty acids accumulating in MTP and LCHAD deficiencies in skeletal muscle. Cecatto C; Godoy KDS; da Silva JC; Amaral AU; Wajner M Toxicol In Vitro; 2016 Oct; 36():1-9. PubMed ID: 27371118 [TBL] [Abstract][Full Text] [Related]
49. A comprehensive HADHA c.1528G>C frequency study reveals high prevalence of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency in Poland. Piekutowska-Abramczuk D; Olsen RK; Wierzba J; Popowska E; Jurkiewicz D; Ciara E; Ołtarzewski M; Gradowska W; Sykut-Cegielska J; Krajewska-Walasek M; Andresen BS; Gregersen N; Pronicka E J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S373-7. PubMed ID: 20814823 [TBL] [Abstract][Full Text] [Related]
50. Impaired Fat Oxidation During Exercise in Long-Chain Acyl-CoA Dehydrogenase Deficiency Patients and Effect of IV-Glucose. Madsen KL; Stemmerik MG; Buch AE; Poulsen NS; Lund AM; Vissing J J Clin Endocrinol Metab; 2019 Sep; 104(9):3610-3613. PubMed ID: 30990523 [TBL] [Abstract][Full Text] [Related]
51. Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency and progressive retinopathy: one case report followed by ERGs, VEPs, EOG over a 17-year period. Rigaudière F; Delouvrier E; Le Gargasson JF; Milani P; Ogier de Baulny H; Schiff M Doc Ophthalmol; 2021 Jun; 142(3):371-380. PubMed ID: 33392894 [TBL] [Abstract][Full Text] [Related]
53. A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women. Ibdah JA; Bennett MJ; Rinaldo P; Zhao Y; Gibson B; Sims HF; Strauss AW N Engl J Med; 1999 Jun; 340(22):1723-31. PubMed ID: 10352164 [TBL] [Abstract][Full Text] [Related]
54. [A case of very long chain acyl-CoA dehydrogenase deficiency diagnosed due to a trigger of hyperemesis gravidarum during pregnancy]. Shiraishi W; Tateishi T; Hayashida S; Tajima G; Tsumura M; Isobe N Rinsho Shinkeigaku; 2023 Oct; 63(10):656-660. PubMed ID: 37779023 [TBL] [Abstract][Full Text] [Related]
55. [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]