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Items: 1 to 20 of 171

1.

Kearns syndrome or Kearns disease. Further evidence of a genuine entity in a case with uncommon features.

Bastiaensen LA, Notermans SL, Ramaekers CH, van Dijke BJ, Joosten EM, Jaspar HH, Stadhouders AM, Beljaars CT.

Ophthalmologica. 1982;184(1):40-50.

PMID:
7054739
2.

[Ptosis as the leading symptom of Kearns-Sayre syndrome. A case report for differential diagnosis of external ophthalmoplegia].

Vock K, Todt H, Fötzsch R, Fischer R.

Kinderarztl Prax. 1990 Feb;58(2):93-7. German.

PMID:
2332951
3.

[Drachman's "ophthalmoplegia plus" or Kearns and Shy syndrome. Apropos of 2 cases with mitochondrial abnormality ultrastructurally demonstrated in the muscle].

Vallat MM, Julien J, Vallat JM, Vital C, Faussier P.

Arch Ophtalmol Rev Gen Ophtalmol. 1975 Jun-Jul;35(6-7):509-20. French.

PMID:
130879
4.

Autosomal dominant Kearns-Sayre syndrome.

Leveille AS, Newell FW.

Ophthalmology. 1980 Feb;87(2):99-108.

PMID:
7383548
5.

[Kearns syndrome. Progressive external ophthalmoplegia, retinal pigment degeneration and heart conduction disorders].

Boltshauser E, Jerusalem F, Niemeyer G, Huber C.

Schweiz Med Wochenschr. 1977 Dec 17;107(50):1880-8. German.

PMID:
594731
6.

Kearns syndrome: a heterogeneous group of disorders with CPEO, or a nosological entity?

Bastiaensen LA, Frenken CW, Ter Laak HJ, Jaspar HH, Stadhouders AM, Ruitenbeek W, Veerkamp JH.

Doc Ophthalmol. 1982 Jan 29;52(3-4):207-25.

PMID:
7067593
7.

[A case of Kearns-Sayre syndrome].

Kokot W, Iwaszkiewicz-Bilikiewiczowa B, Lewczuk A, Sworczak K.

Klin Oczna. 1996;98(4):327-30. Polish.

PMID:
9463130
8.

[Concordance of Kearns-Sayre syndrome and Klinefelter syndrome].

Everding AS, Kurlemann G, Gerding H, Bömbelburg T, Palm DG, Gullotta F, Zierz S.

Monatsschr Kinderheilkd. 1988 Oct;136(10):698-700. German.

PMID:
3237225
9.

Kearns-Sayre syndrome: a case report and review.

Gross-Jendroska M, Schatz H, McDonald HR, Johnson RN.

Eur J Ophthalmol. 1992 Jan-Mar;2(1):15-20. Review.

PMID:
1638160
10.

[Chronic progressive external ophthalmoplegia with atypical retinal pigment dystrophy (author's transl)].

Celić M, Dorn V, Zeskov P, Raić N.

Klin Monbl Augenheilkd. 1980 Dec;177(6):677-83. German.

PMID:
7206551
11.

Myocardial ultrastructure and the development of atrioventricular block in Kearns-Sayre syndrome.

Charles R, Holt S, Kay JM, Epstein EJ, Rees JR.

Circulation. 1981 Jan;63(1):214-9.

PMID:
7438396
12.

Kearns-Sayre syndrome.

Nemet P, Godel V, Lazar M.

Birth Defects Orig Artic Ser. 1982;18(6):263-8.

PMID:
7171761
13.

[PCR-based detection of heteroplasmic deleted mitochondrial DNA in Kearns-Sayre syndrome].

Ramírez-Miranda A, Navas-Pérez A, Gurria-Quintana L, Vargas-Ortega J, Murillo-Correa C, Zenteno JC.

Arch Soc Esp Oftalmol. 2008 Mar;83(3):155-9. Spanish.

14.

[Diagnostic and therapeutic problems in chronic progressive external ophthalmoplegia (CPEO)].

Sommer F, Fötzsch R, Pillunat LE, Wollensak G.

Klin Monbl Augenheilkd. 2003 May;220(5):315-9. German.

PMID:
12766819
15.

[Clinical, morphological and biochemical findings in the Kearns-Sayre syndrome].

Hammerstein W, Mortier W, Noack EA, Frenzel H, Liebert UG, Toyka K, Horstkotte D, Bischof G, Weber U.

Fortschr Ophthalmol. 1983;80(3):193-200. German. No abstract available.

PMID:
6629235
16.

Common deletion of mitochondrial DNA in a 5-year-old girl with failure to thrive, ptosis, ophthalmoplegia and ragged-red fibers.

Seyrantepe V, Kale G, Topaloglu H, Alikasifoglu A, Ozgüc M.

Brain Dev. 1999 Sep;21(6):413-5.

PMID:
10487476
17.

Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation.

Isashiki Y, Nakagawa M, Ohba N, Kamimura K, Sakoda Y, Higuchi I, Izumo S, Osame M.

Acta Ophthalmol Scand. 1998 Feb;76(1):6-13.

18.

Kearns-Sayre syndrome: primarily a mitochondriopathy?

Ketelsen UP, Schmidt D, Beckmann R, Haralambie G.

Dev Ophthalmol. 1982;6:118-37.

PMID:
7095238
19.

Mitochondrial myopathies. A clinico-pathological study of cases with and without extra-ocular muscle involvement.

Mechler F, Mastaglia FL, Serena M, Jenkison M, Johnson MA, Fawcett PR, Hudgson P, Walton JN.

Aust N Z J Med. 1986 Apr;16(2):185-92.

PMID:
3463270
20.

[Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies].

Laforêt P, Eymard B, Danan C, Chevallay M, Rouche A, Frachon P, Fardeau M, Lombès A.

Rev Neurol (Paris). 1997 Feb;153(1):51-8. French.

PMID:
9296156

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