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X
Romero-Cortadellas, L.
33  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

P1475: MUTATIONS IN THE GAP DOMAIN OF RACGAP1 CAUSE DEVELOP..:

Romero-Cortadellas, Lídia ; Bañón, Aitor ; Hernández, Gonzalo...
HemaSphere.  7 (2023)  S3 - p. e01629bb , 2023
Link: https://doi.org/10.1097/..
 
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4

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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5

P1496: TRANSFERRIN NON-CODING VARIANTS CAUSE MRNA DESTABILI..:

Ferrer, Xenia ; Romero-Cortadellas, Lídia ; Diaz-de-Heredia, Cristina...
HemaSphere.  7 (2023)  S3 - p. e7657001 , 2023
Link: https://doi.org/10.1097/..
 
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6

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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7

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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8

Absence of p.R50X Pygm read-through in McArdle disease cell..:

Tarrasó, Guillermo ; Real-Martinez, Alberto ; Parés, Marta...
Disease Models & Mechanisms.  13 (2020)  1 - p. , 2020
Link: https://doi.org/10.1242/..
 
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9

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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10

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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11

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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12

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..
 
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13

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..
 
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14

Haemochromatosis patients' research priorities: Towards an ..:

Romero-Cortadellas, Lídia ; Venturi, Veronica ; Martín-Sánchez, Juan Carlos...
Health Expectations.  , 2023
Link: https://hdl.handle.net/2..
 
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15

P1475: MUTATIONS IN THE GAP DOMAIN OF RACGAP1 CAUSE DEVELOP..:

Romero-Cortadellas, Lídia ; Bañón, Aitor ; Hernández, Gonzalo...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430497/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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