Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Lamberto Camurri"'
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Akademický článek
The contingent use of cell-free fetal DNA for prenatal screening of trisomies 21, 18, 13 in pregnant women within a national health service: A budget impact analysis.
Autor: Federico Prefumo, Davide Paolini, Giulia Speranza, Marilena Palmisano, Matteo Dionisi, Lamberto Camurri
Publikováno v: PLoS ONE, Vol 14, Iss 6, p e0218166 (2019)
ObjectiveNon-invasive prenatal testing (NIPT) based on cell-free fetal DNA (cffDNA) is highly accurate in the detection of common fetal autosomal trisomies. Aim of this project was to investigate short-term costs and clinical outcomes of the continge
Externí odkaz: https://doaj.org/article/2acc5cda08074fccba4ae11eb5438bc1
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2
The contingent use of cell-free fetal DNA for prenatal screening of trisomies 21, 18, 13 in pregnant women within a national health service: A budget impact analysis
Autor: M Dionisi, Lamberto Camurri, Federico Prefumo, Giulia Speranza, Marilena Palmisano, D Paolini
Publikováno v: PLoS ONE
PLoS ONE, Vol 14, Iss 6, p e0218166 (2019)
ObjectiveNon-invasive prenatal testing (NIPT) based on cell-free fetal DNA (cffDNA) is highly accurate in the detection of common fetal autosomal trisomies. Aim of this project was to investigate short-term costs and clinical outcomes of the continge
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e440d615e3cc0132658d2b9034a83f8
https://doi.org/10.1371/journal.pone.0218166
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3
First-trimester fetal reduction to a singleton infant or twins: Outcome in relation to the final number and karyotyping before reduction by transabdominal chorionic villus sampling
Autor: Bruno Brambati, S. Guercilena, Lamberto Camurri, Lucia Tului
Publikováno v: American Journal of Obstetrics and Gynecology. 191:2035-2040
Objective The purpose of this study was to evaluate fetal outcome and maternal complications of multifetal pregnancy reduction to a single fetus or twins. To evaluate safety and efficacy of transabdominal chorionic villus sampling for karyotyping bef
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::652e7695862385f142a236b308e99acf
https://doi.org/10.1016/j.ajog.2004.05.003
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4
Early second trimester (13 to 20 weeks) transabdominal chorionic villus sampling (TA-CVS): a safe and alternative method for both high and low risk populations
Autor: Lucia Tului, Lamberto Camurri, Bruno Brambati, S. Guercilena
Publikováno v: Prenatal diagnosis. 22(10)
Objective To assess feasibility, effectiveness and risk of prenatal diagnosis by TA-CVS at 13–14 and 15–20 weeks' gestation. Methods CVS was performed transabdominally by free-hand single needle insertion technique under continuous ultrasound vis
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a4b1f92529e8e63e8a2882d4e6a7864
https://pubmed.ncbi.nlm.nih.gov/12378575
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5
Are chromosome aberrations in circulating lymphocytes predictive of future cancer onset in humans? Preliminary results of an Italian cohort study
Autor: Angelo Abbondandolo, Daniela Vecchio, Francesca Degrassi, Leda Dal Prá, Stefano Bonassi, Alessandra Forni, Isabella Sbrana, Cecilia Lando, L. Lamberti, Lamberto Camurri, Paola Padovani, Riccardo Puntoni, Marcella De Ferrari
Publikováno v: Cancer genetics and cytogenetics. 79(2)
To investigate the existence of an association between the frequency of chromosome aberrations (CA) in non-target tissues and cancer risk, a historical cohort study was carried out in a group of 1455 subjects screened for CA over the last 20 years in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6565ac4dbbb780e0376c9598a166795
https://pubmed.ncbi.nlm.nih.gov/7889505
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6
D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p)
Autor: Giovanna Floridia, Elena Rossi, Orsetta Zuffardi, Carlo Previde Re, Maurizio Clementi, Stephen Wood, Romano Tenconi, Antonella Minelli, Paola Maraschio, Lamberto Camurri, Franca Bernardi, Cesare Danesino, Heidi Hoeller
Publikováno v: Human genetics. 92(4)
Ten patients with inverted duplication of 8p (inv dup 8p) were studied with cytogenetic, biochemical and molecular techniques. The duplication for the region 8p12-p22 was always associated with a deletion of the locus D8S7 (mapped in 8p23.1) as demon
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2544c8670e395437f800af54bec4e7a0
https://pubmed.ncbi.nlm.nih.gov/7901142
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7
A three-year follow-up on a child with low level trisomy 8 mosaicism which was diagnosed prenatally
Autor: Lamberto Camurri, Annalisa Chiesi
Publikováno v: Prenatal diagnosis. 11(1)
We report on a case of trisomy 8 mosaicism detected prenatally in a single clone of amniotic fluid culture, and confirmed on fetal blood and on peripheral lymphocytes after birth. A follow-up was performed over 3 years, showing a clinically normal fe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e379a3d0ff45b580cf8ca5e2c904abef
https://pubmed.ncbi.nlm.nih.gov/2027856
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