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Artigo de periodico
Reference range of fetal transverse cerebellar diameter between 18 and 24 weeks of pregnancy in a brazilian population (2015)
Araujo Júnior, Edward; Martins, Wellington de Paula; Nardozza, Luciano Marcondes Machado; Pires, Claudio Rodrigues; Zanforlin Filho, Sebastião Marques
Source: Journal of Child Neurology. Unidade: FMRP
Subjects: DESENVOLVIMENTO FETAL, IDADE GESTACIONAL, CEREBELO (MEDIÇÃO), FETO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARAUJO JÚNIOR, Edward et al. Reference range of fetal transverse cerebellar diameter between 18 and 24 weeks of pregnancy in a brazilian population. Journal of Child Neurology, v. 30, n. 2, p. 250-253, 2015Tradução . . Disponível em: https://doi.org/10.1177/0883073814527161. Acesso em: 20 fev. 2026.
APA
Araujo Júnior, E., Martins, W. de P., Nardozza, L. M. M., Pires, C. R., & Zanforlin Filho, S. M. (2015). Reference range of fetal transverse cerebellar diameter between 18 and 24 weeks of pregnancy in a brazilian population. Journal of Child Neurology, 30( 2), 250-253. doi:10.1177/0883073814527161
NLM
Araujo Júnior E, Martins W de P, Nardozza LMM, Pires CR, Zanforlin Filho SM. Reference range of fetal transverse cerebellar diameter between 18 and 24 weeks of pregnancy in a brazilian population [Internet]. Journal of Child Neurology. 2015 ; 30( 2): 250-253.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1177/0883073814527161
Vancouver
Araujo Júnior E, Martins W de P, Nardozza LMM, Pires CR, Zanforlin Filho SM. Reference range of fetal transverse cerebellar diameter between 18 and 24 weeks of pregnancy in a brazilian population [Internet]. Journal of Child Neurology. 2015 ; 30( 2): 250-253.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1177/0883073814527161
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: 20 fev. 2026.
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 2026 fev. 20 ] 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 2026 fev. 20 ] 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: 20 fev. 2026.
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 2026 fev. 20 ]
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 2026 fev. 20 ]
Artigo de periodico
Calpainopathy: focus on a pediatric population (2003)
Kolski, H.; Edmonton, A. B.; Vajsar, J.; Paula, F de; Zatz, Mayana
Source: Journal of Child Neurology. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KOLSKI, H. et al. Calpainopathy: focus on a pediatric population. Journal of Child Neurology, v. 18, n. 3, p. 212, 2003Tradução . . Acesso em: 20 fev. 2026.
APA
Kolski, H., Edmonton, A. B., Vajsar, J., Paula, F. de, & Zatz, M. (2003). Calpainopathy: focus on a pediatric population. Journal of Child Neurology, 18( 3), 212.
NLM
Kolski H, Edmonton AB, Vajsar J, Paula F de, Zatz M. Calpainopathy: focus on a pediatric population. Journal of Child Neurology. 2003 ; 18( 3): 212.[citado 2026 fev. 20 ]
Vancouver
Kolski H, Edmonton AB, Vajsar J, Paula F de, Zatz M. Calpainopathy: focus on a pediatric population. Journal of Child Neurology. 2003 ; 18( 3): 212.[citado 2026 fev. 20 ]
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: 20 fev. 2026.
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 2026 fev. 20 ]
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 2026 fev. 20 ]
Artigo de periodico
Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report (2001)
Yacubian, Elza Márcia T.; Rosemberg, Sérgio; Garrido Neto, Theodomiro L.; Marie, Suely Kazue Nagahashi; Valério, Rosa M. F.; Jorge, Carmen Lisa
Source: Journal of Child Neurology. Unidade: FM
Subjects: NEUROLOGIA, CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
YACUBIAN, Elza Márcia T. et al. Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report. Journal of Child Neurology, v. 16, n. 05, p. 374-377, 2001Tradução . . Acesso em: 20 fev. 2026.
APA
Yacubian, E. M. T., Rosemberg, S., Garrido Neto, T. L., Marie, S. K. N., Valério, R. M. F., & Jorge, C. L. (2001). Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report. Journal of Child Neurology, 16( 05), 374-377.
NLM
Yacubian EMT, Rosemberg S, Garrido Neto TL, Marie SKN, Valério RMF, Jorge CL. Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report. Journal of Child Neurology. 2001 ; 16( 05): 374-377.[citado 2026 fev. 20 ]
Vancouver
Yacubian EMT, Rosemberg S, Garrido Neto TL, Marie SKN, Valério RMF, Jorge CL. Rasmussen encephalitis associated with segmental vitiligo of the scalp: clinicopathologic report. Journal of Child Neurology. 2001 ; 16( 05): 374-377.[citado 2026 fev. 20 ]
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: 20 fev. 2026.
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 2026 fev. 20 ]
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 2026 fev. 20 ]
Artigo de periodico
Childhood degos disease with prominent neurological symptoms: report of a clinicopathological case (1988)
Rosemberg, Sérgio; Lopes, M B S; Sotto, Mírian Nacagami; Graudenz, M S
Source: Journal of Child Neurology. Unidade: FM
Assunto: SINAIS E SINTOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROSEMBERG, Sérgio et al. Childhood degos disease with prominent neurological symptoms: report of a clinicopathological case. Journal of Child Neurology, v. 3 , n. ja 1988, p. 42-6, 1988Tradução . . Acesso em: 20 fev. 2026.
APA
Rosemberg, S., Lopes, M. B. S., Sotto, M. N., & Graudenz, M. S. (1988). Childhood degos disease with prominent neurological symptoms: report of a clinicopathological case. Journal of Child Neurology, 3 ( ja 1988), 42-6.
NLM
Rosemberg S, Lopes MBS, Sotto MN, Graudenz MS. Childhood degos disease with prominent neurological symptoms: report of a clinicopathological case. Journal of Child Neurology. 1988 ;3 ( ja 1988): 42-6.[citado 2026 fev. 20 ]
Vancouver
Rosemberg S, Lopes MBS, Sotto MN, Graudenz MS. Childhood degos disease with prominent neurological symptoms: report of a clinicopathological case. Journal of Child Neurology. 1988 ;3 ( ja 1988): 42-6.[citado 2026 fev. 20 ]

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