Sfoglia per AUTORE
PARABOSCHI EM
Collezione AOU Novara

  

Items : 3

X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis. in Gastroenterology / Gastroenterology. 2021 Jun;160(7):2483-2495.e26. doi: 10.1053/j.gastro.2021.02.061. Epub 2021 Mar 4.
2021
AO Cuneo
AOU Novara

Cardamone G; Carbone M; Siminovitch KA; Hirschfield G; Xiong M; Liu X; Shi Y; Li Z; Tanaka A; Tang R; Nagasaki M; Tokunaga K; Kawashima M; Nishida N; Ueno K; Hitomi Y; Jones DE; Nakamura M; Mells GF; Sandford RN; Cordell HJ; Gerussi A; Asselta R; Paraboschi EM; Duga S; Gershwin ME; Seldin MF; Invernizzi P;

The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS? in Amyotrophic lateral sclerosis & frontotemporal degeneration / Amyotroph Lateral Scler Frontotemporal Degener. 2020 May;21(3-4):273-279. doi: 10.1080/21678421.2019
2020
AOU Novara

Corrado L; Pensato V; Croce R; Di Pierro A; Mellone S; Dalla Bella E; Salsano E; Paraboschi EM; Giordano M; Saraceno M; Mazzini L; Gellera C; D'Alfonso S;

Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. in Human molecular genetics / Hum Mol Genet. 2014 Dec 20;23(25):6746-61. doi: 10.1093/hmg/ddu392. Epub 2014 Jul 30.
2014
AOU Novara

Paraboschi EM; Rimoldi V; Soldà G; Tabaglio T; Dall'Osso C; Saba E; Vigliano M; Salviati A; Leone M; Benedetti MD; Fornasari D; Saarela J; De Jager PL; Patsopoulos NA; D'Alfonso S; Gemmati D; Duga S; Asselta R;