|
1 Kearns TP, Sayre GP. Retinitis pigmentosa, external ophthalmophegia, and complete heart block: Unusual syndrome with histologic study in one of two cases. AMA Arch Ophthalmol, 1958, 60(2): 280–289.
|
|
2 Zhang SQ, ed. Neurology. Beijing: Higher Education Press, 2003, 277–278.[张淑琴,主编. 神经病学. 北京:高等教育出版社,2003, 277–278.]
|
|
3 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.
|
|
4 Yerdelen D, Koc F, Koc Z. Delayed diagnosis of Kearns–Sayre syndrome in a 38–year–old male patient: A case report. Int J Neurosci, 2008,118(2): 267–275.
|
|
5 Nakano T, Imanaka K, Uchida H, et al. Myocardial ultrastructure in Kearns–Sayre syndrome. Angiology, 1987, 38(1): 28–35.
|
|
6 Oginosawa Y, Abe H, Nagatomo T, et al. Sustained polymorphic ventricular tachycardia unassociated with QT prolongation or bradycardia in the Kearns–Sayre syndrome. Pacing Clin Electrophysiol, 2003, 26(9): 1911–1912.
|
|
7 Kosinski C, Mull M, Lethen H, et al. Evidence for cardioembolic stroke in a case of Kearns–Sayre syndrome. Stroke, 1995, 26(10): 1950–1952.
|
|
8 De Block CE, De Leeuw IH, Maassen JA, et al. A novel 7301–bp deletion in mitochondrial DNA in a patient with Kearns–Sayre syndrome, diabetes mellitus, and primary amenorrhoea. Exp Clin Endocrinol Diabetes, 2004, 112(2): 80–83.
|
|
9 Poulton J, O'Rahilly S, Morten KJ, et al. Mitochondrial DNA, diabetes and pancreatic pathology in Kearns–Sayre syndrome. Diabetologia, 1995, 38(7): 868–871.
|
|
10 Kane JM, Rossi J, Tsao S, et al. Metabolic cardiomyopathy and mitochondrial disorders in the pediatric intensive care unit. J Pediatr, 2007, 151(5): 538–541.
|
|
11 Zwirner P, Wilichowski E. Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies. Laryngoscope, 2001, 111(3): 515–521.
|
|
12 Sinnathuray AR, Raut V, Awa A, et al. A review of cochlear implantation in mitochondrial sensorineural hearing loss. Otol Neurotol, 2003, 24(3):418–426.
|
|
13 Boonstra F, Claerhout I, Hol F, et al. Corneal decompensation in a boy with Kearns–Sayre syndrome. Ophthalmic Genet, 2002, 23(4): 247–251.
|
|
14 Bastiaensen LA, Joosten EM, de Rooij JA, et al. Ophthalmoplegia–plus, a real nosological entity. Acta Neurol Scand, 1978, 58(1): 9–34.
|
|
15 Simaan EM, Mikati MA, Touma EH, et al. Unusual presentation of Kearns–Sayre syndrome in early childhood. Pediatr Neurol, 1999, 21(5): 830–831.
|
|
16 Akman CI, Sue CM, Shanske S, et al. Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathy. J Child Neurol, 2004, 19(4): 258–261.
|
|
17 Le Forestier N, Gherardi RK, Meyrignac C, et al. Myasthenic symptoms in patients with mitochondrial myopathies. Muscle Nerve, 1995, 18(11): 1338–1340.
|
|
18 Zoccolella S, Torraco A, Amati A, et al. Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNA. Funct Neurol, 2006, 21(1): 39–41.
|
|
19 Schmiedel J, Jackson S, Schafer J, et al. Mitochondrial cytopathies. J Neurol, 2003, 250(3): 267–277.
|
|
20 Kathleen P. Mitochondrial muscle pathology. Pediatr Develop Pathol, 2004, 7(6): 629–632.
|
|
21 Du Y, Zhang XJ, Zheng GP, et al. Mitochondrial encephalomyopathy–KSS complete type. Nerv Dis Mental Health, 2002, 2(3): 191–192.[杜岩,张晓君,郑国平,等.线粒体脑肌病–KSS完全型(附一例报告). 神经疾病与精神卫生,2002, 2(3): 191–192.]
|
|
22 Chen QT, Li XD, Wu LJ, et al. Mitochondrial gene defect in patients with chronic progressive external ophthalmoplegia. Chin J Med, 1998, 111(6): 500–503.
|