-
1
-
-
0028918471
-
Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects
-
Anan, R., Nakagawa, M., Miyata, M., Higuchi, I., Nakao, S., Suehara, M., Osame, M., & Tanaka, H. (1995). Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects. Circulation, 91(4), 955-61.
-
(1995)
Circulation
, vol.91
, Issue.4
, pp. 955-961
-
-
Anan, R.1
Nakagawa, M.2
Miyata, M.3
Higuchi, I.4
Nakao, S.5
Suehara, M.6
Osame, M.7
Tanaka, H.8
-
2
-
-
0031656184
-
Multiple endocrine involvement in two pediatric patients with Kearns-Sayre syndrome
-
Artuch, R., Pavia, C., Playan, A., Vilaseca, M. A., Colomer, J., Valls, C., Rissech, M., Gonzalez, M. A., Pou, A., Briones, P., Montoya, J., & Pineda, M. (1998). Multiple endocrine involvement in two pediatric patients with Kearns-Sayre syndrome. Hormone Research, 50(2), 99-104.
-
(1998)
Hormone Research
, vol.50
, Issue.2
, pp. 99-104
-
-
Artuch, R.1
Pavia, C.2
Playan, A.3
Vilaseca, M.A.4
Colomer, J.5
Valls, C.6
Rissech, M.7
Gonzalez, M.A.8
Pou, A.9
Briones, P.10
Montoya, J.11
Pineda, M.12
-
3
-
-
0031595077
-
Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison disease
-
Boles, R. G., Roe, T., Senadheera, D., Mahnovski, V., & Wong, L. J. (1998). Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison disease. European Journal of Pediatrics, 157(8), 643-647.
-
(1998)
European Journal of Pediatrics
, vol.157
, Issue.8
, pp. 643-647
-
-
Boles, R.G.1
Roe, T.2
Senadheera, D.3
Mahnovski, V.4
Wong, L.J.5
-
4
-
-
0033761979
-
Mitochondrial DNA mutations in the pathogenesis of human disease
-
Chinnery, P. F., & Turnbull, D. M. (2000). Mitochondrial DNA mutations in the pathogenesis of human disease. Molecular Medicine Today, 6(11), 425-432.
-
(2000)
Molecular Medicine Today
, vol.6
, Issue.11
, pp. 425-432
-
-
Chinnery, P.F.1
Turnbull, D.M.2
-
5
-
-
0033435127
-
MRI of the brain in the Kearns-Sayre syndrome: Report of four cases and a review
-
Chu, B. C., Terae, S., Takahashi, C., Kikuchi, Y., Miyasaka, K., Abe, S., Minowa, K., & Sawamura, T. (1999). MRI of the brain in the Kearns-Sayre syndrome: Report of four cases and a review. Neuroradiology, 41(10), 759-764.
-
(1999)
Neuroradiology
, vol.41
, Issue.10
, pp. 759-764
-
-
Chu, B.C.1
Terae, S.2
Takahashi, C.3
Kikuchi, Y.4
Miyasaka, K.5
Abe, S.6
Minowa, K.7
Sawamura, T.8
-
6
-
-
0025009303
-
Kearns-Sayre syndrome presenting as renal tubular acidosis
-
Eviatar, L., Shanske, S., Gauthier, B., Abrams, C., Maytal, J., Slavin, M., Valderrama, E., & DiMauro, S. (1990). Kearns-Sayre syndrome presenting as renal tubular acidosis. Neurology, 40(11), 1761-1763.
-
(1990)
Neurology
, vol.40
, Issue.11
, pp. 1761-1763
-
-
Eviatar, L.1
Shanske, S.2
Gauthier, B.3
Abrams, C.4
Maytal, J.5
Slavin, M.6
Valderrama, E.7
DiMauro, S.8
-
7
-
-
0026451346
-
Kearns-Sayre syndrome: A case report and review
-
Gross-Jendroska, M., Schatz, H., McDonald, H. R., & Johnson, R. N. (1992). Kearns-Sayre syndrome: A case report and review. Eurepean Journal of Ophthalmology, 2(1), 15-20.
-
(1992)
Eurepean Journal of Ophthalmology
, vol.2
, Issue.1
, pp. 15-20
-
-
Gross-Jendroska, M.1
Schatz, H.2
McDonald, H.R.3
Johnson, R.N.4
-
8
-
-
0026773036
-
Endocrine dysfunction in Kearns-Sayre syndrome
-
Harvey, J. N., & Barnett, D. (1992). Endocrine dysfunction in Kearns-Sayre syndrome. Clinical Endocrinology (Oxf.), 37(1), 97-103.
-
(1992)
Clinical Endocrinology (Oxf.)
, vol.37
, Issue.1
, pp. 97-103
-
-
Harvey, J.N.1
Barnett, D.2
-
9
-
-
18144368445
-
Kearns-Sayre syndrome associated with trifascicular block and QT prolongation
-
Karanikis, P., Korantzopoulos, P., Kountouris, E., Dimitroula, V., Patsouras, D., Pappa, E., & Siogas, K. (2005). Kearns-Sayre syndrome associated with trifascicular block and QT prolongation. International Journal of Cardiology, 101(1), 147-150.
-
(2005)
International Journal of Cardiology
, vol.101
, Issue.1
, pp. 147-150
-
-
Karanikis, P.1
Korantzopoulos, P.2
Kountouris, E.3
Dimitroula, V.4
Patsouras, D.5
Pappa, E.6
Siogas, K.7
-
10
-
-
0036243077
-
Alarming atrioventricular block and mitral valve prolapse in the Kearns-Sayre syndrome
-
Katsanos, K. H., Pappas, C. J., Patsouras, D., Michalis, L. K., Kitsios, G., Elisaf, M., & Tsianos, E. (2002). Alarming atrioventricular block and mitral valve prolapse in the Kearns-Sayre syndrome. International Journal of Cardiology, 83(2), 179-181.
-
(2002)
International Journal of Cardiology
, vol.83
, Issue.2
, pp. 179-181
-
-
Katsanos, K.H.1
Pappas, C.J.2
Patsouras, D.3
Michalis, L.K.4
Kitsios, G.5
Elisaf, M.6
Tsianos, E.7
-
11
-
-
4043063576
-
Kearns-Sayre syndrome. A case with literature review
-
Koc, F., Zorludemir, S., & Sarica, Y. (2003). Kearns-Sayre syndrome. A case with literature review. Marmara Medical Journal, 16, 116-120.
-
(2003)
Marmara Medical Journal
, vol.16
, pp. 116-120
-
-
Koc, F.1
Zorludemir, S.2
Sarica, Y.3
-
12
-
-
0029127326
-
Evidence for cardioembolic stroke in a case of Kearns-Sayre syndrome
-
Kosinski, C., Mull, M., Lethen, H., & Topper, R. (1995). Evidence for cardioembolic stroke in a case of Kearns-Sayre syndrome. Stroke, 26(10), 1950-1952.
-
(1995)
Stroke
, vol.26
, Issue.10
, pp. 1950-1952
-
-
Kosinski, C.1
Mull, M.2
Lethen, H.3
Topper, R.4
-
13
-
-
0016811173
-
Chronic progressive external ophthalmoplegia, pigmentary retinopathy, and heart block (Kearns-Sayre syndrome). Report of a case
-
Lowes, M. (1975). Chronic progressive external ophthalmoplegia, pigmentary retinopathy, and heart block (Kearns-Sayre syndrome). Report of a case. Acta Ophthalmologica (Copenh), 53(4), 610-619.
-
(1975)
Acta Ophthalmologica (Copenh)
, vol.53
, Issue.4
, pp. 610-619
-
-
Lowes, M.1
-
14
-
-
0033251522
-
Kearns-Sayre syndrome "plus." Classical clinical findings and dystonia
-
Marie, S. K., Carvalho, A. A., Fonseca, L. F., Carvalho, M. S., Reed, U. C., & Scaff, M. (1999). Kearns-Sayre syndrome "plus." Classical clinical findings and dystonia. Arquivos de neuro-psiquiatria, 57(4), 1017-1023.
-
(1999)
Arquivos de neuro-psiquiatria
, vol.57
, Issue.4
, pp. 1017-1023
-
-
Marie, S.K.1
Carvalho, A.A.2
Fonseca, L.F.3
Carvalho, M.S.4
Reed, U.C.5
Scaff, M.6
-
15
-
-
0029040769
-
Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndrome
-
Poulton, J., O'Rahilly, S., Morten, K. J., & Clark, A. (1995). Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndrome. Diabetologia, 38(7), 868-871.
-
(1995)
Diabetologia
, vol.38
, Issue.7
, pp. 868-871
-
-
Poulton, J.1
O'Rahilly, S.2
Morten, K.J.3
Clark, A.4
-
16
-
-
0034157274
-
Kearns Sayre syndrome: An atypical presentation
-
Rajakannan, G., Prasad, W., Ramakrishnan, R., & Prajna, N. V. (2000). Kearns Sayre syndrome: An atypical presentation. Indian Journal of Ophthalmology, 48(1), 54-55.
-
(2000)
Indian Journal of Ophthalmology
, vol.48
, Issue.1
, pp. 54-55
-
-
Rajakannan, G.1
Prasad, W.2
Ramakrishnan, R.3
Prajna, N.V.4
-
17
-
-
0030060683
-
Ragged red or ragged blue fibers
-
Reichmann, H., Vogler, L., & Seibel, P. (1996). Ragged red or ragged blue fibers. European Neurology, 36(2), 98-102.
-
(1996)
European Neurology
, vol.36
, Issue.2
, pp. 98-102
-
-
Reichmann, H.1
Vogler, L.2
Seibel, P.3
-
18
-
-
0018420761
-
Familial Kearns-Sayre syndrome
-
Schnitzler, E. R., & Robertson, W. C., Jr.. (1979). Familial Kearns-Sayre syndrome. Neurology, 29(8), 1172-1174.
-
(1979)
Neurology
, vol.29
, Issue.8
, pp. 1172-1174
-
-
Schnitzler, E.R.1
Robertson Jr., W.C.2
-
19
-
-
0343632387
-
Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: A clinical and molecular genetic study of four children with Kearns-Sayre syndrome
-
Wilichowski, E., Gruters, A., Kruse, K., Rating, D., Beetz, R., Korenke, G. C., Ernst, B. P., Christen, H. J., & Hanefeld, F. (1997). Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: A clinical and molecular genetic study of four children with Kearns-Sayre syndrome. Pediatric Research, 41(2), 193-200.
-
(1997)
Pediatric Research
, vol.41
, Issue.2
, pp. 193-200
-
-
Wilichowski, E.1
Gruters, A.2
Kruse, K.3
Rating, D.4
Beetz, R.5
Korenke, G.C.6
Ernst, B.P.7
Christen, H.J.8
Hanefeld, F.9
-
20
-
-
0031732194
-
Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy
-
Zanssen, S., Molnar, M., Buse, G., & Schroder, J. M. (1998). Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy. Clinical Neuropathology, 17(6), 291-296.
-
(1998)
Clinical Neuropathology
, vol.17
, Issue.6
, pp. 291-296
-
-
Zanssen, S.1
Molnar, M.2
Buse, G.3
Schroder, J.M.4
|