Belanger Quintana, Amaya

Publications

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.
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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.
... View more Collapse

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.
... View more Collapse

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.
... View more Collapse

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.
... View more Collapse

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

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.
... View more Collapse

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.
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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.
... View more Collapse

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.
... View more Collapse

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.
... 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