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Resultados de 1 a 10 de 33  para Produção Intelectual da USP

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1
Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy
Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy

Geraldo Antônio Medeiros Neto Z G Zhang; N Lima; A Iacona; A Liberman; M Salvi; J R Wall

v.9 , p.293-300, 1991 Autoimmunity

1991

Localização: FM - Fac. Medicina    (BCSEP 1991 250 )(Acessar)

2
Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy
Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy

Geraldo Antônio Medeiros Neto Z G Zhang; N Lima; A Iacona; A Liberman; M Salvi; J R Wall

v.9 , p.293-300, 1991 Autoimmunity

1991

Localização: FM - Fac. Medicina    (BCSEP 1991 250 )(Acessar)

3
New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
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New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype

Te-Cheng Pan Rui Zhu Zhang; Dominick G Sudano; Suely K Marie; Carsten G Bonnemann; Mon Li Chu

American Journal of Human Genetics Chicago v. 73, p. 355-369, 2003

Chicago 2003

Localização: FM - Fac. Medicina    (FM BCSEP 2003 253 )(Acessar)

4
New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
Material Type:
Artigo 		Adicionar ao Meu Espaço

New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype

Te-Cheng Pan Rui Zhu Zhang; Dominick G Sudano; Suely K Marie; Carsten G Bonnemann; Mon Li Chu

American Journal of Human Genetics Chicago v. 73, p. 355-369, 2003

Chicago 2003

Localização: FM - Fac. Medicina    (FM BCSEP 2003 253 )(Acessar)

5
Involuntary smoking and the risk of head and neck cancer pooled analysis in the INHANCE consortium
Involuntary smoking and the risk of head and neck cancer pooled analysis in the INHANCE consortium
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Involuntary smoking and the risk of head and neck cancer pooled analysis in the INHANCE consortium

Yuan-Chin A. Lee Paolo Boffetta; Erich M Sturgis; Qingyi Wei; Zuo-Feng Zhang; Joshua Muscat; Philip Lazarus; Elena Matos; Richard B Hayes; Deborah M Winn; David Zaridze; Victor Wunsch Filho; José Eluf Neto; Sergio Koifman; Dan Mates; Paula Curado; Ana Menezes; Letícia Fernandez; Alexander W Daudt; Neonilia Szeszenia-Dabrowska; Eleonora Fabinova; Peter Rudnai; Gilles Ferro; Julien Berthiller; Paul Brennan; Mia Hashibe; AACR annual meeting (2008 San Diego, California)

Proceedings Philadelphia v. 49, p. 246, res.1048, abril 2008

Philadelphia 2008

Localização: FM - Fac. Medicina    (FM BCBIB ) e outros locais(Acessar)

6
We thank Dr. Ege for the support and insightful comments regarding the Sleep and Stent Study... [Carta]
We thank Dr. Ege for the support and insightful comments regarding the Sleep and Stent Study... [Carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

We thank Dr. Ege for the support and insightful comments regarding the Sleep and Stent Study... [Carta]

Germaine Loo Chi-Hang Lee; Junjie Zhang; Rishi Sethi; Ruogu Li; Luciano F Drager; Hee-Hwa Ho; Thet Hein; Man-Hong Jim

Clinical Cardiology New York v. 37, n. 10, p. 651, 2014

New York 2014

Localização: FM - Fac. Medicina    (BCSEP 039 2014 )(Acessar)

7
Evaluation for a susceptibility gene for schizophrenia
Evaluation for a susceptibility gene for schizophrenia
Material Type:
Artigo de Jornal 		Adicionar ao Meu Espaço

Evaluation for a susceptibility gene for schizophrenia

Michael E. Talkowski Howard Seltman; Anne S Bassett; Linda M Brzustowicz; Xiangning Chen; Kodavali V Chowdari; David A Collier; Quirino Cordeiro; Aiden P Corvin; Smita N Deshpande; Michael F Egan; Michael Gill; Kenneth S Kendler; George Kirov; Leonard L Heston; Pat Levitt; David A Lewis; Tao Li; Karoly Mirnics; Derek W Morris; Nadine Norton; Michael C O'Donovan; Michael J Owen; Christian Richard; Prachi Semwal; Janet L Sobell; David St Clair; Richard E Straub; B. K Thelma; Homero Vallada; Daniel R Weinberger; Nigel M Williams; Joel wood; Feng Zhang; Bernie Devlin; Vishwajit L Nimgaonkar

Biological Psychiatry New York v. 60, n. 2, p. 152-162, 2006

New Yoork 2006

Acesso online. A biblioteca também possui exemplares impressos.

8
Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT
Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT
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Artigo 		Adicionar ao Meu Espaço

Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT

Rui-Zhu Zhang Yaqun Zou; Te-Cheng Pan; Dessislava Markova; Andrzej Fertala; Ying Hu; Stefano Squarzoni; Umbertina Conti Reed; Suely K. N Marie; Carsten G Bönnemann; Mon-Li Chu

Journal of Biological Chemistry Baltimore v. 285, n. 13, p. 10005-10015, 2010

Baltimore 2010

Acesso online. A biblioteca também possui exemplares impressos.

9
A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties
A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties

Evangelia Charmandari Meilin Zhang; Letícia Gontijo Silveira; Geiorge P Chrousos; Amalia Sertedaki; Ana Claudia Latronico Xavier; Deborah L Segaloff; European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting (9. 2013 Milan, Italy)

Hormone Research in Paediatrics Basel v. 80, suppl. 1, p. 44, res. FC4-164, 2013

Basel 2013

Localização: FM - Fac. Medicina    (BCSEP 418 2013 )(Acessar)

10
Multimodal Magnetic Resonance Imaging Study of Treatment-Naïve Adults with Attention-Deficit/Hyperactivity Disorder
Multimodal Magnetic Resonance Imaging Study of Treatment-Naïve Adults with Attention-Deficit/Hyperactivity Disorder
Material Type:
Artigo 		Adicionar ao Meu Espaço

Multimodal Magnetic Resonance Imaging Study of Treatment-Naïve Adults with Attention-Deficit/Hyperactivity Disorder

Tiffany M. Chaim Tianhao Zhang; Marcus V Zanetti; Maria Aparecida da Silva; Mário R Louzã; Jimit Doshi; Mauricio H Serpa; Fabio L. S Duran; Sheila C Caetano; Christos Davatzikos; Geraldo F Busatto

Plos One San Francisco v. 9, n. 10, p. e110199, 2014

San Francisco 2014

Acesso online. A biblioteca também possui exemplares impressos.

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