THÔNG TIN TÀI LIỆU
146 Carceller AM, Fouron JC, Letarte J, et al Absence of mitral valve prolapse in juvenile hyperthyroidism Am J Cardiol 1984;54:455– 456 147 Pilapil VR, Watson DG Electrocardiogram in hyperthyroid children Am J Dis Child 1979;119:245–248 148 Forfar JC, Muir AL, Sawers SA, Toft AD Abnormal left ventricular function in hyperthyroidism Evidence for a possible reversible cardiomyopathy N Engl J Med 1982;307:1165–1170 149 Cavallo A, Joseph CJ, Casta A Cardiac complications in juvenile hyperthyroidism Am J Dis Child 1984;138:479–482 150 Reddy ER Changes in heart size and volume in certain endocrinal and nutritional deficiency diseases A correlative study in twenty adult patients J Can Assoc Radiol 1984;35(1):17–19 151 Willis FR, Byrne GC, Jones TW Fludrocortisone induced heart failure in Addison's disease J Paediatr Child Health 1994;30(3):280–281 152 Barragan-Campos HM, Barrera-Ramirez CF, Iturralde Torres P, et al Kearns-sayre syndromes an absolute indication for prohylactic implantation of definitive pacemaker? Arch Inst Cardiol Mex 1999;69(6):559–565 153 Subbiah RN, Kuchar D, Baron D Torsades de pointes in a patient with kearns-sayre syndrome: a fortunate finding Pacing Clin Electrophysiol 2007;30(1):137–139 154 Marin-Garcia J, Goldenthal MJ, Filiano JJ Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype J Child Neurol 2002;17(10):759–765 155 Rashid A, Kim MH Kearns-sayre syndrome: association with long QT syndrome? J Cardiovasc Electrophysiol 2002;13(2):184–185 156 Hernandez-Luis C, Garcia-Moran E, Rubio-Sanz J, Fernandez-Aviles F Kearns-sayre syndrome: recurrent syncope and atrial flutter Rev Esp Cardiol 2007;60(1):89–90 157 Katsanos KH, Pappas CJ, Patsouras D, et al Alarming atrioventricular block and mitral valve prolapse in the Kearns-sayre syndrome Int J Cardiol 2002;83(2):179–181 158 Challa S, Kanikannan MA, Murthy JM, Bhoompally VR, Surath M Diagnosis of mitochondrial diseases: clinical and histological study of sixty patients with ragged red fibers Neurol India 2004;52(3):353–358 159 Agapitos E, Pavlopoulos PM, Patsouris E, Davaris P Subacute nectrozing encephalomyelopathy (leigh's disease): a clinicopathologic study of ten cases Gen Diagn Pathol 1997;142(5–6):335–341 160 Clarke SL, Ikon N, Ryan RO Barth syndrome: connecting cardiolipin to cardiomyopathy Lipids 2017;52:99–108 161 Roberts AE, Nixon C, Steward CG, et al The barth syndrome registry: distinguishing disease characteristics and growth data from a longitudinal study Am J Med Genet A 2012;158A:2726–2732 162 Brady AN, Shehata BM, Fernhoff PM X-linked fetal cardiomyopathy caused by a novel mutation in the TAZ gene Prenat Diagn 2006;26:462–465 163 Clarke SL, Bowron A, Gonzalez IL, et al Barth syndrome Orphanet J Rare Dis 2013;8:23 164 Spencer CT, Byrne BJ, Geqitz MH, et al Ventricular arrhythmia in the X-linked cardiomyopathy barth syndrome Pediatr Cardiol 2005;26(5):632–637 165 Desviat LR, Clavero S, Perez-Cerda C, et al New splicing mutations in propionic acidemia J Hum Genet 2006;51(11):992–997 166 Massoud AF, LEanord JV Cardiomyopathy in proprionic acidemia Eur J Pediatr 1993;152(5):441–445 167 Baumgartner D, Scholl-Burgi S, Sass JO, et al
Ngày đăng: 22/10/2022, 13:00
Xem thêm: