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 *

172 related articles for article (PubMed ID: 7581370)

  • 21. Severe lactic acidosis and neonatal death in Pearson syndrome.
    Muraki K; Goto Y; Nishino I; Hayashidani M; Takeuchi S; Horai S; Sakura N; Ueda K
    J Inherit Metab Dis; 1997 Mar; 20(1):43-8. PubMed ID: 9061566
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Recognition of mitochondrial DNA deletion syndrome with non-neuromuscular multisystemic manifestation.
    Wong LJ
    Genet Med; 2001; 3(6):399-404. PubMed ID: 11715003
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Characterization of a 5025 base pair mitochondrial DNA deletion in Kearns-Sayre syndrome.
    Vázquez-Acevedo M; Coria R; González-Astiazarán A; Medina-Crespo V; Ridaura-Sanz C; González-Halphen D
    Biochim Biophys Acta; 1995 Jun; 1271(2-3):363-8. PubMed ID: 7605803
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Deletions of mitochondrial DNA in Kearns-Sayre syndrome].
    Soga F; Ueno S; Yorifuji S
    Nihon Rinsho; 1993 Sep; 51(9):2386-90. PubMed ID: 8411717
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome.
    Shanske S; Tang Y; Hirano M; Nishigaki Y; Tanji K; Bonilla E; Sue C; Krishna S; Carlo JR; Willner J; Schon EA; DiMauro S
    Am J Hum Genet; 2002 Sep; 71(3):679-83. PubMed ID: 12152148
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel mtDNA deletion in an infant with Pearson syndrome.
    Kapsa R; Thompson GN; Thorburn DR; Dahl HH; Marzuki S; Byrne E; Blok RB
    J Inherit Metab Dis; 1994; 17(5):521-6. PubMed ID: 7837757
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Pearson's marrow-pancreas syndrome in 2 Turkish children.
    Gürgey A; Rötig A; Gümrük F; Cemeroğlu P; Sarialioğlu F; Altay C
    Acta Haematol; 1992; 87(4):206-9. PubMed ID: 1519437
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The association between haematological manifestation and mtDNA deletions in Pearson syndrome.
    Muraki K; Nishimura S; Goto Y; Nonaka I; Sakura N; Ueda K
    J Inherit Metab Dis; 1997 Sep; 20(5):697-703. PubMed ID: 9323565
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Kearns-Sayre's syndrome developing in a boy who survived pearson's syndrome caused by mitochondrial DNA deletion.
    Simonsz HJ; Bärlocher K; Rötig A
    Doc Ophthalmol; 1992; 82(1-2):73-9. PubMed ID: 1305030
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A case of Kearns-Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles.
    Mkaouar-Rebai E; Chamkha I; Kammoun T; Chabchoub I; Aloulou H; Fendri N; Hachicha M; Fakhfakh F
    Mitochondrion; 2010 Aug; 10(5):449-55. PubMed ID: 20388556
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies.
    Brockington M; Sweeney MG; Hammans SR; Morgan-Hughes JA; Harding AE
    Nat Genet; 1993 May; 4(1):67-71. PubMed ID: 8513327
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Phylogenetic analysis of mitochondrial DNA in a patient with Kearns-Sayre syndrome containing a novel 7629-bp deletion.
    Montiel-Sosa JF; Herrero MD; Munoz Mde L; Aguirre-Campa LE; Pérez-Ramírez G; García-Ramírez R; Ruiz-Pesini E; Montoya J
    Mitochondrial DNA; 2013 Aug; 24(4):420-31. PubMed ID: 23391298
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [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]  

  • 35. A case of Kearns-Sayre syndrome with the 4,977-bp common deletion associated with a novel 7,704-bp deletion.
    Vázquez-Acevedo M; Vázquez-Memije ME; Mutchinick OM; Morales JJ; García-Ramos G; González-Halphen D
    Neurol Sci; 2002 Dec; 23(5):247-50. PubMed ID: 12522683
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndrome.
    de Vries DD; Buzing CJ; Ruitenbeek W; van der Wouw MP; Sperl W; Sengers RC; Trijbels JM; van Oost BA
    Neuromuscul Disord; 1992; 2(3):185-95. PubMed ID: 1483044
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Whole sequence of the mitochondrial DNA genome of Kearns Sayre Syndrome patients: Identification of deletions and variants.
    Saldaña-Martínez A; Muñoz ML; Pérez-Ramírez G; Montiel-Sosa JF; Montoya J; Emperador S; Ruiz-Pesini E; Cuevas-Covarrubias S; López-Valdez J; Ramírez RG
    Gene; 2019 Mar; 688():171-181. PubMed ID: 30528267
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Progressive external ophthalmoplegia and the Kearns-Sayre syndrome: a clinical and molecular study of 6 cases].
    Barrientos A; Casademont J; Grau JM; Cardellach F; Montoya J; Estivill X; Urbano-Márquez A; Nunes V
    Med Clin (Barc); 1995 Jul; 105(5):180-4. PubMed ID: 7630231
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Pearson's marrow/pancreas syndrome: a histological and genetic study.
    Morikawa Y; Matsuura N; Kakudo K; Higuchi R; Koike M; Kobayashi Y
    Virchows Arch A Pathol Anat Histopathol; 1993; 423(3):227-31. PubMed ID: 8236818
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Paediatric single mitochondrial DNA deletion disorders: an overlapping spectrum of disease.
    Broomfield A; Sweeney MG; Woodward CE; Fratter C; Morris AM; Leonard JV; Abulhoul L; Grunewald S; Clayton PT; Hanna MG; Poulton J; Rahman S
    J Inherit Metab Dis; 2015 May; 38(3):445-57. PubMed ID: 25352051
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.