Área de PDI em Pesquisa, Desenvolvimento e Inovação em Doenças Crônicas e Degenerativas 2011
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Bermejo-Sánchez E, Cuevas L, Amar E, Bakker MK, Bianca S, Bianchi F, Canfield MA, Castilla EE, Clementi M, Cocchi G, Feldkamp ML, Landau D, Leoncini E, Li Z, Lowry RB, Mastroiacovo P, Mutchinick OM, Rissmann A, Ritvanen A, Scarano G, Siffel C, Szabova E, Martínez-Frías ML.2011. Amelia: a multi-center descriptive epidemiologic study in a large dataset from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature. Am J Med Genet C Semin Med Genet. 157C(4):288-304.
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Bermejo-Sánchez E, Cuevas L, Amar E, Bianca S, Bianchi F, Botto LD, Canfield MA, Castilla EE, Clementi M, Cocchi G, Landau D, Leoncini E, Li Z, Lowry RB, Mastroiacovo P, Mutchinick OM, Rissmann A, Ritvanen A, Scarano G, Siffel C, Szabova E, Martínez-Frías ML. 2011. Phocomelia: A worldwide descriptive epidemiologic study in a large series of cases from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature. Am. J. Med. Genet. C. Semin. Med.Genet.157C(4):305-320.
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Botto LD, Feldkamp ML, Amar E, Carey JC, Castilla EE, Clementi M, Cocchi G, de Walle HE, Halliday J, Leoncini E, Li Z, Lowry RB, Marengo LK, Martínez-Frías ML, Merlob P, Morgan M, Muñoz LL, Rissmann A, Ritvanen A, Scarano G, Mastroiacovo P. 2011. Acardia: Epidemiologic findings and literature review from the International Clearinghouse for Birth Defects Surveillance and Research. Am J Med Genet C Semin Med Genet.157C(4):262-73.
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Castilla EE, Mastroiacovo P. 2011. Very rare defects: What can we learn? Am J Med Genet C Semin Med Genet. 157C(4):252-261
de Oliveira Hiragi C, Miranda-Vilela AL, Rocha DM, de Oliveira SF, Hatagima A, de Nazaré Klautau-Guimarães M. 2011. Superoxide dismutase, catalase, glutathione peroxidase and gluthatione S-transferases M1 and T1 gene polymorphisms in three Brazilian population groups. Genet. Mol. Biol.34(1): 11-18.
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Feldkamp ML, Botto LD, Amar E, Bakker MK, Bermejo-Sánchez E, Bianca S, Canfield MA, Castilla EE, Clementi M, Csaky-Szunyogh M, Leoncini E, Li Z, Lowry RB, Mastroiacovo P, Merlob P, Morgan M, Mutchinick OM, Rissmann A, Ritvanen A, Siffel C, Carey JC. 2011. Cloacal exstrophy: An epidemiologic study from the International Clearinghouse of Birth Defects Surveillance and Research. Am. J. Med. Genet. C. Semin. Med. Genet.157C(4):333-343
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Hernandez Mde O, Fulco Tde O, Pinheiro RO, Pereira Rde M, Redner P, Sarno EN, Lopes UG, Sampaio EP. 2011. Thalidomide modulates Mycobacterium leprae-induced NF-kB pathway and lower cytokine response. Eur. J. Pharmacol. 670(1):272-279.
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Jindal A, McMeans M, Narayanan S, Rose EK, Jain S, Marazita ML, Menezes R, Letra A, Carvalho FM, Brandon CA, Resick JM, Mereb JC, Poletta FA, Lopez-Camelo JS, Castilla EE, Orioli IM, Vieira AR. 2011. Women are more susceptible to caries but individuals born with clefts are not. Int J. Dent. 2011:454532.
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Letra A, Menezes R, Cooper ME, Fonseca RF, Tropp S, Govil M, Granjeiro JM, Imoehl SR, Mansilla MA, Murray JC, Castilla EE, Orioli IM, Czeizel AE, Ma L, Chiquet BT, Hecht JT, Vieira AR, Marazita ML. 2011. CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palate. Cleft Palate Craniofac. J. 48 (4): 363-370.
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Orioli IM, Amar E, Bakker MK, Bermejo-Sánchez E, Bianchi F, Canfield MA, Clementi M, Correa A, Csáky-Szunyogh M, Feldkamp ML, Landau D, Leoncini E, Li Z, Lowry RB, Mastroiacovo P, Morgan M, Mutchinick OM, Rissmann A, Ritvanen A, Scarano G, Szabova E, Castilla EE. 2011. Cyclopia: An epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research. Am. J. Med. Genet. C. Semin. Med. Genet. 157C(4):344-357.
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Orioli IM, Lima do Nascimento R, López-Camelo JS, Castilla EE. 2011. Effects of folic acid fortification on spina bifida prevalence in Brazil. Birth Defects Res. A. Clin. Mol. Teratol. 91(9):831-835.
Orioli IM, Camelo JS, Rittler M, Castilla EE. 2011. Sentinel phenotype for rubella embryopathy: time-space distribution in Brazil. Cad. Saude. Publica. 27(10): 1961-1968.
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Orioli IM, Amar E, Arteaga-Vazquez J, Bakker MK, Bianca S, Botto LD, Clementi M, Correa A, Csaky-Szunyogh M, Leoncini E, Li Z, López-Camelo JS, Lowry RB, Marengo L, Martínez-Frías ML, Mastroiacovo P, Morgan M, Pierini A, Ritvanen A, Scarano G, Szabova E, Castilla EE. 2011. Sirenomelia: An epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review. Am. J. Med. Genet. C. Semin. Med.Genet.157C(4):358-373.
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Rittler M, Cosentino V, López-Camelo JS, Murray JC, Wehby G, Castilla EE. 2011. Associated anomalies among infants with oral clefts at birth and during a 1-year follow-up. Am. J. Med. Genet. A. 155A(7):1588-1596.
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Siffel C, Correa A, Amar E, Bakker MK, Bermejo-Sánchez E, Bianca S, Castilla EE, Clementi M, Cocchi G, Csáky-Szunyogh M, Feldkamp ML, Landau D, Leoncini E, Li Z, Lowry RB, Marengo LK, Mastroiacovo P, Morgan M, Mutchinick OM, Pierini A, Rissmann A, Ritvanen A, Scarano G, Szabova E, Olney RS.2011. Bladder exstrophy: an epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature. Am. J. Med. Genet. C. Semin. Med. Genet.157C(4):321-332.
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Vianna FS, Lopez-Camelo JS, Leite JC, Sanseverino MT, Dutra Mda G, Castilla EE, Schüler-Faccini L. 2011. Epidemiological surveillance of birth defects compatible with thalidomide embryopathy in Brazil. PLoS One.6(7):e21735.
Wehby GL, Murray JC, McCarthy AM, Castilla EE. 2011. Racial gaps in child health insurance coverage in four South American countries: The role of wealth, human capital, and other household characteristics. Health Serv. Res.46(6): 2119-2138.
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Werneck MB, Vieira-de-Abreu A, Chammas R, Viola JP., NFAT1 transcription factor is central in the regulation of tissue microenvironment for tumor metastasis, 2011, Cancer Immunology, Immunotherapy, Volume 60, Number 4, pages 537-546.
Atualizado em 29/08/2012.
