576 related articles for article (PubMed ID: 28273704)
1. [Clinical and genetic characteristics of children with Leigh syndrome].
Fang F; Shen Y; Shen DM; Liu ZM; Ding CH; Zhang WC; Sun SZ; Lyu JL; Han TL; Wang XH; Zhang WH; Yang XY; Li JW; Wu HS
Zhonghua Er Ke Za Zhi; 2017 Mar; 55(3):205-209. PubMed ID: 28273704
[No Abstract] [Full Text] [Related]
2. Mitochondrial DNA mutations in late-onset Leigh syndrome.
Wei Y; Cui L; Peng B
J Neurol; 2018 Oct; 265(10):2388-2395. PubMed ID: 30128709
[TBL] [Abstract][Full Text] [Related]
3. [Clinical and genetic characteristics of 62 children with mitochondrial epilepsy].
Han XD; Fang F; Li H; Liu ZM; Shi YQ; Wang JL; Ren XT; Ding CH; Chen CH; Li JW; Zhang WH; Deng J
Zhonghua Er Ke Za Zhi; 2019 Nov; 57(11):844-851. PubMed ID: 31665838
[No Abstract] [Full Text] [Related]
4. Ophthalmological manifestations in patients with Leigh syndrome.
Han J; Lee YM; Kim SM; Han SY; Lee JB; Han SH
Br J Ophthalmol; 2015 Apr; 99(4):528-35. PubMed ID: 25351680
[TBL] [Abstract][Full Text] [Related]
5. The clinical and genetic characteristics in children with mitochondrial disease in China.
Fang F; Liu Z; Fang H; Wu J; Shen D; Sun S; Ding C; Han T; Wu Y; Lv J; Yang L; Li S; Lv J; Shen Y
Sci China Life Sci; 2017 Jul; 60(7):746-757. PubMed ID: 28639102
[TBL] [Abstract][Full Text] [Related]
6. [3-Hydroxy-isobutyryl-CoA hydrolase deficiency in a child with Leigh-like syndrome and literature review].
Zhu H; Bao X; Zhang Y
Zhonghua Er Ke Za Zhi; 2015 Aug; 53(8):626-30. PubMed ID: 26717663
[TBL] [Abstract][Full Text] [Related]
7. Cytochrome C oxydase deficiency: SURF1 gene investigation in patients with Leigh syndrome.
Maalej M; Kammoun T; Alila-Fersi O; Kharrat M; Ammar M; Felhi R; Mkaouar-Rebai E; Keskes L; Hachicha M; Fakhfakh F
Biochem Biophys Res Commun; 2018 Mar; 497(4):1043-1048. PubMed ID: 29481804
[TBL] [Abstract][Full Text] [Related]
8. Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations.
Sonam K; Khan NA; Bindu PS; Taly AB; Gayathri N; Bharath MM; Govindaraju C; Arvinda HR; Nagappa M; Sinha S; Thangaraj K
Brain Dev; 2014 Oct; 36(9):807-12. PubMed ID: 24262866
[TBL] [Abstract][Full Text] [Related]
9. Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations.
Yu XL; Yan CZ; Ji KQ; Lin PF; Xu XB; Dai TJ; Li W; Zhao YY
Chin Med J (Engl); 2018 Nov; 131(22):2705-2712. PubMed ID: 30425197
[TBL] [Abstract][Full Text] [Related]
10. [Diagnosis of mitochondrial disorders in children with next generation sequencing].
Liu Z; Fang F; Ding C; Zhang W; Li J; Yang X; Wang X; Wu Y; Wang H; Liu L; Han T; Wang X; Chen C; Lyu J; Wu H
Zhonghua Er Ke Za Zhi; 2015 Oct; 53(10):747-53. PubMed ID: 26758110
[TBL] [Abstract][Full Text] [Related]
11. [SUCLA2-related encephalomyopathic mitochondrial DNA depletion syndrome: a case report and review of literature].
Liu Z; Fang F; Ding C; Wu H; Lyu J; Wu Y
Zhonghua Er Ke Za Zhi; 2014 Nov; 52(11):817-21. PubMed ID: 25582465
[TBL] [Abstract][Full Text] [Related]
12. Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome.
Zhang Y; Yang YL; Sun F; Cai X; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Zhang YH; Jiang YW; Qin J; Wu XR
J Inherit Metab Dis; 2007 Apr; 30(2):265. PubMed ID: 17323145
[TBL] [Abstract][Full Text] [Related]
13. Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients.
Danis D; Brennerova K; Skopkova M; Kurdiova T; Ukropec J; Stanik J; Kolnikova M; Gasperikova D
Endocr Regul; 2018 Apr; 52(2):110-118. PubMed ID: 29715184
[TBL] [Abstract][Full Text] [Related]
14. Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.
Yang YL; Sun F; Zhang Y; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Qi ZY; Zhang YH; Jiang YW; Bao XH; Qin J; Wu XR
Chin Med J (Engl); 2006 Mar; 119(5):373-7. PubMed ID: 16542579
[TBL] [Abstract][Full Text] [Related]
15. [A case of combined oxidative phosphorylation deficiency 32 caused by MRPS34 gene variation and literature review].
Shen MX; Ji XN; Wu F; Gao YY; Feng S; Xie LN; Zheng P; Mao YY; Chen Q
Zhonghua Er Ke Za Zhi; 2023 Jul; 61(7):642-647. PubMed ID: 37385809
[No Abstract] [Full Text] [Related]
16. Leigh Syndrome: A Study of 209 Patients at the Beijing Children's Hospital.
Stenton SL; Zou Y; Cheng H; Liu Z; Wang J; Shen D; Jin H; Ding C; Tang X; Sun S; Han H; Ma Y; Zhang W; Jin R; Wang H; Sun D; Lv JL; Prokisch H; Fang F
Ann Neurol; 2022 Apr; 91(4):466-482. PubMed ID: 35094435
[TBL] [Abstract][Full Text] [Related]
17. Mortality of Japanese patients with Leigh syndrome: Effects of age at onset and genetic diagnosis.
Ogawa E; Fushimi T; Ogawa-Tominaga M; Shimura M; Tajika M; Ichimoto K; Matsunaga A; Tsuruoka T; Ishige M; Fuchigami T; Yamazaki T; Kishita Y; Kohda M; Imai-Okazaki A; Okazaki Y; Morioka I; Ohtake A; Murayama K
J Inherit Metab Dis; 2020 Jul; 43(4):819-826. PubMed ID: 31967322
[TBL] [Abstract][Full Text] [Related]
18. [Clinical characteristics and genetic analysis of two cases with Leigh syndrome with acute pulmonary hemorrhage as predominant manifestation].
Danqun J; Jie D; Wenjia T; Kefei H
Zhonghua Er Ke Za Zhi; 2015 Apr; 53(4):290-5. PubMed ID: 26182505
[TBL] [Abstract][Full Text] [Related]
19. Genotype-phenotype analysis of MT-ATP6-associated Leigh syndrome.
Na JH; Lee YM
Acta Neurol Scand; 2022 Apr; 145(4):414-422. PubMed ID: 34877647
[TBL] [Abstract][Full Text] [Related]
20. [Clinical manifestation and gene analyses of 15 patients with intellectual disability or developmental delay complicated with congenital nystagmus].
Gao ZJ; Jiang Q; Chen Q; Xu KM; Liu ZQ; Chen XB; Chen XL
Zhonghua Er Ke Za Zhi; 2017 Nov; 55(11):824-829. PubMed ID: 29141312
[No Abstract] [Full Text] [Related]
[Next] [New Search]
