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Artigo de periodico
Telethonin protein expression in neuromuscular disorders (2002)
Vainzof, Mariz ; Moreira, Eloisa S.; Suzuki, Oscar T.; Faulkner, Georgine; Valle, Georgio; Beggs, Alan H.; Carpen, Olli; Ribeiro, Alberto de Freitas ; Zanoteli, Edmar; Gurgel-Gianneti, Juliana; Tsanaclis, Ana Maria Crous; Silva, Helga Cristina Almeida da; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Biochimica et Biophysica Acta. Unidades: IB, FM
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES
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ABNT
VAINZOF, Mariz et al. Telethonin protein expression in neuromuscular disorders. Biochimica et Biophysica Acta, v. 1588, n. 1, p. 33-40, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0925-4439(02)00113-8. Acesso em: 14 ago. 2024.
APA
Vainzof, M., Moreira, E. S., Suzuki, O. T., Faulkner, G., Valle, G., Beggs, A. H., et al. (2002). Telethonin protein expression in neuromuscular disorders. Biochimica et Biophysica Acta, 1588( 1), 33-40. doi:10.1016/s0925-4439(02)00113-8
NLM
Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro A de F, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AMC, Silva HCA da, Passos-Bueno MR, Zatz M. Telethonin protein expression in neuromuscular disorders [Internet]. Biochimica et Biophysica Acta. 2002 ; 1588( 1): 33-40.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/s0925-4439(02)00113-8
Vancouver
Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro A de F, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AMC, Silva HCA da, Passos-Bueno MR, Zatz M. Telethonin protein expression in neuromuscular disorders [Internet]. Biochimica et Biophysica Acta. 2002 ; 1588( 1): 33-40.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/s0925-4439(02)00113-8
Artigo de periodico-carta/editorial
Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta] (2000)
Moreira, Eloisa S.; Wiltshire, Tim J.; Faulkner, Georgine; Nilforoushan, Antje; Vainzof, Mariz ; Suzuki, Oscar T.; Valle, Giorgio; Reeves, Roger; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Jenne, Dieter E.
Source: Nature Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
MOREIRA, Eloisa S. et al. Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]. Nature Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 14 ago. 2024. , 2000
APA
Moreira, E. S., Wiltshire, T. J., Faulkner, G., Nilforoushan, A., Vainzof, M., Suzuki, O. T., et al. (2000). Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]. Nature Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Moreira ES, Wiltshire TJ, Faulkner G, Nilforoushan A, Vainzof M, Suzuki OT, Valle G, Reeves R, Zatz M, Passos-Bueno MR, Jenne DE. Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]. Nature Genetics. 2000 ; 24 163-166.[citado 2024 ago. 14 ]
Vancouver
Moreira ES, Wiltshire TJ, Faulkner G, Nilforoushan A, Vainzof M, Suzuki OT, Valle G, Reeves R, Zatz M, Passos-Bueno MR, Jenne DE. Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]. Nature Genetics. 2000 ; 24 163-166.[citado 2024 ago. 14 ]
Artigo de periodico
Partial 'alfa'-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family (2000)
Vainzof, Mariz ; Moreira, Eloisa S.; Canovas, Marta; Anderson, Louise V. B.; Pavanello, Rita de Cássia M.; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Muscle & Nerve. 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. Partial 'alfa'-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family. Muscle & Nerve, v. 23, n. ju 2000, p. 984-988, 2000Tradução . . Disponível em: https://doi.org/10.1002/(sici)1097-4598(200006)23:6%3C984::aid-mus24%3E3.0.co;2-#. Acesso em: 14 ago. 2024.
APA
Vainzof, M., Moreira, E. S., Canovas, M., Anderson, L. V. B., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (2000). Partial 'alfa'-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family. Muscle & Nerve, 23( ju 2000), 984-988. doi:10.1002/(sici)1097-4598(200006)23:6%3C984::aid-mus24%3E3.0.co;2-#
NLM
Vainzof M, Moreira ES, Canovas M, Anderson LVB, Pavanello R de CM, Passos-Bueno MR, Zatz M. Partial 'alfa'-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family [Internet]. Muscle & Nerve. 2000 ; 23( ju 2000): 984-988.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/(sici)1097-4598(200006)23:6%3C984::aid-mus24%3E3.0.co;2-#
Vancouver
Vainzof M, Moreira ES, Canovas M, Anderson LVB, Pavanello R de CM, Passos-Bueno MR, Zatz M. Partial 'alfa'-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family [Internet]. Muscle & Nerve. 2000 ; 23( ju 2000): 984-988.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/(sici)1097-4598(200006)23:6%3C984::aid-mus24%3E3.0.co;2-#
Artigo de periodico
Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G (1999)
Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Moreira, Eloisa S.; Zatz, Mayana
Source: American Journal of Medical 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. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G. American Journal of Medical Genetics, v. 82, p. 392-398, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0. Acesso em: 14 ago. 2024.
APA
Passos-Bueno, M. R., Vainzof, M., Moreira, E. S., & Zatz, M. (1999). Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G. American Journal of Medical Genetics, 82, 392-398. doi:10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
NLM
Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G [Internet]. American Journal of Medical Genetics. 1999 ; 82 392-398.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
Vancouver
Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G [Internet]. American Journal of Medical Genetics. 1999 ; 82 392-398.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
Trabalho de evento-resumo periodico
Sarcoglycanopathies and limb-girdle syndromes: diagnostic insights (1998)
Zatz, Mayana ; Vainzof, Mariz ; Moreira, Eloisa S.; Passos-Bueno, Maria Rita
Source: Muscle & Nerve. Conference titles: International Congress on Neuromuscular Diseases. 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. Sarcoglycanopathies and limb-girdle syndromes: diagnostic insights. Muscle & Nerve. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 14 ago. 2024. , 1998
APA
Zatz, M., Vainzof, M., Moreira, E. S., & Passos-Bueno, M. R. (1998). Sarcoglycanopathies and limb-girdle syndromes: diagnostic insights. Muscle & Nerve. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Vainzof M, Moreira ES, Passos-Bueno MR. Sarcoglycanopathies and limb-girdle syndromes: diagnostic insights. Muscle & Nerve. 1998 ; 1.[citado 2024 ago. 14 ]
Vancouver
Zatz M, Vainzof M, Moreira ES, Passos-Bueno MR. Sarcoglycanopathies and limb-girdle syndromes: diagnostic insights. Muscle & Nerve. 1998 ; 1.[citado 2024 ago. 14 ]
Artigo de periodico
A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies (1998)
Moreira, Eloisa S.; Vainzof, Mariz ; Marie, Suely Kazue Nagahashi; Nigro, Vicenzo; Zatz, Mayana ; Passos-Bueno, Maria Rita
Source: 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
MOREIRA, Eloisa S. et al. A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies. Journal of Medical Genetics, v. 35, p. 951-953, 1998Tradução . . Disponível em: https://doi.org/10.1136/jmg.35.11.951. Acesso em: 14 ago. 2024.
APA
Moreira, E. S., Vainzof, M., Marie, S. K. N., Nigro, V., Zatz, M., & Passos-Bueno, M. R. (1998). A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies. Journal of Medical Genetics, 35, 951-953. doi:10.1136/jmg.35.11.951
NLM
Moreira ES, Vainzof M, Marie SKN, Nigro V, Zatz M, Passos-Bueno MR. A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies [Internet]. Journal of Medical Genetics. 1998 ; 35 951-953.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1136/jmg.35.11.951
Vancouver
Moreira ES, Vainzof M, Marie SKN, Nigro V, Zatz M, Passos-Bueno MR. A first missense mutation in the 'delta' sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies [Internet]. Journal of Medical Genetics. 1998 ; 35 951-953.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1136/jmg.35.11.951
Trabalho de evento-resumo periodico
Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex (1998)
Vainzof, Mariz ; Moreira, Eloisa S.; Passos-Bueno, Maria Rita ; Marie, Suely Kazue Nagahashi; Zatz, Mayana
Source: Muscle & Nerve. Conference titles: International Congress on Neuromuscular Diseases. 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. Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex. Muscle & Nerve. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 14 ago. 2024. , 1998
APA
Vainzof, M., Moreira, E. S., Passos-Bueno, M. R., Marie, S. K. N., & Zatz, M. (1998). Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex. Muscle & Nerve. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Moreira ES, Passos-Bueno MR, Marie SKN, Zatz M. Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex. Muscle & Nerve. 1998 ; 1.[citado 2024 ago. 14 ]
Vancouver
Vainzof M, Moreira ES, Passos-Bueno MR, Marie SKN, Zatz M. Further evidence for the organization of the four sarcoglycan proteins within the dystrophin-glycoprotein complex. Muscle & Nerve. 1998 ; 1.[citado 2024 ago. 14 ]
Artigo de periodico
Deficiency of 'alfa'-actinin-3 (ACTN3) Occurs in different forms of muscular dystrophy (1997)
Vainzof, Mariz ; Costa, C. S.; Marie, Suely Kazue Nagahashi; Moreira, Eloisa S.; Reed, Umbertina Conti; Passos-Bueno, Maria Rita ; Beggs A. H.; Zatz, Mayana
Source: Neuropediatrics. Unidades: FM, IB
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 'alfa'-actinin-3 (ACTN3) Occurs in different forms of muscular dystrophy. Neuropediatrics, v. 28, p. 223-228, 1997Tradução . . Acesso em: 14 ago. 2024.
APA
Vainzof, M., Costa, C. S., Marie, S. K. N., Moreira, E. S., Reed, U. C., Passos-Bueno, M. R., et al. (1997). Deficiency of 'alfa'-actinin-3 (ACTN3) Occurs in different forms of muscular dystrophy. Neuropediatrics, 28, 223-228.
NLM
Vainzof M, Costa CS, Marie SKN, Moreira ES, Reed UC, Passos-Bueno MR, Beggs A. H., Zatz M. Deficiency of 'alfa'-actinin-3 (ACTN3) Occurs in different forms of muscular dystrophy. Neuropediatrics. 1997 ; 28 223-228.[citado 2024 ago. 14 ]
Vancouver
Vainzof M, Costa CS, Marie SKN, Moreira ES, Reed UC, Passos-Bueno MR, Beggs A. H., Zatz M. Deficiency of 'alfa'-actinin-3 (ACTN3) Occurs in different forms of muscular dystrophy. Neuropediatrics. 1997 ; 28 223-228.[citado 2024 ago. 14 ]

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