Similar articles for PMID: 29895548

Year	Number of Results
1976	1
1979	3
1980	2
1982	2
1983	1
1984	1
1985	2
1986	2
1987	2
1989	1
1993	2
1999	1
2002	2
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2013	14
2014	11
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2016	7
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2018	15
2019	14
2020	14
2021	12
2022	13
2023	3
2024	0

1

Primary carnitine deficiency in a 57-year-old patient with recurrent exertional rhabdomyolysis.

Echaniz-Laguna A, Biancalana V, Gaignard P, Chanson JB. Echaniz-Laguna A, et al. BMJ Case Rep. 2018 Jun 11;2018:bcr2018224272. doi: 10.1136/bcr-2018-224272. BMJ Case Rep. 2018. PMID: 29895548 Free PMC article.

2

Dilated Cardiomyopathy as the Only Clinical Manifestation of Carnitine Transporter Deficiency.

Papadopoulou-Legbelou K, Gogou M, Dokousli V, Eboriadou M, Evangeliou A. Papadopoulou-Legbelou K, et al. Indian J Pediatr. 2017 Mar;84(3):231-233. doi: 10.1007/s12098-016-2250-8. Epub 2016 Nov 3. Indian J Pediatr. 2017. PMID: 27807682

3

Primary Carnitine Deficiency - A Rare Treatable Cause of Cardiomyopathy and Massive Hepatomegaly.

Deswal S, Bijarnia-Mahay S, Manocha V, Hara K, Shigematsu Y, Saxena R, Verma IC. Deswal S, et al. Indian J Pediatr. 2017 Jan;84(1):83-85. doi: 10.1007/s12098-016-2227-7. Epub 2016 Sep 1. Indian J Pediatr. 2017. PMID: 27581592

4

[A cause of dilated cardiomyopathy in a child: primary carnitine deficiency].

Baragou S, Pio M, Di Bernardo S, Ksontini TB, Dommange SJ, Bonafe L, Meijboom E, Sekarski N. Baragou S, et al. Ann Cardiol Angeiol (Paris). 2014 Apr;63(2):107-10. doi: 10.1016/j.ancard.2011.12.006. Epub 2011 Dec 27. Ann Cardiol Angeiol (Paris). 2014. PMID: 22260907 French.

5

Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up.

Yilmaz BS, Kor D, Mungan NO, Erdem S, Ceylaner S. Yilmaz BS, et al. J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):1179-81. doi: 10.1515/jpem-2014-0528. J Pediatr Endocrinol Metab. 2015. PMID: 26030785

6

Thirty-year follow-up of carnitine supplementation in two siblings with hypertrophic cardiomyopathy caused by primary systemic carnitine deficiency.

Kishimoto S, Suda K, Yoshimoto H, Teramachi Y, Nishino H, Koteda Y, Itoh S, Kudo Y, Iemura M, Matsuishi T. Kishimoto S, et al. Int J Cardiol. 2012 Aug 9;159(1):e14-5. doi: 10.1016/j.ijcard.2011.11.010. Epub 2011 Dec 6. Int J Cardiol. 2012. PMID: 22154200 No abstract available.

7

A newborn with seizures born to a mother diagnosed with primary carnitine deficiency.

Chen S, Hu Y, Huang Y, Nan Y, Zhou X, Chen S, Lin J, Lin Z. Chen S, et al. BMC Pediatr. 2019 Mar 18;19(1):79. doi: 10.1186/s12887-019-1452-4. BMC Pediatr. 2019. PMID: 30885166 Free PMC article.

8

Fever, Fasting, and Rhabdomyolysis in an Adult Male.

Shukla SG, Verma A. Shukla SG, et al. Neurol India. 2020 Jan-Feb;68(1):182-184. doi: 10.4103/0028-3886.279697. Neurol India. 2020. PMID: 32129275 Free article.

9

SLC22A5 mutations in a patient with systemic primary carnitine deficiency: the first Korean case confirmed by biochemical and molecular investigation.

Yoon YA, Lee DH, Ki CS, Lee SY, Kim JW, Lee YW, Park HD. Yoon YA, et al. Ann Clin Lab Sci. 2012 Fall;42(4):424-8. Ann Clin Lab Sci. 2012. PMID: 23090741

10

Carnitine uptake defect due to a 5'UTR mutation in a pedigree with false positives and false negatives on Newborn screening.

Verbeeten KC, Lamhonwah AM, Bulman D, Faghfoury H, Chakraborty P, Tein I, Geraghty MT. Verbeeten KC, et al. Mol Genet Metab. 2020 Mar;129(3):213-218. doi: 10.1016/j.ymgme.2019.12.006. Epub 2019 Dec 10. Mol Genet Metab. 2020. PMID: 31864849

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