Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
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neonatal screening

62 articoli — 1997-2025

RI Articolo speciale
Screening genomici neonatali: opportunità e sfide etiche

De Curtis M.

2025/10 — pag. 643-645 — DOI

Neonatal screening is one of the most significant achievements in preventive medicine that enables the early detection and treatment of many rare metabolic and genetic disorders. The introduction of exome (WES) and genome (WGS) sequencing now offers ...

RI Pagine elettroniche
Un caso di FPIES in paziente alimentata con latte di formula per galattosemia

Fumagalli R, Crescitelli V, Barzaghi S, Pretese R, Lazzerotti A, Gasperini S.

2024/9 — pag. 597-600 — DOI

Soy-derived proteins are a known trigger for Food Protein Induced Enterocolitis Syndrome. The authors present the case of a sly onset of chronic FPIES in a newborn fed by soy-based formula. The baby’s nutrition was switched to infant formula to avoid...

EL Caso contributivo
Un caso di FPIES in paziente alimentata con latte di formula per galattosemia

Fumagalli R, Crescitelli V, Barzaghi S, Pretese R, Lazzerotti A, Gasperini S

2024/9 — pag. 168-170 — DOI

Soy-derived proteins are a known trigger for Food Protein Induced Enterocolitis Syndrome. The authors present the case of a sly onset of chronic FPIES in a newborn fed by soy-based formula. The baby’s nutrition was switched to infant formula to avoid...

EL I Poster degli specializzandi
Accesso libero
Anticipare il futuro (di circa otto anni) per provare a cambiarlo

Di Cataldo G, Gauci MC, Gammeri C, Dierna F, Ferrera G, Gambilonghi F, Meli C

2024/7 — pag. 141-141 — DOI

A 14-day-old infant was diagnosed with classical homocystinuria through extended newborn screening after detecting hypermethioninemia and elevated homocysteine levels. The infant exhibited feeding difficulties and poor general health. Following a low...

EL Ricerca
Infezione congenita da citomegalovirus e ipoacusia

Gambacorta V, Orzan E, Lapenna R, Ricci G

2022/10 — pag. 195-199 — DOI

Background - Cytomegalovirus (CMV) infection is the most common of congenital infections, with a prevalence of 0.3-1.2% in industrialized countries and is the most frequent non-genetic cause of permanent hearing loss in children, with an incidence ra...

RI Problemi speciali
AAA tiroide cercasi

A. Trombetta, G. Tamaro, F. Alberti, G. Tornese

2019/9 — pag. 573-576

The paper presents the case of a newborn with congenital hypothyroidism and iatrogenic hyperthyroidism after replacement treatment at proper dosage was started. Laboratory findings suggested the diagnosis of ectopic thyroid gland that was confirmed...

EL Casi indimenticabili
Galattosemia e lieto fine: importanza dello screening neonatale allargato

L. Pecoraro, E. Rigotti, A. Dianin, G. Gugelmo, G. Rodella, I. Monge, E. Tadiotto, M. Clemente, A. Bordugo

2019/1 — pag. 12-12

RI Editoriali
La fibrosi cistica nel 2017

B.M. Assael

2017/2 — pag. 75-77

RI Pediatria flash
Glutarico-aciduria di tipo 1

V. Carrato

2017/1 — pag. 44-46

RI Casi indimenticabili
Persone dietro lo screening... per la fibrosi cistica

G. Boschi

2016/9 — pag. 596-598

EL I Poster degli specializzandi
Accesso libero
Screening e sorveglianza dell’ipoacusia in Friuli Venezia Giulia

M. Gregori

2016/6

EL Casi indimenticabili
Un colpo d’occhio… siculo

M.C. Lia, I. Giuseppin, A. Tonetto, P.G. Flora

2015/7

RI Aggiornamento
Ipoacusia infantile permanente

E. Orzan, E. Ciciriello, R. Marchi, F. Ruta, F. Ceschin, C. Marchese, C. Falzone, G. Canteri, P. Bolzonello

2014/6 — pag. 361-368

Newborn hearing screening programmes, voluntarily carried out or regulated by regional norms, have developed themselves into a standardized health organization system in several Italian regions in a few years. Hospital-based programmes are generall...

EL Caso contributivo
Diagnosi di malattia di Pompe nel neonato

C. Amador, M. Sacchini, E. Agostini, E. Procopio, E. Laudani, P. Fiorini

2014/6

Pompe disease is an autosomal recessive storage disorder caused by a deficiency in the enzyme α-glucosidase, resulting in intralysosomal glycogen accumulation in skeletal and cardiac muscle. The classic infantile form is characterized by progres...

RI Casi indimenticabili
La fibrosi cistica al tempo dello screening

F. Marchetti, G. Vieni, F. Pugliese, I. Venturi, V. Poletti, M. Ambroni, F. Battistini

2014/1 — pag. 49-51

EL Casi indimenticabili
Uno screening traditore

I. Giuseppin

2011/9

RI Pediatria flash
La fenilchetonuria

2010/7 — pag. 461-462

EL Appunti di Terapia
Accesso libero
Il riflesso rosso nel neonato, nel lattante e nel bambino

G. Bartolozzi

2009/1

RI Linee guida
Accesso libero
Il test del sudore

A CURA DELLA SOCIETÀ ITALIANA FIBROSI CISTICA

2007/8 — pag. 512-516

The quantitative measurement of sweat electrolytes following stimulation by pilocarpine iontophoresis remains the gold standard for the diagnosis of both classical, atypical forms of CF and the so called CF related diseases also in the genomic era. I...

EL Protocolli di diagnosi e terapia
Accesso libero
Le Raccomandazioni italiane sul Test del Sudore

A cura della Società Italiana Fibrosi Cistica

2007/7

EL Pediatria per l'ospedale
Accesso libero
Il Neuroblastoma (parte prima)

G. Bartolozzi

2007/7

EL Contributi Originali - Ricerca
Accesso libero
Screening per la displasia evolutiva dell'ancaImpatto sull'outcome diagnostico e terapeutico su una popolazione di 6152 bambini

E. Mazzoleni, F. Braga, R. Pelizzari

2007/1

RI Pagine elettroniche ; Ricerca
Screening per la displasia evolutiva dell’anca

E. Mazzoleni, F. Braga, R. Pelizzari

2007/1 — pag. 51-53

Developmental Dysplasia of the Hip (DDH) is the most important congenital deformity with regard to its incidence, functional and aesthetical consequences and treatment difficulties. The objective of our study was to evaluate a population-based scr...

RI Focus
Quello che un pediatra deve sapere sulla fibrosi cistica

G. Magazzù e collaboratori

2006/3 — pag. 155-173

The medical care of the patient with CF is ideally carried out with the joint efforts of the CF Center specialists and the patient’s primary care physician (PCP). The implementation of a nation-wide neonatal screening may represent a unique opportuni...

RI Aggiornamento monografico
Sindrome adreno-genitale congenita da deficit di 21-idrossilasi

A. Balsamo, A. Cicognani

2005/5 — pag. 293-301

Congenital adrenal hyperplasia (CAH) refers to a group of inherited disorders of adrenal steroidogenesis. More than 90% of CAH is due to 21-hydroxylase deficiency (21-OH-D), found in 1:10.000 to 1:15.000 live births as classical form and detected i...

EL Seminari degli specializzandi
Accesso libero
L'ipotiroidismo dalla nascita in poi

I. Berti, I. Giuseppin, R. Meneghetti

2005/3

RI ABC
Il test del sudore

V. Kiren, L. Travan, E. Barth

2004/9 — pag. 573-577

RI Editoriali
La legge inversa dell’evidenza

G. Tamburlini

2003/1 — pag. 7-8

EL Contributi Originali - Ricerca
Accesso libero
Lo screening uditivo neonatale: un'esperienza a misura di Nido

M. C. Alberelli, L. Pavanello, E. Orzan.

2002/5

RI Pagine elettroniche
Accesso libero
Lo screening uditivo neonatale: una esperienza a misura di Nido

2002/5 — pag. 325-326

Report of an otoacoustic emissions screening carried out at a nursery. The cost calculated for each case of deep hearing loss identified at birth ranges from 1200 to 2400 Italian euro....

RI Aggiornamento monografico
Accesso libero
L’ipotiroidismo congenito

G. Tonini, M. Lazzerini

1999/8 — pag. 481-488

The incidence of Primary Congenital Hypothyroidism (PCH) is about 1:2000. Most cases are due to a dysgenetic/ectopic thyroid. Only in a small minority of cases a defect in the iodine metabolism is present. Congenital hypothyroidism secondary to a d...

RI Organizzazione sanitaria
Accesso libero
I tre paradossi della dimissione precoce

D. Baronciani, R. Bellu’, R. Zanini

1999/3 — pag. 181-183

The evidence on the health consequences of early newborn discharge are reviewed. Most of the studies on early discharge are aimed at showing that early discharge is safe and that no serious negative side effects are produced, rather than showing an...

EL Contributi Originali - Casi contributivi
Accesso libero
Fibrolipomatosi precalcaneale congenita:una curiosità che deve essere riconosciuta a prima vista

M. Cutrone

1999/1

RI Aggiornamento monografico
Accesso libero
La displasia evolutiva dell’anca

G. Atti, P. Farina, P. Varni

1998/7 — pag. 431-438

Developmental dysplasia of the hip (DDH) describes a wide range of hip abnormalities, from a shallow acetabulum to a dislocated hip. The abnormality can be present at birth but also occur at later stages. Without therapy, patients with completel...

RI Screening: luci e ombre
Accesso libero
Appunti per una nuova rubrica

D. Baronciani

1998/2 — pag. 109-112

RI Prevenzione
Accesso libero
A proposito dello screening uditivo

S. Chiappe

1997/3 — pag. 180-182

Although a screening approach is widely accepted as the method of choice for early detection of hearing loss in infants, in spite of recurring proposals of new methods, the “ideal” procedure has not yet been found. Thus, only limited success has...