Sfoglia per AUTORE
DELLEPIANE RM
Collezione AOU Novara
Items : 3
Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family. in Medicina (Kaunas, Lithuania) / Medicina (Kaunas). 2020 Mar 10;56(3):120. doi: 10.3390/medicina56030120.
2020
AOU Novara
AOU Novara
Dellepiane RM; Baselli LA; Cazzaniga M; Lougaris V; Macor P; Giordano M; Gualtierotti R; Cugno M;
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome. in The journal of allergy and clinical immunology. In practice / J Allergy Clin Immunol Pract. 2019 Sep-Oct;7(7):2369-2376. doi: 10.1016/j.jaip.2019.03.014. Epub 201
2019
AOU Novara
AOU Novara
Martire B; Duse M; Gattorno M; Consolini R; Dellepiane RM; Bossi G; Azzari C; Baselli LA; Volpi S; Ricci S; Giardino G; Leonardi L; Conti F; Amodio D; Giancotta C; Scaioli G; Ferro F; Ricotti E; Di Cesare S; Robasto F; Licciardi F; Marolda A; Montin D; Putti MC; Soresina A; Plebani A; Ramenghi U; Martino S; Pignata C; et alii...
Invasive meningococcal disease in three siblings with hereditary deficiency of the 8(th) component of complement: evidence for the importance of an early diagnosis. in Orphanet journal of rare diseases / Orphanet J Rare Dis. 2016 May 17;11(1):64. doi: 10.1186/s13023-016-0448-5.
2016
AOU Novara
AOU Novara
Dellepiane RM; Dell'Era L; Pavesi P; Macor P; Giordano M; De Maso L; Pietrogrande MC; Cugno M;