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Belanger Quintana, Amaya

Medicina y Especialidades Médicas / Universidad de Alcalá

Publications

Mitochondrial bioenergetic is impaired in Monocarboxylate transporter 1 deficiency: a new clinical case and review of the literature

  • Stanescu, S.
  • Bravo-Alonso, I.
  • Belanger-Quintana, A.
  • Pérez, B.
  • Medina-Diaz, M.
  • Ruiz-Sala, P.
  • Flores, N.P.
  • Buenache, R.
  • Arrieta, F.
  • Rodríguez-Pombo, P.
... View more Collapse

Orphanet Journal Of Rare Diseases - 1/12/2022

Editor: BioMed Central Ltd

10.1186/s13023-022-02389-4 View at source

  • ISSN 17501172
  • ISSN/ISBN 1750-1172

Severe anemia in patients with Propionic acidemia is associated with branched-chain amino acid imbalance

  • Stanescu, S.
  • Belanger-Quintana, A.
  • Fernandez-Felix, B.M.
  • Arrieta, F.
  • Quintero, V.
  • Maldonado, M.S.
  • Alcaide, P.
  • Martínez-Pardo, M.
... View more Collapse

Orphanet Journal of Rare Diseases - 2021

Editor: BioMed Central Ltd

10.1186/s13023-021-01865-7 View at source

  • ISSN/ISBN 1750-1172

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

Erratum: PKU dietary handbook to accompany PKU guidelines (Orphanet Journal of Rare Diseases (2020) 15 (171) DOI: 10.1186/s13023-020-01391-y)

  • 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.
  • Romani, C.
  • Trefz, F.
  • Van Spronsen, F.J.
... View more Collapse

Orphanet Journal of Rare Diseases - 2020

Editor: BioMed Central Ltd

10.1186/s13023-020-01486-6 View at source

  • ISSN/ISBN 1750-1172

Special low protein foods for phenylketonuria: Availability in Europe and an examination of their nutritional profile

  • Pena, M.J.
  • 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.
... View more Collapse

Orphanet Journal of Rare Diseases - 2015

Editor: BioMed Central Ltd.

10.1186/s13023-015-0378-7 View at source

  • ISSN/ISBN 1750-1172

The complete European guidelines on phenylketonuria: Diagnosis and treatment

  • Van Wegberg, A.M.J.
  • MacDonald, A.
  • Ahring, K.
  • Bélanger-Quintana, A.
  • Blau, N.
  • Bosch, A.M.
  • Burlina, A.
  • Campistol, J.
  • Feillet, F.
  • Giżewska, M.
  • Huijbregts, S.C.
  • Kearney, S.
  • Leuzzi, V.
  • Maillot, F.
  • Muntau, A.C.
  • Van Rijn, M.
  • Trefz, F.
  • Walter, J.H.
  • Van Spronsen, F.J.
... View more Collapse

Orphanet Journal of Rare Diseases - 2017

Editor: BioMed Central Ltd.

10.1186/s13023-017-0685-2 View at source

  • ISSN/ISBN 1750-1172

Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases

  • Martín-Hernández, E.
  • Aldámiz-Echevarría, L.
  • Castejón-Ponce, E.
  • Pedrón-Giner, C.
  • Couce, M.L.
  • Serrano-Nieto, J.
  • Pintos-Morell, G.
  • Bélanger-Quintana, A.
  • Martínez-Pardo, M.
  • García-Silva, M.T.
  • Quijada-Fraile, P.
  • Vitoria-Miñana, I.
  • Dalmau, J.
  • Lama-More, R.A.
  • Bueno-Delgado, M.A.
  • Del Toro-Riera, M.
  • García-Jiménez, I.
  • Sierra-Córcoles, C.
  • Ruiz-Pons, M.
  • Peña-Quintana, L.J.
  • Vives-Piñera, I.
  • Moráis, A.
  • Balmaseda-Serrano, E.
  • Meavilla, S.
  • Sanjurjo-Crespo, P.
  • Pérez-Cerdá, C.
... View more Collapse

Orphanet journal of rare diseases (p. 187) - 2014

10.1186/s13023-014-0187-4 View at source

  • ISSN/ISBN 1750-1172

Pediatric renovascular hypertension (multiple letters) [3]

  • Estepa, R.
  • Gallego, N.
  • Orte, L.
  • Belanger, A.
  • Aracil, E.
  • Ortuño, J.
  • McTaggart, S.J.
  • Jones, C.L.
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Pediatric Nephrology (p. 529-531) - 2001

  • ISSN/ISBN 0931-041X

Challenges and pitfalls in the management of phenylketonuria

  • Feillet, F.
  • Van Spronsen, F.J.
  • MacDonald, A.
  • Trefz, F.K.
  • Demirkol, M.
  • Giovannini, M.
  • Bélanger-Quintana, A.
  • Blau, N.
... View more Collapse

Pediatrics (p. 333-341) - 2010

10.1542/peds.2009-3584 View at source

  • ISSN/ISBN 0031-4005

Long-term follow-up and outcome of phenylketonuria patients on sapropterin: A retrospective study

  • Keil, S.
  • Anjema, K.
  • Van Spronsen, F.J.
  • Lambruschini, N.
  • Burlina, A.
  • Bélanger-Quintana, A.
  • Couce, M.L.
  • Feillet, F.
  • Cerone, R.
  • Lotz-Havla, A.S.
  • Muntau, A.C.
  • Bosch, A.M.
  • Meli, C.A.P.
  • De Villemeur, T.B.
  • Kern, I.
  • Riva, E.
  • Giovannini, M.
  • Damaj, L.
  • Leuzzi, V.
  • Blau, N.
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Pediatrics - 2013

10.1542/peds.2012-3291 View at source

  • ISSN/ISBN 0031-4005

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.
... 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

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

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