Belanger Quintana, Amaya

Publications

Diet in phenylketonuria: A snapshot of special dietary costs and reimbursement systems in 10 international centers

  • Belanger-Quintana, A.
  • Dokoupil, K.
  • Gokmen-Ozel, H.
  • Lammardo, A.M.
  • MacDonald, A.
  • Motzfeldt, K.
  • Nowacka, M.
  • Robert, M.
  • Van Rijn, M.
  • Ahring, K.
... View more Collapse

Molecular Genetics and Metabolism (p. 390-394) - 2012

10.1016/j.ymgme.2011.12.004 View at source

  • ISSN/ISBN 1096-7192

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

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

Optimizing the use of sapropterin (BH4) in the management of phenylketonuria

  • Blau, N.
  • Bélanger-Quintana, A.
  • Demirkol, M.
  • Feillet, F.
  • Giovannini, M.
  • MacDonald, A.
  • Trefz, F.K.
  • van Spronsen, F.J.
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Molecular Genetics and Metabolism (p. 158-163) - 2009

10.1016/j.ymgme.2009.01.002 View at source

  • ISSN/ISBN 1096-7192

Management of early treated adolescents and young adults with phenylketonuria: Development of international consensus recommendations using a modified Delphi approach

  • Burton, B.K.
  • Hermida, Á.
  • Bélanger-Quintana, A.
  • Bell, H.
  • Bjoraker, K.J.
  • Christ, S.E.
  • Grant, M.L.
  • Harding, C.O.
  • Huijbregts, S.C.J.
  • Longo, N.
  • McNutt, M.C.
  • Nguyen-Driver, M.D.
  • Santos Pessoa, A.L.
  • Rocha, J.C.
  • Sacharow, S.
  • Sanchez-Valle, A.
  • Sivri, H.S.
  • Vockley, J.
  • Walterfang, M.
  • Whittle, S.
  • Muntau, A.C.
... View more Collapse

Molecular Genetics and Metabolism (p. 114-126) - 2022

Editor: Academic Press Inc.

10.1016/j.ymgme.2022.07.012 View at source

  • ISSN/ISBN 1096-7206

Spanish BH4-responsive phenylalanine hydroxylase-deficient patients: evolution of seven patients on long-term treatment with tetrahydrobiopterin

  • Bélanger-Quintana, A.
  • García, M.J.
  • Castro, M.
  • Desviat, L.R.
  • Pérez, B.
  • Mejía, B.
  • Ugarte, M.
  • Martínez-Pardo, M.
... View more Collapse

Molecular Genetics And Metabolism (p. S61-S66) - 1/1/2005

Editor: Academic Press Inc.

10.1016/j.ymgme.2005.07.024 View at source

  • ISSN 10967192
  • ISSN/ISBN 1096-7206

Tetrahydrobiopterin responsiveness: results of the BH4 loading test in 31 Spanish PKU patients and correlation with their genotype

  • Desviat, L.R.
  • Pérez, B.
  • Bèlanger-Quintana, A.
  • Castro, M.
  • Aguado, C.
  • Sánchez, A.
  • García, M.J.
  • Martínez-Pardo, M.
  • Ugarte, M.
... View more Collapse

Molecular Genetics And Metabolism (p. 157-162) - 1/9/2004

10.1016/j.ymgme.2004.06.007 View at source

  • ISSN 10967192
  • ISSN/ISBN 1096-7192

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

"Lymphonodular hyperplasia as a sign of food allergy in children".

  • Suárez Cortina, L.
  • Bélanger-Quintana, A.

Journal of Pediatric Gastroenterology and Nutrition (p. 351) - 2000

  • ISSN/ISBN 0277-2116

Newborn screening for propionic, methylmalonic acidemia and vitamin B12 deficiency. Analysis of 588,793 newborns

  • Rivada, Á.M.
  • Conejero, A.C.
  • Martín-Hernández, E.
  • Quijada-Fraile, P.
  • Bellusci, M.
  • Calzada, S.C.
  • López, A.M.
  • Martínez, A.B.
  • Bélanger-Quintana, A.
  • Stanescu, S.
  • Casanova, M.M.-P.
  • Villarroya, E.C.
  • Pedrón-Giner, C.
  • Ruíz-Sala, P.
  • Ugarte, M.
  • González, B.P.
... View more Collapse

Journal of Pediatric Endocrinology and Metabolism (p. 1223-1231) - 2022

Editor: De Gruyter Open Ltd

10.1515/jpem-2022-0340 View at source

  • ISSN/ISBN 2191-0251

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.
... View more Collapse

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.
... 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