284 related articles for article (PubMed ID: 7484086)
1. 3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome.
Klopstock T; Bischof F; Gerok K; Deuschl G; Seibel P; Ketelsen UP; Reichmann H
Acta Neuropathol; 1995; 90(2):126-9. PubMed ID: 7484086
[TBL] [Abstract][Full Text] [Related]
2. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.
Shoffner JM; Lott MT; Voljavec AS; Soueidan SA; Costigan DA; Wallace DC
Proc Natl Acad Sci U S A; 1989 Oct; 86(20):7952-6. PubMed ID: 2554297
[TBL] [Abstract][Full Text] [Related]
3. Kearns-Sayre syndrome case presenting a mitochondrial DNA deletion with unusual direct repeats and a rudimentary RNAase mitochondrial ribonucleotide processing target sequence.
Remes AM; Peuhkurinen KJ; Herva R; Majamaa K; Hassinen IE
Genomics; 1993 Apr; 16(1):256-8. PubMed ID: 7683627
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.
Nelson I; Degoul F; Obermaier-Kusser B; Romero N; Borrone C; Marsac C; Vayssiere JL; Gerbitz K; Fardeau M; Ponsot G; Lestienne P
Nucleic Acids Res; 1989 Oct; 17(20):8117-24. PubMed ID: 2813058
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. [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]
8. [Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].
Wang ZX; Yuan Y; Gao F; Qi Y; Shen DG; Chen QT
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):273-8. PubMed ID: 12903032
[TBL] [Abstract][Full Text] [Related]
9. [Mitochondrial DNA deletions in Kearns-Sayre syndrome].
Carod-Artal FJ; Lopez Gallardo E; Solano A; Dahmani Y; Herrero MD; Montoya J
Neurologia; 2006 Sep; 21(7):357-64. PubMed ID: 16977556
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samples.
De Coo IF; Gussinklo T; Arts PJ; Van Oost BA; Smeets HJ
J Neurol Sci; 1997 Jul; 149(1):37-40. PubMed ID: 9168163
[TBL] [Abstract][Full Text] [Related]
12. A topoisomerase II cleavage site is associated with a novel mitochondrial DNA deletion.
Blok RB; Thorburn DR; Thompson GN; Dahl HH
Hum Genet; 1995 Jan; 95(1):75-81. PubMed ID: 7814031
[TBL] [Abstract][Full Text] [Related]
13. Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.
Degoul F; Nelson I; Lestienne P; Francois D; Romero N; Duboc D; Eymard B; Fardeau M; Ponsot G; Paturneau-Jouas M
J Neurol Sci; 1991 Feb; 101(2):168-77. PubMed ID: 1851820
[TBL] [Abstract][Full Text] [Related]
14. Kearns-Sayre syndrome case. Novel 5,9 kb mtDNA deletion.
Grigalionienė K; Burnytė B; Balkelienė D; Ambrozaitytė L; Utkus A
Mol Genet Genomic Med; 2023 Jan; 11(1):e2059. PubMed ID: 36181358
[TBL] [Abstract][Full Text] [Related]
15. Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?
Poulton J; Morten KJ; Weber K; Brown GK; Bindoff L
Hum Mol Genet; 1994 Jun; 3(6):947-51. PubMed ID: 7951243
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Duplications of mitochondrial DNA in Kearns-Sayre syndrome.
Poulton J; Morten KJ; Marchington D; Weber K; Brown GK; Rötig A; Bindoff L
Muscle Nerve Suppl; 1995; 3():S154-8. PubMed ID: 7603518
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial genome analysis in Kearns-Sayre syndrome.
Lertrit P; Atchaneeyasakul L; Devahastin V; Saechan V; Sangruchi T; Neungton N; Lekhakula S
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():162-5. PubMed ID: 8629098
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial DNA deletion and duplication in Kearns-Sayre Syndrome (KSS) with initial presentation as Pearson Marrow-Pancreas Syndrome (PMPS): Two case reports in Barranquilla, Colombia.
Sabella-Jiménez V; Otero-Herrera C; Silvera-Redondo C; Garavito-Galofre P
Mol Genet Genomic Med; 2020 Nov; 8(11):e1509. PubMed ID: 33030289
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]