Author/Creator: Debellis, Lucantonio - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Debellis, Lucantonio

1. Cardiofaciocutaneous syndrome with rare structural variant in DOCK8 gene associated with neurodevelopmental disorders. Issue 3 (14th February 2020)

Authors:: Dell'Edera, Domenico; Debellis, Lucantonio; Mitidieri, Angela; Anna Epifania, Annunziata; Cuscianna, Eustachio; Allegretti, Arianna
Journal:: Clinical case reports
Issue:: Volume 8:Issue 3(2020)
Page Start:: 539
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. NKCC2 activity is inhibited by the Bartter's syndrome type 5 gain‐of‐function CaR‐A843E mutant in renal cells. (12th March 2015)

Authors:: Carmosino, Monica; Gerbino, Andrea; Hendy, Geoffrey N.; Torretta, Silvia; Rizzo, Federica; Debellis, Lucantonio; Procino, Giuseppe; Svelto, Maria
Journal:: Biology of the cell
Issue:: Volume 107:Number 4(2015:Apr.)
Page Start:: 98
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗