diagnosi prenatale

Diagnosi e gestione precoce del neonato con familiarità per disordine congenito dell'immunità

Laudante U, Falco G, Ferrandino C, Romano AC, Turchetti F, Romano R, Giardino G

2026/1 — pag. 23-23 — DOI

This study examines the role of early diagnosis in managing inborn errors of immunity, which are often characterised by early onset and high mortality. By analysing data from 15 patients with a positive family history, the research evaluated the util...

Fidarsi o non fidarsi del test prenatale non invasivo. Riflessioni a partire da un caso di falso negativo

Neirotti A, Bombaci S, Rubino C

2024/9 — pag. 183-186 — DOI

Non-invasive prenatal testing (NIPT) is a screening for foetal chromosomal abnormalities that identifies at-risk pregnancies and is used to propose a possible invasive genetic confirmation testing in case of its positive results. For Down syndrome (t...

Un vomito tanto precoce: la spia di un’atresia intestinale

G. Ferrara, T. Stampalija, D. Codrich, C. Simionato, A. Taddio, L. Travan

2016/4 — pag. 259-261

Small bowel atresia is a congenital obstruction of the lumen of the duodenum, jejunum or ileum and is one of the most common causes of neonatal bowel obstruction. It usually arises with vomiting in the first 48 h of life, but more and more frequen...

La diagnosi prenatale... ci azzecca sempre?

A. Barachino

2014/8

La falsa sicurezza dell’amniocentesi

F. Marolla

2014/1 — pag. 49-51

L’etica in medicinaIntervista a Sandro Spinsanti

2011/6 — pag. 387-388

La fibrosi cistica, lo screening neonatalee lo screening del portatore Intervista a Carlo Castellani

2011/3 — pag. 180-181

Dalla diagnosi prenatale al management post natale delle malformazioni polmonari: suggerimenti per i pediatri

F. Gobbo, G. Pelizzo, J. Schleef

2010/2

Dalla diagnosi prenatale al management post-natale delle malformazioni polmonari

F. Gobbo, G. Pelizzo, J. Schleef

2010/2 — pag. 125-126

Congenital pulmonary airway malformations (CPAM) include a wide spectrum of developmental anomalies. Almost 50% of the cases are diagnosed in utero. These appear as hyperechoic, cystic or mixed lesions. Prenatal clinical course varies from seriou...

Talassemia e bambini non natiCure semi-intensive e bisogni di salute inevasiFluoro nelle falde acquifere

2009/1 — pag. 13-15

Le prove di laboratorio per la diagnosi di toxoplasmosi congenita

2001/5

IL DESTINO NEL DNAI geni della felicità

M.C. Fulchignoni, L. Greco

2001/1 — pag. 20-29

The genes of happiness are the best candidates for coding dopamine receptors, whereas the genes of sadness are the best candidates for coding serotonin metabolism and re-uptake. In fact, several studies on separately grown homozygous twins demonstr...

Fenilchetonuria materna

G. Nassimbeni

1997/4 — pag. 251-253