Electrocardiography as an early cardiac screening test in children with mitochondrial disease
Ran Baik (Baik R), Jung Hyun Chae (Chae JH), Young Mock Lee (Lee YM), Hoon Chul Kang (Kang HC), Joon Soo Lee (Lee JS), Heung Dong Kim (Kim HD)
Clin Exp Pediatr. 2010;53(5):644-647. Published online 2010 May 31 DOI: https://doi.org/10.3345/kjp.2010.53.5.644
|
Citations to this article as recorded by
Cardiovascular Involvement in mtDNA Disease
Michele Lioncino, Emanuele Monda, Martina Caiazza, Adelaide Fusco, Annapaola Cirillo, Francesca Dongiglio, Vicenzo Simonelli, Simone Sampaolo, Lucia Ruggiero, Gioacchino Scarano, Vicenzo Pota, Giulia Frisso, Cristina Mazzaccara, Giulia D'Amati, Gerardo Ni
Heart Failure Clinics.2022; 18(1): 51. CrossRef Cardiac complications in inherited mitochondrial diseases
Mohaddeseh Behjati, Mohammad Reza Sabri, Masood Etemadi Far, Majid Nejati
Heart Failure Reviews.2021; 26(2): 391. CrossRef Bedaquiline inhibits the yeast and human mitochondrial ATP synthases
Min Luo, Wenchang Zhou, Hiral Patel, Anurag P. Srivastava, Jindrich Symersky, Michał M. Bonar, José D. Faraldo-Gómez, Maofu Liao, David M. Mueller
Communications Biology.2020;[Epub] CrossRef Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathy
Asfia Quadir, Carly Sabine Pontifex, Helen Lee Robertson, Christopher Labos, Gerald Pfeffer
Neurology Genetics.2019;[Epub] CrossRef Chronic maternal hypercortisolemia in late gestation alters fetal cardiac function at birth
Andrew Antolic, Charles E. Wood, Maureen Keller-Wood
American Journal of Physiology-Regulatory, Integra.2018; 314(3): R342. CrossRef Inhibition of aldose-reductase-2 by a benzofuroxane derivative bf-5m increases the expression of kcne1, kcnq1 in high glucose cultured H9c2 cardiac cells and sudden cardiac death
Maria Consiglia Trotta, Monica Salerno, Anna Lisa Brigida, Vincenzo Monda, Antonietta Messina, Carmela Fiore, Roberto Avola, Renato Bernardini, Francesco Sessa, Gabriella Marsala, Guido N. Zanghì, Giovanni Messina, Michele D’Amico, Clara Di Filippo
Oncotarget.2018; 9(25): 17257. CrossRef The association of uncoupling protein 2 (UCP2) exon 8 insertion/deletion polymorphism and ECG derived QRS duration: A cross-sectional study in an Australian rural population
Yvonne Yin Leng Lee, Yuling Zhou, Herbert F Jelinek, Brett D Hambly, Craig S McLachlan
International Journal of Cardiology.2017; 228: 507. CrossRef Characteristic cardiac phenotypes are detected by cardiovascular magnetic resonance in patients with different clinical phenotypes and genotypes of mitochondrial myopathy
Anca Florian, Anna Ludwig, Bianca Stubbe-Dräger, Matthias Boentert, Peter Young, Johannes Waltenberger, Sabine Rösch, Udo Sechtem, Ali Yilmaz
Journal of Cardiovascular Magnetic Resonance.2015; 17(1): 40. CrossRef Diagnosis and treatment of mitochondrial myopathies
Gerald Pfeffer, Patrick F. Chinnery
Annals of Medicine.2013; 45(1): 4. CrossRef Regain of visuospatial capacity after coenzyme Q10 in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes: a case report
Che-Sheng Chu, Chin-Liang Chu, Hong-Ern Liu, Ti Lu
Acta Neuropsychiatrica.2012; 24(3): 186. CrossRef Early cardiac evaluation in children with non‐specific mitochondrial disease with isolated mitochondrial respiratory chain complex I defect
Ran Baik, Rita Yu, Young Mock Lee, Hoon Chul Kang, Joon Soo Lee, Heung Dong Kim
Journal of Paediatrics and Child Health.2012; 48(11): 1016. CrossRef
|