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Ferrer-Cortès, Xenia
17
results:
OpenAccess-fulltext X
Sorted by: Relevance
Sorted by: Year
?
1
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..
?
2
A mutation in the iron-responsive element of ALAS2 is a mod..:
Ducamp, Sarah
;
Luscieti, Sara
;
Ferrer-Cortès, Xènia
...
Haematologica. , 2024
Link:
https://hdl.handle.net/2..
?
3
New cases of hypochromic microcytic anemia due to mutations..:
Romero-Cortadellas, Lídia
;
Hernández, Gonzalo
;
Ferrer-Cortès, Xènia
...
International Journal of Molecular Sciences. , 2024
Link:
https://hdl.handle.net/2..
?
4
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..
?
5
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...
?
6
Mutations in the RACGAP1 gene cause autosomal recessive con..:
Hernández, Gonzalo
;
Romero-Cortadellas, Lídia
;
Ferrer-Cortès, Xènia
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890003/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
7
A mutation in the iron-responsive element of ALAS2 is a mod..:
Ducamp, Sarah
;
Luscieti, Sara
;
Ferrer-Cortès, Xènia
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252951/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
8
Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L ..:
Celma Nos, Ferran
;
Hernández, Gonzalo
;
Ferrer-Cortès, Xènia
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196845/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
9
New Mutations in HFE2 and TFR2 Genes Causing Non HFE-Relate..:
Hernández, Gonzalo
;
Ferrer-Cortès, Xenia
;
Venturi, Veronica
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702017/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
10
New Cases and Mutations in SEC23B Gene Causing Congenital D..:
Melina Mara Musri
;
Veronica Venturi
;
Xènia Ferrer-Cortès
...
Molecular Pathology, Diagnostics, and Therapeutics. , 2023
Link:
https://doi.org/10.3390/..
?
11
New Cases and Mutations in SEC23B Gene Causing Congenital D..:
Melina Mara Musri
;
Veronica Venturi
;
Xènia Ferrer-Cortès
...
https://www.mdpi.com/1422-0067/24/12/9935. , 2023
Link:
https://doi.org/10.3390/..
?
12
New Cases of Hypochromic Microcytic Anemia Due to Mutations..:
Lídia Romero-Cortadellas
;
Gonzalo Hernández
;
Xènia Ferrer-Cortès
...
Molecular Endocrinology and Metabolism. , 2022
Link:
https://doi.org/10.3390/..
?
13
New Cases of Hypochromic Microcytic Anemia Due to Mutations..:
Lídia Romero-Cortadellas
;
Gonzalo Hernández
;
Xènia Ferrer-Cortès
...
https://www.mdpi.com/1422-0067/23/8/4406. , 2022
Link:
https://doi.org/10.3390/..
?
14
Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L ..:
Ferran Celma Nos
;
Gonzalo Hernández
;
Xènia Ferrer-Cortès
...
Molecular Pathology, Diagnostics, and Therapeutics. , 2021
Link:
https://doi.org/10.3390/..
?
15
Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L ..:
Ferran Celma Nos
;
Gonzalo Hernández
;
Xènia Ferrer-Cortès
...
https://www.mdpi.com/1422-0067/22/11/5451. , 2021
Link:
https://doi.org/10.3390/..
1-15