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Trabalho de evento-resumo periodico
Clinical variability in calpainopathy: what makes the difference? (2002)
Paula, F de; Vainzof, Mariz ; Moreira, Edson Dias; Passos-Bueno, Maria Rita ; Pavanello, Rita de Cássia M.; Matioli, Sergio Russo ; Nigro, Vicenzo; Zatz, Mayana
Source: Journal of the Neurological Sciences. Conference titles: International Congress on Neuromuscular Diseases. Unidades: IB, FM
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA
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ABNT
PAULA, F de et al. Clinical variability in calpainopathy: what makes the difference?. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 16 nov. 2024. , 2002
APA
Paula, F. de, Vainzof, M., Moreira, E. D., Passos-Bueno, M. R., Pavanello, R. de C. M., Matioli, S. R., et al. (2002). Clinical variability in calpainopathy: what makes the difference? Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo.
NLM
Paula F de, Vainzof M, Moreira ED, Passos-Bueno MR, Pavanello R de CM, Matioli SR, Nigro V, Zatz M. Clinical variability in calpainopathy: what makes the difference? Journal of the Neurological Sciences. 2002 ; 199 S57.[citado 2024 nov. 16 ]
Vancouver
Paula F de, Vainzof M, Moreira ED, Passos-Bueno MR, Pavanello R de CM, Matioli SR, Nigro V, Zatz M. Clinical variability in calpainopathy: what makes the difference? Journal of the Neurological Sciences. 2002 ; 199 S57.[citado 2024 nov. 16 ]
Trabalho de evento-resumo periodico
Looking for one more autosomal recessive limb girdle muscular dystrophy gene (2002)
Starling, A.; Vainzof, Mariz ; Canovas, Marta; Pavanello, Rita de Cássia M.; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Journal of the Neurological Sciences. Conference titles: International Congress on Neuromuscular Diseases. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES
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ABNT
STARLING, A. et al. Looking for one more autosomal recessive limb girdle muscular dystrophy gene. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 16 nov. 2024. , 2002
APA
Starling, A., Vainzof, M., Canovas, M., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (2002). Looking for one more autosomal recessive limb girdle muscular dystrophy gene. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo.
NLM
Starling A, Vainzof M, Canovas M, Pavanello R de CM, Passos-Bueno MR, Zatz M. Looking for one more autosomal recessive limb girdle muscular dystrophy gene. Journal of the Neurological Sciences. 2002 ; 199 S57.[citado 2024 nov. 16 ]
Vancouver
Starling A, Vainzof M, Canovas M, Pavanello R de CM, Passos-Bueno MR, Zatz M. Looking for one more autosomal recessive limb girdle muscular dystrophy gene. Journal of the Neurological Sciences. 2002 ; 199 S57.[citado 2024 nov. 16 ]
Trabalho de evento-resumo periodico
Partial telethonin deficiency in severely affected north american LGMD patients (2002)
Houston, Ronnie; Muirhead, David; Elmonoufy, Nora; Cornelia, Reuel; Faulkner, Georgine; Valle, Giorgio; Zatz, Mayana ; Vainzof, Mariz ; Iannaccone, Susan
Source: Journal of the Neurological Sciences. Conference titles: International Congress on Neuromuscular Diseases. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HOUSTON, Ronnie et al. Partial telethonin deficiency in severely affected north american LGMD patients. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 16 nov. 2024. , 2002
APA
Houston, R., Muirhead, D., Elmonoufy, N., Cornelia, R., Faulkner, G., Valle, G., et al. (2002). Partial telethonin deficiency in severely affected north american LGMD patients. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo.
NLM
Houston R, Muirhead D, Elmonoufy N, Cornelia R, Faulkner G, Valle G, Zatz M, Vainzof M, Iannaccone S. Partial telethonin deficiency in severely affected north american LGMD patients. Journal of the Neurological Sciences. 2002 ; 199 S58.[citado 2024 nov. 16 ]
Vancouver
Houston R, Muirhead D, Elmonoufy N, Cornelia R, Faulkner G, Valle G, Zatz M, Vainzof M, Iannaccone S. Partial telethonin deficiency in severely affected north american LGMD patients. Journal of the Neurological Sciences. 2002 ; 199 S58.[citado 2024 nov. 16 ]
Trabalho de evento-resumo periodico
Sarcomeric myopalladin study in limb girdle muscular dystrophies (2002)
Vainzof, Mariz ; Canovas, Marta; Labeit, Siegfried; Bang, Marie Louise; Faulkner, Georgine; Valle, G.; Zatz, Mayana
Source: Journal of the Neurological Sciences. Conference titles: International Congress on Neuromuscular Diseases. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Sarcomeric myopalladin study in limb girdle muscular dystrophies. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 16 nov. 2024. , 2002
APA
Vainzof, M., Canovas, M., Labeit, S., Bang, M. L., Faulkner, G., Valle, G., & Zatz, M. (2002). Sarcomeric myopalladin study in limb girdle muscular dystrophies. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Canovas M, Labeit S, Bang ML, Faulkner G, Valle G, Zatz M. Sarcomeric myopalladin study in limb girdle muscular dystrophies. Journal of the Neurological Sciences. 2002 ; 199 S33.[citado 2024 nov. 16 ]
Vancouver
Vainzof M, Canovas M, Labeit S, Bang ML, Faulkner G, Valle G, Zatz M. Sarcomeric myopalladin study in limb girdle muscular dystrophies. Journal of the Neurological Sciences. 2002 ; 199 S33.[citado 2024 nov. 16 ]
Artigo de periodico
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population (1999)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Pavanello, Rita de Cássia M; Marie, Suely Kazue Nagahashi; Oliveira, Acary B. S.; Zatz, Mayana
Source: Journal of the Neurological Sciences. 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. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population. Journal of the Neurological Sciences, v. 164, p. 44-49, 1999Tradução . . Disponível em: https://doi.org/10.1016/s0022-510x(99)00040-4. Acesso em: 16 nov. 2024.
APA
Vainzof, M., Passos-Bueno, M. R., Pavanello, R. de C. M., Marie, S. K. N., Oliveira, A. B. S., & Zatz, M. (1999). Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population. Journal of the Neurological Sciences, 164, 44-49. doi:10.1016/s0022-510x(99)00040-4
NLM
Vainzof M, Passos-Bueno MR, Pavanello R de CM, Marie SKN, Oliveira ABS, Zatz M. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population [Internet]. Journal of the Neurological Sciences. 1999 ; 164 44-49.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/s0022-510x(99)00040-4
Vancouver
Vainzof M, Passos-Bueno MR, Pavanello R de CM, Marie SKN, Oliveira ABS, Zatz M. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population [Internet]. Journal of the Neurological Sciences. 1999 ; 164 44-49.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/s0022-510x(99)00040-4
Artigo de periodico
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the brazilian population (1999)
Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Pavanello, Rita C. M; Oliveira, Acary S. B.; Zatz, Mayana ; Marie, Suely Kazue Nagahashi
Source: Journal of the Neurological Sciences. Unidades: FM, IB
Assunto: NEUROLOGIA
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 in the brazilian population. Journal of the Neurological Sciences, v. 164, p. 44-49, 1999Tradução . . Disponível em: https://doi.org/10.1016/s0022-510x(99)00040-4. Acesso em: 16 nov. 2024.
APA
Vainzof, M., Passos-Bueno, M. R., Pavanello, R. C. M., Oliveira, A. S. B., Zatz, M., & Marie, S. K. N. (1999). Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the brazilian population. Journal of the Neurological Sciences, 164, 44-49. doi:10.1016/s0022-510x(99)00040-4
NLM
Vainzof M, Passos-Bueno MR, Pavanello RCM, Oliveira ASB, Zatz M, Marie SKN. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the brazilian population [Internet]. Journal of the Neurological Sciences. 1999 ; 164 44-49.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/s0022-510x(99)00040-4
Vancouver
Vainzof M, Passos-Bueno MR, Pavanello RCM, Oliveira ASB, Zatz M, Marie SKN. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the brazilian population [Internet]. Journal of the Neurological Sciences. 1999 ; 164 44-49.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/s0022-510x(99)00040-4
Artigo de periodico
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (lgmd2a) (1997)
Spencer, M J; Tidball, J G; Anderson, L V B; Bushby, K M D; Harris, J B; Passos-Bueno, Maria Rita ; Somer, H; Vainzof, Mariz ; Zatz, Mayana
Source: Journal of the Neurological Sciences. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
SPENCER, M J et al. Absence of calpain 3 in a form of limb-girdle muscular dystrophy (lgmd2a). Journal of the Neurological Sciences, v. 146, p. 173-8, 1997Tradução . . Acesso em: 16 nov. 2024.
APA
Spencer, M. J., Tidball, J. G., Anderson, L. V. B., Bushby, K. M. D., Harris, J. B., Passos-Bueno, M. R., et al. (1997). Absence of calpain 3 in a form of limb-girdle muscular dystrophy (lgmd2a). Journal of the Neurological Sciences, 146, 173-8.
NLM
Spencer MJ, Tidball JG, Anderson LVB, Bushby KMD, Harris JB, Passos-Bueno MR, Somer H, Vainzof M, Zatz M. Absence of calpain 3 in a form of limb-girdle muscular dystrophy (lgmd2a). Journal of the Neurological Sciences. 1997 ;146 173-8.[citado 2024 nov. 16 ]
Vancouver
Spencer MJ, Tidball JG, Anderson LVB, Bushby KMD, Harris JB, Passos-Bueno MR, Somer H, Vainzof M, Zatz M. Absence of calpain 3 in a form of limb-girdle muscular dystrophy (lgmd2a). Journal of the Neurological Sciences. 1997 ;146 173-8.[citado 2024 nov. 16 ]
Trabalho de evento-resumo periodico
Correlation of DNA expansion and systemic manifestations in myotonic dystrophy (1997)
Teixeira, V. G; Zatz, Mayana ; Marie, Suely Kazue Nagahashi; Passos-Bueno, Maria Rita ; Reed, Umbertina Conti
Source: Journal of the 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
TEIXEIRA, V. G et al. Correlation of DNA expansion and systemic manifestations in myotonic dystrophy. Journal of the Neurological Sciences. Amsterdam: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 16 nov. 2024. , 1997
APA
Teixeira, V. G., Zatz, M., Marie, S. K. N., Passos-Bueno, M. R., & Reed, U. C. (1997). Correlation of DNA expansion and systemic manifestations in myotonic dystrophy. Journal of the Neurological Sciences. Amsterdam: Faculdade de Medicina, Universidade de São Paulo.
NLM
Teixeira VG, Zatz M, Marie SKN, Passos-Bueno MR, Reed UC. Correlation of DNA expansion and systemic manifestations in myotonic dystrophy. Journal of the Neurological Sciences. 1997 ; 150( suppl): S324.[citado 2024 nov. 16 ]
Vancouver
Teixeira VG, Zatz M, Marie SKN, Passos-Bueno MR, Reed UC. Correlation of DNA expansion and systemic manifestations in myotonic dystrophy. Journal of the Neurological Sciences. 1997 ; 150( suppl): S324.[citado 2024 nov. 16 ]
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(95)00104-a
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(94)90213-5
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: 16 nov. 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 nov. 16 ] 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 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(93)90189-6
Artigo de periodico
Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein (1991)
Vainzof, Mariz ; Zubrzycka-Gaarn, E E; Rapaport, D; Passos-Bueno, Maria Rita ; Pavanello, R C M; Pavanello Filho, I; 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. Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein. Journal of the Neurological Sciences, v. 101, p. 141-7, 1991Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(91)90038-9. Acesso em: 16 nov. 2024.
APA
Vainzof, M., Zubrzycka-Gaarn, E. E., Rapaport, D., Passos-Bueno, M. R., Pavanello, R. C. M., Pavanello Filho, I., & Zatz, M. (1991). Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein. Journal of the Neurological Sciences, 101, 141-7. doi:10.1016/0022-510x(91)90038-9
NLM
Vainzof M, Zubrzycka-Gaarn EE, Rapaport D, Passos-Bueno MR, Pavanello RCM, Pavanello Filho I, Zatz M. Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein [Internet]. Journal of the Neurological Sciences. 1991 ;101 141-7.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(91)90038-9
Vancouver
Vainzof M, Zubrzycka-Gaarn EE, Rapaport D, Passos-Bueno MR, Pavanello RCM, Pavanello Filho I, Zatz M. Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein [Internet]. Journal of the Neurological Sciences. 1991 ;101 141-7.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(91)90038-9
Artigo de periodico
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27 (1991)
Passos-Bueno, Maria Rita ; Byth, B; Love, D; Terwilliger, J; Ott, J; Rapaport, D; Vainzof, Mariz ; Zatz, Mayana ; Davies, K E
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
PASSOS-BUENO, Maria Rita et al. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27. Journal of the Neurological Sciences, v. 102, p. 206-8, 1991Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(91)90070-n. Acesso em: 16 nov. 2024.
APA
Passos-Bueno, M. R., Byth, B., Love, D., Terwilliger, J., Ott, J., Rapaport, D., et al. (1991). Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27. Journal of the Neurological Sciences, 102, 206-8. doi:10.1016/0022-510x(91)90070-n
NLM
Passos-Bueno MR, Byth B, Love D, Terwilliger J, Ott J, Rapaport D, Vainzof M, Zatz M, Davies KE. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27 [Internet]. Journal of the Neurological Sciences. 1991 ;102 206-8.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(91)90070-n
Vancouver
Passos-Bueno MR, Byth B, Love D, Terwilliger J, Ott J, Rapaport D, Vainzof M, Zatz M, Davies KE. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27 [Internet]. Journal of the Neurological Sciences. 1991 ;102 206-8.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(91)90070-n
Artigo de periodico
Limb-girdle syndrome: a genetic study of 22 large brazilian families comparison with x-linked duchenne and becker dystrophies (1991)
Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Pavanello, R C M; Pavanello Filho, I; Lima, M A B O; 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
PASSOS-BUENO, Maria Rita et al. Limb-girdle syndrome: a genetic study of 22 large brazilian families comparison with x-linked duchenne and becker dystrophies. Journal of the Neurological Sciences, v. 103, p. 65-75, 1991Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(91)90286-g. Acesso em: 16 nov. 2024.
APA
Passos-Bueno, M. R., Vainzof, M., Pavanello, R. C. M., Pavanello Filho, I., Lima, M. A. B. O., & Zatz, M. (1991). Limb-girdle syndrome: a genetic study of 22 large brazilian families comparison with x-linked duchenne and becker dystrophies. Journal of the Neurological Sciences, 103, 65-75. doi:10.1016/0022-510x(91)90286-g
NLM
Passos-Bueno MR, Vainzof M, Pavanello RCM, Pavanello Filho I, Lima MABO, Zatz M. Limb-girdle syndrome: a genetic study of 22 large brazilian families comparison with x-linked duchenne and becker dystrophies [Internet]. Journal of the Neurological Sciences. 1991 ;103 65-75.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(91)90286-g
Vancouver
Passos-Bueno MR, Vainzof M, Pavanello RCM, Pavanello Filho I, Lima MABO, Zatz M. Limb-girdle syndrome: a genetic study of 22 large brazilian families comparison with x-linked duchenne and becker dystrophies [Internet]. Journal of the Neurological Sciences. 1991 ;103 65-75.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(91)90286-g
Artigo de periodico
Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a brazilian study (1990)
Vainzof, Mariz ; Pavanello, R C M; Pavanello Filho, I; Passos-Bueno, Maria Rita ; Rapaport, D; Hsi, C T; 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. Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a brazilian study. Journal of the Neurological Sciences, v. 98, p. 221-33, 1990Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(90)90263-m. Acesso em: 16 nov. 2024.
APA
Vainzof, M., Pavanello, R. C. M., Pavanello Filho, I., Passos-Bueno, M. R., Rapaport, D., Hsi, C. T., & Zatz, M. (1990). Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a brazilian study. Journal of the Neurological Sciences, 98, 221-33. doi:10.1016/0022-510x(90)90263-m
NLM
Vainzof M, Pavanello RCM, Pavanello Filho I, Passos-Bueno MR, Rapaport D, Hsi CT, Zatz M. Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a brazilian study [Internet]. Journal of the Neurological Sciences. 1990 ;98 221-33.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(90)90263-m
Vancouver
Vainzof M, Pavanello RCM, Pavanello Filho I, Passos-Bueno MR, Rapaport D, Hsi CT, Zatz M. Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a brazilian study [Internet]. Journal of the Neurological Sciences. 1990 ;98 221-33.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(90)90263-m
Artigo de periodico
Effect of age on the detection rate in Duchenne muscular dystrophy (1980)
Zatz, Mayana ; Otto, Paulo A
Source: Journal of the Neurological Sciences. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e OTTO, Paulo A. Effect of age on the detection rate in Duchenne muscular dystrophy. Journal of the Neurological Sciences, v. 47, n. 3, p. 407-410, 1980Tradução . . Disponível em: https://doi.org/10.1016/0022-510X(80)90093-3. Acesso em: 16 nov. 2024.
APA
Zatz, M., & Otto, P. A. (1980). Effect of age on the detection rate in Duchenne muscular dystrophy. Journal of the Neurological Sciences, 47( 3), 407-410. doi:10.1016/0022-510X(80)90093-3
NLM
Zatz M, Otto PA. Effect of age on the detection rate in Duchenne muscular dystrophy [Internet]. Journal of the Neurological Sciences. 1980 ; 47( 3): 407-410.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510X(80)90093-3
Vancouver
Zatz M, Otto PA. Effect of age on the detection rate in Duchenne muscular dystrophy [Internet]. Journal of the Neurological Sciences. 1980 ; 47( 3): 407-410.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510X(80)90093-3
Artigo de periodico
Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker) (1980)
Zatz, Mayana ; Shapiro, Larry J.; Campion, David; Kaback, Michael M.; Otto, Paulo A
Source: Journal of the Neurological Sciences. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker). Journal of the Neurological Sciences, v. 46, n. 3, p. 267-279, 1980Tradução . . Disponível em: https://doi.org/10.1016/0022-510x(80)90051-9. Acesso em: 16 nov. 2024.
APA
Zatz, M., Shapiro, L. J., Campion, D., Kaback, M. M., & Otto, P. A. (1980). Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker). Journal of the Neurological Sciences, 46( 3), 267-279. doi:10.1016/0022-510x(80)90051-9
NLM
Zatz M, Shapiro LJ, Campion D, Kaback MM, Otto PA. Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker) [Internet]. Journal of the Neurological Sciences. 1980 ; 46( 3): 267-279.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(80)90051-9
Vancouver
Zatz M, Shapiro LJ, Campion D, Kaback MM, Otto PA. Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker) [Internet]. Journal of the Neurological Sciences. 1980 ; 46( 3): 267-279.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/0022-510x(80)90051-9

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