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Items: 1 to 20 of 139

1.
2.

A case of polimalformed fetus with a microdeletion of CTNNA3 gene.

Cancemi D, Urciuoli M, Morelli F, Lonardo MC, Lonardo V, Spampanato C, Ventruto M, Ventruto V, Sica C.

J Prenat Med. 2016 Jul-Dec;10(3-4):20-22. doi: 10.11138/jpm/2016.10.3.020.

3.

Fetal-MRI prenatal diagnosis of severe bilateral lung hypoplasia: alveolar capillary dysplasia case report.

Zirpoli S, Munari AM, Rustico M, Bulfamante G, Lista G, Spaccini L, Cesaretti C.

J Prenat Med. 2016 Jul-Dec;10(3-4):15-19. doi: 10.11138/jpm/2016.10.3.015.

4.

Conservative management in a case of uncomplicated trap sequence: a case report and brief literature review.

Pepe F, Teodoro MC, Luca C, Privitera F.

J Prenat Med. 2015 Jul-Dec;9(3-4):29-34. doi: 10.11138/jpm/2015.9.3.029.

5.

First trimester fetal anatomy study and identification of major anomalies using 10 standardized scans.

Colosi E, Musone R, Filardi G, Fabbo A.

J Prenat Med. 2015 Jul-Dec;9(3-4):24-8. doi: 10.11138/jpm/2015.9.3.024.

6.

Alpha-fetoprotein and its value for predicting pregnancy outcomes - a re-evaluation.

Darouich AA, Liehr T, Weise A, Schlembach D, Schleußner E, Kiehntopf M, Schreyer I.

J Prenat Med. 2015 Jul-Dec;9(3-4):18-23. doi: 10.11138/jpm/2015.9.3.018.

7.

Ultrasound prenatal diagnosis of congenital primary aphakia: case report.

Di Meglio F, Vascone C, Di Meglio L, Turco LC, Vitale SG, Cignini P, Valenti G, Gulino FA, Rapisarda AM, Cianci S.

J Prenat Med. 2015 Jan-Jun;9(1-2):16-7. doi: 10.11138/jpm/2015.9.1.016.

8.

A comparison between amniotic fluid index and the single deepest vertical pocket technique in predicting adverse outcome in prolonged pregnancy.

Rosati P, Guariglia L, Cavaliere AF, Ciliberti P, Buongiorno S, Ciardulli A, Cianci S, Vitale SG, Cignini P, Mappa I.

J Prenat Med. 2015 Jan-Jun;9(1-2):12-5. doi: 10.11138/jpm/2015.9.1.012.

9.

A new case of interstitial 1q 25.3-32.1 deletion: cytogenetic analysis molecular characterization and ultrasound findings.

Libotte F, Bizzoco D, Gabrielli I, Tamburrino C, Ernandez C, Carpineto L, D'Aleo MP, Cima A, Mesoraca A, Cignini P, Aloisi A, Angioli R, Vitale SG, Giorlandino C.

J Prenat Med. 2015 Jan-Jun;9(1-2):8-11. doi: 10.11138/jpm/2015.9.1.008.

10.

Supplementation with a dietary multicomponent (Lafergin(®)) based on Ferric Sodium EDTA (Ferrazone(®)): results of an observational study.

Cignini P, Mangiafico L, Padula F, D'Emidio L, Dugo N, Aloisi A, Giorlandino C, Vitale SG.

J Prenat Med. 2015 Jan-Jun;9(1-2):1-7. doi: 10.11138/jpm/2015.9.1.001.

11.

Management, prognosis and reproductive outcomes of borderline ovarian tumor relapse during pregnancy: from diagnosis to potential treatment options.

Cosentino F, Turco LC, Cianci S, Fanfani F, Fagotti A, Alletti SG, Vizzielli G, Vitale SG, Laganà AS, Padula F, Coco C, Pisconti S, Scambia G.

J Prenat Med. 2016 Jan-Jun;10(1-2):8-14. doi: 10.11138/jpm/2016.10.1.008. Review.

12.

Congenital high airway obstruction syndrome (CHAOS): discussing the role and limits of prenatal diagnosis starting from a single-center case series.

D'Eufemia MD, Cianci S, Di Meglio F, Di Meglio L, Di Meglio L, Vitale SG, Laganà AS, Chiofato B, Rapisarda AMC, Padula F, La Rosa V, Coco C, Vascone C.

J Prenat Med. 2016 Jan-Jun;10(1-2):4-7. doi: 10.11138/jpm/2016.10.1.004. Review.

13.

US-color Doppler early diagnosis of uterine rupture with protrusion of umbilical cord.

Del Vecchio V, Chincoli A, Caradonna F, Vimercati A.

J Prenat Med. 2016 Jan-Jun;10(1-2):1-3. doi: 10.11138/jpm/2016.10.1.001.

14.

Six consecutive false positive cases from cell-free fetal DNA testing in a single referring centre.

Dugo N, Padula F, Mobili L, Brizzi C, D'Emidio L, Cignini P, Mesoraca A, Bizzoco D, Cima A, Giorlandino C.

J Prenat Med. 2014 Jan-Mar;8(1-2):31-5.

15.

Level of C - reactive protein as an indicator for prognosis of premature uterine contractions.

Najat Nakishbandy BM, Barawi SA.

J Prenat Med. 2014 Jan-Mar;8(1-2):25-30.

16.

Next generation sequencing in the identification of a rare genetic disease from preconceptional couple screening to preimplantation genetic diagnosis.

Dello Russo C, Di Giacomo G, Mesoraca A, D'Emidio L, Iaconianni P, Minutolo E, Lippa A, Giorlandino C.

J Prenat Med. 2014 Jan-Mar;8(1-2):17-24.

17.

Newborns with congenital heart diseases: epidemiological data from a single reference center in Brazil.

Silva KP, Rocha LA, Leslie AT, Guinsburg R, Silva CM, Nardozza LM, Moron AF, Araujo Júnior E.

J Prenat Med. 2014 Jan-Mar;8(1-2):11-6.

18.

Introducing the next generation sequencing in genomic amnio and villuos sampling. The so called "Next Generation Prenatal Diagnosis" (NGPD).

Giorlandino C, Mesoraca A, Bizzoco D, Dello Russo C, Cima A, Di Giacomo G, Cignini P, Padula F, Dugo N, D'Emidio L, Brizzi C, Raffio R, Milite V, Mangiafico L, Coco C, Carcioppolo O, Vigna R, Mastrandrea M, Mobili L.

J Prenat Med. 2014 Jan-Mar;8(1-2):1-10. No abstract available.

19.

Antenatal diagnosis of Seckel Syndrome: a rare case report.

Vascone C, Di Meglio F, Di Meglio L, Turco LC, Vitale SG, Cignini P, Marilli I, Rapisarda AM, Valenti G, Cianci S.

J Prenat Med. 2014 Apr-Jun;8(3-4):70-2.

20.

Comparative study of aCGH and Next Generation Sequencing (NGS) for chromosomal microdeletion and microduplication screening.

Russo CD, Di Giacomo G, Cignini P, Padula F, Mangiafico L, Mesoraca A, D'Emidio L, McCluskey MR, Paganelli A, Giorlandino C.

J Prenat Med. 2014 Apr-Jun;8(3-4):57-69.

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