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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STAT3 Transcription Factor

6 articoli — 2011-2024

RI Pagine elettroniche
Un inspirio insolito: la vocal cord dysfunction

Fracas D.

2024/3 — pag. 189-192 — DOI

The diagnosis of vocal cord dysfunction was eventually made in a 10-year-old boy with repeated self-limited episodes of inspiratory dyspnoea....

RI Pagine elettroniche
Quando il polmone ci suggerisce una immunodeficienza

Lo Scalzo L, Tumminello M, Corsello G

2024/3 — pag. 189-192 — DOI

A neonate affected by a severe respiratory infection was eventually diagnosed with severe combined immunodeficiency with hyper-IgE (Job syndrome)....

EL I Poster degli specializzandi
Accesso libero
Quando il polmone ci suggerisce una immunodeficienza

Lo Scalzo L, Tumminello M, Corsello G

2024/3 — pag. 58-58 — DOI

A neonate affected by a severe respiratory infection was eventually diagnosed with severe combined immunodeficiency with hyper-IgE (Job syndrome)....

EL I Poster degli specializzandi
Accesso libero
Un caso complesso di citopenia trilineare ed epatite gigantocellulare

Comella M, Licciardello M, Miraglia V, Russo G

2023/8 — pag. 165-165 — DOI

The case of a five-year-old boy presenting with autoimmune anaemia, neutropenia and thrombocytopenia associated to giant cell hepatitis is described. The diagnosis of ALPS-like syndrome was eventually made....

RI Percorsi clinici
La diagnosi differenziale delle malattie che si presentano con IgE alte

G. Patelli, S. Farimbella, M. Cortesi, R. Badolato

2017/1 — pag. 39-43

Elevated IgE levels (higher than 1500 UI) can be detected in multiple conditions observed in childhood, including atopic dermatitis, infectious diseases or primary immunodeficiencies. This article describes the case of a child who in the first year...

RI Pillole: per capire
Dermatite e IgE alte

R. Badolato

2011/2 — pag. 107-109

A case of Job syndrome is presented. Job syndrome is linked to a dominant autosomal disorder of the gene that codifies an intracellular protein whose function is the transduction of receptorial signals from the membrane to the nucleus. This central...