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
Dietary practices in methylmalonic acidaemia: A European survey
- Pinto, A.
- Evans, S.
- Daly, A.
- Almeida, M.F.
- Assoun, M.
- Belanger-Quintana, A.
- Bernabei, S.M.
- Bollhalder, S.
- Cassiman, D.
- Champion, H.
- Chan, H.
- Corthouts, K.
- Dalmau, J.
- Boer, F.D.
- Laet, C.D.
- Meyer, A.D.
- Desloovere, A.
- Dianin, A.
- Dixon, M.
- Dokoupil, K.
- Dubois, S.
- Eyskens, F.
- Faria, A.
- Fasan, I.
- Favre, E.
- Feillet, F.
- Fekete, A.
- Gallo, G.
- Gingell, C.
- Gribben, J.
- Hansen, K.K.
- Horst, N.T.
- Jankowski, C.
- Janssen-Regelink, R.
- Jones, I.
- Jouault, C.
- Kahrs, G.E.
- Kok, I.
- Kowalik, A.
- Laguerre, C.
- Verge, S.L.
- Liguori, A.
- Lilje, R.
- Maddalon, C.
- Mayr, D.
- Meyer, U.
- Micciche, A.
- Och, U.
- Robert, M.
- Rocha, J.C.
- Rogozinski, H.
- Rohde, C.
- Ross, K.
- Saruggia, I.
- Schlune, A.
- Singleton, K.
- Sjoqvist, E.
- Skeath, R.
- Stolen, L.H.
- Terry, A.
- Timmer, C.
- Tomlinson, L.
- Tooke, A.
- Kerckhove, K.V.
- Van Dam, E.
- Hurk, D.V.D.
- Ploeg, L.V.D.
- Van Driessche, M.
- Van Rijn, M.
- Wegberg, A.V.
- Vasconcelos, C.
- Vestergaard, H.
- Vitoria, I.
- Webster, D.
- White, F.
- White, L.
- Zweers, H.
- Macdonald, A.
Journal of Pediatric Endocrinology and Metabolism (p. 147-155) - 2020
Editor: De Gruyter Open Ltd
10.1515/jpem-2019-0277 View at source
- ISSN/ISBN 2191-0251
A series of three case reports in patients with phenylketonuria performing regular exercise: First steps in dietary adjustment
- Rocha, J.C.
- Van Dam, E.
- Ahring, K.
- Almeida, M.F.
- Bélanger-Quintana, A.
- Dokoupil, K.
- Gökmen-Özel, H.
- Robert, M.
- Heidenborg, C.
- Harbage, E.
- Macdonald, A.
Journal of Pediatric Endocrinology and Metabolism (p. 635-641) - 2019
Editor: De Gruyter
10.1515/jpem-2018-0492 View at source
- ISSN/ISBN 2191-0251
Outcomes of phenylketonuria with relevance to follow-up
- van Spronsen, F.J.
- Bélanger-Quintana, A.
Journal of Inherited Metabolic Disease (p. 49-55) - 2011
Editor: Kluwer Academic Publishers
10.1007/8904_2011_16 View at source
- ISSN/ISBN 1573-2665
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
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
Ataxia with isolated vitamin E deficiency: case report and review of the literature
- Aparicio, J.M.
- Bélanger-Quintana, A.
- Suárez, L.
- Mayo, D.
- Benítez, J.
- Díaz, M.
- Escobar, H.
Journal Of Pediatric Gastroenterology And Nutrition (p. 206-210) - 1/1/2001
Editor: Lippincott Williams and Wilkins
10.1097/00005176-200108000-00022 View at source
- ISSN 15364801
- ISSN/ISBN 0277-2116
- Dialnet
- iMarina
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
Diagnosis of inborn errors of metabolism within the expanded newborn screening in the Madrid region
- Martín-Rivada, Á.
- Palomino Pérez, L.
- Ruiz-Sala, P.
- Navarrete, R.
- Cambra Conejero, A.
- Quijada Fraile, P.
- Moráis López, A.
- Belanger-Quintana, A.
- Martín-Hernández, E.
- Bellusci, M.
- Cañedo Villaroya, E.
- Chumillas Calzada, S.
- García Silva, M.T.
- Bergua Martínez, A.
- Stanescu, S.
- Martínez-Pardo Casanova, M.
- Ruano, M.L.F.
- Ugarte, M.
- Pérez, B.
- Pedrón-Giner, C.
JIMD Reports (p. 146-161) - 2022
Editor: John Wiley and Sons Inc
10.1002/jmd2.12265 View at source
- ISSN/ISBN 2192-8312
Long-term follow-up with filter paper samples in patients with propionic acidemia
- Stanescu, S.
- Belanger-Quintana, A.
- Fernández-Felix, B.M.
- Pérez-Cerdá, C.
- Merinero, B.
- Ruiz-Sala, P.
- Arrieta, F.
- Martínez-Pardo, M.
JIMD Reports (p. 44-51) - 2021
Editor: John Wiley and Sons Inc
10.1002/jmd2.12166 View at source
- ISSN/ISBN 2192-8312
Pathogenic variants of DNAJC12 and evaluation of the encoded cochaperone as a genetic modifier of hyperphenylalaninemia
- Gallego, D.
- Leal, F.
- Gámez, A.
- Castro, M.
- Navarrete, R.
- Sanchez-Lijarcio, O.
- Vitoria, I.
- Bueno-Delgado, M.
- Belanger-Quintana, A.
- Morais, A.
- Pedrón-Giner, C.
- García, I.
- Campistol, J.
- Artuch, R.
- Alcaide, C.
- Cornejo, V.
- Gil, D.
- Yahyaoui, R.
- Desviat, L.R.
- Ugarte, M.
- Martínez, A.
- Pérez, B.
Human Mutation (p. 1329-1338) - 1/7/2020
Editor: John Wiley and Sons Inc.
10.1002/humu.24026 View at source
- ISSN 10597794
- ISSN/ISBN 1098-1004
This researcher has no books.
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
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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