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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Histocompatibility Antigens

Biological Factors Antigens Antigens, Surface Histocompatibility Antigens

31 articoli — 1997-2025 Include sottocategorie MeSH

RI Aggiornamento
Le spondiloartropatie giovanili

Ballaben A, Vrinceanu A, Pastore S, Taddio A.

2025/9 — pag. 563-567 — DOI

Juvenile spondyloarthropathies (JSpA) are a heterogeneous group of chronic inflammatory diseases, including enthesitis-related arthritis (ERA), juvenile psoriatic arthritis (JPsA) and undifferentiated arthritis. Many clinical features overlap with ot...

EL I Poster degli specializzandi
Accesso libero
Dal rene all'occhio: che cos'è la TINU?

Sapienza GM, Greco M, Cardilicchia M, Lo Scalzo L, Spallino E, Corrado C, Pavone G, Cusumano R, Sapia MC, D'Alessandro MM, Corsello G

2024/26 — pag. 2-2 — DOI

An eight-year-old boy presenting with interstitial nephritis (abdominal pain, microhematuria, glycosuria, proteinuria, elevated urinary beta2-microglobulin levels) was eventually diagnosed with TINU syndrome (tubulointerstitial nephritis associated w...

RI Digest
Cellule CAR T: universo in espansione

Moretti A, Biondi A.

2024/5 — pag. 309-312 — DOI

RI Rubrica iconografica
Il dolore alla schiena in un adolescente

Bontempo C, Lama C, Mambelli L, Feletti F, Lotta C, Marchetti F.

2023/2 — pag. 116-118 — DOI

EL I Poster degli specializzandi
Accesso libero
A caval donato... guarda anche in bocca!

Gustuti V

2022/5 — pag. 114-114 — DOI

A 15-year-old girl with vulvar ulcers previously attributed to recurrent herpetic infection is presented. Aphthous oral ulcers were also present and the diagnosis of Behçet disease was eventually made....

EL I Poster degli specializzandi
Accesso libero
Non ti scordar del tubulo: la malattia di Dent

Benvenuto S, Bossini B

2022/5 — pag. 112-112 — DOI

The case of a 12-year-old boy with proteinuria, microhaematuria and nephrocalcinosis with normal glomerular function is described. A diagnosis of Dent disease was eventually made and confirmed by the genetic test....

RI Linee guida
Le nuove linee guida ESPGHAN 2020 per la diagnosi di celiachia: passo dopo passo

Mandile R, Auricchio R.

2022/1 — pag. 26-28 — DOI

In 2020 new guidelines for the diagnosis of paediatric coeliac disease were published by the ESPGHAN Society. Just one algorithm is indicated for both symptomatic and asymptomatic patients, HLA haplotype typing is no more suggested and anti-tissue tr...

RI Percorsi clinici
Una PFAPA che diventa un Behçet

Cafolla C, Iacono A, Guiducci C, Mambelli L, Marchetti F

2021/4 — pag. 226-229 — DOI

PFAPA syndrome (periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis) is the most common periodic fever syndrome in children. The disease appears to cluster in families, but the pathogenesis is unknown. The paper reports the descrip...

EL Casi indimenticabili
Ancora il ribollir del TINU

A. Filpo

2016/8

RI Focus
La diagnosi e il follow-up della celiachia

Tavolo Tecnico del Ministero della Salute

2016/3 — pag. 159-176

RI Focus
CELIACHIA 2016: DALLA TEORIA ALLA PRATICA

2016/3 — pag. 159-176

EL I Poster degli specializzandi
Accesso libero
Il difetto di IgA: da un’analisi clinico-epidemiologica alla proposta di un protocollo ospedaliero

I. Della Libera

2013/10

EL Casi indimenticabili
Una strana vulvovaginite ricorrente

F. De Maddi, F. Pellegrini, R. Sottile, R. Dinardo

2013/9

EL Contributi Originali - Ricerca
Accesso libero
Cercare la celiachia con il test rapido: l'esperienza brasiliana

S. Crovella, L. Brandao, R. Guimaraes, J. de Lima Filho, L.C. Arraes, A. Ventura, T. Not

2008/6

RI Aggiornamento monografico
Le spondiloartropatie in età pediatrica

A. Lenhardt e collaboratori

2006/7 — pag. 429-437

Spondyloarthropathies are a heterogeneous group of morbid conditions, characterized by familiarity, by their association with specific HLA and by extra-articular localisations. In the present article the different morbid conditions, their most recent...

RI Focus
Screening e malattia celiaca

T. Not

2005/7 — pag. 449-455

From the clinical and the epidemiological point of view, celiac disease may represent an appropriate disease model to apply a population based screening strategy. In the literature, the use of human tTG antibodies is described as an efficient scree...

EL Caso Clinico Interattivo
Accesso libero
Diabete insulino-dipendente in fase di cattivo controllo

M. Lazzerini

2003/9

EL Caso Clinico Interattivo
Accesso libero
Diabete insulino-dipendente in fase di cattivo controllo

M. Lazzerini

2003/9

RI Focus
Malattie cutanee autoimmuni e genoma

V. Leone, F. Panizon

2003/4 — pag. 235-241

Some auto-immune skin diseases are heritable. The most common among these is psoriasis, which has an incidence of 15% if one parent is affected and of 50% if both parents are affected. Six loci (PSORS 1 to 6) are involved, and the main one (PSORS 1...

RI Focus
Accesso libero
Celiachia e autoimmunità

A. Ventura

1998/2 — pag. 98-101

RI Focus
Accesso libero
Celiachia: diagnosi genetica?

L. Greco, B. Di Caprio

1998/2 — pag. 96-101

RI Editoriali
Accesso libero
Autoimmunità, transglutaminasi tissutale e malattia celiaca

M. Maki

1998/2 — pag. 75-77