Detalhe da pesquisa
1.
Long-term screening for primary mitochondrial DNA variants associated with Leber hereditary optic neuropathy: incidence, penetrance and clinical features.
Mitochondrion
; 54: 128-132, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32861874
2.
Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection.
J Clin Neurosci
; 16(9): 1223-5, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19502062
3.
DNA electroporation in vivo targets mature fibres in dystrophic mdx muscle.
Neuromuscul Disord
; 15(9-10): 630-41, 2005 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16084723
4.
Writer's cramp in an Australian pedigree with DYT1 dystonia.
J Clin Neurosci
; 11(5): 537-9, 2004 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15177405
5.
Late-adult onset Leigh syndrome.
J Clin Neurosci
; 19(2): 195-202, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22273117
6.
Novel single base pair COX III subunit deletion of mitochondrial DNA associated with rhabdomyolysis.
J Clin Neurosci
; 18(2): 290-2, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21163656
7.
Dominant inheritance of premature ovarian failure associated with mutant mitochondrial DNA polymerase gamma.
Hum Reprod
; 21(10): 2467-73, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16595552