Multi-system neurological disease is common in patients with OPA1 mutations (2010)
- Authors:
- Man, P. Yu Wai
- Griffiths, P. G.
- Gorman, G. S.
- Lourenço, C. M.
- Wright, A. F.
- Grumbach, M. Auer
- Toscano, A.
- Musumeci, O.
- Valentino, M. L.
- Caporali, L.
- Lamperti, C.
- Tallaksen, C. M.
- Duffey, P.
- Miller, J.
- Whittaker, R. G.
- Baker, M. R.
- Jackson, M. J.
- Clarke, M. P.
- Dhillon, B.
- Czermin, B.
- Stewart, J. D.
- Hudson, G.
- Reynier, P.
- Bonneaus, D.
- Marques Júnior, Wilson
- Lenaers, G.
- McFarland, R.
- Taylor, R. W.
- Turnbull, D. M.
- Votruba, M.
- Zeviani, M.
- Carelli, V.
- Bindoff, L. A.
- Horvath, R.
- Bonneau, P. Amati
- Chinnery, P. F.
- Autor USP: MARQUES JÚNIOR, WILSON - FMRP
- Unidade: FMRP
- DOI: 10.1093/brain/awq007
- Assunto: DOENÇAS NEURODEGENERATIVAS
- Language: Inglês
- Imprenta:
- Source:
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
MAN, P. Yu Wai et al. Multi-system neurological disease is common in patients with OPA1 mutations. Brain, v. 133, n. 3, p. 771-786, 2010Tradução . . Disponível em: https://doi.org/10.1093/brain/awq007. Acesso em: 25 fev. 2026. -
APA
Man, P. Y. W., Griffiths, P. G., Gorman, G. S., Lourenço, C. M., Wright, A. F., Grumbach, M. A., et al. (2010). Multi-system neurological disease is common in patients with OPA1 mutations. Brain, 133( 3), 771-786. doi:10.1093/brain/awq007 -
NLM
Man PYW, Griffiths PG, Gorman GS, Lourenço CM, Wright AF, Grumbach MA, Toscano A, Musumeci O, Valentino ML, Caporali L, Lamperti C, Tallaksen CM, Duffey P, Miller J, Whittaker RG, Baker MR, Jackson MJ, Clarke MP, Dhillon B, Czermin B, Stewart JD, Hudson G, Reynier P, Bonneaus D, Marques Júnior W, Lenaers G, McFarland R, Taylor RW, Turnbull DM, Votruba M, Zeviani M, Carelli V, Bindoff LA, Horvath R, Bonneau PA, Chinnery PF. Multi-system neurological disease is common in patients with OPA1 mutations [Internet]. Brain. 2010 ; 133( 3): 771-786.[citado 2026 fev. 25 ] Available from: https://doi.org/10.1093/brain/awq007 -
Vancouver
Man PYW, Griffiths PG, Gorman GS, Lourenço CM, Wright AF, Grumbach MA, Toscano A, Musumeci O, Valentino ML, Caporali L, Lamperti C, Tallaksen CM, Duffey P, Miller J, Whittaker RG, Baker MR, Jackson MJ, Clarke MP, Dhillon B, Czermin B, Stewart JD, Hudson G, Reynier P, Bonneaus D, Marques Júnior W, Lenaers G, McFarland R, Taylor RW, Turnbull DM, Votruba M, Zeviani M, Carelli V, Bindoff LA, Horvath R, Bonneau PA, Chinnery PF. Multi-system neurological disease is common in patients with OPA1 mutations [Internet]. Brain. 2010 ; 133( 3): 771-786.[citado 2026 fev. 25 ] Available from: https://doi.org/10.1093/brain/awq007 - Does pregnancy change the natural history of CMT1A neuropathy?
- Mutational analysis of LITAF, EGR2 and NEFL genes in a Brazilian population of Charcot-Marie-Tooth neuropathy type I
- Hydroxicloroquine in the treatment of painful leprosy neuropathy
- Leprosy neuropathy
- Análise da qualidade de vida de pacientes com a doença de Charcot-Marie-Tooth tipo 1a
- Identification of five novel mutations in brazilian families with X-linked CMT
- Screening of HINT1 mutations associated with recessive axonal neuropathy in a brazilian cohort
- Central nervous system involvement in a new connexin32 mutation affecting identical twins
- Does pregnancy change the natural history of CMT1A neuropathy ?
- Tractography imaging: a useful method in the peripheral neuropathy diagnosis
Informações sobre o DOI: 10.1093/brain/awq007 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
