Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marilisa Salemi"'
Autor:
Giuseppina Colonna-Romano, Vito M. R. Muggeo, Francesco Arcoleo, Marilisa Salemi, V. Mandalà, Salvatore Milano, Gabriella Misiano, Enrico Cillari
Hereditary angioedema (HAE) is a rare autosomal dominant disorder, due to C1-inhibitor deficiency, which causes episodic swellings of subcutaneous tissues, bowel walls and upper airways which are disabling and potentially life-threatening. We evaluat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53619fe625a3f725c8cbe6650be3cf84
http://hdl.handle.net/10447/224470
http://hdl.handle.net/10447/224470
Publikováno v:
La Rivista Italiana della Medicina di Laboratorio - Italian Journal of Laboratory Medicine. 8:131-137
L’angioedema ereditario e causato da una carenza genetica di C1-inibitore, fattore che regola una serie di pathways infiammatori. I pazienti affetti da HAE hanno crisi intermittenti caratterizzate da edemi cutanei o mucosali legati a un malfunziona
Autor:
Marco Cicardi, Francesco Arcoleo, Francesca Di Bella, Roberto Perricone, Antonino Miragliotta, Valentina Selvaggio, Maria Domenica Guarino, Andrea Zanichelli, Marilisa Salemi, Enrico Cillari
Publikováno v:
Journal of Psychology & Psychotherapy.
Objectives: Hereditary Angioedema (HAE) is a rare serious medical condition caused by a deficiency of C1-inhibitor, due to mutations in its structural gene. The disease appears clinically as cutaneous swelling of the extremities, face, genitals, and
Autor:
Antonio La Porta, Salvatore Milano, Marilisa Salemi, Gabriella Misiano, Valentina Selvaggio, Giuseppina Colonna Romano, Francesco Arcoleo, Vitalba Mandalà, Vito M. R. Muggeo, Enrico Cillari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6934430c1e83517859a7c751be98fa3
http://hdl.handle.net/10447/99916
http://hdl.handle.net/10447/99916