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Similar articles for PubMed (Select 23391298)

1.

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. doi: 10.3109/19401736.2012.760550. Epub 2013 Feb 8.

PMID:
23391298
2.

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.

PMID:
7484086
3.

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 9;1271(2-3):363-8.

PMID:
7605803
4.

Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCR.

Kleinle S, Wiesmann U, Superti-Furga A, Krähenbühl S, Boltshauser E, Reichen J, Liechti-Gallati S.

Hum Genet. 1997 Oct;100(5-6):643-50.

PMID:
9341886
6.

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.

PMID:
12522683
7.

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.

PMID:
7814031
8.

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. doi: 10.1016/j.mito.2010.04.003. Epub 2010 Apr 11.

PMID:
20388556
9.

Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome.

Fischel-Ghodsian N, Bohlman MC, Prezant TR, Graham JM Jr, Cederbaum SD, Edwards MJ.

Pediatr Res. 1992 Jun;31(6):557-60.

PMID:
1635816
10.

[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. Spanish.

PMID:
16977556
11.

Characterisation of repeat and palindrome elements in patients harbouring single deletions of mitochondrial DNA.

Solano A, Gámez J, Carod FJ, Pineda M, Playán A, López-Gallardo E, Andreu AL, Montoya J.

J Med Genet. 2003 Jul;40(7):e86. No abstract available.

12.

Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes.

Sadikovic B, Wang J, El-Hattab A, Landsverk M, Douglas G, Brundage EK, Craigen WJ, Schmitt ES, Wong LJ.

PLoS One. 2010 Dec 20;5(12):e15687. doi: 10.1371/journal.pone.0015687.

13.

[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 1;105(5):180-4. Spanish.

PMID:
7630231
14.
15.

Multiple short direct repeats associated with single mtDNA deletions.

Larsson NG, Holme E.

Biochim Biophys Acta. 1992 Aug 25;1139(4):311-4.

PMID:
1325186
16.

Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion.

Becher MW, Wills ML, Noll WW, Hurko O, Price DL.

Hum Pathol. 1999 May;30(5):577-81.

PMID:
10333230
17.

A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

Schon EA, Rizzuto R, Moraes CT, Nakase H, Zeviani M, DiMauro S.

Science. 1989 Apr 21;244(4902):346-9.

PMID:
2711184
18.

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 25;17(20):8117-24.

19.

[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. Chinese.

PMID:
12903032
20.

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.

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