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
Early feeding practices in infants with phenylketonuria across 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. 82-89) - 2018
Editor: Elsevier Inc.
10.1016/j.ymgmr.2018.07.008 View at source
- ISSN/ISBN 2214-4269
Erratum: PKU dietary handbook to accompany PKU guidelines (Orphanet Journal of Rare Diseases (2020) 15 (171) DOI: 10.1186/s13023-020-01391-y)
- MacDonald, A.
- Van Wegberg, A.M.J.
- Ahring, K.
- Beblo, S.
- Bélanger-Quintana, A.
- Burlina, A.
- Campistol, J.
- Coşkun, T.
- Feillet, F.
- Giżewska, M.
- Huijbregts, S.C.
- Leuzzi, V.
- Maillot, F.
- Muntau, A.C.
- Rocha, J.C.
- Romani, C.
- Trefz, F.
- Van Spronsen, F.J.
Orphanet Journal of Rare Diseases - 2020
Editor: BioMed Central Ltd
10.1186/s13023-020-01486-6 View at source
- ISSN/ISBN 1750-1172
Fluctuations in phenylalanine concentrations in phenylketonuria: A review of possible relationships with outcomes
- Cleary, M.
- Trefz, F.
- Muntau, A.C.
- Feillet, F.
- van Spronsen, F.J.
- Burlina, A.
- Bélanger-Quintana, A.
- Gizewska, M.
- Gasteyger, C.
- Bettiol, E.
- Blau, N.
- MacDonald, A.
Molecular Genetics and Metabolism (p. 418-423) - 2013
Editor: Academic Press Inc.
10.1016/j.ymgme.2013.09.001 View at source
- ISSN/ISBN 1096-7206
GLUT1 and COVID-19 deficiency syndrome
- Arrieta Blanco, F.
- Bélanger Quintana, A.
- Bengoa Rojano, N.
- Stanescu, S.
- Martinez Pardo, M.
Endocrinologia, Diabetes y Nutricion (p. 514-515) - 2021
Editor: Elsevier Doyma
10.1016/j.endinu.2020.07.001 View at source
- ISSN/ISBN 2530-0172
Genes and Variants Underlying Human Congenital Lactic Acidosis-From Genetics to Personalized Treatment
- Bravo-Alonso, I.
- Navarrete, R.
- Vega, A.I.
- Ruíz-Sala, P.
- Silva, M.T.G.
- Martín-Hernández, E.
- Quijada-Fraile, P.
- Belanger-Quintana, A.
- Stanescu, S.
- Bueno, M.
- Vitoria, I.
- Toledo, L.
- Couce, M.L.
- García-Jiménez, I.
- Ramos-Ruiz, R.
- Martín, M.Á.
- Desviat, L.R.
- Ugarte, M.
- Pérez-Cerdá, C.
- Merinero, B.
- Pérez, B.
- Rodríguez-Pombo, P.
Journal Of Clinical Medicine - 1/11/2019
Editor: MDPI
10.3390/jcm8111811 View at source
- ISSN 20770383
- ISSN/ISBN 2077-0383
Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia
- Couce, M.L.
- Aldamiz-Echevarría, L.
- Bueno, M.A.
- Barros, P.
- Belanger-Quintana, A.
- Blasco, J.
- García-Silva, M.-T.
- Márquez-Armenteros, A.M.
- Vitoria, I.
- Vives, I.
- Navarrete, R.
- Fernández-Marmiesse, A.
- Pérez, B.
- Pérez-Cerdá, C.
Journal of Human Genetics (p. 355-360) - 2017
Editor: Nature Publishing Group
10.1038/jhg.2016.144 View at source
- ISSN/ISBN 1435-232X
Glycerol kinase deficiency in adult patient: Hypertriglyceridemia resistance to diet and pharmacological treatment
- Arrieta, F.
- Ojeda, S.
- Rueda, Á.
- Stanescu, S.
- Belanger-Quintana, A.
- Martínez-Pardo, M.
Nutricion Hospitalaria (p. 993-995) - 2018
Editor: ARAN Ediciones S.A.
10.20960/nh.1921 View at source
- ISSN/ISBN 1699-5198
Hyperammonaemia as a cause of psychosis in an adolescent
- Bélanger-Quintana, A.
- Martínez-Pardo, M.
- García, M.J.
- Wermuth, B.
- Torres, J.
- Pallarés, E.
- Ugarte, M.
European Journal of Pediatrics (p. 773-775) - 2003
Editor: Springer Verlag
10.1007/s00431-002-1126-2 View at source
- ISSN/ISBN 0340-6199
Importancia del diagnóstico precoz de fenilcetonuria en la mujer y del control de los niveles de fenilalanina en la gestación
- Arrieta Blanco, F.
- Bélanger Quintana, A.
- Vázquez Martínez, C.
- Martínez Pardo, M.
Nutricion Hospitalaria (p. 1658-1661) - 2012
10.3305/nh.2012.27.5.5945 View at source
- ISSN/ISBN 0212-1611
International best practice for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria
- Muntau, A.C.
- Adams, D.J.
- Bélanger-Quintana, A.
- Bushueva, T.V.
- Cerone, R.
- Chien, Y.-H.
- Chiesa, A.
- Coşkun, T.
- de las Heras, J.
- Feillet, F.
- Katz, R.
- Lagler, F.
- Piazzon, F.
- Rohr, F.
- van Spronsen, F.J.
- Vargas, P.
- Wilcox, G.
- Bhattacharya, K.
Molecular Genetics and Metabolism (p. 1-11) - 2019
Editor: Academic Press Inc.
10.1016/j.ymgme.2019.04.004 View at source
- ISSN/ISBN 1096-7206
This researcher has no books.
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
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
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
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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