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Área de PDI em doenças crônicas, degenerativas e genéticas 2008

 Pubmed
Pubmed
Bezerra FF, Cabello GM, Mendonça LM, Donangelo CM. 2008. Bone mass and breast milk calcium concentration are associated with vitamin D receptor gene polymorphisms in adolescent mothers.The Journal of Nutrition.138,277-281.

 doi
doi
Bloch M, Althabe F, Onyamboko M, Kaseba-Sata C, Castilla EE, Freire S, Garces AL, Parida S, Goudar SS, Kadir MM, Goco N, Thornberry J, Daniels M, Bartz J, Hartwell T, Moss N, Goldenberg R. 2008. Tobacco use and secondhand smoke exposure during pregnancy: An investigative survey of women in 9 developing nations. American Journal of Public Health. 98, 1833-1840.

 doi
doi
Castilla EE, Mastroiacovo P, López-Camelo JS, Saldarriaga W, Isaza C, Orioli IM. 2008. Sirenomelia and cyclopia cluster in Cali, Colombia. American Journal of Medical Genetics Part A. 146A, 2626-2636.

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doi
Castilla EE, Mastroiacovo P, Orioli IM. 2008. Gastroschisis: International epidemiology and public health perspectives. American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 148 C, 162 – 179.

 doi
doi
Hatagima A , Costa ECB, Marques CFS, Koifman RJ, Boffetta P, Koifman S.2008. Glutathione S-transferase polymorphisms and oral cancer: A case-control study in Rio de Janeiro, Brazil. 44, 200-207.

 doi
doi
Leoncini E, Baranello G, Orioli IM, Annerén G, Bakker M, Bianchi F, Bower C, Canfield MA, Castilla EE, Cocchi G, Correa A, De Vigan C, Doray B, Feldkamp ML, Gatt M, Irgens LM, Lowry RB, Maraschini A, Mc Donnell R, Morgan M, Mutchinick O, Poetzsch S, Riley M, Ritvanen A, Gnansia ER, Scarano G, Sipek A, Tenconi R, Mastroiacovo P. 2008. Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations. Birth Defects Research Part A: Clinical and Molecular Teratology. 82, 585-591.

 doi
doi
Rittler M, Lopez-Camelo JS, Castilla EE, Bermejo E, Cocchi G, Correa A, Csaky-Szunyogh M, Danderfer R, De Vigan C, De Walle H, Dutra MD, Hirahara F, Martinez-Frias ML, Merlob P,Mutchinick O, Ritvanen A, Robert-Gnansia E, Scarano G, Siffel C, Stoll C, Mastroiacovo P.2008. Preferential associations between oral clefts and other major congenital anomalies. 45, 525-532.

 doi
doi
Varela-Lema L, Taioli E, Ruano-Ravina A, Barros-Dios JM, Anantharaman D, Benhamou S, Boccia S, Bhisey RA, Cadoni G, Capoluongo E, Chen CJ, Foulkes WD, Goloni-Bertollo EM, Hatagima A, Hayes RB, Katoh T, Koifman S, Lazarus P, Manni JJ, Mahimkar M, Morita S, Park J,Park KK, Bertelli ECP, Ribeiro EMDSF,Roy B, Spitz MR, Strange RC, Wei QY, Ragin CC. 2008. Meta-analysis and pooled analysis of GSTM1 and CYP1A1 polymorphisms and oral and pharyngeal cancers: a HuGE-GSEC review.10, 369-384.

 Scielo
Scielo
Vieira AR, Cooper ME, Marazita ML, Castilla EE, Orioli IM. 2008. Reduced folate carrier 1 (RFC1) is associated with cleft of the lip only. 41, 689-693.

 doi
doi
Weinberg SM, Brandon CA, McHenry TH, Neiswanger K, Deleyiannis FW, de Salamanca JE, Castilla EE, Czeizel AE, Vieira AR, Marazita ML. 2008. Rethinking isolated cleft palate: evidence of occult lip defects in a subset of cases. American Journal of Medical Genetics Part A. 146A, 1670-1675.

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