I agree that this site is using cookies. You can find further informations here.
X
Venturi, Veronica
49  results:
Search for persons X
?
1

New Cases and Mutations in SEC23B Gene Causing Congenital D..:

Musri, Melina Mara ; Venturi, Veronica ; Ferrer-Cortès, Xènia...
International Journal of Molecular Sciences.  24 (2023)  12 - p. 9935 , 2023
Link: https://doi.org/10.3390/..
 
?
2

Haemochromatosis patients' research priorities: Towards an ..:

Romero‐Cortadellas, Lídia ; Venturi, Veronica ; Martín‐Sánchez, Juan Carlos...
Health Expectations.  26 (2023)  6 - p. 2293-2301 , 2023
Link: https://doi.org/10.1111/..
 
?
3

Mutations in the RACGAP1 gene cause autosomal recessive con..:

Hernández, Gonzalo ; Romero-Cortadellas, Lídia ; Ferrer-Cortès, Xènia...
Haematologica.  108 (2022)  2 - p. 581-587 , 2022
Link: https://doi.org/10.3324/..
 
?
4

Huntington's disease brain-derived small RNAs recapitulate ..:

Creus-Muncunill, Jordi ; Guisado-Corcoll, Anna ; Venturi, Veronica...
Acta Neuropathologica.  141 (2021)  4 - p. 565-584 , 2021
Link: https://doi.org/10.1007/..
 
?
5

New Mutations in HFE2 and TFR2 Genes Causing Non HFE-Relate..:

Hernández, Gonzalo ; Ferrer-Cortès, Xenia ; Venturi, Veronica...
Genes.  12 (2021)  12 - p. 1980 , 2021
Link: https://doi.org/10.3390/..
 
?
6

CoDysAn: A Telemedicine Tool to Improve Awareness and Diagn..:

Tornador, Cristian ; Sánchez-Prados, Edgar ; Cadenas, Beatriz...
Frontiers in Physiology.  10 (2019)  - p. , 2019
Link: https://doi.org/10.3389/..
 
?
7

Characterisation of the biological response of Saccharomyce..:

Venturi, Veronica ; Little, Richard ; Bircham, Peter W....
Biochemical and Biophysical Research Communications.  496 (2018)  4 - p. 1082-1087 , 2018
Link: https://doi.org/10.1016/..
 
?
8

Distinct recruitment of human eIF4E isoforms to processing ..:

Frydryskova, Klara ; Masek, Tomas ; Borcin, Katerina...
BMC Molecular Biology.  17 (2016)  1 - p. , 2016
Link: https://doi.org/10.1186/..
 
?
9

The protein synthesis inhibitors mycalamides A and E have l..:

Venturi, Veronica ; Davies, Carolina ; Singh, A. Jonathan...
Journal of Biochemical and Molecular Toxicology.  26 (2011)  3 - p. 94-100 , 2011
Link: https://doi.org/10.1002/..
 
?
10

Mutations in the RACGAP1 gene cause autosomal recessive con..:

Hernández, Gonzalo ; Romero-Cortadellas, Lídia ; Ferrer-Cortès, Xènia...
Haematologica.  , 2024
Link: https://hdl.handle.net/2..
 
?
11

Haemochromatosis patients' research priorities: Towards an ..:

Romero-Cortadellas, Lídia ; Venturi, Veronica ; Martín-Sánchez, Juan Carlos...
Health Expectations.  , 2023
Link: https://hdl.handle.net/2..
 
?
12

New cases and mutations in SEC23B gene causing congenital d..:

Mara Musri, Melina ; Venturi, Veronica ; Ferrer-Cortès, Xènia...
International Journal of Molecular Sciences.  , 2023
Link: https://hdl.handle.net/2..
 
?
13

New Cases and Mutations in SEC23B Gene Causing Congenital D..:

Musri, Melina Mara ; Venturi, Veronica ; Ferrer-Cortès, Xènia...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298408/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
?
14

New Cases and Mutations in SEC23B Gene Causing Congenital D..:

Musri, Melina Mara ; Venturi, Veronica ; Ferrer, Xènia...
International Journal of Molecular Sciences;24(12).  , 2023
Link: https://hdl.handle.net/1..
 
?
15

Haemochromatosis patients' research priorities: Towards an ..:

Romero‐Cortadellas, Lídia ; Venturi, Veronica ; Martín‐Sánchez, Juan Carlos...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632644/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
1-15