Artuch R - Search Results

1

Pediatric Gaucher disease with intermediate type 2-3 phenotype associated with parkinsonian features and levodopa responsiveness.

Darling A, Irún P, Giraldo P, Armstrong J, Gort L, Díaz-Conradi Á, Yubero D, De Oryazábal Sanz AL, Ormazábal A, Artuch R, García-Cazorla À, O'Callaghan M. Darling A, et al. Among authors: artuch r. Parkinsonism Relat Disord. 2021 Oct;91:19-22. doi: 10.1016/j.parkreldis.2021.08.010. Epub 2021 Aug 19. Parkinsonism Relat Disord. 2021. PMID: 34454394

2

[Pathogenetic mechanisms in phenylketonuria: disorders affecting the metabolism of neurotransmitters and the antioxidant system].

Ormazábal A, Artuch R, Vilaseca MA, García-Cazorla A, Campistol J. Ormazábal A, et al. Among authors: artuch r. Rev Neurol. 2004 Nov 16-30;39(10):956-61. Rev Neurol. 2004. PMID: 15573314 Free article. Review. Spanish.

3

HPLC with electrochemical and fluorescence detection procedures for the diagnosis of inborn errors of biogenic amines and pterins.

Ormazabal A, García-Cazorla A, Fernández Y, Fernández-Alvarez E, Campistol J, Artuch R. Ormazabal A, et al. Among authors: artuch r. J Neurosci Methods. 2005 Mar 15;142(1):153-8. doi: 10.1016/j.jneumeth.2004.08.007. J Neurosci Methods. 2005. PMID: 15652629

4

Congenital disorder of glycosylation type Ia revealed by hypertransaminasemia and failure to thrive in a young boy with normal neurodevelopment.

Pancho C, Garcia-Cazorla A, Varea V, Artuch R, Ferrer I, Vilaseca MA, Briones P, Campistol J. Pancho C, et al. Among authors: artuch r. J Pediatr Gastroenterol Nutr. 2005 Feb;40(2):230-2. doi: 10.1097/00005176-200502000-00030. J Pediatr Gastroenterol Nutr. 2005. PMID: 15699704 No abstract available.

5

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: artuch r. 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

6

[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: artuch r. Rev Neurol. 2005 Jul 16-31;41(2):99-108. Rev Neurol. 2005. PMID: 16028189 Free article. Review. Spanish.

7

Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion.

Pineda M, Ormazabal A, López-Gallardo E, Nascimento A, Solano A, Herrero MD, Vilaseca MA, Briones P, Ibáñez L, Montoya J, Artuch R. Pineda M, et al. Among authors: artuch r. Ann Neurol. 2006 Feb;59(2):394-8. doi: 10.1002/ana.20746. Ann Neurol. 2006. PMID: 16365882

8

Cerebrospinal fluid concentrations of folate, biogenic amines and pterins in Rett syndrome: treatment with folinic acid.

Ormazabal A, Artuch R, Vilaseca MA, Aracil A, Pineda M. Ormazabal A, et al. Among authors: artuch r. Neuropediatrics. 2005 Dec;36(6):380-5. doi: 10.1055/s-2005-873078. Neuropediatrics. 2005. PMID: 16429378 Clinical Trial.

9

Platelet serotonin concentrations in PKU patients under dietary control and tetrahydrobiopterin treatment.

Ormazabal A, Vilaseca MA, Pérez-Dueñas B, Lambruschini N, Gómez L, Campistol J, Artuch R. Ormazabal A, et al. Among authors: artuch r. J Inherit Metab Dis. 2005;28(6):863-70. doi: 10.1007/s10545-005-0153-3. J Inherit Metab Dis. 2005. PMID: 16435178

10

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: artuch r. 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

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