182 related articles for article (PubMed ID: 1978558)
1. Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.
Zeviani M; Bresolin N; Gellera C; Bordoni A; Pannacci M; Amati P; Moggio M; Servidei S; Scarlato G; DiDonato S
Am J Hum Genet; 1990 Dec; 47(6):904-14. PubMed ID: 1978558
[TBL] [Abstract][Full Text] [Related]
2. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia.
Moslemi AR; Melberg A; Holme E; Oldfors A
Ann Neurol; 1996 Nov; 40(5):707-13. PubMed ID: 8957011
[TBL] [Abstract][Full Text] [Related]
3. Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies.
Servidei S; Zeviani M; Manfredi G; Ricci E; Silvestri G; Bertini E; Gellera C; Di Mauro S; Di Donato S; Tonali P
Neurology; 1991 Jul; 41(7):1053-9. PubMed ID: 2067633
[TBL] [Abstract][Full Text] [Related]
4. Marked decrease of mitochondrial DNA with multiple deletions in a patient with familial mitochondrial myopathy.
Otsuka M; Niijima K; Mizuno Y; Yoshida M; Kagawa Y; Ohta S
Biochem Biophys Res Commun; 1990 Mar; 167(2):680-5. PubMed ID: 2322247
[TBL] [Abstract][Full Text] [Related]
5. Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy.
Bohlega S; Tanji K; Santorelli FM; Hirano M; al-Jishi A; DiMauro S
Neurology; 1996 May; 46(5):1329-34. PubMed ID: 8628476
[TBL] [Abstract][Full Text] [Related]
6. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.
Zeviani M; Servidei S; Gellera C; Bertini E; DiMauro S; DiDonato S
Nature; 1989 May; 339(6222):309-11. PubMed ID: 2725645
[TBL] [Abstract][Full Text] [Related]
7. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.
Holt IJ; Harding AE; Morgan-Hughes JA
Nature; 1988 Feb; 331(6158):717-9. PubMed ID: 2830540
[TBL] [Abstract][Full Text] [Related]
8. Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses.
Carrozzo R; Hirano M; Fromenty B; Casali C; Santorelli FM; Bonilla E; DiMauro S; Schon EA; Miranda AF
Neurology; 1998 Jan; 50(1):99-106. PubMed ID: 9443465
[TBL] [Abstract][Full Text] [Related]
9. Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy.
Cormier V; Rotig A; Tardieu M; Colonna M; Saudubray JM; Munnich A
Am J Hum Genet; 1991 Apr; 48(4):643-8. PubMed ID: 2014791
[TBL] [Abstract][Full Text] [Related]
10. A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies.
Hammans SR; Sweeney MG; Wicks DA; Morgan-Hughes JA; Harding AE
Brain; 1992 Apr; 115 ( Pt 2)():343-65. PubMed ID: 1606473
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes.
Gerbitz KD; Obermaier-Kusser B; Zierz S; Pongratz D; Müller-Höcker J; Lestienne P
J Neurol; 1990 Feb; 237(1):5-10. PubMed ID: 2156958
[TBL] [Abstract][Full Text] [Related]
12. [Multiple mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO)].
Kawashima S; Nishizawa M
Nihon Rinsho; 1993 Sep; 51(9):2391-5. PubMed ID: 8411718
[TBL] [Abstract][Full Text] [Related]
13. RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy.
Reyes A; Melchionda L; Nasca A; Carrara F; Lamantea E; Zanolini A; Lamperti C; Fang M; Zhang J; Ronchi D; Bonato S; Fagiolari G; Moggio M; Ghezzi D; Zeviani M
Am J Hum Genet; 2015 Jul; 97(1):186-93. PubMed ID: 26094573
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial encephalomyopathy with autosomal dominant inheritance: a clinical and genetic entity of mitochondrial diseases.
Kawai H; Akaike M; Yokoi K; Nishida Y; Kunishige M; Mine H; Saito S
Muscle Nerve; 1995 Jul; 18(7):753-60. PubMed ID: 7783765
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Mitochondrial DNA deletions in mitochondrial cytopathies: observations in 19 patients.
Yamamoto M; Clemens PR; Engel AG
Neurology; 1991 Nov; 41(11):1822-8. PubMed ID: 1682853
[TBL] [Abstract][Full Text] [Related]
17. Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadism.
Melberg A; Arnell H; Dahl N; Stålberg E; Raininko R; Oldfors A; Bakall B; Lundberg PO; Holme E
Muscle Nerve; 1996 Dec; 19(12):1561-9. PubMed ID: 8941270
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.
Suomalainen A; Majander A; Wallin M; Setälä K; Kontula K; Leinonen H; Salmi T; Paetau A; Haltia M; Valanne L; Lonnqvist J; Peltonen L; Somer H
Neurology; 1997 May; 48(5):1244-53. PubMed ID: 9153451
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Cytoplasmic body and mitochondrial DNA deletion.
Sahashi K; Ohno K; Tanaka M; Ibi T; Yamamoto T; Tashiro M; Sato W; Takahashi A; Ozawa T
J Neurol Sci; 1990 Nov; 99(2-3):291-300. PubMed ID: 1964959
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]