These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 10683696)

  • 21. Kearns Sayre Syndrome--case report with review of literature.
    Phadke M; Lokeshwar MR; Bhutada S; Tampi C; Saxena R; Kohli S; Shah KN
    Indian J Pediatr; 2012 May; 79(5):650-4. PubMed ID: 22231766
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Severe cardiac failure in Kearns-Sayre syndrome].
    Consalvo D; Villegas F; Villa AM; Köhler G; Molina H; Benchuga E; Chamoles N; Sanz OP; Sica RE
    Medicina (B Aires); 1997; 57(1):67-71. PubMed ID: 9435373
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Exophthalmos in Kearns-Sayre syndrome.
    Tauber J; Polla DJ; Park S
    J AAPOS; 2019 Oct; 23(5):295-297. PubMed ID: 31158487
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Kearns Sayre syndrome: an unusual form of mitochondrial diabetes.
    Laloi-Michelin M; Virally M; Jardel C; Meas T; Ingster-Moati I; Lombès A; Massin P; Chabriat H; Tielmans A; Mikol J; Guillausseau PJ
    Diabetes Metab; 2006 Apr; 32(2):182-6. PubMed ID: 16735969
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndrome.
    Poulton J; O'Rahilly S; Morten KJ; Clark A
    Diabetologia; 1995 Jul; 38(7):868-71. PubMed ID: 7556992
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Kearns-Sayre syndrome and complex II deficiency.
    Rivner MH; Shamsnia M; Swift TR; Trefz J; Roesel RA; Carter AL; Yanamura W; Hommes FA
    Neurology; 1989 May; 39(5):693-6. PubMed ID: 2710360
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Detection of deleted mitochondrial DNA in Kearns-Sayre syndrome using laser capture microdissection.
    Pistilli D; di Gioia CR; D'Amati G; Sciacchitano S; Quaglione R; Quitadamo R; Casali C; Gallo P; Santorelli FM
    Hum Pathol; 2003 Oct; 34(10):1058-61. PubMed ID: 14608542
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome.
    Moraes CT; Schon EA; DiMauro S; Miranda AF
    Biochem Biophys Res Commun; 1989 Apr; 160(2):765-71. PubMed ID: 2541710
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Progression in a case of Kearns-Sayre syndrome.
    Ishikawa Y; Goto Y; Ishikawa Y; Minami R
    J Child Neurol; 2000 Nov; 15(11):750-5. PubMed ID: 11108509
    [TBL] [Abstract][Full Text] [Related]  

  • 31. "Bartter-like" phenotype in Kearns-Sayre syndrome.
    Emma F; Pizzini C; Tessa A; Di Giandomenico S; Onetti-Muda A; Santorelli FM; Bertini E; Rizzoni G
    Pediatr Nephrol; 2006 Mar; 21(3):355-60. PubMed ID: 16382326
    [TBL] [Abstract][Full Text] [Related]  

  • 32. MERRF and Kearns-Sayre overlap syndrome due to the mitochondrial DNA m.3291T>C mutation.
    Emmanuele V; Silvers DS; Sotiriou E; Tanji K; DiMauro S; Hirano M
    Muscle Nerve; 2011 Sep; 44(3):448-51. PubMed ID: 21996807
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [A case of incomplete Kearns-Sayre syndrome with a stroke like episode].
    Furuya H; Sugimura T; Yamada T; Hayashi K; Kobayashi T
    Rinsho Shinkeigaku; 1997 Aug; 37(8):680-4. PubMed ID: 9404143
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
    Mita S; Schmidt B; Schon EA; DiMauro S; Bonilla E
    Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9509-13. PubMed ID: 2556715
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Clinical and Brain Magnetic Resonance Imaging Features in a Cohort of Chinese Patients with Kearns-Sayre Syndrome.
    Yu M; Zhang Z; Wang QQ; Liu J; Zuo YH; Yu L; Xiao JX; Zhang W; Yuan Y; Wang ZX
    Chin Med J (Engl); 2016 Jun; 129(12):1419-24. PubMed ID: 27270536
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Loss of myelin-associated glycoprotein in kearns-sayre syndrome.
    Lax NZ; Campbell GR; Reeve AK; Ohno N; Zambonin J; Blakely EL; Taylor RW; Bonilla E; Tanji K; DiMauro S; Jaros E; Lassmann H; Turnbull DM; Mahad DJ
    Arch Neurol; 2012 Apr; 69(4):490-9. PubMed ID: 22491194
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues.
    Ponzetto C; Bresolin N; Bordoni A; Moggio M; Meola G; Bet L; Prelle A; Scarlato G
    J Neurol Sci; 1990 May; 96(2-3):207-10. PubMed ID: 2376752
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Kearns-Sayre syndrome: ophthalmic manifestations].
    Bande Rodriguez M; Pose Bazarra S; Treus Suarez A; Abraldes Lopez-Veiga M; Fernandez Rodriguez MI; Rodriguez Cid MJ
    An Pediatr (Barc); 2015 Jan; 82(1):e151-3. PubMed ID: 25441208
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome].
    Capková M; Tesarová M; Wenchich L; Cerná L; Hansíková H; Hůlková H; Hrubá E; Elleder M; Zeman J
    Cas Lek Cesk; 2002 Feb; 141(2):51-4. PubMed ID: 11925663
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Kearns-Sayre syndrome with a novel mitochondrial DNA deletion.
    Marin-Garcia J; Goldenthal MJ; Sarnat HB
    J Child Neurol; 2000 Aug; 15(8):555-8. PubMed ID: 10961796
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.