Mitochondrial encephalomyopathies. a comparison of Kearns-Sayre syndrome, MELAS and MERRF
Zenner, K.; Gold, R.; Meurers, B.; Reichmann, H.
Der Nervenarzt 61(10): 597-603
1990
ISSN/ISBN: 0028-2804 PMID: 2177152 Document Number: 351231
Document emailed within 1 workday
Related Documents
Byrne, E.; Marzuki, S.; Sattayasai, N.; Dennett, X.; Trounce, I. 1987: Mitochondrial studies in Kearns-Sayre syndrome: normal respiratory chain function with absence of a mitochondrial translation product Neurology 37(9): 1530-1534Soga, F.; Ueno, S.; Yorifuji, S. 1993: Deletions of mitochondrial DNA in Kearns-Sayre syndrome Nihon Rinsho. Japanese Journal of Clinical Medicine 51(9): 2386-2390
Perocchio, M.; Caponnetto, S. 1992: Mitochondrial myopathy and the heart. Kearns-Sayre syndrome Cardiologia 37(5): 373-377
Goto, Y. 1997: Mitochondrial DNA mutations and three major forms of mitochondrial myopathies: CPEO, MELAS and MERRF Nihon Rinsho. Japanese Journal of Clinical Medicine 55(12): 3259-3264
Nemet, P.; Godel, V.; Lazar, M. 1982: Kearns-Sayre syndrome Birth Defects Original Article Series 18(6): 263-268
Simon, K.; Solti, F.; Sótonyi, P.; Rényi Vámos, F.; Vecsey, T.; Szelier, A. 1989: New aspects of the Kearns-Sayre syndrome Orvosi Hetilap 130(8): 405-409
Kokot, W.; Iwaszkiewicz-Bilikiewiczowa, B.; Lewczuk, A.; Sworczak, K. 1996: A case of Kearns-Sayre syndrome Klinika Oczna 98(4): 327-330
Usui, M.; Takagi, Y.; Masumoto, H.; Ueda, U. 2002: Pacemaker therapy in Kearns-Sayre syndrome Kyobu Geka. Japanese Journal of Thoracic Surgery 55(13): 1112-1114
Consalvo, D.; Villegas, F.; Villa, A.M.; Köhler, G.; Molina, H.; Benchuga, E.; Chamoles, N.; Sanz, O.P.; Sica, R.E. 1997: Severe cardiac failure in Kearns-Sayre syndrome Medicina 57(1): 67-71
Tamai, A.; Holland, M.G. 1976: Electrophysiological studies on a case of Kearns-Sayre syndrome Nippon Ganka Gakkai Zasshi 80(2): 71-75
Everding, A.S.; Kurlemann, G.; Gerding, H.; Bömbelburg, T.; Palm, D.G.; Gullotta, F.; Zierz, S. 1988: Concordance of Kearns-Sayre syndrome and Klinefelter syndrome Monatsschrift Kinderheilkunde: Organ der Deutschen Gesellschaft für Kinderheilkunde 136(10): 698-700
Gillet, J.M.; Toppet, M.; Gallez, A.; Bernard, R. 1978: Conduction abnormalities in Kearns-Sayre syndrome. Observation of 2 clinical cases Acta Cardiologica 33(5): 323-329
Gal, R.; Lahat, E. 2000: Progressive ptosis in children as a presenting sign of Kearns-Sayre syndrome Harefuah 138(2): 108
Rubí-Palomares, I.; Martínez-León, M.I.; Vera-Medialdea, R.; Delgado-Marqués, M.P.; López-Ruiz, P. 2002: Kearns-Sayre syndrome: pediatric neuroradiologic findings in computed tomography and magnetic resonance imaging Anales Espanoles de Pediatria 56(2): 180-184
Cesneková, T.; Jurecka, T.; Skorkovská, K.; Tesarová, M.; Hanisková, H.; Wenchich, L.; Zámecník, J.; Zeman, J. 2011: Corneal ulceration complicating surgical correction of ptosis in patient with Kearns-Sayre syndrome--a case report Ceska a Slovenska Oftalmologie: Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti 67(4): 133-135
Berio, A.; Piazzi, A. 2007: Facial anomalies in a patient with cytochrome-oxidase deficiency and subsequent Kearns-Sayre syndrome with growth hormone deficiency Minerva Medica 98(1): 81-85
Mochizuki, H.; Joh, K.; Kawame, H.; Imadachi, A.; Nozaki, H.; Ohashi, T.; Usui, N.; Eto, Y.; Kanetsuna, Y.; Aizawa, S. 1996: Mitochondrial encephalomyopathies preceded by de-Toni-Debré-Fanconi syndrome or focal segmental glomerulosclerosis Clinical Nephrology 46(5): 347-352
Yamamoto, M.; Shimokawa, M.; Hamada, K. 1997: Application of long PCR method to detection of mitochondrial DNA deletions in mitochondrial encephalomyopathies Nihon Rinsho. Japanese Journal of Clinical Medicine 55(12): 3282-3285
Song, D.; Zhang, Y.; Shi, J. 2001: The study of point mutation of muscular mitochondrial DNA from patients with mitochondrial encephalomyopathies Zhonghua Yi Xue Za Zhi 81(11): 659-661
Prayson, R.A.; Wang, N. 1998: Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report Archives of Pathology and Laboratory Medicine 122(11): 978-981