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Ceberio-Hualde, Leticia
24
results:
Search for persons
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Format
Online (24)
Mediatypes
Articles (Online) (21)
Bookchapter (Online) (2)
OpenAccess-fulltext (1)
Sorted by: Relevance
Sorted by: Year
?
1
Pearls & Oy-sters: Challenges and Controversies in Wilson D..:
Ruiz-Lopez, Marta
;
Moreno Estébanez, Ana
;
Tijero, Beatriz
...
Neurology. 99 (2022) 6 - p. 251-255 , 2022
Link:
https://doi.org/10.1212/..
?
2
Clinical characteristics of patients with lysosomal disease..:
Pérez-López, Jordi
;
Ceberio-Hualde, Leticia
;
García-Morillo, José Salvador
...
Molecular Genetics and Metabolism. 120 (2017) 1-2 - p. S106-S107 , 2017
Link:
https://doi.org/10.1016/..
?
3
Transition process from paediatric to adult care in patient..:
Pérez-López, Jordi
;
Ceberio-Hualde, Leticia
;
García Morillo, José Salvador
...
Medicina Clínica (English Edition). 147 (2016) 11 - p. 506.e1-506.e7 , 2016
Link:
https://doi.org/10.1016/..
?
4
Pearls & Oy-sters: Challenges and Controversies in Wilson D..:
Ruiz-Lopez, Marta
;
Moreno Estébanez, Ana
;
Tijero, Beatriz
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442620/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
5
Long-term safety and efficacy of DTX301 in adults with late..:
Thomas, Janet
;
Tan, Wen-Hann
;
Khan, Aneal
...
Molecular Genetics and Metabolism. 141 (2024) 4 - p. 108266 , 2024
Link:
https://doi.org/10.1016/..
?
6
Efficacy of Idursulfase therapy in patients with Mucopolysa..:
Pérez-López, J.
;
Moltó-Abad, M.
;
Muñoz-Delgado, C.
...
Molecular Genetics and Metabolism. 124 (2018) 3 - p. 216-227 , 2018
Link:
https://doi.org/10.1016/..
?
7
Clinical characteristics of adult patients with inborn erro..:
Pérez-López, J.
;
Ceberio-Hualde, L.
;
García-Morillo, J.S.
...
Molecular Genetics and Metabolism Reports. 10 (2017) - p. 92-95 , 2017
Link:
https://doi.org/10.1016/..
?
8
Analysis of the manifestations and treatment of tuberous sc..:
Gutiérrez Zurimendi, G.
;
Olmo Velasco, M.
;
De Frutos Muñoyerro, G.
...
European Urology Open Science. 19 (2020) - p. e716 , 2020
Link:
https://doi.org/10.1016/..
?
9
Correction: Vitamin C and folate status in hereditary fruct..:
Cano, Ainara
;
Alcalde, Carlos
;
Belanger-Quintana, Amaya
...
European Journal of Clinical Nutrition. 77 (2023) 11 - p. 1102-1103 , 2023
Link:
https://doi.org/10.1038/..
?
10
Adult acid sphingomyelinase deficiency (Niemann-Pick diseas..:
Villarrubia, Jesús
;
Muñoz, Gloria
;
Ciubotariu, Crina
...
Molecular Genetics and Metabolism. 135 (2022) 2 - p. S125 , 2022
Link:
https://doi.org/10.1016/..
?
11
Vitamin C and folate status in hereditary fructose intolera..:
Cano, Ainara
;
Alcalde, Carlos
;
Belanger-Quintana, Amaya
...
European Journal of Clinical Nutrition. 76 (2022) 12 - p. 1733-1739 , 2022
Link:
https://doi.org/10.1038/..
?
12
Genetic screening of lysosomal disorders: An account of fiv..:
del Castillo, Francisco J.
;
Muñoz, Gloria
;
Gandía, Marta
...
Molecular Genetics and Metabolism. 135 (2022) 2 - p. S36 , 2022
Link:
https://doi.org/10.1016/..
?
13
NGS-based panel screening of suspected lysosomal disease ca..:
del Castillo, Francisco J.
;
Muñoz, Gloria
;
Domínguez-Ruiz, María
...
Molecular Genetics and Metabolism. 135 (2022) 2 - p. S36 , 2022
Link:
https://doi.org/10.1016/..
?
14
Transferrin Isoforms, Old but New Biomarkers in Hereditary ..:
Cano, Ainara
;
Alcalde, Carlos
;
Belanger-Quintana, Amaya
...
Journal of Clinical Medicine. 10 (2021) 13 - p. 2932 , 2021
Link:
https://doi.org/10.3390/..
?
15
Urine Phenylacetylglutamine Determination in Patients with ..:
Andrade, Fernando
;
Cano, Ainara
;
Unceta Suarez, María
...
Journal of Clinical Medicine. 10 (2021) 16 - p. 3674 , 2021
Link:
https://doi.org/10.3390/..
1-15