Ieda M Orioli

Summary

Affiliation: Rio de Janeiro
Country: Brazil

Publications

  1. pmc The effect of systematic pediatric care on neonatal mortality and hospitalizations of infants born with oral clefts
    George L Wehby
    Department of Pediatrics, University of Iowa, Iowa City, IA, USA
    BMC Pediatr 11:121. 2011
  2. pmc Description of the methodology used in an ongoing pediatric care interventional study of children born with cleft lip and palate in South America [NCT00097149]
    George L Wehby
    Department of Health Management and Policy, University of Iowa, Iowa City, USA
    BMC Pediatr 6:9. 2006
  3. doi Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research
    Ieda M Orioli
    Estudo Colaborativo Latino Americano de Malformações Congênitas at Departamento de Genética, Instituto de Biologia, Rio de Janeiro, Brazil
    Am J Med Genet C Semin Med Genet 157:344-57. 2011
  4. doi Sirenomelia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review
    Ieda M Orioli
    Estudo Colaborativo Latino Americano de Malformações Congênitas at Departamento de Genética, Instituto de Biologia, Rio de Janeiro, Brazil
    Am J Med Genet C Semin Med Genet 157:358-73. 2011
  5. doi Effects of folic acid fortification on spina bifida prevalence in Brazil
    Iêda Maria Orioli
    Estudio Colaborativo Latino Americano de Malformaciones Congénitas, at Departamento de Genética, Universidade Federal do Rio de Janeiro
    Birth Defects Res A Clin Mol Teratol 91:831-5. 2011
  6. doi Epidemiology of holoprosencephaly: Prevalence and risk factors
    Ieda M Orioli
    Federal University of Rio de Janeiro, Brazil
    Am J Med Genet C Semin Med Genet 154:13-21. 2010
  7. ncbi Clinical and epidemiological studies of amniotic deformity, adhesion, and mutilation (ADAM) sequence in a South American (ECLAMC) population
    Ieda M Orioli
    Estudo Colaborativo Latino Americano de Malformações Congênitas ECLAMC at Departamento de Genética, Curso de Pós Graduação em Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
    Am J Med Genet A 118:135-45. 2003
  8. doi Clusters of sirenomelia in South America
    Ieda M Orioli
    ECLAMC Latin American Collaborative Study of Congenital Malformations, Departamento de Genetica, Universidade Federal do Rio de Janeiro, Brazil
    Birth Defects Res A Clin Mol Teratol 85:112-8. 2009
  9. ncbi Clinical epidemiologic study of holoprosencephaly in South America
    Ieda M Orioli
    Estudo Colaborativo Latino Americano de Malformações Congênitas ECLAMC at Departamento de Genética, Curso de Pós Graduação em Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
    Am J Med Genet A 143:3088-99. 2007
  10. pmc Is there a familial link between Down's syndrome and neural tube defects? Population and familial survey
    Marcia R Amorim
    ECLAMC at Departamento de Genética, Universidade Federal do Rio de Janeiro, Caixa Postal 68 011, 21944 970, Rio de Janeiro, Brazil
    BMJ 328:84. 2004

Collaborators

Detail Information

Publications18

  1. pmc The effect of systematic pediatric care on neonatal mortality and hospitalizations of infants born with oral clefts
    George L Wehby
    Department of Pediatrics, University of Iowa, Iowa City, IA, USA
    BMC Pediatr 11:121. 2011
    ..This study aimed at assessing the effects of systematic pediatric care on neonatal mortality and hospitalizations of infants with cleft lip and/or palate (CL/P) in South America...
  2. pmc Description of the methodology used in an ongoing pediatric care interventional study of children born with cleft lip and palate in South America [NCT00097149]
    George L Wehby
    Department of Health Management and Policy, University of Iowa, Iowa City, USA
    BMC Pediatr 6:9. 2006
    ..As other mortality and morbidity causes including infections, hygiene, prematurity, and nutrition are eradicated in less developed countries, the burden of birth defects will increase proportionally...
  3. doi Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research
    Ieda M Orioli
    Estudo Colaborativo Latino Americano de Malformações Congênitas at Departamento de Genética, Instituto de Biologia, Rio de Janeiro, Brazil
    Am J Med Genet C Semin Med Genet 157:344-57. 2011
    ..The heterogeneous etiology with a high prevalence of chromosomal abnormalities, and female predominance in HPE, were confirmed, but no effect of increased maternal age or association with twinning was observed...
  4. doi Sirenomelia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review
    Ieda M Orioli
    Estudo Colaborativo Latino Americano de Malformações Congênitas at Departamento de Genética, Instituto de Biologia, Rio de Janeiro, Brazil
    Am J Med Genet C Semin Med Genet 157:358-73. 2011
    ..The application of the new biological network analysis approach, including molecular results, to these associated very rare diseases is suggested for future studies...
  5. doi Effects of folic acid fortification on spina bifida prevalence in Brazil
    Iêda Maria Orioli
    Estudio Colaborativo Latino Americano de Malformaciones Congénitas, at Departamento de Genética, Universidade Federal do Rio de Janeiro
    Birth Defects Res A Clin Mol Teratol 91:831-5. 2011
    ..To assess spina bifida birth prevalence changes after folic acid fortification of wheat and maize flours began in Brazil in June 2004...
  6. doi Epidemiology of holoprosencephaly: Prevalence and risk factors
    Ieda M Orioli
    Federal University of Rio de Janeiro, Brazil
    Am J Med Genet C Semin Med Genet 154:13-21. 2010
    ..The variable female predominance, found in different HPE studies, could also depend on the proportion of early conceptions in each study sample, as males are more likely to be lost through spontaneous abortions...
  7. ncbi Clinical and epidemiological studies of amniotic deformity, adhesion, and mutilation (ADAM) sequence in a South American (ECLAMC) population
    Ieda M Orioli
    Estudo Colaborativo Latino Americano de Malformações Congênitas ECLAMC at Departamento de Genética, Curso de Pós Graduação em Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
    Am J Med Genet A 118:135-45. 2003
    ..The observed geographic difference in birth prevalence could be a useful indication to study specific genetic and environmental candidate factors to ADAM susceptibility...
  8. doi Clusters of sirenomelia in South America
    Ieda M Orioli
    ECLAMC Latin American Collaborative Study of Congenital Malformations, Departamento de Genetica, Universidade Federal do Rio de Janeiro, Brazil
    Birth Defects Res A Clin Mol Teratol 85:112-8. 2009
    ..One hospital in the city of Cali, Colombia, of the ECLAMC (Latin-American Collaborative Study of Congenital Malformations) network, reported the unusual occurrence of four cases of sirenomelia within a 55-day period...
  9. ncbi Clinical epidemiologic study of holoprosencephaly in South America
    Ieda M Orioli
    Estudo Colaborativo Latino Americano de Malformações Congênitas ECLAMC at Departamento de Genética, Curso de Pós Graduação em Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
    Am J Med Genet A 143:3088-99. 2007
    ..Cyclopia was not associated with oral clefts; 6 of 8 cases of ethmocephaly had cleft palate; 6 of 20 cases of cebocephaly had oral clefts; 4 of 20 cases had premaxillary agenesis; and 2 of 20 cases had cleft palate...
  10. pmc Is there a familial link between Down's syndrome and neural tube defects? Population and familial survey
    Marcia R Amorim
    ECLAMC at Departamento de Genética, Universidade Federal do Rio de Janeiro, Caixa Postal 68 011, 21944 970, Rio de Janeiro, Brazil
    BMJ 328:84. 2004
    ..To verify whether Down's syndrome and neural tube defects arise more often in the same family than expected by chance...
  11. doi Sirenomelia and cyclopia cluster in Cali, Colombia
    Eduardo E Castilla
    ECLAMC Latin American Collaborative Study of Congenital Malformations, FIOCRUZ Instituto Oswaldo Cruz, Rio de Janeiro, Brazil
    Am J Med Genet A 146:2626-36. 2008
    ..The time-space cluster is nonrandom for sirenomelia, and possibly random for cyclopia. The polluting landfill remains as a possible etiological factor...
  12. ncbi Preliminary data on changes in neural tube defect prevalence rates after folic acid fortification in South America
    Eduardo E Castilla
    ECLAMC at Instituto Oswaldo Cruz, FIOCRUZ, CP 926, Rio de Janeiro, RJ 20001 970 Brazil
    Am J Med Genet A 123:123-8. 2003
    ....
  13. doi Gastroschisis: international epidemiology and public health perspectives
    Eduardo E Castilla
    ECLAMC GENETICA FIOCRUZ, Av Brasil 4365, Pav 26, sala 617, 21045 900 Rio de Janeiro, Brazil
    Am J Med Genet C Semin Med Genet 148:162-79. 2008
    ..The increasing prevalence of gastroschisis combined with improved medical techniques to reduce morbidity and mortality are also increasing the burden and costs of this anomaly on health systems...
  14. ncbi Single median maxillary central incisor: new data and mutation review
    Kenia B El-Jaick
    Estudo Latino Americano de Malformações Congênitas, Departamento de Genetica, Universidade Federal do Rio de Janeiro, Brazil
    Birth Defects Res A Clin Mol Teratol 79:573-80. 2007
    ..Families with SMMCI, without HPE cases, are difficult to counsel for the risk of HPE in future generations because the same midline defects described as part of the "SMMCI syndrome" can also be part of the HPE spectrum...
  15. ncbi ECLAMC: the Latin-American collaborative study of congenital malformations
    Eduardo E Castilla
    ECLAMC, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil, Argentina
    Community Genet 7:76-94. 2004
    ..ECLAMC can be defined as a continental network of persons interested in research and prevention of birth defects...
  16. doi Second case of Beare-Stevenson syndrome with an FGFR2 Ser372Cys mutation
    Renata Fonseca
    ECLAMC Estudo Colaborativo Latino Americano de Malformações Congênitas at Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
    Am J Med Genet A 146:658-60. 2008
    ..Reported causes are an FGFR2 Tyr375Cys mutation in nine cases and an FGFR2 Ser372Cys mutation in one case. Here, we report on a second patient with the FGFR2 Ser372Cys mutation...
  17. doi MTHFR 677C-->T and 1298A-->C polymorphisms in children with Down syndrome and acute myeloid leukemia in Brazil
    Marcia R Amorim
    Pediatric Hematology Oncology Program, Instituto Nacional de Cancer, Rio de Janeiro, Brazil
    Pediatr Hematol Oncol 25:744-50. 2008
    ..The present study failed to reveal any association between these polymorphisms and risk of AML in DS children. The data also indicate that MTHFR polymorphisms are not associated with risk of being a DS child...
  18. ncbi Non-Latin European descent could be a requirement for association of NTDs and MTHFR variant 677C > T: a meta-analysis
    Marcia R Amorim
    Estudo Colaborativo Latino Americano de Malformações Congênitas ECLAMC at Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
    Am J Med Genet A 143:1726-32. 2007
    ....