Risultati ricerca pubblicazioni

The burden of common variable immunodeficiency disorders: a retrospective analysis of the European Society for Immunodeficiency (ESID) registry data

pubblicato su: ORPHANET JOURNAL OF RARE DISEASES - 2018

Odnoletkova Irina, Kindle Gerhard, Quinti Isabella, Grimbacher Bodo, Knerr Viviane, Gathmann Benjamin, Ehl Stephan, Mahlaoui Nizar, Van Wilder Philippe, Bogaerts Kris, de Vries Esther

Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations

pubblicato su: ORPHANET JOURNAL OF RARE DISEASES - 2019

Calcagni G., Digilio M. C., Marino B., Tartaglia M.

Ocular manifestations in Gorlin-Goltz syndrome

pubblicato su: ORPHANET JOURNAL OF RARE DISEASES - 2019

Moramarco A., Himmelblau E., Miraglia E., Mallone F., Roberti V., Franzone F., Iacovino C., Giustini S., Lambiase A.