Campistol J - Search Results

1

Creatine transporter deficiency: prevalence among patients with mental retardation and pitfalls in metabolite screening.

Arias A, Corbella M, Fons C, Sempere A, García-Villoria J, Ormazabal A, Poo P, Pineda M, Vilaseca MA, Campistol J, Briones P, Pàmpols T, Salomons GS, Ribes A, Artuch R. Arias A, et al. Among authors: campistol j. Clin Biochem. 2007 Nov;40(16-17):1328-31. doi: 10.1016/j.clinbiochem.2007.07.010. Epub 2007 Aug 10. Clin Biochem. 2007. PMID: 17825809

2

Ubiquinone-10 content in lymphocytes of phenylketonuric patients.

Colomé C, Artuch R, Vilaseca MA, Sierra C, Brandi N, Cambra FJ, Lambruschini N, Campistol J. Colomé C, et al. Among authors: campistol j. Clin Biochem. 2002 Feb;35(1):81-4. doi: 10.1016/s0009-9120(02)00278-3. Clin Biochem. 2002. PMID: 11937084

3

Hurler's syndrome, West's syndrome, and vitamin D-dependent rickets.

Gudiño MA, Campistol J, Chavez B, Conill J, Hernández S, Vilaseca MA. Gudiño MA, et al. Among authors: campistol j. J Child Neurol. 2002 Feb;17(2):149-51. doi: 10.1177/088307380201700214. J Child Neurol. 2002. PMID: 11952079

4

Lipophilic antioxidants in patients with phenylketonuria.

Colomé C, Artuch R, Vilaseca MA, Sierra C, Brandi N, Lambruschini N, Cambra FJ, Campistol J. Colomé C, et al. Among authors: campistol j. Am J Clin Nutr. 2003 Jan;77(1):185-8. doi: 10.1093/ajcn/77.1.185. Am J Clin Nutr. 2003. PMID: 12499340

5

Spectrum of CBS mutations in 16 homocystinuric patients from the Iberian Peninsula: high prevalence of T191M and absence of I278T or G307S.

Urreizti R, Balcells S, Rodés M, Vilarinho L, Baldellou A, Couce ML, Muñoz C, Campistol J, Pintó X, Vilaseca MA, Grinberg D. Urreizti R, et al. Among authors: campistol j. Hum Mutat. 2003 Jul;22(1):103. doi: 10.1002/humu.9153. Hum Mutat. 2003. PMID: 12815602

6

A longitudinal study of antioxidant status in phenylketonuric patients.

Artuch R, Colomé C, Sierra C, Brandi N, Lambruschini N, Campistol J, Ugarte D, Vilaseca MA. Artuch R, et al. Among authors: campistol j. Clin Biochem. 2004 Mar;37(3):198-203. doi: 10.1016/j.clinbiochem.2003.10.017. Clin Biochem. 2004. PMID: 14972641

7

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: campistol j. Clin Biochem. 2004 Dec;37(12):1083-90. doi: 10.1016/j.clinbiochem.2004.09.005. Clin Biochem. 2004. PMID: 15589814 Clinical Trial.

8

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: campistol j. J Neurosci Methods. 2005 Mar 15;142(1):153-8. doi: 10.1016/j.jneumeth.2004.08.007. J Neurosci Methods. 2005. PMID: 15652629

9

Cognitive functions in classic phenylketonuria and mild hyperphenylalaninaemia: experience in a paediatric population.

Gassió R, Artuch R, Vilaseca MA, Fusté E, Boix C, Sans A, Campistol J. Gassió R, et al. Among authors: campistol j. Dev Med Child Neurol. 2005 Jul;47(7):443-8. doi: 10.1017/s0012162205000861. Dev Med Child Neurol. 2005. PMID: 15991863 Free article. Clinical Trial.

10

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: campistol j. J Neurol. 2005 Nov;252(11):1328-34. doi: 10.1007/s00415-005-0860-6. Epub 2005 Jul 5. J Neurol. 2005. PMID: 15995796

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