Belanger Quintana, Amaya
Publications
- Articles 85
- Books 0
- Book chapters 3
- Conferences 0
- Working papers 0
- Technical reports 0
- Research projects 0
- Supervised theses 0
- Patent or software license 0
When should social service referral be considered in phenylketonuria?
- Van Rijn, M.
- Ahring, K.
- Bélanger-Quintana, A.
- Dokoupil, K.
- Ozel, H.G.
- Lammardo, A.M.
- Robert, M.
- Rocha, J.C.
- Macdonald, A.
Molecular Genetics and Metabolism Reports (p. 85-88) - 2015
Editor: Elsevier Inc.
10.1016/j.ymgmr.2015.01.002 View at source
- ISSN/ISBN 2214-4269
Weight Management in Phenylketonuria: What Should Be Monitored?
- César Rocha, J.
- Van Rijn, M.
- Van Dam, E.
- Ahring, K.
- Bélanger-Quintana, A.
- Dokoupil, K.
- Gokmen Ozel, H.
- Lammardo, A.M.
- Robert, M.
- Heidenborg, C.
- MacDonald, A.
Annals of Nutrition and Metabolism (p. 60-65) - 2016
Editor: S. Karger AG
10.1159/000442304 View at source
- ISSN/ISBN 1421-9697
Weaning practices in phenylketonuria vary between health professionals in Europe
- Pinto, A.
- Adams, S.
- Ahring, K.
- Allen, H.
- Almeida, M.F.
- Garcia-Arenas, D.
- Arslan, N.
- Assoun, M.
- Atik Altınok, Y.
- Barrio-Carreras, D.
- Belanger Quintana, A.
- Bernabei, S.M.
- Bontemps, C.
- Boyle, F.
- Bruni, G.
- Bueno-Delgado, M.
- Caine, G.
- Carvalho, R.
- Chrobot, A.
- Chyż, K.
- Cochrane, B.
- Correia, C.
- Corthouts, K.
- Daly, A.
- De Leo, S.
- Desloovere, A.
- De Meyer, A.
- De Theux, A.
- Didycz, B.
- Dijsselhof, M.E.
- Dokoupil, K.
- Drabik, J.
- Dunlop, C.
- Eberle-Pelloth, W.
- Eftring, K.
- Ekengren, J.
- Errekalde, I.
- Evans, S.
- Foucart, A.
- Fokkema, L.
- François, L.
- French, M.
- Forssell, E.
- Gingell, C.
- Gonçalves, C.
- Gökmen Özel, H.
- Grimsley, A.
- Gugelmo, G.
- Gyüre, E.
- Heller, C.
- Hensler, R.
- Jardim, I.
- Joost, C.
- Jörg-Streller, M.
- Jouault, C.
- Jung, A.
- Kanthe, M.
- Koç, N.
- Kok, I.L.
- Kozanoğlu, T.
- Kumru, B.
- Lang, F.
- Lang, K.
- Liegeois, I.
- Liguori, A.
- Lilje, R.
- Ļubina, O.
- Manta-Vogli, P.
- Mayr, D.
- Meneses, C.
- Newby, C.
- Meyer, U.
- Mexia, S.
- Nicol, C.
- Och, U.
- Olivas, S.M.
- Pedrón-Giner, C.
- Pereira, R.
- Plutowska-Hoffmann, K.
- Purves, J.
- Re Dionigi, A.
- Reinson, K.
- Robert, M.
- Robertson, L.
- Rocha, J.C.
- Rohde, C.
- Rosenbaum-Fabian, S.
- Rossi, A.
- Ruiz, M.
- Saligova, J.
- Gutiérrez-Sánchez, A.
- Schlune, A.
- Schulpis, K.
- Serrano-Nieto, J.
- Skarpalezou, A.
- Skeath, R.
- Slabbert, A.
- Straczek, K.
- Giżewska, M.
- Terry, A.
- Thom, R.
- Tooke, A.
- Tuokkola, J.
- van Dam, E.
- van den Hurk, T.A.M.
- van der Ploeg, E.M.C.
- Vande Kerckhove, K.
- Van Driessche, M.
- van Wegberg, A.M.J.
- van Wyk, K.
- Vasconcelos, C.
- Velez García, V.
- Wildgoose, J.
- Winkler, T.
- Żółkowska, J.
- Zuvadelli, J.
- MacDonald, A.
Molecular Genetics and Metabolism Reports (p. 39-44) - 2019
Editor: Elsevier Inc.
10.1016/j.ymgmr.2018.11.003 View at source
- ISSN/ISBN 2214-4269
Vitamin C and folate status in hereditary fructose intolerance
- Cano, A.
- Alcalde, C.
- Belanger-Quintana, A.
- Cañedo-Villarroya, E.
- Ceberio, L.
- Chumillas-Calzada, S.
- Correcher, P.
- Couce, M.L.
- García-Arenas, D.
- Gómez, I.
- Hernández, T.
- Izquierdo-García, E.
- Chicano, D.M.
- Morales, M.
- Pedrón-Giner, C.
- Jáuregui, E.P.
- Peña-Quintana, L.
- Sánchez-Pintos, P.
- Serrano-Nieto, J.
- Suarez, M.U.
- Miñana, I.V.
- de las Heras, J.
European Journal of Clinical Nutrition (p. 1733-1739) - 2022
Editor: Springer Nature
10.1038/s41430-022-01178-3 View at source
- ISSN/ISBN 1476-5640
Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program
- Navarrete, R.
- Leal, F.
- Vega, A.I.
- Morais-López, A.
- Garcia-Silva, M.T.
- Martín-Hernández, E.
- Quijada-Fraile, P.
- Bergua, A.
- Vives, I.
- García-Jiménez, I.
- Yahyaoui, R.
- Pedrón-Giner, C.
- Belanger-Quintana, A.
- Stanescu, S.
- Cañedo, E.
- García-Campos, O.
- Bueno-Delgado, M.
- Delgado-Pecellín, C.
- Vitoria, I.
- Rausell, M.D.
- Balmaseda, E.
- Couce, M.L.
- Desviat, L.R.
- Merinero, B.
- Rodríguez-Pombo, P.
- Ugarte, M.
- Pérez-Cerdá, C.
- Pérez, B.
European Journal Of Human Genetics (p. 556-562) - 1/4/2019
Editor: Nature Publishing Group
10.1038/s41431-018-0330-0 View at source
- ISSN 10184813
- ISSN/ISBN 1476-5438
Use of sapropterin in the management of phenylketonuria: Seven case reports
- Gokmen Ozel, H.
- Lammardo, A.M.
- Motzfeldt, K.
- Robert, M.
- Rocha, J.C.
- van Rijn, M.
- Ahring, K.
- Bélanger-Quintana, A.
- MacDonald, A.
- Dokoupil, K.
Molecular Genetics and Metabolism (p. 109-111) - 2013
10.1016/j.ymgme.2012.11.012 View at source
- ISSN/ISBN 1096-7192
Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases
- Martín-Hernández, E.
- Aldámiz-Echevarría, L.
- Castejón-Ponce, E.
- Pedrón-Giner, C.
- Couce, M.L.
- Serrano-Nieto, J.
- Pintos-Morell, G.
- Bélanger-Quintana, A.
- Martínez-Pardo, M.
- García-Silva, M.T.
- Quijada-Fraile, P.
- Vitoria-Miñana, I.
- Dalmau, J.
- Lama-More, R.A.
- Bueno-Delgado, M.A.
- Del Toro-Riera, M.
- García-Jiménez, I.
- Sierra-Córcoles, C.
- Ruiz-Pons, M.
- Peña-Quintana, L.J.
- Vives-Piñera, I.
- Moráis, A.
- Balmaseda-Serrano, E.
- Meavilla, S.
- Sanjurjo-Crespo, P.
- Pérez-Cerdá, C.
Orphanet journal of rare diseases (p. 187) - 2014
10.1186/s13023-014-0187-4 View at source
- ISSN/ISBN 1750-1172
Up to date knowledge on different treatment strategies for phenylketonuria
- Bélanger-Quintana, A.
- Burlina, A.
- Harding, C.O.
- Muntau, A.C.
Molecular Genetics and Metabolism - 2011
10.1016/j.ymgme.2011.08.009 View at source
- ISSN/ISBN 1096-7192
Trasplante de progenitores hematopoyéticos en las inmunodeficiencias primarias
- Bélanger-Quintana, A.
- Romero, M.S.J.
Revista Espanola de Pediatria (p. 355-361) - 2001
- ISSN/ISBN 0034-947X
Transferrin isoforms, old but new biomarkers in hereditary fructose intolerance
- Cano, A.
- Alcalde, C.
- Belanger-Quintana, A.
- Cañedo-Villarroya, E.
- Ceberio, L.
- Chumillas-Calzada, S.
- Correcher, P.
- Couce, M.L.
- García-Arenas, D.
- Gómez, I.
- Hernández, T.
- Izquierdo-García, E.
- Chicano, D.M.
- Morales, M.
- Pedrón-Giner, C.
- Jáuregui, E.P.
- Peña-Quintana, L.
- Sánchez-Pintos, P.
- Serrano-Nieto, J.
- Suarez, M.U.
- Miñana, I.V.
- de las Heras, J.
Journal of Clinical Medicine - 2021
Editor: MDPI
10.3390/jcm10132932 View at source
- ISSN/ISBN 2077-0383
This researcher has no books.
The Kuvan® adult maternal paediatric european registry (KAMPER) multinational observational study: Baseline and 1-year data in phenylketonuria patients responsive to sapropterin
- Trefz, F.K.
- Muntau, A.C.
- Lagler, F.B.
- Moreau, F.
- Alm, J.
- Burlina, A.
- Rutsch, F.
- Bélanger-Quintana, A.
- Feillet, F.
JIMD Reports (p. 35-43) - 2015
Editor: Springer
10.1007/8904_2015_425 View at source
- ISSN/ISBN 2192-8312
Hígado. Hepatopatías de la etiología metabólica
- Amaya Bélanger Quintana
- Mercedes Martínez-Pardo Casanova
Tratado de gastroenterología, hepatología y nutrición pediátrica aplicada de la SEGHNP (p. 454-473) - 2010
Editor: Ergon
- ISSN/ISBN 978-84-8473-891-6
Four years’ experience in the diagnosis of very long-chain acyl-coa dehydrogenase deficiency in infants detected in three spanish newborn screening centers
- Merinero, B.
- Alcaide, P.
- Martín-Hernández, E.
- Morais, A.
- García-Silva, M.T.
- Quijada-Fraile, P.
- Pedrón-Giner, C.
- Dulin, E.
- Yahyaoui, R.
- Egea, J.M.
- Belanger-Quintana, A.
- Blasco-Alonso, J.
- Fernandez Ruano, M.L.
- Besga, B.
- Ferrer-López, I.
- Leal, F.
- Ugarte, M.
- Ruiz-Sala, P.
- Pérez, B.
- Pérez-Cerdá, C.
JIMD Reports (p. 63-74) - 2018
Editor: Springer
10.1007/8904_2017_40 View at source
- ISSN/ISBN 2192-8312
This researcher has no conferences.
This researcher has no working papers.
This researcher has no technical reports.
This researcher has no research projects.
This researcher has no supervised thesis.
This researcher has no patents or software licenses.
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