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106 results

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Page 1
Cerebrospinal fluid synaptic proteins as useful biomarkers in tyrosine hydroxylase deficiency.
Ortez C, Duarte ST, Ormazábal A, Serrano M, Pérez A, Pons R, Pineda M, Yapici Z, Fernández-Álvarez E, Domingo-Jiménez R, De Castro P, Artuch R, García-Cazorla A. Ortez C, et al. Among authors: ormazabal a. Mol Genet Metab. 2015 Jan;114(1):34-40. doi: 10.1016/j.ymgme.2014.10.014. Epub 2014 Oct 31. Mol Genet Metab. 2015. PMID: 25468651 Free article.
Malabsorption of carbohydrates and depression in children and adolescents.
Varea V, de Carpi JM, Puig C, Alda JA, Camacho E, Ormazabal A, Artuch R, Gómez L. Varea V, et al. Among authors: ormazabal a. J Pediatr Gastroenterol Nutr. 2005 May;40(5):561-5. doi: 10.1097/01.mpg.0000153005.61234.28. J Pediatr Gastroenterol Nutr. 2005. PMID: 15861016
[Inborn errors of neurotransmitters in neuropaediatrics].
García-Cazorla A, Ormazábal A, Artuch R, Pérez-Dueñas B, López-Casas J, Fernández-Alvarez E, Campistol J. García-Cazorla A, et al. Among authors: ormazabal a. Rev Neurol. 2005 Jul 16-31;41(2):99-108. Rev Neurol. 2005. PMID: 16028189 Free article. Review. Spanish.
Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency.
Møller LB, Romstad A, Paulsen M, Hougaard P, Ormazabal A, Pineda M, Blau N, Güttler F, Artuch R. Møller LB, et al. Among authors: ormazabal a. Prenat Diagn. 2005 Aug;25(8):671-5. doi: 10.1002/pd.1193. Prenat Diagn. 2005. PMID: 16049992
Methods for the diagnosis of creatine deficiency syndromes: a comparative study.
Arias A, Ormazabal A, Moreno J, González B, Vilaseca MA, García-Villoria J, Pàmpols T, Briones P, Artuch R, Ribes A. Arias A, et al. Among authors: ormazabal a. J Neurosci Methods. 2006 Sep 30;156(1-2):305-9. doi: 10.1016/j.jneumeth.2006.03.005. Epub 2006 Apr 18. J Neurosci Methods. 2006. PMID: 16621013
106 results