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Author/Creator Gentile, M

3. Changes in markers of subclinical atherosclerosis in patients with familial hypercholesterolemia treated with evolocumab: a prospective cohort study. (25th November 2020)

Authors:
Calcaterra, I; Di Minno, A; Gentile, M; Tripaldella, M; Buonaiuto, A; Forte, F; Di Taranto, M.D; Giacobbe, C; Iannuzzo, G; Rubba, P.O.F; Di Minno, M.N.D
Journal:
European heart journal
Issue:
Volume 41:(2020)Supplement 2
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

6. Correlation between different LDL-R mutations and response to ab-PCSK9 therapy in a group of patient with genetic diagnosis of Familial Hypercholesterolemia. Preliminary report. (25th November 2020)

Authors:
Buonaiuto, A; Gentile, M; Calcaterra, I.L; Giacobbe, C; Tripaldella, M; Forte, F; Iannuzzo, G; Di Minno, M.N.D; Fortunato, G; Rubba, P.O.F
Journal:
European heart journal
Issue:
Volume 41:(2020)Supplement 2
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

10. Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis). Issue 1 (1st July 2009)

Authors:
Doherty, D; Parisi, M A; Finn, L S; Gunay-Aygun, M; Al-Mateen, M; Bates, D; Clericuzio, C; Demir, H; Dorschner, M; van Essen, A J; Gahl, W A; Gentile, M; Gorden, N T; Hikida, A; Knutzen, D; Özyurek, H; Phelps, I; Rosenthal, P; Verloes, A; Weigand, H
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 1(2010)
Page Start:
8
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗