Developmental Disabilities

La sindrome di Koolen-De Vries

Bergo E, Selicorni A.

2026/3 — pag. 179-181 — DOI

La sindrome di Malan

Ramazzotti S, Nuvoli V, Baldo F.

2026/2 — pag. 114-117 — DOI

"Amici per la pelle": un caso di leishmaniosi

Fantasia M, Vecchi M, Cavalleri L, Bruni F, Provenzi M

2025/4 — pag. 81-85 — DOI

Leishmaniasis is an infectious disease caused by protozoa of the Leishmania genus, parasites of humans and several domestic and wild animals, and transmitted via vectors. The authors describe the case of an 18-month-old girl, presenting to the Emerge...

Cosa deve sapere il pediatra sui DSA Intervista ad Antonella Gagliano, neuropsichiatra infantile

2024/8 — pag. 525-527 — DOI

La sindrome di Sotos

Scupilliti S, Selicorni A.

2024/2 — pag. 113-115 — DOI

Lo spettro della sindrome Cornelia de Lange

Prada E, Mariani M, Selicorni A.

2023/3 — pag. 183-185 — DOI

Sindrome dell’X fragile

Carrer A, Mariani M, Selicorni A.

2023/2 — pag. 119-120 — DOI

L’integrazione di differenti prospettive sullo sviluppo del bambino: l’osservazione del genitore e quella del pediatra

Clavenna A, Segre G, Roberti E, Costantino I, Scarpellini F, Tessarollo V, Bonati M

2023/1 — pag. 55-58 — DOI

Objective - To assess the feasibility of a shared approach that combines the clinical expertise of family paediatricians and the perspectives of parents in the early identification of potential disorders in children using standard clinical practice t...

L’integrazione di differenti prospettive sullo sviluppo del bambino: l’osservazione del genitore e quella del pediatra

Clavenna A, Segre G, Roberti E, Costantino I, Scarpellini F, Tessarollo V, Bonati M

2023/1 — pag. 1-3 — DOI

Objective - To assess the feasibility of a shared approach that combines the clinical expertise of family paediatricians and the perspectives of parents in the early identification of potential disorders in children using standard clinical practice t...

Uno sguardo al neurosviluppo raggiunto ai 2 anni di età

Segre G, Costantino I, Scarpellini F, Tessarollo V, Clavenna A, Bonati M.

2022/5 — pag. 313-323 — DOI

When a child develops a psychological disorder, even a mild one, early diagnosis is essential to provide a timely and appropriate intervention that can improve the child’s symptoms and development. Early identification can prevent consequences of dif...

L’omocistinuria classica in età pediatrica

Ravaglia A, Costagliola G, Spada M

2021/10 — pag. 309-313 — DOI

Classical homocystinuria is an inborn error of methionin metabolism. It is characterized by an accumulation of homocysteine, due to a deficiency of the enzyme involved in its metabolism, namely cystathionine beta synthase. If not treated, the increas...

Cosa deve sapere ogni pediatra sulla comunicazione aumentativa alternativa (CAA)

C. La Manna, I. Prina, M. Cavalleri, P. Conti, A. Selicorni

2020/8 — pag. 513-517 — DOI

Augmentative Alternative Communication (AAC) is an area of clinical practice that tries to compensate for the temporary or permanent disability of individuals with complex communication needs. It uses gestures or signs and images and utilises a doubl...

Sindrome dello spettro autistico: il vomito rivelatore

A. Velkoski

2020/7 — pag. 195-195 — DOI

Guide for Monitoring Child Development

G. Tamburlini, I. Ertem

2019/2 — pag. 91-96

Monitoring and promoting early child development is an increasingly important task of paediatric primary care services. There is consensus that the most effective approach includes both longitudinal surveillance and monitoring rather than one-shot ...

Sindrome di Prader-Willi

P. Cianci, A. Bosco, M. Ferrario, A. Selicorni

2019/1 — pag. 49-51

Spettro autistico: M-CHAT o M-CHAT R/F I medici non leggono più riviste scientifiche? Il dibattito Il consenso informato e la recente legislazione italiana Il sorriso di Giannina

2018/7 — pag. 420-422

La sindrome di Williams

A. Fornari, P. Cianci, A. Selicorni

2018/2 — pag. 111-113

Screening per i disordini del neurosviluppo

2017/9 — pag. 591-592

La sindrome CHARGE

S. Tajè, P. Cianci, A. Selicorni

2017/9 — pag. 585-586

Diagnosi precoce dei disturbi dello spettro autistico

R. Devescovi, L. Monasta, A. Mancini, M. Bin, C. Zago, M. Carrozzi, Gruppo Terapisti ESDM - Trieste e Gorizia

2017/8 — pag. 511-517

Background - Early diagnosis combined with an early intervention programme, such as the Early Start Denver Model (ESDM), can positively influence the early natural history of autism spectrum disorders. This study evaluated the effectiveness of an e...

Sviluppo precoce del bambino e pediatriadello sviluppo

G. Tamburlini, A. Alushaj, E. Flaugnacco, T. Gerarduzzi

2016/6 — pag. 365-372

Families are encountering increasing difficulties in receiving information and advice regarding both typical and atypical development of young children. Primary care paediatricians should be able to assess and promote early child development and to...

Fetal alcohol syndrome sì, fetal alcohol syndrome no, fetal alcohol syndrome un cavolo!

L. Longoni, S. Maitz, A. Cereda, M. Mariani, F. Crosti, A. Selicorni

2016/4

La sindrome feto-alcolica: un approccio clinico per il pediatra

L. Tarani, M. Martini, F, Marolla, M. Fiore, M. Ceccanti

2015/2 — pag. 87-93

Fetal alcohol syndrome (FAS) is a complex malformative condition due to the teratogenic effect of alcohol consumed during pregnancy. Several epidemiological studies have shown that maternal alcohol use during pregnancy is the most common preventabl...

Non sempre l’appetito è indice di “benessere”

C. Cubaiu, G. Masia

2013/7

Cosa deve sapere il pediatra delle sindromi

A. Selicorni

2013/2 — pag. 114-115

I disturbi del neurosviluppo

C. Calzone

2012/7 — pag. 444-447

In clinical practice the onset of a new pathology mostly draws the patients’ and physician’s attention. New manifestations that interrupt the pre-existing healthy condition of a child are easily noticed by their parents or paediatricians, but the b...

Guida pratica per il bambino con sindrome di Prader-Willi

G. Tornese, S. Pastore, G. Tonini

2012/3 — pag. 195-196

Although Prader-Willi syndrome is a rare disease, it provides an excellent example of how early diagnosis and meticulous management can significantly improve long-term prognosis of some genetic diseases. These guidelines, particularly addressed t...

Il ruolo del pediatra nella cura del bambino con autismo

C. Raffin

2012/3 — pag. 174-177

Guida pratica per il bambino con sindrome di Prader-Willi

G. Tornese, S. Pastore, G. Tonini

2012/3

Although Prader-Willi syndrome is a rare disease, it provides an excellent example of how early diagnosis and meticulous management can significantly improve long-term prognosis of some genetic diseases. These guidelines, particularly addressed to fa...

Prevenzione dei disturbi dello sviluppo del bambino

M. Guerriero, M. Faberi, S. Bush, M. Sandri, M. Castagnini

2011/5

Introduction: The literature and current experience tend to doubt the usefulness of the psychomotor rehabilitation in the cases of pre-perinatal neurodamage. The characteristics of brain development undoubtedly indicate that the first year of life an...

Il ruolo del pediatra nell’individuazione dei segni premonitori dell’autismo

S. Cremaschi, E. Alberini, G. Zappulla

2008/8 — pag. 504-509

Autism is a syndrome caused by a biologically determined developmental disorder. It develops in the first years of life and it mainly affects mutual social interaction, the ability of communicating ideas and emotions and of establishing relationshi...

I gemelli: eterogeneità clinica e approccio multidisciplinare

E. Piro, G. Corsello

2008/6 — pag. 375-380

The incidence of multiple pregnancy has increased during the last 15 years, particularly in relation to the advances in assisted reproductive technologies. Twins are conceived in about 1 in 80 pregnancies. Multiple gestations are high risk pregnanc...

Outcome della nascita pretermine: una breve review

M. Chiavarini, L. Minelli

2008/4 — pag. 235-238

In the last twenty years the survival of the premature babies has improved. The obstetricneonatal care has been effective in increasing survival among prematures, unfortunately they are not so effective to reduce the outcomes among the survivors (p...

Autismo e medicine alternative

D. Mariani Cerati, C. Hanau

2005/7 — pag. 465-468

Autism is an oligogenic disease, the phenotipic expression of which depends on post-conceptional factors not yet identified. To identify these factors, as well as possible palliative treatments, is among the expectations of parents of autistic chil...

La neuropsichiatria infantile nell’ultimo decennio

F. Bouquet, P. Costa, M. Paci

2001/7 — pag. 429-434

The article offers an overview of the most important advances of the neuro-sciences over the last 10 years and discusses some of their implications for child neurology and psychiatry. Particular emphasis is given to the progress in the management o...

Marco

R. Salvadori

2000/7 — pag. 460-462

La carenza di ferro Parte II: Clinica, prevenzione e terapia

C. Vullo

1998/6 — pag. 359-374

Part II of the review on iron deficiency (ID) is devoted to clinical manifestations, prevention and treatment. Pallor and fatigue are increasingly rare as presenting signs and symptoms of ID in industrialized countries. More subtle conditions su...