GTP Phosphohydrolases

Diagnostica ambulatoriale nella gestione delle infezioni respiratorie acute nelle cure primarie pediatriche

Reggiani L.

2025/9 — pag. 573-582 — DOI

In recent years, the possibility of performing diagnostic tests in the physician’s office (Point of Care) has made countless advances: both in the etiological investigation of viruses or bacteria through pharyngeal or nasopharyngeal swabs or via bloo...

Macrotrombocitopenia, dismorfismi facciali e ritardo dello sviluppo psicomotorio: alla scoperta del gene CDC42

Fabbri E, Giardinelli S, Filippini B, Gasperini P, Mazzocco M, Radice C, Marchetti F, Pericoli R

2022/9 — pag. 181-186 — DOI

Cell Division Control 42 (CDC42) gene encodes for a small GTPase with a fundamental role in controlling intracellular signaling pathway. Gene mutations can cause different phenotypic manifestations, which reflect the variety of the role of this media...

Sindrome di Costello

C. Leoni, P. Cianci, G. Zampino, A. Selicorni

2019/6 — pag. 383-386

Troppo stanca troppo presto: la leucemia mielomonocitica giovanile

S. Contorno

2019/4 — pag. 95-95

Un’impensata pubertà

L. Baggio, M. Mauro, P. Cavarzere

2017/2

Inspiegabili bernoccoli

M.C. Pellegrin, A. Delise, D. Sanabor, E. Faleschini, I. Bruno

2015/3 — pag. 193-195

Fibrous dysplasia (FD) is a nonhereditary benign condition in which medullary bone is replaced by immature bone and fibrous tissue. It accounts for 7% of all benign bone tumours and usually presents in the first three decades of life. FD arises f...

Inspiegabili bernoccoli

M.C. Pellegrin, A. Delise, D. Sanabor, E. Faleschini, I. Bruno

2015/3

Fibrous dysplasia (FD) is a nonhereditary benign condition in which medullary bone is replaced by immature bone and fibrous tissue. It accounts for 7% of all benign bone tumours and usually presents in the first three decades of life. FD arises f...

Displasia fibrosa poliostotica

E. Benelli, G. Tornese, M. Maschio

2015/1

Eteroplasia ossificante progressiva: una nuova mutazione del gene GNAS1 e rassegna della letteratura

S. Mattia, G. Mantovani, N. Guaraldi, R. Pagano, A. Venuta, P. Ferrari

2008/3 — pag. 193-194

Progressive osseous heteroplasia (PHO) is a recently described genetic disorder of mesenchymal differentiation characterized by dermal ossification during infancy and by progressive heterotopic ossification of cutaneous, subcutaneous and deep con...

Eteroplasia ossificante progressiva: una nuova mutazione del gene GNAS1 e review della letteratura

S. Mattia, G. Mantovani, N. Guaral, R. Pagano, A. Venuta, P. Ferrari

2008/3

Inibizione dell'apoptosi da parte degli anticorpi monoclonali umani anti-transglutaminasili

A. Tommasini, M. Soban, I. Berti, C. Trevisiol, E. Panfili, D. Santon, V. Baldas, E. Fragonas

2000/6