Similar articles for PMID: 15065573

Year	Number of Results
1967	4
1972	2
1982	1
1983	1
1984	3
1985	2
1987	1
1988	1
1991	4
1992	1
1993	5
1994	4
1995	2
1996	3
1997	3
1998	1
1999	4
2000	4
2001	2
2002	2
2003	2
2004	4
2005	1
2006	3
2007	5
2008	2
2010	4
2011	2
2012	2
2013	1
2014	3
2017	5
2018	5
2019	2
2021	1
2024	0

1

Straight-chain acyl-CoA oxidase deficiency presenting with dysmorphia, neurodevelopmental autistic-type regression and a selective pattern of leukodystrophy.

Kurian MA, Ryan S, Besley GT, Wanders RJ, King MD. Kurian MA, et al. J Inherit Metab Dis. 2004;27(1):105-8. doi: 10.1023/b:boli.0000016687.88818.6d. J Inherit Metab Dis. 2004. PMID: 15065573

2

Peroxisomal acyl-CoA-oxidase deficiency: two new cases.

Carrozzo R, Bellini C, Lucioli S, Deodato F, Cassandrini D, Cassanello M, Caruso U, Rizzo C, Rizza T, Napolitano ML, Wanders RJ, Jakobs C, Bruno C, Santorelli FM, Dionisi-Vici C, Bonioli E. Carrozzo R, et al. Am J Med Genet A. 2008 Jul 1;146A(13):1676-81. doi: 10.1002/ajmg.a.32298. Am J Med Genet A. 2008. PMID: 18536048

3

Effects of hematopoietic stem cell transplantation on acyl-CoA oxidase deficiency: a sibling comparison study.

Wang RY, Monuki ES, Powers J, Schwartz PH, Watkins PA, Shi Y, Moser A, Shrier DA, Waterham HR, Nugent DJ, Abdenur JE. Wang RY, et al. J Inherit Metab Dis. 2014 Sep;37(5):791-9. doi: 10.1007/s10545-014-9698-3. Epub 2014 Mar 12. J Inherit Metab Dis. 2014. PMID: 24619150 Free PMC article.

4

Is autism a disorder of fatty acid metabolism? Possible dysfunction of mitochondrial beta-oxidation by long chain acyl-CoA dehydrogenase.

Clark-Taylor T, Clark-Taylor BE. Clark-Taylor T, et al. Med Hypotheses. 2004;62(6):970-5. doi: 10.1016/j.mehy.2004.01.011. Med Hypotheses. 2004. PMID: 15142659

5

Selective screening for inborn errors of metabolism on clinical patients using tandem mass spectrometry in China: a four-year report.

Han LS, Ye J, Qiu WJ, Gao XL, Wang Y, Gu XF. Han LS, et al. J Inherit Metab Dis. 2007 Aug;30(4):507-14. doi: 10.1007/s10545-007-0543-9. Epub 2007 Mar 8. J Inherit Metab Dis. 2007. PMID: 17347912

6

Inborn Errors of Bile Acid Metabolism.

Heubi JE, Setchell KDR, Bove KE. Heubi JE, et al. Clin Liver Dis. 2018 Nov;22(4):671-687. doi: 10.1016/j.cld.2018.06.006. Epub 2018 Aug 22. Clin Liver Dis. 2018. PMID: 30266156 Review.

7

Milder childhood form of very long-chain acyl-CoA dehydrogenase deficiency in a 6-year-old Japanese boy.

Doi T, Abo W, Tateno M, Hayashi K, Hori T, Nakada T, Fukao T, Takahashi Y, Terada N. Doi T, et al. Eur J Pediatr. 2000 Dec;159(12):908-11. doi: 10.1007/pl00008368. Eur J Pediatr. 2000. PMID: 11131350

8

Pitfall in metabolic screening in a patient with fatal peroxisomal beta-oxidation defect.

Rosewich H, Waterham HR, Wanders RJ, Ferdinandusse S, Henneke M, Hunneman D, Gärtner J. Rosewich H, et al. Neuropediatrics. 2006 Apr;37(2):95-8. doi: 10.1055/s-2006-923943. Neuropediatrics. 2006. PMID: 16773508

9

Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card.

Wood JC, Magera MJ, Rinaldo P, Seashore MR, Strauss AW, Friedman A. Wood JC, et al. Pediatrics. 2001 Jul;108(1):E19. doi: 10.1542/peds.108.1.e19. Pediatrics. 2001. PMID: 11433098

10

Bilateral intracranial vertebral artery dissection presenting as sudden bilateral hearing loss.

Shibata K, Matsui K, Ito H, Ito E, Nishimura Y, Kondo H, Sunose H, Otuka K. Shibata K, et al. Clin Neurol Neurosurg. 2012 Nov;114(9):1266-9. doi: 10.1016/j.clineuro.2012.02.044. Epub 2012 Mar 22. Clin Neurol Neurosurg. 2012. PMID: 22445621 No abstract available.

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