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X
Ferrer-Cortès, X.
387  Ergebnisse:
Personensuche X
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1

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/..
 
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2

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/..
 
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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...
 
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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/..
 
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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/..
 
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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..
 
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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/..
 
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9

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/..
 
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10

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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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