ReP USP - Resultado da busca

Trabalho de evento-resumo periodico
Heterozygote advantage of the MTHFR gene: are heterozygous C677T/MTHFR womem at lower risk of having children with nonsyndromic cleft lip with/without cleft palate? (1999)
Gaspar, D A; Pavanello, R C M; André, M; Steman, S; Zatz, Mayana ; Wyszynski, Diego F; Matioli, Sergio Russo ; Passos-Bueno, Maria Rita
Source: American Journal of Human Genetics. Conference titles: American Society of Human Genetics. Unidades: FO, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GASPAR, D A et al. Heterozygote advantage of the MTHFR gene: are heterozygous C677T/MTHFR womem at lower risk of having children with nonsyndromic cleft lip with/without cleft palate?. American Journal of Human Genetics. San Francisco: Faculdade de Odontologia, Universidade de São Paulo. . Acesso em: 17 jul. 2024. , 1999
APA
Gaspar, D. A., Pavanello, R. C. M., André, M., Steman, S., Zatz, M., Wyszynski, D. F., et al. (1999). Heterozygote advantage of the MTHFR gene: are heterozygous C677T/MTHFR womem at lower risk of having children with nonsyndromic cleft lip with/without cleft palate? American Journal of Human Genetics. San Francisco: Faculdade de Odontologia, Universidade de São Paulo.
NLM
Gaspar DA, Pavanello RCM, André M, Steman S, Zatz M, Wyszynski DF, Matioli SR, Passos-Bueno MR. Heterozygote advantage of the MTHFR gene: are heterozygous C677T/MTHFR womem at lower risk of having children with nonsyndromic cleft lip with/without cleft palate? American Journal of Human Genetics. 1999 ; 65( 4):[citado 2024 jul. 17 ]
Vancouver
Gaspar DA, Pavanello RCM, André M, Steman S, Zatz M, Wyszynski DF, Matioli SR, Passos-Bueno MR. Heterozygote advantage of the MTHFR gene: are heterozygous C677T/MTHFR womem at lower risk of having children with nonsyndromic cleft lip with/without cleft palate? American Journal of Human Genetics. 1999 ; 65( 4):[citado 2024 jul. 17 ]
Trabalho de evento-resumo periodico
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy (1998)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Pavanello, R C M; Marie, Suely Kazue Nagahashi; Oliveira, A. S. B.; Zatz, Mayana
Source: Neuromuscular disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy. Neuromuscular disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 17 jul. 2024. , 1998
APA
Vainzof, M., Passos-Bueno, M. R., Pavanello, R. C. M., Marie, S. K. N., Oliveira, A. S. B., & Zatz, M. (1998). Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy. Neuromuscular disorders. Oxford: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Passos-Bueno MR, Pavanello RCM, Marie SKN, Oliveira ASB, Zatz M. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy. Neuromuscular disorders. 1998 ; 8( 3/4):[citado 2024 jul. 17 ]
Vancouver
Vainzof M, Passos-Bueno MR, Pavanello RCM, Marie SKN, Oliveira ASB, Zatz M. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy. Neuromuscular disorders. 1998 ; 8( 3/4):[citado 2024 jul. 17 ]
Trabalho de evento-resumo periodico
Mutações diferentes em pacientes com distrofia muscular do tipo duchenne pertencentes a uma mesma família (1997)
Sumita, D R; Campiotto, S; Cerqueira, A M P; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Pavanello, R C M; Zatz, Mayana
Source: Brazilian Journal of Genetics = Revista Brasileira de Genética. Conference titles: Congresso Nacional de Genética. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SUMITA, D R et al. Mutações diferentes em pacientes com distrofia muscular do tipo duchenne pertencentes a uma mesma família. Brazilian Journal of Genetics = Revista Brasileira de Genética. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 17 jul. 2024. , 1997
APA
Sumita, D. R., Campiotto, S., Cerqueira, A. M. P., Passos-Bueno, M. R., Vainzof, M., Pavanello, R. C. M., & Zatz, M. (1997). Mutações diferentes em pacientes com distrofia muscular do tipo duchenne pertencentes a uma mesma família. Brazilian Journal of Genetics = Revista Brasileira de Genética. Instituto de Biociências, Universidade de São Paulo.
NLM
Sumita DR, Campiotto S, Cerqueira AMP, Passos-Bueno MR, Vainzof M, Pavanello RCM, Zatz M. Mutações diferentes em pacientes com distrofia muscular do tipo duchenne pertencentes a uma mesma família. Brazilian Journal of Genetics = Revista Brasileira de Genética. 1997 ; 20( 3 suppl.): 222.[citado 2024 jul. 17 ]
Vancouver
Sumita DR, Campiotto S, Cerqueira AMP, Passos-Bueno MR, Vainzof M, Pavanello RCM, Zatz M. Mutações diferentes em pacientes com distrofia muscular do tipo duchenne pertencentes a uma mesma família. Brazilian Journal of Genetics = Revista Brasileira de Genética. 1997 ; 20( 3 suppl.): 222.[citado 2024 jul. 17 ]
Trabalho de evento-resumo
Genomic screening for beta and gamma-sarcoglycan gene mutations (1996)
Bonnemann, C G; Mcnally, E M; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Moreira, E S; Pavanello, R C M; Marie, Suely Kazue Nagahashi; Othmane, K B; Denton, P H; Vance, J M; Noguchi, S; Ozawa, E
Source: Abstracts. Conference titles: Limb Girdle Muscular Dystrophies Genetics Workshop. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BONNEMANN, C G et al. Genomic screening for beta and gamma-sarcoglycan gene mutations. 1996, Anais.. Tunis: Instituto de Biociências, Universidade de São Paulo, 1996. . Acesso em: 17 jul. 2024.
APA
Bonnemann, C. G., Mcnally, E. M., Passos-Bueno, M. R., Vainzof, M., Moreira, E. S., Pavanello, R. C. M., et al. (1996). Genomic screening for beta and gamma-sarcoglycan gene mutations. In Abstracts. Tunis: Instituto de Biociências, Universidade de São Paulo.
NLM
Bonnemann CG, Mcnally EM, Passos-Bueno MR, Vainzof M, Moreira ES, Pavanello RCM, Marie SKN, Othmane KB, Denton PH, Vance JM, Noguchi S, Ozawa E. Genomic screening for beta and gamma-sarcoglycan gene mutations. Abstracts. 1996 ;[citado 2024 jul. 17 ]
Vancouver
Bonnemann CG, Mcnally EM, Passos-Bueno MR, Vainzof M, Moreira ES, Pavanello RCM, Marie SKN, Othmane KB, Denton PH, Vance JM, Noguchi S, Ozawa E. Genomic screening for beta and gamma-sarcoglycan gene mutations. Abstracts. 1996 ;[citado 2024 jul. 17 ]
Artigo de periodico
Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e) (1996)
Bonnemann, C G; Passos-Bueno, Maria Rita ; Mcnally, E M; Vainzof, Mariz ; Moreira, E S; Marie, Suely Kazue Nagahashi; Pavanello, R C M; Noguchi, S; Ozawa, E; Zatz, Mayana ; Kunkel, L M
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BONNEMANN, C G et al. Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e). Human Molecular Genetics, v. 5 , n. 12, p. 1953-61, 1996Tradução . . Acesso em: 17 jul. 2024.
APA
Bonnemann, C. G., Passos-Bueno, M. R., Mcnally, E. M., Vainzof, M., Moreira, E. S., Marie, S. K. N., et al. (1996). Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e). Human Molecular Genetics, 5 ( 12), 1953-61.
NLM
Bonnemann CG, Passos-Bueno MR, Mcnally EM, Vainzof M, Moreira ES, Marie SKN, Pavanello RCM, Noguchi S, Ozawa E, Zatz M, Kunkel LM. Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e). Human Molecular Genetics. 1996 ;5 ( 12): 1953-61.[citado 2024 jul. 17 ]
Vancouver
Bonnemann CG, Passos-Bueno MR, Mcnally EM, Vainzof M, Moreira ES, Marie SKN, Pavanello RCM, Noguchi S, Ozawa E, Zatz M, Kunkel LM. Genomic screening for 'BETA'-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e). Human Molecular Genetics. 1996 ;5 ( 12): 1953-61.[citado 2024 jul. 17 ]
Artigo de periodico
Is dystrophin always altered in becker muscular dystrophy patients? (1995)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Pavanello, R C M; Zatz, Mayana
Source: Journal of the Neurological Sciences. Unidade: IB
Subjects: GENÉTICA MÉDICA, NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Is dystrophin always altered in becker muscular dystrophy patients?. Journal of the Neurological Sciences, v. 131, p. 99-104, 1995Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(95)00104-a. Acesso em: 17 jul. 2024.
APA
Vainzof, M., Passos-Bueno, M. R., Pavanello, R. C. M., & Zatz, M. (1995). Is dystrophin always altered in becker muscular dystrophy patients? Journal of the Neurological Sciences, 131, 99-104. doi:10.1016/0022-510x(95)00104-a
NLM
Vainzof M, Passos-Bueno MR, Pavanello RCM, Zatz M. Is dystrophin always altered in becker muscular dystrophy patients? [Internet]. Journal of the Neurological Sciences. 1995 ;131 99-104.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/0022-510x(95)00104-a
Vancouver
Vainzof M, Passos-Bueno MR, Pavanello RCM, Zatz M. Is dystrophin always altered in becker muscular dystrophy patients? [Internet]. Journal of the Neurological Sciences. 1995 ;131 99-104.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/0022-510x(95)00104-a
Artigo de periodico
Analysis of the ctg repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? (1995)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Cerqueira, A M P; Marie, Suely Kazue Nagahashi; Vainzof, Mariz ; Pavanello, R C M
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Analysis of the ctg repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?. Human Molecular Genetics, v. 4 , n. 3 , p. 401-6, 1995Tradução . . Disponível em: https://doi.org/10.1093/hmg/4.3.401. Acesso em: 17 jul. 2024.
APA
Zatz, M., Passos-Bueno, M. R., Cerqueira, A. M. P., Marie, S. K. N., Vainzof, M., & Pavanello, R. C. M. (1995). Analysis of the ctg repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? Human Molecular Genetics, 4 ( 3 ), 401-6. doi:10.1093/hmg/4.3.401
NLM
Zatz M, Passos-Bueno MR, Cerqueira AMP, Marie SKN, Vainzof M, Pavanello RCM. Analysis of the ctg repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? [Internet]. Human Molecular Genetics. 1995 ;4 ( 3 ): 401-6.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/hmg/4.3.401
Vancouver
Zatz M, Passos-Bueno MR, Cerqueira AMP, Marie SKN, Vainzof M, Pavanello RCM. Analysis of the ctg repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? [Internet]. Human Molecular Genetics. 1995 ;4 ( 3 ): 401-6.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/hmg/4.3.401
Trabalho de evento-resumo periodico
Avaliacao da alteracao quantitativa de distrofina na distrofia muscular tipo becker (1995)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Pavanello, R C M; Zatz, Mayana
Source: Revista Brasileira de Genetica = Brazilian Journal of Genetics. Conference titles: Congresso Nacional de Genetica. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Avaliacao da alteracao quantitativa de distrofina na distrofia muscular tipo becker. Revista Brasileira de Genetica = Brazilian Journal of Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 17 jul. 2024. , 1995
APA
Vainzof, M., Passos-Bueno, M. R., Pavanello, R. C. M., & Zatz, M. (1995). Avaliacao da alteracao quantitativa de distrofina na distrofia muscular tipo becker. Revista Brasileira de Genetica = Brazilian Journal of Genetics. Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Passos-Bueno MR, Pavanello RCM, Zatz M. Avaliacao da alteracao quantitativa de distrofina na distrofia muscular tipo becker. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1995 ;18( 3 suppl.): se 1995.[citado 2024 jul. 17 ]
Vancouver
Vainzof M, Passos-Bueno MR, Pavanello RCM, Zatz M. Avaliacao da alteracao quantitativa de distrofina na distrofia muscular tipo becker. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1995 ;18( 3 suppl.): se 1995.[citado 2024 jul. 17 ]
Artigo de periodico
Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations (1995)
Vainzof, Mariz ; Marie, Suely Kazue Nagahashi; Reed, Umbertina Conti; Schwartzman, J S; Pavanello, R C M; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Neuropediatrics. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations. Neuropediatrics, v. 26, p. 293-7, 1995Tradução . . Acesso em: 17 jul. 2024.
APA
Vainzof, M., Marie, S. K. N., Reed, U. C., Schwartzman, J. S., Pavanello, R. C. M., Passos-Bueno, M. R., & Zatz, M. (1995). Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations. Neuropediatrics, 26, 293-7.
NLM
Vainzof M, Marie SKN, Reed UC, Schwartzman JS, Pavanello RCM, Passos-Bueno MR, Zatz M. Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations. Neuropediatrics. 1995 ;26 293-7.[citado 2024 jul. 17 ]
Vancouver
Vainzof M, Marie SKN, Reed UC, Schwartzman JS, Pavanello RCM, Passos-Bueno MR, Zatz M. Deficiency of merosin (laminin m or 'ALFA'2) in congenital muscular dystrophy associated with cerebral white matter alterations. Neuropediatrics. 1995 ;26 293-7.[citado 2024 jul. 17 ]
Trabalho de evento-resumo periodico
Deficiencia de merosina na distrofia muscular congenita associada a alteracao da substancia branca cerebral (1995)
Vainzof, Mariz ; Marie, Suely Kazue Nagahashi; Reed, Umbertina Conti; Schwartzman, J S; Pavanello, R C M; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Revista Brasileira de Genetica = Brazilian Journal of Genetics. Conference titles: Congresso Nacional de Genetica. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Deficiencia de merosina na distrofia muscular congenita associada a alteracao da substancia branca cerebral. Revista Brasileira de Genetica = Brazilian Journal of Genetics. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 17 jul. 2024. , 1995
APA
Vainzof, M., Marie, S. K. N., Reed, U. C., Schwartzman, J. S., Pavanello, R. C. M., Passos-Bueno, M. R., & Zatz, M. (1995). Deficiencia de merosina na distrofia muscular congenita associada a alteracao da substancia branca cerebral. Revista Brasileira de Genetica = Brazilian Journal of Genetics. Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Marie SKN, Reed UC, Schwartzman JS, Pavanello RCM, Passos-Bueno MR, Zatz M. Deficiencia de merosina na distrofia muscular congenita associada a alteracao da substancia branca cerebral. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1995 ;18( 3 suppl.): se 1995.[citado 2024 jul. 17 ]
Vancouver
Vainzof M, Marie SKN, Reed UC, Schwartzman JS, Pavanello RCM, Passos-Bueno MR, Zatz M. Deficiencia de merosina na distrofia muscular congenita associada a alteracao da substancia branca cerebral. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1995 ;18( 3 suppl.): se 1995.[citado 2024 jul. 17 ]
Artigo de periodico
Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy (1994)
Zatz, Mayana ; Matsumura, K; Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Pavanello, R C M; Marie, Suely Kazue Nagahashi; Campbell, K P
Source: Journal of the Neurological Sciences. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy. Journal of the Neurological Sciences, v. 123, p. 122-8, 1994Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(94)90213-5. Acesso em: 17 jul. 2024.
APA
Zatz, M., Matsumura, K., Vainzof, M., Passos-Bueno, M. R., Pavanello, R. C. M., Marie, S. K. N., & Campbell, K. P. (1994). Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy. Journal of the Neurological Sciences, 123, 122-8. doi:10.1016/0022-510x(94)90213-5
NLM
Zatz M, Matsumura K, Vainzof M, Passos-Bueno MR, Pavanello RCM, Marie SKN, Campbell KP. Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy [Internet]. Journal of the Neurological Sciences. 1994 ;123 122-8.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/0022-510x(94)90213-5
Vancouver
Zatz M, Matsumura K, Vainzof M, Passos-Bueno MR, Pavanello RCM, Marie SKN, Campbell KP. Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy [Internet]. Journal of the Neurological Sciences. 1994 ;123 122-8.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/0022-510x(94)90213-5
Trabalho de evento-resumo periodico
Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy (1993)
Passos-Bueno, Maria Rita ; Cerqueira, A; Takata, R I; Pavanello, R C M; Eggers, S.; Marie, Suely Kazue Nagahashi; Levy, J A; Zatz, Mayana
Source: Canadian Journal of Neurological Sciences. Conference titles: World Congress of Neurology. Unidades: FM, IB
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 17 jul. 2024. , 1993
APA
Passos-Bueno, M. R., Cerqueira, A., Takata, R. I., Pavanello, R. C. M., Eggers, S., Marie, S. K. N., et al. (1993). Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo.
NLM
Passos-Bueno MR, Cerqueira A, Takata RI, Pavanello RCM, Eggers S, Marie SKN, Levy JA, Zatz M. Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2024 jul. 17 ]
Vancouver
Passos-Bueno MR, Cerqueira A, Takata RI, Pavanello RCM, Eggers S, Marie SKN, Levy JA, Zatz M. Correlation between ctg trinucleotide repeat length and clinical picture in brazilian patients affected with myotonic dystrophy. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2024 jul. 17 ]
Artigo de periodico
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype (1993)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Takata, R I; Pavanello, R C M; Zatz, Mayana
Source: Journal of the Neurological Sciences. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype. Journal of the Neurological Sciences, v. 119, p. 38-42, 1993Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(93)90189-6. Acesso em: 17 jul. 2024.
APA
Vainzof, M., Passos-Bueno, M. R., Takata, R. I., Pavanello, R. C. M., & Zatz, M. (1993). Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype. Journal of the Neurological Sciences, 119, 38-42. doi:10.1016/0022-510x(93)90189-6
NLM
Vainzof M, Passos-Bueno MR, Takata RI, Pavanello RCM, Zatz M. Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype [Internet]. Journal of the Neurological Sciences. 1993 ;119 38-42.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/0022-510x(93)90189-6
Vancouver
Vainzof M, Passos-Bueno MR, Takata RI, Pavanello RCM, Zatz M. Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype [Internet]. Journal of the Neurological Sciences. 1993 ;119 38-42.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/0022-510x(93)90189-6
Artigo de periodico
No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers (1993)
Passos-Bueno, Maria Rita ; Wijmenga, C; Takata, R I; Marie, Suely Kazue Nagahashi; Vainzof, Mariz ; Pavanello, R C M; Hewitt, J E; Bakker, E; Carvalho, A.; Akiyama, J; Frants, R R
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers. Human Molecular Genetics, v. 2 , n. 5 , p. 557-62, 1993Tradução . . Disponível em: https://doi.org/10.1093/hmg/2.5.557. Acesso em: 17 jul. 2024.
APA
Passos-Bueno, M. R., Wijmenga, C., Takata, R. I., Marie, S. K. N., Vainzof, M., Pavanello, R. C. M., et al. (1993). No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers. Human Molecular Genetics, 2 ( 5 ), 557-62. doi:10.1093/hmg/2.5.557
NLM
Passos-Bueno MR, Wijmenga C, Takata RI, Marie SKN, Vainzof M, Pavanello RCM, Hewitt JE, Bakker E, Carvalho A, Akiyama J, Frants RR. No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers [Internet]. Human Molecular Genetics. 1993 ;2 ( 5 ): 557-62.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/hmg/2.5.557
Vancouver
Passos-Bueno MR, Wijmenga C, Takata RI, Marie SKN, Vainzof M, Pavanello RCM, Hewitt JE, Bakker E, Carvalho A, Akiyama J, Frants RR. No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers [Internet]. Human Molecular Genetics. 1993 ;2 ( 5 ): 557-62.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/hmg/2.5.557
Artigo de periodico
Is the maintanance of the c-terminus domain of dystrophin enough to ensure a milder becker muscular dystrophy phenotype? (1993)
Vainzof, Mariz ; Takata, R I; Passos-Bueno, Maria Rita ; Pavanello, R C M; Zatz, Mayana
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Is the maintanance of the c-terminus domain of dystrophin enough to ensure a milder becker muscular dystrophy phenotype?. Human Molecular Genetics, v. 2 , n. 1 , p. 39-42, 1993Tradução . . Disponível em: https://doi.org/10.1093/hmg/2.1.39. Acesso em: 17 jul. 2024.
APA
Vainzof, M., Takata, R. I., Passos-Bueno, M. R., Pavanello, R. C. M., & Zatz, M. (1993). Is the maintanance of the c-terminus domain of dystrophin enough to ensure a milder becker muscular dystrophy phenotype? Human Molecular Genetics, 2 ( 1 ), 39-42. doi:10.1093/hmg/2.1.39
NLM
Vainzof M, Takata RI, Passos-Bueno MR, Pavanello RCM, Zatz M. Is the maintanance of the c-terminus domain of dystrophin enough to ensure a milder becker muscular dystrophy phenotype? [Internet]. Human Molecular Genetics. 1993 ;2 ( 1 ): 39-42.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/hmg/2.1.39
Vancouver
Vainzof M, Takata RI, Passos-Bueno MR, Pavanello RCM, Zatz M. Is the maintanance of the c-terminus domain of dystrophin enough to ensure a milder becker muscular dystrophy phenotype? [Internet]. Human Molecular Genetics. 1993 ;2 ( 1 ): 39-42.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/hmg/2.1.39
Trabalho de evento-resumo periodico
Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families (1993)
Passos-Bueno, Maria Rita ; Wijmenga, C; Takata, R I; Marie, Suely Kazue Nagahashi; Vainzof, Mariz ; Pavanello, R C M; Hewitt, J E; Bakker, E; Carvalho, A A S; Akiyama, J; Frants, R R
Source: Canadian Journal of Neurological Sciences. Conference titles: World Congress of Neurology. Unidades: FM, IB
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 17 jul. 2024. , 1993
APA
Passos-Bueno, M. R., Wijmenga, C., Takata, R. I., Marie, S. K. N., Vainzof, M., Pavanello, R. C. M., et al. (1993). Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. Calgary: Faculdade de Medicina, Universidade de São Paulo.
NLM
Passos-Bueno MR, Wijmenga C, Takata RI, Marie SKN, Vainzof M, Pavanello RCM, Hewitt JE, Bakker E, Carvalho AAS, Akiyama J, Frants RR. Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2024 jul. 17 ]
Vancouver
Passos-Bueno MR, Wijmenga C, Takata RI, Marie SKN, Vainzof M, Pavanello RCM, Hewitt JE, Bakker E, Carvalho AAS, Akiyama J, Frants RR. Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families. Canadian Journal of Neurological Sciences. 1993 ;20( suppl.4): s30.[citado 2024 jul. 17 ]
Artigo de periodico
Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families (1993)
Passos-Bueno, Maria Rita ; Bakker, E; Marie, Suely Kazue Nagahashi; Pavanello, R C M; Vainzof, Mariz ; Carvalho, A. A.; Cohen, D; Beckmann, J S; Zatz, Mayana
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families. Human Molecular Genetics, v. 2 , n. 2 , p. 201-2, 1993Tradução . . Disponível em: https://doi.org/10.1093/hmg/2.2.201. Acesso em: 17 jul. 2024.
APA
Passos-Bueno, M. R., Bakker, E., Marie, S. K. N., Pavanello, R. C. M., Vainzof, M., Carvalho, A. A., et al. (1993). Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families. Human Molecular Genetics, 2 ( 2 ), 201-2. doi:10.1093/hmg/2.2.201
NLM
Passos-Bueno MR, Bakker E, Marie SKN, Pavanello RCM, Vainzof M, Carvalho AA, Cohen D, Beckmann JS, Zatz M. Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families [Internet]. Human Molecular Genetics. 1993 ;2 ( 2 ): 201-2.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/hmg/2.2.201
Vancouver
Passos-Bueno MR, Bakker E, Marie SKN, Pavanello RCM, Vainzof M, Carvalho AA, Cohen D, Beckmann JS, Zatz M. Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families [Internet]. Human Molecular Genetics. 1993 ;2 ( 2 ): 201-2.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/hmg/2.2.201
Artigo de periodico
Sarcolemmal distribution of abnormal dystrophin in xp21 carriers (1993)
Vainzof, Mariz ; Nicholson, L V B; Bulman, D E; Tsanaclis, Ana Maria Crous; Passos-Bueno, Maria Rita ; Pavanello, R C M; Zatz, Mayana
Source: Neuromuscular Disorders. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Sarcolemmal distribution of abnormal dystrophin in xp21 carriers. Neuromuscular Disorders, v. 3 , n. 2 , p. 135-40, 1993Tradução . . Disponível em: https://doi.org/10.1016/0960-8966(93)90005-5. Acesso em: 17 jul. 2024.
APA
Vainzof, M., Nicholson, L. V. B., Bulman, D. E., Tsanaclis, A. M. C., Passos-Bueno, M. R., Pavanello, R. C. M., & Zatz, M. (1993). Sarcolemmal distribution of abnormal dystrophin in xp21 carriers. Neuromuscular Disorders, 3 ( 2 ), 135-40. doi:10.1016/0960-8966(93)90005-5
NLM
Vainzof M, Nicholson LVB, Bulman DE, Tsanaclis AMC, Passos-Bueno MR, Pavanello RCM, Zatz M. Sarcolemmal distribution of abnormal dystrophin in xp21 carriers [Internet]. Neuromuscular Disorders. 1993 ;3 ( 2 ): 135-40.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/0960-8966(93)90005-5
Vancouver
Vainzof M, Nicholson LVB, Bulman DE, Tsanaclis AMC, Passos-Bueno MR, Pavanello RCM, Zatz M. Sarcolemmal distribution of abnormal dystrophin in xp21 carriers [Internet]. Neuromuscular Disorders. 1993 ;3 ( 2 ): 135-40.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1016/0960-8966(93)90005-5
Artigo de periodico
Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? (1993)
Passos-Bueno, Maria Rita ; Byth, B C; Rosemberg, Sérgio; Takata, R I; Bakker, E; Beggs, A H; Pavanello, R C M; Vainzof, Mariz ; Davies, K E; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidades: FM, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation?. American Journal of Medical Genetics, v. 46, n. 2 , p. 172-5, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460214. Acesso em: 17 jul. 2024.
APA
Passos-Bueno, M. R., Byth, B. C., Rosemberg, S., Takata, R. I., Bakker, E., Beggs, A. H., et al. (1993). Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? American Journal of Medical Genetics, 46( 2 ), 172-5. doi:10.1002/ajmg.1320460214
NLM
Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1002/ajmg.1320460214
Vancouver
Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1002/ajmg.1320460214
Trabalho de evento-resumo
Unexpected findings in a large study of brazilian patients with xp21 muscular dystrophies (1992)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Takata, R I; Lima, M A B O; Rapaport, D; Schreiber, R; Pavanello, R C M
Source: Programa e Resumos. Conference titles: Reuniao Anual da Sociedade Brasileira de Bioquimica e Biologia Molecular - Sbbq. Unidade: IB
Assunto: GENÉTICA ANIMAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Unexpected findings in a large study of brazilian patients with xp21 muscular dystrophies. 1992, Anais.. Caxambu: Sbbq, 1992. . Acesso em: 17 jul. 2024.
APA
Zatz, M., Passos-Bueno, M. R., Vainzof, M., Takata, R. I., Lima, M. A. B. O., Rapaport, D., et al. (1992). Unexpected findings in a large study of brazilian patients with xp21 muscular dystrophies. In Programa e Resumos. Caxambu: Sbbq.
NLM
Zatz M, Passos-Bueno MR, Vainzof M, Takata RI, Lima MABO, Rapaport D, Schreiber R, Pavanello RCM. Unexpected findings in a large study of brazilian patients with xp21 muscular dystrophies. Programa e Resumos. 1992 ;[citado 2024 jul. 17 ]
Vancouver
Zatz M, Passos-Bueno MR, Vainzof M, Takata RI, Lima MABO, Rapaport D, Schreiber R, Pavanello RCM. Unexpected findings in a large study of brazilian patients with xp21 muscular dystrophies. Programa e Resumos. 1992 ;[citado 2024 jul. 17 ]

USP Schools

ReP

Filtros

Departament

Authors

USP affiliated authors

Date published

Subjects

Source title

Conference titles

Countries/Territories