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
Overweight and obesity in PKU: The results from 8 centres in Europe and Turkey
- Gokmen Ozel, H.
- Ahring, K.
- Bélanger-Quintana, A.
- Dokoupil, K.
- Lammardo, A.M.
- Robert, M.
- Rocha, J.C.
- Almeida, M.F.
- Van Rijn, M.
- MacDonald, A.
Molecular Genetics and Metabolism Reports (p. 483-486) - 2014
Editor: Elsevier Inc.
10.1016/j.ymgmr.2014.11.003 View at source
- ISSN/ISBN 2214-4269
PKU dietary handbook to accompany PKU guidelines
- 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.
- Rocha, J.C.
- Romani, C.
- Trefz, F.
- Van Spronsen, F.J.
Orphanet Journal of Rare Diseases - 2020
Editor: BioMed Central Ltd
10.1186/s13023-020-01391-y View at source
- ISSN/ISBN 1750-1172
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
Pediatric renovascular hypertension (multiple letters) [3]
- Estepa, R.
- Gallego, N.
- Orte, L.
- Belanger, A.
- Aracil, E.
- Ortuño, J.
- McTaggart, S.J.
- Jones, C.L.
Pediatric Nephrology (p. 529-531) - 2001
- ISSN/ISBN 0931-041X
Persistent increase of plasma butyryl/isobutyrylcarnitine concentrations as marker of SCAD defect and ethylmalonic encephalopathy.
- Merinero, B.
- Pérez-Cerdá, C.
- Ruiz Sala, P.
- Ferrer, I.
- García, M.J.
- Martínez Pardo, M.
- Belanger-Quintana, A.
- de la Mota, J.L.
- Martin-Hernández, E.
- Vianey-Saban, C.
- Bischoff, C.
- Gregersen, N.
- Ugarte, M.
Journal of inherited metabolic disease (p. 685) - 2006
10.1007/s10545-006-0342-8 View at source
- ISSN/ISBN 0141-8955
Physical development in patients with phenylketonuria on dietary treatment: A retrospective study
- Belanger-Quintana, A.
- Martínez-Pardo, M.
Molecular Genetics and Metabolism (p. 480-484) - 2011
10.1016/j.ymgme.2011.08.002 View at source
- ISSN/ISBN 1096-7192
Plasma CoQ10 Status in Patients with Propionic Acidaemia and Possible Benefit of Treatment with Ubiquinol
- Stanescu, S.
- Belanger-Quintana, A.
- Fernández-Felix, B.M.
- Ruiz-Sala, P.
- Alcaide, P.
- Arrieta, F.
- Martínez-Pardo, M.
Antioxidants - 2022
Editor: MDPI
10.3390/antiox11081588 View at source
- ISSN/ISBN 2076-3921
Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approach
- Aguiar, A.
- Ahring, K.
- Almeida, M.F.
- Assoun, M.
- Belanger Quintana, A.
- Bigot, S.
- Bihet, G.
- Blom Malmberg, K.
- Burlina, A.
- Bushueva, T.
- Caris, A.
- Chan, H.
- Clark, A.
- Clark, S.
- Cochrane, B.
- Corthouts, K.
- Dalmau, J.
- Dassy, M.
- De Meyer, A.
- Didycz, B.
- Diels, M.
- Dokupil, K.
- Dubois, S.
- Eftring, K.
- Ekengren, J.
- Ellerton, C.
- Evans, S.
- Faria, A.
- Fischer, A.
- Ford, S.
- Freisinger, P.
- Gizewska, M.
- Gokmen-Ozel, H.
- Gribben, J.
- Gunden, F.
- Heddrich-Ellerbrok, M.
- Heiber, S.
- Heidenborg, C.
- Jankowski, C.
- Janssen-Regelink, R.
- Jones, I.
- Jonkers, C.
- Joerg-Streller, M.
- Kaalund-Hansen, K.
- Kiss, E.
- Lammardo, A.M.
- Lang, K.
- Lier, D.
- Lilje, R.
- Lowry, S.
- Luyten, K.
- MacDonald, A.
- Meyer, U.
- Moor, D.
- Pal, A.
- Robert, M.
- Robertson, L.
- Rocha, J.C.
- Rohde, C.
- Ross, K.
- Saruhan, S.
- Sjöqvist, E.
- Skeath, R.
- Stoelen, L.
- Ter Horst, N.M.
- Terry, A.
- Timmer, C.
- Tuncer, N.
- Vande Kerckhove, K.
- van der Ploeg, L.
- van Rijn, M.
- van Spronsen, F.J.
- van Teeffelen-Heithoff, A.
- van Wegberg, A.
- van Wyk, K.
- Vasconcelos, C.
- Vitoria, I.
- Wildgoose, J.
- Webster, D.
- White, F.J.
- Zweers, H.
Molecular Genetics and Metabolism (p. 17-22) - 2015
Editor: Academic Press Inc.
10.1016/j.ymgme.2015.03.006 View at source
- ISSN/ISBN 1096-7206
Protein substitutes for phenylketonuria in Europe: Access and nutritional composition
- Pena, M.J.
- De Almeida, M.F.
- Van Dam, E.
- Ahring, K.
- Bélanger-Quintana, A.
- Dokoupil, K.
- Gokmen-Ozel, H.
- Lammardo, A.M.
- MacDonald, A.
- Robert, M.
- Rocha, J.C.
European Journal of Clinical Nutrition (p. 785-789) - 2016
Editor: Nature Publishing Group
10.1038/ejcn.2016.54 View at source
- ISSN/ISBN 1476-5640
Recommendations for the Diagnosis and Therapeutic Management of Hyperammonaemia in Paediatric and Adult Patients
- Bélanger-Quintana, A.
- Blanco, F.A.
- Barrio-Carreras, D.
- Martínez, A.B.
- Villarroya, E.C.
- García-Silva, M.T.
- More, R.L.
- Martín-Hernández, E.
- López, A.M.
- Morales-Conejo, M.
- Pedrón-Giner, C.
- Quijada-Fraile, P.
- Stanescu, S.
- Casanova, M.M.-P.
Nutrients - 2022
Editor: MDPI
10.3390/nu14132755 View at source
- ISSN/ISBN 2072-6643
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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