Belanger Quintana, Amaya

Publications

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.
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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.
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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.
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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.
... View more Collapse

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.
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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.
... View more Collapse

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.
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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.
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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.
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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.
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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.
... View more Collapse

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.

Last data update: 4/24/24 1:18 PM