Browsing by Author Zanoteli, E.

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Showing results 1 to 11 of 11
Issue DateTitleAuthor(s)
1-Oct-2012Centronuclear and myotubular myopathies: Clinical, histological and molecular findings in a large series of Brazilian patientsAbath, O.; Silva, M. R. [UNIFESP]; Pesquero, J. B. [UNIFESP]; Oliveira, A. S. B. [UNIFESP]; Carvalho, M.; Chadi, G.; Reed, U. C.; Zanoteli, E.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)
11-Jun-1998Centronuclear myopathy: Clinical aspects of ten Brazilian patients with childhood onsetZanoteli, E.; Oliveira, ASB; Schmidt, B.; Gabbai, Alberto Alain [UNIFESP]; Universidade Federal de São Paulo (UNIFESP)
1-Feb-2003Deficiency of muscle alpha-actinin-3 is compatible with high muscle performanceZanoteli, E.; Lotuffo, R. M.; Oliveira, ASB; Beggs, A. H.; Canovas, M.; Zatz, M.; Vainof, M.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP); Harvard Univ
30-Apr-2005Deletion of both MTM1 and MTMR1 genes in a boy with myotubular myopathyZanoteli, E.; Oliveira, ASB; Gabbai, Alberto Alain [UNIFESP]; Laporte, J.; Kretz, C.; Mandel, J. L.; Buj-Bello, A.; Rocha, JCC; Perez, ABA; Universidade Federal de São Paulo (UNIFESP); Coll France
1-Oct-2011The effects of Omega-3 fatty acid on skeletal muscle atrophy induced by DexamethasoneFappi, A.; Godoy, T. S. [UNIFESP]; Venancio, D. P. [UNIFESP]; Chadi, G.; Zanoteli, E.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)
1-Aug-2002Fukuyama-type congenital muscular dystrophy: a case report in the Japanese population living in BrazilZanoteli, E.; Rocha, JCC; Narumia, L. K.; Fireman, MAT; Moura, L. S.; Oliveira, ASB; Gabbai, Alberto Alain [UNIFESP]; Fukuda, Y.; Kinoshita, M.; Toda, T.; Universidade Federal de São Paulo (UNIFESP); Otsuka Pharmaceut Co Ltd; Osaka Univ
1-Mar-2001Nebulin expression in patients with nemaline myopathyGurgel-Giannetti, J.; Reed, U.; Bang, M. L.; Pelin, K.; Donner, K.; Marie, S. K.; Carvalho, M.; Fireman, MAT; Zanoteli, E.; Oliveira, ASB; Zatz, M.; Wallgren-Pettersson, C.; Labeit, S.; Vainzof, M.; Universidade de São Paulo (USP); European Mol Biol Lab; Univ Helsinki; Universidade Federal de São Paulo (UNIFESP)
1-Sep-2004Protein and DNA analysis for the prenatal diagnosis of alpha 2-laminin-deficient congenital muscular dystrophyYamamoto, L. U.; Gollop, T. R.; Naccache, N. F.; Pavanello, RCM; Zanoteli, E.; Zatz, M.; Vainzof, M.; Universidade de São Paulo (USP); Inst Med Fetal & Genet Humana; Universidade Federal de São Paulo (UNIFESP)
1-Aug-2002Temporomandibular joint and masticatory muscle involvement in myotonic dystrophy: A study by magnetic resonance imagingZanoteli, E.; Yamashita, H. K.; Suzuki, H.; Oliveira, ASB; Gabbai, Alberto Alain [UNIFESP]; Universidade Federal de São Paulo (UNIFESP); Associacao Cirurgioes Dent Campinas
1-Jul-2000Temporomandibular joint involvement in a patient with centronuclear myopathyZanoteli, E.; Guimaraes, A. S.; Martins, R. J.; Yamashita, H. K.; Toledo, C. S.; Oliveira, ASB; Gabbai, Alberto Alain [UNIFESP]; Universidade Federal de São Paulo (UNIFESP); Hosp Samaritano
1-Jan-2014Whole-body magnetic resonance imaging in the assessment of muscular involvement in juvenile dermatomyositis/polymyositis patientsCastro, T. C. M. [UNIFESP]; Lederman, H. [UNIFESP]; Terreri, M. T. [UNIFESP]; Caldana, W. I. [UNIFESP]; Zanoteli, E.; Hilario, M. O. E. [UNIFESP]; Universidade Federal de São Paulo (UNIFESP); Universidade de São Paulo (USP)