Artuch R - Search Results

1

Childhood chorea with cerebral hypotrophy: a treatable GLUT1 energy failure syndrome.

Pérez-Dueñas B, Prior C, Ma Q, Fernández-Alvarez E, Setoain X, Artuch R, Pascual JM. Pérez-Dueñas B, et al. Among authors: artuch r. Arch Neurol. 2009 Nov;66(11):1410-4. doi: 10.1001/archneurol.2009.236. Arch Neurol. 2009. PMID: 19901175

2

Tetrahydrobiopterin responsiveness in patients with phenylketonuria.

Pérez-Dueñas B, Vilaseca MA, Mas A, Lambruschini N, Artuch R, Gómez L, Pineda J, Gutiérrez A, Mila M, Campistol J. Pérez-Dueñas B, et al. Among authors: artuch r. Clin Biochem. 2004 Dec;37(12):1083-90. doi: 10.1016/j.clinbiochem.2004.09.005. Clin Biochem. 2004. PMID: 15589814 Clinical Trial.

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

Characterization of tremor in phenylketonuric patients.

Pérez-Dueñas B, Valls-Solé J, Fernández-Alvarez E, Conill J, Vilaseca MA, Artuch R, Campistol J. Pérez-Dueñas B, et al. Among authors: artuch r. J Neurol. 2005 Nov;252(11):1328-34. doi: 10.1007/s00415-005-0860-6. Epub 2005 Jul 5. J Neurol. 2005. PMID: 15995796

5

[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.

6

Clinical and nutritional evaluation of phenylketonuric patients on tetrahydrobiopterin monotherapy.

Lambruschini N, Pérez-Dueñas B, Vilaseca MA, Mas A, Artuch R, Gassió R, Gómez L, Gutiérrez A, Campistol J. Lambruschini N, et al. Among authors: artuch r. Mol Genet Metab. 2005 Dec;86 Suppl 1:S54-60. doi: 10.1016/j.ymgme.2005.05.014. Epub 2005 Jul 22. Mol Genet Metab. 2005. PMID: 16040265

7

Is deoxypyridinoline a good resorption marker to detect osteopenia in phenylketonuria?

Millet P, Vilaseca MA, Valls C, Pérez-Dueñas B, Artuch R, Gómez L, Lambruschini N, Campistol J. Millet P, et al. Among authors: artuch r. Clin Biochem. 2005 Dec;38(12):1127-32. doi: 10.1016/j.clinbiochem.2005.09.002. Epub 2005 Oct 27. Clin Biochem. 2005. PMID: 16256974

8

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

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

Global and regional volume changes in the brains of patients with phenylketonuria.

Pérez-Dueñas B, Pujol J, Soriano-Mas C, Ortiz H, Artuch R, Vilaseca MA, Campistol J. Pérez-Dueñas B, et al. Among authors: artuch r. Neurology. 2006 Apr 11;66(7):1074-8. doi: 10.1212/01.wnl.0000204415.39853.4a. Neurology. 2006. PMID: 16606920

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