Belanger-Quintana A - Search Results

1

Plasma CoQ10 Status in Patients with Propionic Acidaemia and Possible Benefit of Treatment with Ubiquinol.

Stanescu S, Belanger-Quintana A, Fernández-Felix BM, Ruiz-Sala P, Alcaide P, Arrieta F, Martínez-Pardo M. Stanescu S, et al. Antioxidants (Basel). 2022 Aug 16;11(8):1588. doi: 10.3390/antiox11081588. Antioxidants (Basel). 2022. PMID: 36009307 Free PMC article.

2

Management of phenylketonuria in European PKU centres remains heterogeneous.

Ahring K, Bélanger-Quintana A, Burlina A, Giżewska M, Maillot F, Muntau A, Roscher A, MacDonald A. Ahring K, et al. Among authors: belanger quintana a. Mol Genet Metab. 2024 Jan;141(1):108120. doi: 10.1016/j.ymgme.2023.108120. Epub 2023 Dec 23. Mol Genet Metab. 2024. PMID: 38159545

3

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

Suárez Cortina L, Bélanger-Quintana A. Suárez Cortina L, et al. J Pediatr Gastroenterol Nutr. 2000 Mar;30(3):351. doi: 10.1097/00005176-200003000-00032. J Pediatr Gastroenterol Nutr. 2000. PMID: 10749430 No abstract available.

4

Hyperammonaemia as a cause of psychosis in an adolescent.

Bélanger-Quintana A, Martínez-Pardo M, García MJ, Wermuth B, Torres J, Pallarés E, Ugarte M. Bélanger-Quintana A, et al. Eur J Pediatr. 2003 Nov;162(11):773-5. doi: 10.1007/s00431-002-1126-2. Epub 2003 Aug 27. Eur J Pediatr. 2003. PMID: 12942317

5

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

Desviat LR, Pérez B, Bèlanger-Quintana A, Castro M, Aguado C, Sánchez A, García MJ, Martínez-Pardo M, Ugarte M. Desviat LR, et al. Mol Genet Metab. 2004 Sep-Oct;83(1-2):157-62. doi: 10.1016/j.ymgme.2004.06.007. Mol Genet Metab. 2004. PMID: 15464430

6

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

Bélanger-Quintana A, García MJ, Castro M, Desviat LR, Pérez B, Mejía B, Ugarte M, Martínez-Pardo M. Bélanger-Quintana A, et al. Mol Genet Metab. 2005 Dec;86 Suppl 1:S61-6. doi: 10.1016/j.ymgme.2005.07.024. Epub 2005 Sep 13. Mol Genet Metab. 2005. PMID: 16165389

7

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 MJ, Martínez Pardo M, Belanger-Quintana A, de la Mota JL, Martin-Hernández E, Vianey-Saban C, Bischoff C, Gregersen N, Ugarte M. Merinero B, et al. J Inherit Metab Dis. 2006 Oct;29(5):685. doi: 10.1007/s10545-006-0342-8. Epub 2006 Aug 12. J Inherit Metab Dis. 2006. PMID: 16906473

8

BH4 responsiveness associated to a PKU mutation with decreased binding affinity for the cofactor.

Aguado C, Pérez B, García MJ, Bélanger-Quintana A, Martínez-Pardo M, Ugarte M, Desviat LR. Aguado C, et al. Clin Chim Acta. 2007 May 1;380(1-2):8-12. doi: 10.1016/j.cca.2007.02.034. Clin Chim Acta. 2007. PMID: 17408607

9

Physical development in patients with phenylketonuria on dietary treatment: a retrospective study.

Belanger-Quintana A, Martínez-Pardo M. Belanger-Quintana A, et al. Mol Genet Metab. 2011 Dec;104(4):480-4. doi: 10.1016/j.ymgme.2011.08.002. Epub 2011 Aug 10. Mol Genet Metab. 2011. PMID: 21878401

10

[Importance of early diagnosis of phenylketonuria in women and control of phenylalanine levels during pregnancy].

Arrieta Blanco F, Bélanger Quintana A, Vázquez Martínez C, Martínez Pardo M. Arrieta Blanco F, et al. Nutr Hosp. 2012 Sep-Oct;27(5):1658-61. doi: 10.3305/nh.2012.27.5.5945. Nutr Hosp. 2012. PMID: 23478721 Spanish.

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