Consensus statement on standard of care for congenital myopathies (2012)
- Authors:
- Wang, Ching H
- Dowling, James J - University of Michigan (UM)
- North, Kathryn
- Schroth, Mary K
- Sejersen, Thomas
- Shapiro, Frederic
- Bellini, Jonathan
- Weiss, Hali
- Guillet, Marc
- Amburgey, Kimberly - University of Michigan (UM)
- Apkon, Susan
- Bertini, Enrico
- Bonnemann, Carsten - National Institutes of Health (NIH)
- Clarke, Nigel
- Connolly, Anne M
- Estournet-Mathiaud, Brigitte
- Fitzgerald, Dominic
- Florence, Julaine M
- Gee, Richard
- Gurgel Giannetti, Juliana - Universidade Federal de Minas Gerais (UFMG)
- Glanzman, Allan M
- Hofmeister, Brittany
- Jungbluth, Heinz
- Koumbourlis, Anastassios C
- Laing, Nigel G
- Main, Marion
- Morrison, Leslie A
- Munns, Craig
- Rose, Kristy
- Schuler, Pamela M
- Sewry, Caroline
- Storhaug, Kari
- Vainzof, Mariz
- Yuan, Nanci
- Autor USP: VAINZOF, MARIZ - IB
- Unidade: IB
- DOI: 10.1177/0883073812436605
- Subjects: DOENÇAS MUSCULARES; NEUROLOGIA; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Publisher place: Thousand Oaks, CA
- Date published: 2012
- Source:
- Título do periódico: Journal of Child Neurology
- ISSN: 0883-0738
- Volume/Número/Paginação/Ano: v. 37, n. 3, p. 363-382, 2012
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: green
-
ABNT
WANG, Ching H; DOWLING, James J; NORTH, Kathryn; et al. Consensus statement on standard of care for congenital myopathies. Journal of Child Neurology, Thousand Oaks, CA, v. 37, n. 3, p. 363-382, 2012. Disponível em: < http://dx.doi.org/10.1177/0883073812436605 > DOI: 10.1177/0883073812436605. -
APA
Wang, C. H., Dowling, J. J., North, K., Schroth, M. K., Sejersen, T., Shapiro, F., et al. (2012). Consensus statement on standard of care for congenital myopathies. Journal of Child Neurology, 37( 3), 363-382. doi:10.1177/0883073812436605 -
NLM
Wang CH, Dowling JJ, North K, Schroth MK, Sejersen T, Shapiro F, Bellini J, Weiss H, Guillet M, Amburgey K, Apkon S, Bertini E, Bonnemann C, Clarke N, Connolly AM, Estournet-Mathiaud B, Fitzgerald D, Florence JM, Gee R, Gurgel Giannetti J, Glanzman AM, Hofmeister B, Jungbluth H, Koumbourlis AC, Laing NG, Main M, Morrison LA, Munns C, Rose K, Schuler PM, Sewry C, Storhaug K, Vainzof M, Yuan N. Consensus statement on standard of care for congenital myopathies [Internet]. Journal of Child Neurology. 2012 ; 37( 3): 363-382.Available from: http://dx.doi.org/10.1177/0883073812436605 -
Vancouver
Wang CH, Dowling JJ, North K, Schroth MK, Sejersen T, Shapiro F, Bellini J, Weiss H, Guillet M, Amburgey K, Apkon S, Bertini E, Bonnemann C, Clarke N, Connolly AM, Estournet-Mathiaud B, Fitzgerald D, Florence JM, Gee R, Gurgel Giannetti J, Glanzman AM, Hofmeister B, Jungbluth H, Koumbourlis AC, Laing NG, Main M, Morrison LA, Munns C, Rose K, Schuler PM, Sewry C, Storhaug K, Vainzof M, Yuan N. Consensus statement on standard of care for congenital myopathies [Internet]. Journal of Child Neurology. 2012 ; 37( 3): 363-382.Available from: http://dx.doi.org/10.1177/0883073812436605 - Estudo da atividade de quatro enzimas em tecido muscular de heterozigotas certas e afetadas por distrofias musculares progressivas: correlação com achados histológicos
- Therapeutic potential of murine mesenchymal stem cells (MSC) from adipose tissue in the treatment of muscular dystrophy in the new double mutant mouse model for the genes dystrophin and large
- Achados histológicos em biópsia muscular de eqüino com alterações neuromusculares
- The contribution of muscle protein analysis in the diagnosis of genetic myopathies and in the understanding of the organization and maintenance of muscle fiber integrity
- Reviewing large LAMA2 deletions and duplications in congenital muscular dystrophy patients
- Behavioral responses in animal model of congenital muscular dystrophy 1D
- The mdx/SJL mouse: a new double mutant model for neuromuscular disorders with mutations in the dystrophin and dysferlin genes
- Heterozygous mutations in putative glycosyltransferase modulating the severity of the phenotype of muscular dystrophies
- Effects of steroid hormones on myostatin expression and on genes of muscle regeneration pathway
- 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017
Informações sobre o DOI: 10.1177/0883073812436605 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
