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1
Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients
Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients
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Conference Paper 		Add to e-Shelf

Molecular-genetic defects in AICDA gene confirms clinical spectrum of autosomal hyper igm syndrome in brazilian patients

S. Klaver B Carvalho; F Tavares; S Lima; J Ferreira; E Mansur; P Roxo-Junior; A Durandy; Antonio Condino-Neto; Biennial Meenting of the European Society for Immunodeficiencies (ESID) (15. 2012 Florença); Meeting of the International Patient Organisation for Primary Immunodeficiences (IPOPI) (12. 2012 Florença); Meeting of the International Nursing Group for Immunodeficiencies (INGID) (10. 2012 Florença)

Resumos Florença: The European Society for Immunodeficiencies

Florença The European Society for Immunodeficiencies 2012

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2
Role of inflammasome genetics in susceptibility to HPV infection and cervical cancer development
Role of inflammasome genetics in susceptibility to HPV infection and cervical cancer development
Material Type:
Article 		Add to e-Shelf

Role of inflammasome genetics in susceptibility to HPV infection and cervical cancer development

Alessandra Pontillo P Bricher; V. N. C Leal; S Lima; P. R. E Souza; S Crovella

Journal of Medical Virology New York v. 88, n. 9, p. 1646-1651, 2016

New York 2016

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3
Deteccao de mutacoes no exon 24 do gen c3 em crianca deficiente desta proteina
Deteccao de mutacoes no exon 24 do gen c3 em crianca deficiente desta proteina
Material Type:
Conference Paper 		Add to e-Shelf

Deteccao de mutacoes no exon 24 do gen c3 em crianca deficiente desta proteina

A S Lima D S Caramico; M Pereira; Lourdes Isaac; Simposio de Iniciacao Cientifica da Universidade de São Paulo (3. 1995 Ribeirao Preto)

Sao Paulo : Usp, 1995 Resumos

São Paulo Usp 1995

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4
Molecular bases of human complement component C3 deficiency
Molecular bases of human complement component C3 deficiency
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Molecular bases of human complement component C3 deficiency

G V Baracho E S Reis; G V Baracho; A S Lima; Lourdes Isaac; Congresso do Instituto de Ciências Biomédicas (3. 2001 São Paulo)

Resumos São Paulo: Comissão de Cultura e Extensão Universitária do ICB/USP, 2001

São Paulo Comissão de Cultura e Extensão Universitária do ICB/USP 2001

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5
A stop codon in exon 13 causes the complete lack of human complement component C3 deficiency
A stop codon in exon 13 causes the complete lack of human complement component C3 deficiency
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A stop codon in exon 13 causes the complete lack of human complement component C3 deficiency

E S Reis G V Baracho; A S Lima; Lourdes Isaac; European Meeting on Complement in Human Disease (1. 2001 Strasbourg)

Molecular Immunology v.38, p.118, 2001

Strasbourg 2001

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6
Estudo molecular parcial da imunodeficiência do componente C3 do sistema complemento humano
Estudo molecular parcial da imunodeficiência do componente C3 do sistema complemento humano
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Estudo molecular parcial da imunodeficiência do componente C3 do sistema complemento humano

A S Lima R Ulbricht; Lourdes Isaac; Simpósio de Iniciação Científica da Universidade de São Paulo (5. 1997 São Paulo)

Resumos São Paulo : USP, 1997

São Paulo USP 1997

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7
Analise molecular preliminar de uma deficiencia de c3 humano
Analise molecular preliminar de uma deficiencia de c3 humano
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Analise molecular preliminar de uma deficiencia de c3 humano

A S Lima M P C Florido; Geraldo Aleixo Silva Passos; Nancy Starobinas; P E M Andrade; Lourdes Isaac; Simpósio de Iniciação Cientifica da Universidade de São Paulo (4. 1996 Ribeirão Preto)

São Paulo : USP, 1996 [Resumos]

São Paulo Usp 1996

Available at FMRP - Fac. Medicina de Ribeirão Preto    (pcd E 016 p.232 914929 ) and other locations(GetIt)

8
Disfunções primárias de neutrófilos
Disfunções primárias de neutrófilos
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Article 		Add to e-Shelf

Disfunções primárias de neutrófilos

R Bellinati-Pires M. M. S Carneiro-Sampaio; Maria Lima A. S Araújo

Cadernos de Imunoalergologia Pediatrica Lisboa v. 6, p. 5-14, 1991

Lisboa 1991

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9
Disfunções primárias de neutrófilos
Disfunções primárias de neutrófilos
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Article 		Add to e-Shelf

Disfunções primárias de neutrófilos

R Bellinati-Pires M. M. S Carneiro-Sampaio; Maria Lima A. S Araújo

Cadernos de Imunoalergologia Pediatrica Lisboa v. 6, p. 5-14, 1991

Lisboa 1991

Available at ICB - Inst. Ciências Biomédicas    (PC-ICB BMI SEP 1991 )(GetIt)

10
First report of the hyper-IgM syndrome registry of the Latin American Society for Immunodeficiencies novel mutations, unique infections, and outcomes
First report of the hyper-IgM syndrome registry of the Latin American Society for Immunodeficiencies novel mutations, unique infections, and outcomes
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First report of the hyper-IgM syndrome registry of the Latin American Society for Immunodeficiencies novel mutations, unique infections, and outcomes

Otavio Cabral-Marques Stefanie Klaver; Lena Schimke; Évelyn H Ascendino; Taj Ali Khan; Paulo Vitor Soeiro Pereira; Angela Falcai; Alexander Vargas-Hernández; Leopoldo Santos-Argumedo; Liliana Bezrodnik; Ileana Moreira; Gisela Seminario; Daniela Di Giovanni; Andrea Gómez Raccio; Oscar Porras; Cristina Worm Weber; Janaíra Fernandes Ferreira; Fabiola Scancetti Tavares; Elisa de Carvalho; Claudia França Cavalcante Valente; Gisele Kuntze; Miguel Galicchio; Alejandra King; Nelson Augusto Rosário-Filho; Milena Baptistella Grota; Maria Marluce dos Santos Vilela; Regina Sumiko Watanabe Di Gesu; Simone Lima; Leiva de Souza Moura; Eduardo Talesnik; Eli Mansour; Persio Roxo Junior; Juan Carlos Aldave; Ekaterine Goudouris; Fernanda Pinto-Mariz; Laura Berrón-Ruiz; Tamara Staines-Boone; Wilmer O. Córdova Calderón; María del Carmen Zarate-Hernández; Anete S Grumach; Ricardo Sorensen; Anne Durandy; Troy R Torgerson; Beatriz Tavares Costa Carvalho; Francisco Espinosa-Rosales; Hans D Ochs; Antonio Condino-Neto

Journal of Clinical Immunology New York v. 34, n. 2, p. 146-156, 2014

New York 2014

Available at FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2496917 Estantes Deslizantes )(GetIt)

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