173 related articles for article (PubMed ID: 29071542)
1. 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]
2. 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
Indian J Pediatr; 2017 Jan; 84(1):83-85. PubMed ID: 27581592
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. 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]
6. [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]
7. 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]
8. 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]
9. MRI findings in encephalopathy with primary carnitine deficiency: a case report.
Yilmaz TF; Atay M; Toprak H; Guler S; Aralasmak A; Alkan A
J Neuroimaging; 2015; 25(2):325-328. PubMed ID: 24612242
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [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
Ann Cardiol Angeiol (Paris); 2014 Apr; 63(2):107-10. PubMed ID: 22260907
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. [Screening for fatty acid oxidation disorders of newborns in Zhejiang province:prevalence, outcome and follow-up].
Zheng J; Zhang Y; Hong F; Yang J; Tong F; Mao H; Huang X; Zhou X; Yang R; Zhao Z; Huang X
Zhejiang Da Xue Xue Bao Yi Xue Ban; 2017 May; 46(3):248-255. PubMed ID: 29039165
[TBL] [Abstract][Full Text] [Related]
15. Hypoglycemia Due to Acquired Carnitine Deficiency in a Pediatric Patient Receiving Chemotherapy.
Vasta LM; Reynolds SM; Sami S; Schacht JP; Emerick JE; Parekh DS; Vogt KS
J Pediatr Hematol Oncol; 2022 Mar; 44(2):e496-e499. PubMed ID: 33661167
[TBL] [Abstract][Full Text] [Related]
16. Intracellular in vitro probe acylcarnitine assay for identifying deficiencies of carnitine transporter and carnitine palmitoyltransferase-1.
Purevsuren J; Kobayashi H; Hasegawa Y; Yamada K; Takahashi T; Takayanagi M; Fukao T; Fukuda S; Yamaguchi S
Anal Bioanal Chem; 2013 Feb; 405(4):1345-51. PubMed ID: 23143007
[TBL] [Abstract][Full Text] [Related]
17. Carnitine deficiency induces a short QT syndrome.
Roussel J; Labarthe F; Thireau J; Ferro F; Farah C; Roy J; Horiuchi M; Tardieu M; Lefort B; François Benoist J; Lacampagne A; Richard S; Fauconnier J; Babuty D; Le Guennec JY
Heart Rhythm; 2016 Jan; 13(1):165-74. PubMed ID: 26190315
[TBL] [Abstract][Full Text] [Related]
18. Functional and molecular studies in primary carnitine deficiency.
Frigeni M; Balakrishnan B; Yin X; Calderon FRO; Mao R; Pasquali M; Longo N
Hum Mutat; 2017 Dec; 38(12):1684-1699. PubMed ID: 28841266
[TBL] [Abstract][Full Text] [Related]
19. Primary carnitine deficiency in a 57-year-old patient with recurrent exertional rhabdomyolysis.
Echaniz-Laguna A; Biancalana V; Gaignard P; Chanson JB
BMJ Case Rep; 2018 Jun; 2018():. PubMed ID: 29895548
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
