E-LIB Suche - Ergebnisse für: Casari, Giorgio

1

115 The mannose-binding lectin (MBL) in MIS-C: relationship..:

Stravalaci, Matteo ; Pagani, Isabel ; Zhong, Hang...
Immunobiology. 228 (2023) 5 - p. 152566 , 2023

Link: https://doi.org/10.1016/..

2

Whole exome data prioritization unveils the hidden weight o..:

Quarantani, Gioia ; Sorgente, Anna ; Alfano, Massimo...
PLOS ONE. 18 (2023) 8 - p. e0288336 , 2023

Link: https://doi.org/10.1371/..

3

Studying severe long COVID to understand post-infectious di..:

Brodin, Petter ; Casari, Giorgio ; Townsend, Liam...
Nature Medicine. 28 (2022) 5 - p. 879-882 , 2022

Link: https://doi.org/10.1038/..

4

VarGenius-HZD Allows Accurate Detection of Rare Homozygous ..:

Musacchia, Francesco ; Karali, Marianthi ; Torella, Annalaura...
Genes. 12 (2021) 12 - p. 1979 , 2021

Link: https://doi.org/10.3390/..

5

Specific activation of GluN1-N2B NMDA receptors underlies f..:

Crivellaro, Giovanna ; Tottene, Angelita ; Vitale, Marina...
Neurobiology of Disease. 156 (2021) - p. 105419 , 2021

Link: https://doi.org/10.1016/..

6

Novel SCN5A p.Val1667Asp Missense Variant Segregation and C..:

Monasky, Michelle M. ; Micaglio, Emanuele ; Ciconte, Giuseppe...
International Journal of Molecular Sciences. 22 (2021) 9 - p. 4700 , 2021

Link: https://doi.org/10.3390/..

7

Immunosuppressive therapy in childhood‐onset arrhythmogenic..:

Peretto, Giovanni ; Barzaghi, Federica ; Cicalese, Maria Pia...
Pacing and Clinical Electrophysiology. 44 (2021) 3 - p. 552-556 , 2021

Link: https://doi.org/10.1111/..

8

Brugada syndrome genetics is associated with phenotype seve..:

Ciconte, Giuseppe ; Monasky, Michelle M ; Santinelli, Vincenzo...
European Heart Journal. 42 (2020) 11 - p. 1082-1090 , 2020

Link: https://doi.org/10.1093/..

9

Cavitating and tigroid‐like leukoencephalopathy in a case o..:

Alagia, Marianna ; Cappuccio, Gerarda ; Torella, Annalaura...
JIMD Reports. 52 (2020) 1 - p. 11-16 , 2020

Link: https://doi.org/10.1002/..

10

A Global Effort to Define the Human Genetics of Protective ..:

Casanova, Jean-Laurent ; Su, Helen C. ; Abel, Laurent...
Cell. 181 (2020) 6 - p. 1194-1199 , 2020

Link: https://doi.org/10.1016/..

11

Novel SCN5A p.V1429M Variant Segregation in a Family with B..:

Monasky, Michelle M. ; Micaglio, Emanuele ; Ciconte, Giuseppe...
International Journal of Molecular Sciences. 21 (2020) 16 - p. 5902 , 2020

Link: https://doi.org/10.3390/..

12

Impaired flickering of the permeability transition pore cau..:

Sambri, Irene ; Massa, Filomena ; Gullo, Francesca...
EBioMedicine. 61 (2020) - p. 103050 , 2020

Link: https://doi.org/10.1016/..

13

Retinal dystrophy in an individual carrying a de novo misse..:

Cappuccio, Gerarda ; Brunetti‐Pierri, Raffaella ; Torella, Annalaura...
Molecular Genetics & Genomic Medicine. 7 (2019) 6 - p. , 2019

Link: https://doi.org/10.1002/..

14

Differential effect of FHM2 mutation on synaptic plasticity..:

Iure, Antonio de ; Mazzocchetti, Petra ; Bastioli, Guendalina...
Cephalalgia. 39 (2019) 10 - p. 1333-1338 , 2019

Link: https://doi.org/10.1177/..

15

Consolidating the Role of TDP2 Mutations in Recessive Spino..:

TUDP Study Group ; Ciaccio, Claudia ; Castello, Raffaele...
The Cerebellum. 18 (2019) 5 - p. 972-975 , 2019

Link: https://doi.org/10.1007/..