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7. Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscle. Romero NB; Lestienne P; Marsac C; Paturneau-Jouas M; Nelson I; François D; Eymard B; Fardeau M J Neurol Sci; 1989 Nov; 93(2-3):297-309. PubMed ID: 2556504 [TBL] [Abstract][Full Text] [Related]
8. [Disorders of folate metabolism in the Kearns-Sayre syndrome]. Macron JM; Mizon JP; Rosa A Rev Neurol (Paris); 1983; 139(11):673-7. PubMed ID: 6677979 [TBL] [Abstract][Full Text] [Related]
9. A case of lipid storage myopathy with carnitine deficiency. Biochemical and electromyographic correlations. Scarlato G; Albizzati MG; Bassi S; Cerri C; Frattola L Eur Neurol; 1977; 16(1-6):222-9. PubMed ID: 615713 [TBL] [Abstract][Full Text] [Related]
10. Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome. Goto Y; Itami N; Kajii N; Tochimaru H; Endo M; Horai S J Pediatr; 1990 Jun; 116(6):904-10. PubMed ID: 2161456 [TBL] [Abstract][Full Text] [Related]
12. Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome. Shanske S; Moraes CT; Lombes A; Miranda AF; Bonilla E; Lewis P; Whelan MA; Ellsworth CA; DiMauro S Neurology; 1990 Jan; 40(1):24-8. PubMed ID: 2296377 [TBL] [Abstract][Full Text] [Related]
13. [31P-NMR spectroscopy of mitochondrial myopathies: the relation between abnormal energy metabolism and muscle biopsy findings]. Kawai M; Itoh M; Okazawa H; Kamakura K Rinsho Shinkeigaku; 1989 Feb; 29(2):167-71. PubMed ID: 2546706 [TBL] [Abstract][Full Text] [Related]
14. [Disorders of folate metabolism in the Kearns-Sayre syndrome]. Laplane D; Hasboun D Rev Otoneuroophtalmol; 1984; 56(2):199-202. PubMed ID: 6474025 [No Abstract] [Full Text] [Related]
15. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 34-1987. A 30-year-old woman with an ocular motility disturbance, myopathy, and hypocalcemia. N Engl J Med; 1987 Aug; 317(8):493-501. PubMed ID: 3614294 [No Abstract] [Full Text] [Related]
16. Kearns-Sayre syndrome: biochemical studies of mitochondrial metabolism. Martens ME; Peterson PL; Lee CP; Nigro MA; Hart Z; Glasberg M; Hatfield JS; Chang CH Ann Neurol; 1988 Nov; 24(5):630-7. PubMed ID: 2849368 [TBL] [Abstract][Full Text] [Related]
17. Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromes. Zupanc ML; Moraes CT; Shanske S; Langman CB; Ciafaloni E; DiMauro S Ann Neurol; 1991 Jun; 29(6):680-3. PubMed ID: 1892371 [TBL] [Abstract][Full Text] [Related]
18. Folate metabolism disorder in Kearns-Sayre syndrome. Dougados M; Zittoun J; Laplane D; Castaigne P Ann Neurol; 1983 Jun; 13(6):687. PubMed ID: 6881934 [No Abstract] [Full Text] [Related]
19. High CSF lactate and pyruvate content in Kearns-Sayre syndrome. Kuriyama M; Suehara M; Marume N; Osame M; Igata A Neurology; 1984 Feb; 34(2):253-5. PubMed ID: 6538023 [TBL] [Abstract][Full Text] [Related]
20. Coenzyme Q in serum and muscle of 5 patients with Kearns-Sayre syndrome and 12 patients with ophthalmoplegia plus. Zierz S; Jahns G; Jerusalem F J Neurol; 1989 Feb; 236(2):97-101. PubMed ID: 2709060 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]