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Ferrer-Cortès, X.
390
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Search for persons
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Online (390)
Mediatypes
E-Books (1)
Articles (Online) (375)
Bookchapter (Online) (9)
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1
P1431: MOLECULAR CHARACTERIZATION AND LENTIVIRAL CORRECTION..:
Hernández, G.
;
Romero-Cortadellas, L.
;
Ferrer-Cortès, X.
...
HemaSphere. 6 (2022) - p. 1314-1315 , 2022
Link:
https://doi.org/10.1097/..
?
2
S274: A NOVEL SUBTYPE OF ANEMIA CAUSED BY MUTATIONS IN TFRC..:
Colucci, S.
;
Venturi, V.
;
Nicole, F.
...
HemaSphere. 6 (2022) - p. 175-176 , 2022
Link:
https://doi.org/10.1097/..
?
3
P1431: MOLECULAR CHARACTERIZATION AND LENTIVIRAL CORRECTION..:
Hernández, G
;
Romero-Cortadellas, L
;
Ferrer-Cortès, X
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429535/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
4
S274: A NOVEL SUBTYPE OF ANEMIA CAUSED BY MUTATIONS IN TFRC..:
S. Colucci
;
V. Venturi
;
F. Nicole
...
http://journals.lww.com/10.1097/01.HS9.0000843988.71420.55. , 2022
Link:
https://doi.org/10.1097/..
?
5
P1431: MOLECULAR CHARACTERIZATION AND LENTIVIRAL CORRECTION..:
G. Hernández
;
L. Romero-Cortadellas
;
X. Ferrer-Cortès
...
http://journals.lww.com/10.1097/01.HS9.0000848580.75298.51. , 2022
Link:
https://doi.org/10.1097/..
?
6
Impacto de la intervención con una adaptación grupal del mé..:
March Luján, Vicente Alejandro
;
de la Rubia Ortí, José Enrique
;
Huguet, José María
...
http://hdl.handle.net/20.500.12466/3483. , 2018
Link:
https://hdl.handle.net/2..
?
7
Strategies to reengage patients lost to follow up in HIV ca..:
Palacio Vieira, Jorge
;
Reyes Urueña, Juliana Maria
;
Imaz, Arkaitz
...
Reproducció del document publicat a: https://doi.org/10.1186/s12889-021-11613-y. , 2021
Link:
http://hdl.handle.net/24..
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8
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/..
?
9
New Cases of Hypochromic Microcytic Anemia Due to Mutations..:
Romero-Cortadellas, Lídia
;
Hernández, Gonzalo
;
Ferrer-Cortès, Xènia
...
International Journal of Molecular Sciences. 23 (2022) 8 - p. 4406 , 2022
Link:
https://doi.org/10.3390/..
?
10
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/..
?
11
Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L ..:
Celma Nos, Ferran
;
Hernández, Gonzalo
;
Ferrer-Cortès, Xènia
...
International Journal of Molecular Sciences. 22 (2021) 11 - p. 5451 , 2021
Link:
https://doi.org/10.3390/..
?
12
A mutation in the iron-responsive element of ALAS2 is a mod..:
Ducamp, Sarah
;
Luscieti, Sara
;
Ferrer-Cortès, Xènia
...
Haematologica. 106 (2021) 7 - p. 2030-2033 , 2021
Link:
https://doi.org/10.3324/..
?
13
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/..
?
14
Biallelic mutations in NDUFA8 cause complex I deficiency in..:
Tort, Frederic
;
Barredo, Estibaliz
;
Parthasarathy, Ranjani
...
Molecular Genetics and Metabolism. 131 (2020) 3 - p. 349-357 , 2020
Link:
https://doi.org/10.1016/..
?
15
A leaky splicing mutation in NFU1 is associated with a part..:
Ferrer-Cortès, Xènia
;
Narbona, Juan
;
Bujan, Núria
...
Mitochondrion. 26 (2016) - p. 72-80 , 2016
Link:
https://doi.org/10.1016/..
1-15