Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Amanda B Freitas"'
Autor:
Lucas A M Franco, Ana Paula V D Alves, Mara Sandra Hoshida, José Eduardo Levi, Amanda B Freitas, Rossana Pulcineli Vieira Francisco, Mário Henrique Burlacchini de Carvalho, Elizabeth González Patiño, Antonio Gomes de Amorim Filho
Publikováno v:
Journal of Perinatal Medicine. 49:553-558
Objectives To investigate the association between selected single nucleotide polymorphisms (SNPs) with cervical insufficiency and its relationship with obstetric history. Methods Twenty-eight women with cervical insufficiency (case group) and 29 non-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6c4c1473d95e2a7ccbca11a6b586a08
https://doi.org/10.1515/jpm-2020-0320
https://doi.org/10.1515/jpm-2020-0320
Autor:
Sandra F Centofanti, Samar N. Chehimi, Amanda B Freitas, Rossana Pulcineli Vieira Francisco, J. G. Damasceno, Leslie Domenici Kulikowski, Maria de Lourdes Brizot, Gilmar de Souza Osmundo-Junior
Publikováno v:
Prenatal Diagnosis. 41:449-456
Objective The purpose of this study was to describe the genomic deoxyribonucleic acid (DNA) methylation profile in fetuses with gastroschisis, determine whether the profile was inherited, and investigate any possible correlations with maternal risk f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c38dcee7777d86a12ad01acf5e0b216
https://doi.org/10.1002/pd.5881
https://doi.org/10.1002/pd.5881
Autor:
Chong Ae Kim, Guilherme L. Yamamoto, Rachel Sayuri Honjo, José Ricardo Magliocco Ceroni, Débora Romeo Bertola, Alexander A. L. Jorge, Michele M Buscarilli, Alexsandra C. Malaquias, Maria Rita Passos-Bueno, Alexandre C. Pereira, Amanda B Freitas, Matheus Augusto Araujo Castro
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical geneticsREFERENCES. 184(4)
We report the clinical and molecular data of a large cohort comprising 242 individuals with RASopathies, from a single Tertiary Center in Brazil, the largest study from Latin America. Noonan syndrome represented 76% of the subjects, with heterozygous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5f3498406cd6b957ded0dbbd09e037
https://pubmed.ncbi.nlm.nih.gov/33128510
https://pubmed.ncbi.nlm.nih.gov/33128510
Autor:
Sandra F Centofanti, Gilmar de Souza Osmundo-Junior, Maria de Lourdes Brizot, Agatha Sacramento Rodrigues, Amanda B Freitas, Rossana Pulcineli Vieira Francisco
Publikováno v:
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and ObstetricsReferences. 149(3)
To evaluate risk factors associated with fetal gastroschisis.As a secondary aim of a larger case-control study, pregnant women attending the Fetal Medicine Unit at the Department of Obstetrics and Gynecology at Hospital das Clinicas, Sao Paulo Univer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bfe75635ae51fb2686992d03bae1088
https://pubmed.ncbi.nlm.nih.gov/32115707
https://pubmed.ncbi.nlm.nih.gov/32115707