BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 2177152)

  • 1. [Mitochondrial encephalomyopathies. A comparison of Kearns-Sayre syndrome, MELAS and MERRF].
    Zenner K; Gold R; Meurers B; Reichmann H
    Nervenarzt; 1990 Oct; 61(10):597-603. PubMed ID: 2177152
    [No Abstract]   [Full Text] [Related]  

  • 2. [Familial cases of mitochondrial cytopathy].
    Ishitsu T; Matsuda I; Kitano A; Shimoji A; Kimura H
    Rinsho Shinkeigaku; 1987 Aug; 27(8):983-9. PubMed ID: 3121229
    [No Abstract]   [Full Text] [Related]  

  • 3. [Mitochondrial myopathy and abnormal mitochondrial DNA].
    Takeshita K
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):834-8. PubMed ID: 3152098
    [No Abstract]   [Full Text] [Related]  

  • 4. [Kearns-Sayre syndrome: mitochondrial encephalomyopathy caused by deficiency of the respiratory chain].
    Desnuelle C; Pellissier JF; Serratrice G; Pouget J; Turnbull DM
    Rev Neurol (Paris); 1989; 145(12):842-50. PubMed ID: 2559448
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial angiopathy in a family with MELAS.
    Förster C; Hübner G; Müller-Höcker J; Pongratz D; Baierl P; Senger R; Ruitenbeek W
    Neuropediatrics; 1992 Jun; 23(3):165-8. PubMed ID: 1322508
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literature.
    van Hellenberg Hubar JL; Gabreëls FJ; Ruitenbeek W; Sengers RC; Renier WO; Thijssen HO; ter Laak HJ
    Neuropediatrics; 1991 Feb; 22(1):10-4. PubMed ID: 1903852
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mitochondrial encephalomyopathy--MERRF and MELAS are clinicopathologically distinctive entities].
    Tanaka K; Nishizawa M; Miyatake T; Takeda S; Ohama E
    Rinsho Shinkeigaku; 1987 Nov; 27(11):1468-73. PubMed ID: 3129227
    [No Abstract]   [Full Text] [Related]  

  • 9. [A case of myoclonus epilepsy associated with ragged-red fibers (MERRF) with cytochrome c oxidase deficiency].
    Taniwaki T; Yamashita Y; Ohshima Y; Habara S; Nagao H
    Rinsho Shinkeigaku; 1988 Aug; 28(8):902-9. PubMed ID: 2853657
    [No Abstract]   [Full Text] [Related]  

  • 10. [A patient with Kearns-Sayre syndrome].
    Spina G; Capone A
    Klin Monbl Augenheilkd; 1994 May; 204(5):462-4. PubMed ID: 8051900
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Mitochondrial encephalomyopathy].
    Ozawa T; Tanaka M
    Tanpakushitsu Kakusan Koso; 1990 May; 35(7 Suppl):1236-45. PubMed ID: 2162552
    [No Abstract]   [Full Text] [Related]  

  • 12. Kearns Sayre syndrome: an atypical presentation.
    Rajakannan ; Gayathri ; Prasad W; Ramakrishnan R; Prajna NV
    Indian J Ophthalmol; 2000 Mar; 48(1):54-5. PubMed ID: 11271939
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Progressive ptosis in children as a presenting sign of Kearns-Sayre syndrome].
    Gal R; Lahat E
    Harefuah; 2000 Jan; 138(2):108-10, 174. PubMed ID: 10883071
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Kearns-Sayre syndrome. A case report.
    Altunbaşak S; Bingöl G; Ozbarlas N; Akçören Z; Hergüner O
    Turk J Pediatr; 1998; 40(2):255-9. PubMed ID: 9677732
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Peripheral neuropathy of mitochondrial myopathies.
    Mizusawa H; Ohkoshi N; Watanabe M; Kanazawa I
    Rev Neurol (Paris); 1991; 147(6-7):501-7. PubMed ID: 1660182
    [TBL] [Abstract][Full Text] [Related]  

  • 16. EEG findings in children and adolescents with mitochondrial encephalomyopathies: a study of 25 cases.
    Tulinius MH; Hagne I
    Brain Dev; 1991 May; 13(3):167-73. PubMed ID: 1928609
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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. PubMed ID: 6629235
    [No Abstract]   [Full Text] [Related]  

  • 18. Kearns-Sayre syndrome associated with de Toni-Debré-Fanconi syndrome due to cytochrome-c-oxidase (COX) deficiency.
    Berio A; Piazzi A
    Panminerva Med; 2001 Sep; 43(3):211-4. PubMed ID: 11579332
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial encephalomyopathies preceded by de-Toni-Debré-Fanconi syndrome or focal segmental glomerulosclerosis.
    Mochizuki H; Joh K; Kawame H; Imadachi A; Nozaki H; Ohashi T; Usui N; Eto Y; Kanetsuna Y; Aizawa S
    Clin Nephrol; 1996 Nov; 46(5):347-52. PubMed ID: 8953126
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial encephalomyopathies.
    Scarlato G; Moggio M; Bet L; Gallanti A; Bresolin N
    Acta Neurol (Napoli); 1989 Oct; 11(5):322-9. PubMed ID: 2603778
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.