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Resultados de 1 a 10 de 39  para Produção Intelectual da USP

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1
Osteopontin expression during chronic and acute muscle injury
Osteopontin expression during chronic and acute muscle injury
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Osteopontin expression during chronic and acute muscle injury

L Tasaki R Ishiba; D Ayub-Guerrieri; C Almeida; S Fernandes; A Ribeiro Jr.; L Galleni; L Souza; A Santos; Mariz Vainzof; International Congress of the World Muscle Society (22. 2017 St. Malo, France)

Neuromuscular Disorders London v. 27, Suppl. 2, p. S193, Abstr. P.320, Oct. 2017

London 2017

Item não circula. Consulte sua biblioteca.(Acessar)

2
Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies
Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies
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Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies

D Ayub-Guerrieri A Ribeiro Junior; R Ishiba; L Yumi; P Semedo-Kuriki; Mariz Vainzof; International Congress of the World Muscle Society (21. (2016 Granada)

Neuromuscular Disorders London v. 26, suppl. 2, p.S128, res. P135, Oct. 2016

London 2016

Item não circula. Consulte sua biblioteca.(Acessar)

3
Muscle NMR imaging in the rare E650K mutation in the DNM2 gene in a centronuclear myopathy patient
Muscle NMR imaging in the rare E650K mutation in the DNM2 gene in a centronuclear myopathy patient
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Muscle NMR imaging in the rare E650K mutation in the DNM2 gene in a centronuclear myopathy patient

Mariz Vainzof P Calyjur; M.C.G Otaduy; C.F. et al Almeida; International Congress of The World Muscle Society Asilomar 2013 18

Neuromuscular Disorders v. 23, n. 9-10, p. 763, res. P.4.13, Oct. 2013

Oxford 2013

Item não circula. Consulte sua biblioteca.(Acessar)

4
Why is LGMD2G rare?
Why is LGMD2G rare?
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Why is LGMD2G rare?

C.F. Almeida P.C.G. Onofre Oliveira; Mayana Zatz; L Negrao; Mariz Vainzof; International Congress of The World Muscle Society Asilomar 2013 18

Neuromuscular Disorders v. 23, n. 9-10, p. 766, res. P.5.8, Oct. 2013

Oxford 2013

Item não circula. Consulte sua biblioteca.(Acessar)

5
Association of two mutations in the RYR1 gene in central core disease recessive or modifying effect?
Association of two mutations in the RYR1 gene in central core disease recessive or modifying effect?
Material Type:
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Association of two mutations in the RYR1 gene in central core disease recessive or modifying effect?

T. Cuperman S Alcântara; M Canovas; L.U Yamamoto; R.C Pavanello; Mayana Zatz; A.S Oliveira; Mariz Vainzof; International Congress of The World Muscle Society Asilomar 2013 18

Neuromuscular Disorders v. 23, n. 9-10, p. 763, res. P.4.12, Oct. 2013

Oxford 2013

Item não circula. Consulte sua biblioteca.(Acessar)

6
Central core disease (CCD) improving the screening for mutations in RYR1 gene
Central core disease (CCD) improving the screening for mutations in RYR1 gene
Material Type:
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Central core disease (CCD) improving the screening for mutations in RYR1 gene

T. Cuperman S Alcântara; N.C.V Lourenço; L.U Yamamoto; R.C Pavanello; H.C Silva; J. Gurgel Gianetti; Mayana Zatz; A.S Oliveira; Mariz Vainzof; International Congress of The World Muscle Society Asilomar 2013 18

Neuromuscular Disorders v. 23, n. 9-10, p. 763, res. P.4.13, Oct. 2013

Oxford 2013

Item não circula. Consulte sua biblioteca.(Acessar)

7
K7del is a recurrent TPM2 nemaline myopathy mutation associated with joint contractures and increased calcium sensitivity
K7del is a recurrent TPM2 nemaline myopathy mutation associated with joint contractures and increased calcium sensitivity
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K7del is a recurrent TPM2 nemaline myopathy mutation associated with joint contractures and increased calcium sensitivity

N. Mokbel B Ilkovski; M Memo; Mariz Vainzof; International Congress of The World Muscle Society Perth 2012 17

Neuromuscular Disorders v. 22, n. 9-10, oct. p. 845, G.P. 15, 2012

Oxford 2012

Item não circula. Consulte sua biblioteca.(Acessar)

8
LGMD2G with clinical presentation of congenital muscular dystrophy a rare phenotype
LGMD2G with clinical presentation of congenital muscular dystrophy a rare phenotype
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

LGMD2G with clinical presentation of congenital muscular dystrophy a rare phenotype

C.F. Almeida B.L Lima; P.C.G. Onofre Oliveira; R.C.M Pavanello; Mayana Zatz; Mariz Vainzof; International Congress of The World Muscle Society Perth 2012 17

Neuromuscular Disorders v. 22, n. 9-10, p. 831, res. G.P. 40, Oct. 2012

Perth 2012

Item não circula. Consulte sua biblioteca.(Acessar)

9
Expression analysis of x-dystroglycosyltransferases in distinct murine muscular dystrophies models
Expression analysis of x-dystroglycosyltransferases in distinct murine muscular dystrophies models
Material Type:
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Expression analysis of x-dystroglycosyltransferases in distinct murine muscular dystrophies models

D. Ayub Guerrieri P. Priscila Calyjur; P.C.M Martins; P.C.G. Onofre Oliveira; Mariz Vainzof; International Congress of The World Muscle Society Perth 2012 17

Neuromuscular Disorders v. 22, n. 9-10, p. 814, res. G.P. 8, Oct. 2012

Perth 2012

Item não circula. Consulte sua biblioteca.(Acessar)

10
Effects of steroid hormones on myostatin expression and on genes of muscle regeneration pathway
Effects of steroid hormones on myostatin expression and on genes of muscle regeneration pathway
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Effects of steroid hormones on myostatin expression and on genes of muscle regeneration pathway

A. L. F Santos P. C Calyjur; D Zilberztajn; P C G Onofre-Oliveira; P. C. M Martins; L. U Yamamoto; Mariz Vainzof; International Congress of the World Muscle Society (17. 2012 Perth, Austrália)

Neuromuscular Disorders London v. 22, n. 9-10, p. 864 T.P.38, Oct. 2012

London 2012

Item não circula. Consulte sua biblioteca.(Acessar)

Resultados de 1 a 10 de 39  para Produção Intelectual da USP

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