Similar articles for PMID: 24585816

Year	Number of Results
1981	1
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1992	1
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1998	2
1999	1
2002	1
2003	1
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2012	5
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2014	14
2015	10
2016	4
2017	4
2018	7
2019	6
2020	3
2021	2

1

Index of suspicion. Case 1: fever, diarrhea, jaundice, and confusion in an 18-year-old male. Case 2: severe anemia in a 6-month-old girl. Case 3: red urine in a 4-month-old boy.

Ku E, Thomas M, Ho CH, Whipple NS, Abdul-Rahman O, Megason GC, Herrington BL, Carmody JB, Charlton JR. Ku E, et al. Pediatr Rev. 2014 Mar;35(3):129-35. doi: 10.1542/pir.35-3-129. Pediatr Rev. 2014. PMID: 24585816 No abstract available.

2

Pearson Syndrome, A Medical Diagnosis Difficult to Sustain Without Genetic Testing.

Sur L, Floca E, Samasca G, Lupan I, Aldea C, Sur G. Sur L, et al. Clin Lab. 2018 Mar 1;64(3):375-377. doi: 10.7754/Clin.Lab.2017.171017. Clin Lab. 2018. PMID: 29739102

3

A primigravida with very-long-chain acyl-CoA dehydrogenase deficiency.

Murata KY, Sugie H, Nishino I, Kondo T, Ito H. Murata KY, et al. Muscle Nerve. 2014 Feb;49(2):295-6. doi: 10.1002/mus.24055. Muscle Nerve. 2014. PMID: 23966064 No abstract available.

4

Hypotonia and Lethargy in a Two-Day-Old Male Infant.

Long AH, Fiore JG, Gillani R, Douglass LM, Fujii AM, Hoffman JD. Long AH, et al. Pediatrics. 2019 Jul;144(1):e20180788. doi: 10.1542/peds.2018-0788. Pediatrics. 2019. PMID: 31227563 Free article.

5

Breath-holding spell and macrocytic anaemia in a toddler.

Ramachandran S, Alessandri A, Price J, Balasubramaniam S. Ramachandran S, et al. Br J Haematol. 2014 Jul;166(2):156. doi: 10.1111/bjh.12927. Epub 2014 May 5. Br J Haematol. 2014. PMID: 24797152 No abstract available.

6

Early presentation of very long chain acyl-CoA dehydrogenase deficiency: nursing action resulting in a positive outcome.

Sedgwick ER. Sedgwick ER. J Pediatr Nurs. 2013 Jul-Aug;28(4):379-82. doi: 10.1016/j.pedn.2012.11.002. Epub 2012 Dec 10. J Pediatr Nurs. 2013. PMID: 23238219 Review.

7

Successful management of pregnancy with very-long-chain acyl-coenzyme A dehydrogenase deficiency.

Yamamoto H, Tachibana D, Tajima G, Shigematsu Y, Hamasaki T, Tanaka A, Koyama M. Yamamoto H, et al. J Obstet Gynaecol Res. 2015 Jul;41(7):1126-8. doi: 10.1111/jog.12672. Epub 2015 Feb 6. J Obstet Gynaecol Res. 2015. PMID: 25655073

8

Pearson Syndrome: A Rare Cause of Failure to Thrive in Infants.

Pronman L, Rondinelli M, Burkardt DD, Velayuthan S, Khalili AS, Bedoyan JK. Pronman L, et al. Clin Pediatr (Phila). 2019 Jun;58(7):819-824. doi: 10.1177/0009922819834285. Epub 2019 Mar 7. Clin Pediatr (Phila). 2019. PMID: 30845838 No abstract available.

9

Very long-chain acyl-coenzyme A dehydrogenase deficiency in Chinese patients: eight case reports, including one case of prenatal diagnosis.

Li X, Ding Y, Ma Y, Liu Y, Wang Q, Song J, Yang Y. Li X, et al. Eur J Med Genet. 2015 Mar;58(3):134-9. doi: 10.1016/j.ejmg.2015.01.005. Epub 2015 Jan 31. Eur J Med Genet. 2015. PMID: 25652019

10

[Mass Screening for Inborn Errors of Metabolism].

Ito T. Ito T. Rinsho Byori. 2015 Apr;63(4):441-9. Rinsho Byori. 2015. PMID: 26536777 Review. Japanese.

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