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Refinado por: autor: Vainzof, M remover
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1
Partial 'alfa'-sarcoglycan ('alfa'-SG) deficiency associated with the retention of the SG complex in a LGMD2D family
Partial 'alfa'-sarcoglycan ('alfa'-SG) deficiency associated with the retention of the SG complex in a LGMD2D family
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Artigo de Congresso 		Adicionar ao Meu Espaço

Partial 'alfa'-sarcoglycan ('alfa'-SG) deficiency associated with the retention of the SG complex in a LGMD2D family

Mariz Vainzof E S Moreira; M Canovas; Oscar T Suzuki; Rita de Cássia M Pavanello; Maria Rita Passos-Bueno; Mayana Zatz; American Society of Human Genetics (49. 1999 San Francisco)

American Journal of Human Genetics Baltimore v. 65, n. 4, suppl., res.2815, oct. 1999

San Francisco 1999

Item não circula. Consulte sua biblioteca.(Acessar)

2
Deficiência parcial de A-sarcoglicana (A-SG) associada à manutenção do complexo sarcoglicano em uma família com forma 2D de distrofia muscular das cinturas (DMC)
Deficiência parcial de A-sarcoglicana (A-SG) associada à manutenção do complexo sarcoglicano em uma família com forma 2D de distrofia muscular das cinturas (DMC)
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Deficiência parcial de A-sarcoglicana (A-SG) associada à manutenção do complexo sarcoglicano em uma família com forma 2D de distrofia muscular das cinturas (DMC)

Mariz Vainzof Eloisa S Moreira; Marta Canovas; Oscar T Suzuki; Rita de Cássia M Pavanello; Cleber S Costa; Maria Rita Passos-Bueno; Mayana Zatz; Congresso Nacional de Genética (45. 1999 Gramado)

Genetics and Molecular Biology Ribeirão Preto v. 22, n. 3, suppl., res.05-122, 1999

Gramado 1999

Item não circula. Consulte sua biblioteca.(Acessar)

3
Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]
Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]
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Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]

Eloisa S. Moreira Tim J Wiltshire; Georgine Faulkner; Antje Nilforoushan; Mariz Vainzof; Oscar T Suzuki; Giorgio Valle; Roger Reeves; Mayana Zatz; Maria Rita Passos-Bueno; Dieter E Jenne

Nature Genetics v. 24, p. 163-166, Feb. 2000

New York 2000

Item não circula. Consulte sua biblioteca.(Acessar)

4
Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]
Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]

Eloisa S. Moreira Tim J Wiltshire; Georgine Faulkner; Antje Nilforoushan; Mariz Vainzof; Oscar T Suzuki; Giorgio Valle; Roger Reeves; Mayana Zatz; Maria Rita Passos-Bueno; Dieter E Jenne

Nature Genetics v. 24, p. 163-166, Feb. 2000

New York 2000

Item não circula. Consulte sua biblioteca.(Acessar)

5
Partial telethonin deficiency in severely affected North American limb girdle muscular dystrophy patients
Partial telethonin deficiency in severely affected North American limb girdle muscular dystrophy patients
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Artigo de Congresso 		Adicionar ao Meu Espaço

Partial telethonin deficiency in severely affected North American limb girdle muscular dystrophy patients

S. T. Iannaccone David Muirhead; Nora Elmonoufy; Reuel Cornelia; Georgine Faulkner; G Valle; Oscar T Suzuki; Mayana Zatz; Mariz Vainzof; International Congress of the World Muscle Society (7. 2002 Rotterdam)

Neuromuscular Disorders v. 12, n. 7-8, p. 732, oct. 2002

Oxford 2002

Item não circula. Consulte sua biblioteca.(Acessar)

6
Telethonin protein expression in neuromuscular disorders
Telethonin protein expression in neuromuscular disorders
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Telethonin protein expression in neuromuscular disorders

Mariz Vainzof Eloisa S Moreira; Oscar T Suzuki; Georgine Faulkner; Georgio Valle; Alan H Beggs; Olli Carpen; Alberto de Freitas Ribeiro; Edmar Zanoteli; Juliana Gurgel-Gianneti; Ana Maria Crous Tsanaclis; Helga Cristina Almeida da Silva; Maria Rita Passos-Bueno; Mayana Zatz

Biochimica et Biophysica Acta v. 1588, n. 1, p. 33-40, 2002

Amsterdam 2002

Item não circula. Consulte sua biblioteca.(Acessar)

7
Telethonin protein expression in neuromuscular disorders
Telethonin protein expression in neuromuscular disorders
Material Type:
Artigo 		Adicionar ao Meu Espaço

Telethonin protein expression in neuromuscular disorders

Mariz Vainzof Eloisa S Moreira; Oscar T Suzuki; Georgine Faulkner; Georgio Valle; Alan H Beggs; Olli Carpen; Alberto de Freitas Ribeiro; Edmar Zanoteli; Juliana Gurgel-Gianneti; Ana Maria Crous Tsanaclis; Helga Cristina Almeida da Silva; Maria Rita Passos-Bueno; Mayana Zatz

Biochimica et Biophysica Acta v. 1588, n. 1, p. 33-40, 2002

Amsterdam 2002

Item não circula. Consulte sua biblioteca.(Acessar)

8
Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12]
Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12]
Material Type:
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Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12]

E. S. Moreira Mariz Vainzof; Oscar T Suzuki; Rita de Cássia M Pavanello; Mayana Zatz; Maria Rita Passos-Bueno

Journal of Medical Genetics v. 40, p. e12, 2003

London 2003

Item não circula. Consulte sua biblioteca.(Acessar)

9
Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12]
Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12]

E. S. Moreira Mariz Vainzof; Oscar T Suzuki; Rita de Cássia M Pavanello; Mayana Zatz; Maria Rita Passos-Bueno

Journal of Medical Genetics v. 40, p. e12, 2003

London 2003

Item não circula. Consulte sua biblioteca.(Acessar)

10
Preclinical studies with umbilical cord mesenchymal stromal cells in different animal models for muscular dystrophy
Preclinical studies with umbilical cord mesenchymal stromal cells in different animal models for muscular dystrophy
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Preclinical studies with umbilical cord mesenchymal stromal cells in different animal models for muscular dystrophy

Eder Zucconi Natassia Moreira da Silva Vieira; Carlos Roberto Bueno Jr.; Mariane Secco; Tatiana Jazedje; Marcos Costa Valadares; Miriam Fussae Suzuki; Paolo Bartolini; Mariz Vainzof; Mayana Zatz

Journal of Biomedicine and Biotechnology New york online, p. on-line, July 2011

New York 2011

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Zatz, M
  2. Vainzof, M
  3. Suzuki, O
  4. Moreira, E
  5. Passos-Bueno, M

Neste Assunto:

  1. Distrofia Muscular
  2. Genética Médica
  3. Mutação Genética
  4. Modelos Animais
  5. Transplante De Medula Óssea

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

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