145 related articles for article (PubMed ID: 25229968)
1. [Primary carnitine deficiency in an infant].
Cheng C; Zhang XY; Li JJ
Zhongguo Dang Dai Er Ke Za Zhi; 2014 Sep; 16(9):952-4. PubMed ID: 25229968
[No Abstract] [Full Text] [Related]
2. [Primary carnitine deficiency in a neonate].
Sun ZX; Lan JH
Zhongguo Dang Dai Er Ke Za Zhi; 2013 Jan; 15(1):75-6. PubMed ID: 23336175
[No Abstract] [Full Text] [Related]
3. Cardiac magnetic resonance findings in a case of carnitine deficiency.
Ascunce RR; Nayar AC; Phoon CK; Srichai MB
Tex Heart Inst J; 2013; 40(1):104-5. PubMed ID: 23468586
[No Abstract] [Full Text] [Related]
4. Infant with hepatomegaly and hypoglycemia: A setting for fatty acid oxidation defects.
Ravindranath A; Pai G; Srivastava A; Poddar U; Yachha SK
Indian J Gastroenterol; 2017 Sep; 36(5):429-434. PubMed ID: 29071542
[TBL] [Abstract][Full Text] [Related]
5. Importance of molecular diagnosis in the accurate diagnosis of systemic carnitine deficiency.
Hitomi T; Matsuura N; Shigematsu Y; Okano Y; Shinozaki E; Kawai M; Kobayashi H; Harada KH; Koizumi A
J Genet; 2015 Mar; 94(1):147-50. PubMed ID: 25846890
[No Abstract] [Full Text] [Related]
6. Dilated Cardiomyopathy With Short QT Interval Suggests Primary Carnitine Deficiency.
Perin F; Rodríguez-Vázquez Del Rey MDM; Carreras-Blesa C; Arrabal-Fernández L; Jiménez-Jáimez J; Tercedor L
Rev Esp Cardiol (Engl Ed); 2018 Dec; 71(12):1074-1075. PubMed ID: 29198778
[No Abstract] [Full Text] [Related]
7. Primary carnitine deficiency cardiomyopathy.
Wang SS; Rao J; Li YF; Zhang ZW; Zeng GH
Int J Cardiol; 2014 Jun; 174(1):171-3. PubMed ID: 24746540
[No Abstract] [Full Text] [Related]
8. Successful perioperative management of a patient with primary systemic carnitine deficiency: a case report.
Kato K; Mizota T; Hirota K; Fukuda K
J Anesth; 2013 Feb; 27(1):141-2. PubMed ID: 22996439
[No Abstract] [Full Text] [Related]
9. [Primary carnitine deficiency in 17 patients: diagnosis, treatment and follow up].
Han LS; Ye J; Qiu WJ; Zhang HW; Wang Y; Ji WJ; Gao XL; Li XY; Jin J; Gu XF
Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):405-9. PubMed ID: 22931933
[TBL] [Abstract][Full Text] [Related]
10. Dilated Cardiomyopathy as the Only Clinical Manifestation of Carnitine Transporter Deficiency.
Papadopoulou-Legbelou K; Gogou M; Dokousli V; Eboriadou M; Evangeliou A
Indian J Pediatr; 2017 Mar; 84(3):231-233. PubMed ID: 27807682
[TBL] [Abstract][Full Text] [Related]
11. Clinical features and genotyping of patients with primary carnitine deficiency identified by newborn screening.
Sun Y; Wang YY; Jiang T
J Pediatr Endocrinol Metab; 2017 Aug; 30(8):879-883. PubMed ID: 28753539
[TBL] [Abstract][Full Text] [Related]
12. Primary Carnitine Deficiency and Newborn Screening for Disorders of the Carnitine Cycle.
Longo N
Ann Nutr Metab; 2016; 68 Suppl 3():5-9. PubMed ID: 27931018
[TBL] [Abstract][Full Text] [Related]
13. Carnitine Profile by Tandem Mass Spectrometry and Dialysis Patients.
Kamei D; Kamei Y; Tanaka N; Tsukada M; Miwa N; Hanafusa N; Mineshima M; Nitta K; Tsuchiya K
Contrib Nephrol; 2019; 198():73-77. PubMed ID: 30991404
[TBL] [Abstract][Full Text] [Related]
14. Lipid storage myopathies: Current treatments and future directions.
Vasiljevski ER; Summers MA; Little DG; Schindeler A
Prog Lipid Res; 2018 Oct; 72():1-17. PubMed ID: 30099045
[TBL] [Abstract][Full Text] [Related]
15. Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California.
Gallant NM; Leydiker K; Wilnai Y; Lee C; Lorey F; Feuchtbaum L; Tang H; Carter J; Enns GM; Packman S; Lin HJ; Wilcox WR; Cederbaum SD; Abdenur JE
Mol Genet Metab; 2017 Nov; 122(3):76-84. PubMed ID: 28711408
[TBL] [Abstract][Full Text] [Related]
16. Cardiomyopathy, carnitine deficiency, and celiac disease.
Boutrid N; Rahmoune H
Eur J Pediatr; 2024 May; 183(5):2507-2508. PubMed ID: 38358548
[No Abstract] [Full Text] [Related]
17. Acquired encephalopathy associated with carnitine deficiency after cefditoren pivoxil administration.
Kim H; Chu K; Jung KH; Lee ST; Kim JM; Lee SK
Neurol Sci; 2012 Dec; 33(6):1393-6. PubMed ID: 22258360
[TBL] [Abstract][Full Text] [Related]
18. 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
BMC Pediatr; 2019 Mar; 19(1):79. PubMed ID: 30885166
[TBL] [Abstract][Full Text] [Related]
19. 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
Mol Genet Metab; 2020 Mar; 129(3):213-218. PubMed ID: 31864849
[TBL] [Abstract][Full Text] [Related]
20. [Correlation between serum L-carnitine concentration and neutrophil engraftment in patients treated with cord blood transplantation].
Sano F; Kondo T; Matsuhashi Y; Hyo R; Koresawa R; Susuki S; Hayashi K; Tasaka T; Wada H; Sugihara T
Rinsho Ketsueki; 2016 Feb; 57(2):165-70. PubMed ID: 26935634
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]