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Artigo de periodico
Consensus statement on standard of care for congenital myopathies (2012)
Wang, Ching H; Dowling, James J; North, Kathryn; Schroth, Mary K; Sejersen, Thomas; Shapiro, Frederic; Bellini, Jonathan; Weiss, Hali; Guillet, Marc; Amburgey, Kimberly; Apkon, Susan; Bertini, Enrico; Bonnemann, Carsten; Clarke, Nigel; Connolly, Anne M; Estournet-Mathiaud, Brigitte; Fitzgerald, Dominic; Florence, Julaine M; Gee, Richard; Gurgel Giannetti, Juliana; 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
Source: Journal of Child Neurology. Unidade: IB
Subjects: DOENÇAS MUSCULARES, NEUROLOGIA, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WANG, Ching H et al. Consensus statement on standard of care for congenital myopathies. Journal of Child Neurology, v. 37, n. 3, p. 363-382, 2012Tradução . . Disponível em: https://doi.org/10.1177/0883073812436605. Acesso em: 06 maio 2024.
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.[citado 2024 maio 06 ] Available from: https://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.[citado 2024 maio 06 ] Available from: https://doi.org/10.1177/0883073812436605
Artigo de periodico
Diagnosis and molecular characterization of non-classic forms of Tay-Sachs disease in Brazil (2006)
Rozenberg, Roberto; Kok, Fernando; Burin, Maira Graeff; Miranda, M. C. Sá; Vasques, C.; Henriques-Souza, A. M. M.; Gugliani, R.; Vainzof, Mariz ; Pereira, Lygia da Veiga
Source: Journal of Child Neurology. Unidade: IB
Subjects: DOENÇAS METABÓLICAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROZENBERG, Roberto et al. Diagnosis and molecular characterization of non-classic forms of Tay-Sachs disease in Brazil. Journal of Child Neurology, v. 21, n. 6, p. 540-544, 2006Tradução . . Acesso em: 06 maio 2024.
APA
Rozenberg, R., Kok, F., Burin, M. G., Miranda, M. C. S., Vasques, C., Henriques-Souza, A. M. M., et al. (2006). Diagnosis and molecular characterization of non-classic forms of Tay-Sachs disease in Brazil. Journal of Child Neurology, 21( 6), 540-544.
NLM
Rozenberg R, Kok F, Burin MG, Miranda MCS, Vasques C, Henriques-Souza AMM, Gugliani R, Vainzof M, Pereira L da V. Diagnosis and molecular characterization of non-classic forms of Tay-Sachs disease in Brazil. Journal of Child Neurology. 2006 ; 21( 6): 540-544.[citado 2024 maio 06 ]
Vancouver
Rozenberg R, Kok F, Burin MG, Miranda MCS, Vasques C, Henriques-Souza AMM, Gugliani R, Vainzof M, Pereira L da V. Diagnosis and molecular characterization of non-classic forms of Tay-Sachs disease in Brazil. Journal of Child Neurology. 2006 ; 21( 6): 540-544.[citado 2024 maio 06 ]
Artigo de periodico
Rod distribution and muscle fiber type modification in the progression of nemaline myopathy (2003)
Gurgel-Giannetti, J.; Zanoteli, E.; Werneck, L. C.; Reed, Umbertina Conti; Beggs, A. H.; Marie, Suely Kazue Nagahashi; Fireman, M. A. T.; Oliveira, A. S. B.; Zatz, Mayana ; Vainzof, Mariz
Source: Journal of Child Neurology. Unidades: FM, IB
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GURGEL-GIANNETTI, J. et al. Rod distribution and muscle fiber type modification in the progression of nemaline myopathy. Journal of Child Neurology, v. 18, n. 3, p. 235-240, 2003Tradução . . Acesso em: 06 maio 2024.
APA
Gurgel-Giannetti, J., Zanoteli, E., Werneck, L. C., Reed, U. C., Beggs, A. H., Marie, S. K. N., et al. (2003). Rod distribution and muscle fiber type modification in the progression of nemaline myopathy. Journal of Child Neurology, 18( 3), 235-240.
NLM
Gurgel-Giannetti J, Zanoteli E, Werneck LC, Reed UC, Beggs AH, Marie SKN, Fireman MAT, Oliveira ASB, Zatz M, Vainzof M. Rod distribution and muscle fiber type modification in the progression of nemaline myopathy. Journal of Child Neurology. 2003 ; 18( 3): 235-240.[citado 2024 maio 06 ]
Vancouver
Gurgel-Giannetti J, Zanoteli E, Werneck LC, Reed UC, Beggs AH, Marie SKN, Fireman MAT, Oliveira ASB, Zatz M, Vainzof M. Rod distribution and muscle fiber type modification in the progression of nemaline myopathy. Journal of Child Neurology. 2003 ; 18( 3): 235-240.[citado 2024 maio 06 ]
Artigo de periodico
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases (2000)
Reed, Umbertina Conti; Marie, Suely Kazue Nagahashi; Vainzof, Mariz ; Gobbo, L. F.; Gurgel, J. E. P.; Carvalho, M. S.; Resende, M. B. D.; Espindola, A. A.; Zatz, Mayana ; Diament, Aron Judka
Source: Journal of Child Neurology. Unidades: FM, IB
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REED, Umbertina Conti et al. Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases. Journal of Child Neurology, v. 15, n. 3, p. 172-8, 2000Tradução . . Acesso em: 06 maio 2024.
APA
Reed, U. C., Marie, S. K. N., Vainzof, M., Gobbo, L. F., Gurgel, J. E. P., Carvalho, M. S., et al. (2000). Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases. Journal of Child Neurology, 15( 3), 172-8.
NLM
Reed UC, Marie SKN, Vainzof M, Gobbo LF, Gurgel JEP, Carvalho MS, Resende MBD, Espindola AA, Zatz M, Diament AJ. Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases. Journal of Child Neurology. 2000 ; 15( 3): 172-8.[citado 2024 maio 06 ]
Vancouver
Reed UC, Marie SKN, Vainzof M, Gobbo LF, Gurgel JEP, Carvalho MS, Resende MBD, Espindola AA, Zatz M, Diament AJ. Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases. Journal of Child Neurology. 2000 ; 15( 3): 172-8.[citado 2024 maio 06 ]

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