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Refinado por: autor: International Congress of the World Muscle Society remover autor: Marie, S remover
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1
The lack of the C-terminal domain of nebulin in patients with nemaline myopathy
The lack of the C-terminal domain of nebulin in patients with nemaline myopathy
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

The lack of the C-terminal domain of nebulin in patients with nemaline myopathy

J. Gurgel-Giannetti Suely Kazue Nagahashi Marie; Umbertina Conti Reed; M Canovas; M. L Bang; Mayana Zatz; S Labeit; Mariz Vainzof; International Congress of the World Muscle Society (6. 2001 Utah)

Neuromuscular Disorders v. 11, n. 6-7, p. 657

2001

Localização: FM - Fac. Medicina    (BCSEP 2001 175 ) e outros locais(Acessar)

2
Nebulin expression in patients with nemaline myopathy
Nebulin expression in patients with nemaline myopathy
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Nebulin expression in patients with nemaline myopathy

J. E. P Gurgel Umbertina Conti Reed; Suely Kazue Nagahashi Marie; M Carvalho; E Zanoteli; M. A. T Fireman; A. S. B Oliveira; Mayana Zatz; Mariz Vainzof; International Congress of the World Muscle Society (4. 1999 Estados Unidos)

Neuromuscular Disorders Estados Unidos v. 09, n. 06-07, p. 513, res. G.P.5.2, 1999

Estados Unidos 1999

Localização: FM - Fac. Medicina    (BCSEP 247 1999 ) e outros locais(Acessar)

3
Rod distribution and muscles fibers type modification in the progression of nemaline myopathy
Rod distribution and muscles fibers type modification in the progression of nemaline myopathy
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Rod distribution and muscles fibers type modification in the progression of nemaline myopathy

J. Gurgel-Giannetti E Zanoteli; L. C Werneck; Umbertina Conti Reed; A. H Beggs; Suely Kazue Nagahashi Marie; M. A. T Fireman; A. S. B Oliveira; Mayana Zatz; Mariz Vainzof; International Congress of the World Muscle Society (7. 2002 Rotterdam)

Neuromuscular Disorders v. 12, n. 7-8, p. 767 res. G.P.6.11, Oct. 2002

Oxford 2002

Localização: FM - Fac. Medicina    (BCSEP 2002 44 ) e outros locais(Acessar)

4
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy

Mariz Vainzof Maria Rita Passos-Bueno; R C M Pavanello; Suely Kazue Nagahashi Marie; A. S. B Oliveira; Mayana Zatz; International Congress of the World Muscle Society (3. 1998 Naples)

Neuromuscular disorders Oxford v. 8, n. 3/4, res. GP2.6, 1998

Oxford 1998

Item não circula. Consulte sua biblioteca.(Acessar)

5
Congenital muscular dystrophy (CMD) clinical-immunochemical correlation in a Brazilian casuistic 40 cases
Congenital muscular dystrophy (CMD) clinical-immunochemical correlation in a Brazilian casuistic 40 cases
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Congenital muscular dystrophy (CMD) clinical-immunochemical correlation in a Brazilian casuistic 40 cases

Umbertina Conti Reed Mariz Vainzof; M.B.D Resende; M.S Carvalho; Aron Judka Diament; Milberto Scaff; Suely Kazue Nagahashi Marie; International Congress of the World Muscle Society (5. 2000 South Africa)

Neuromuscular Disorders v. 10, n. 4-5, p. 381, June 2000

Kidlington Oxford 2000

Localização: FM - Fac. Medicina    (BCSEP 2000 21 )(Acessar)

6
The limb-girdle muscular dystrophy 2G (LGMD2G) phenotype
The limb-girdle muscular dystrophy 2G (LGMD2G) phenotype
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

The limb-girdle muscular dystrophy 2G (LGMD2G) phenotype

Maria Rita Passos-Bueno E De Sá Moreira; Suely Kazue Nagahashi Marie; R.C.M Pavanello; E Zanoteli; Mariz Vainzof; Mayana Zatz; International Congress of the World Muscle Society (5. 2000 South Africa)

Neuromuscular Disorders v. 10, n. 4-5, p. 346, June 2000

Kidlington Oxford 2000

Localização: FM - Fac. Medicina    (BCSEP 2000 21 )(Acessar)

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Deste Autor:

  1. Vainzof, M
  2. International Congress of the World Muscle Society
  3. Marie, S
  4. Zatz, M
  5. Reed, U

Neste Assunto:

  1. Neurologia
  2. Genética Médica

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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