Vilaseca MA - Search Results

1

3-phosphoglycerate dehydrogenase deficiency in a patient with West syndrome.

Pineda M, Vilaseca MA, Artuch R, Santos S, García González MM, Aracil A, Van Schaftingen E, Jaeken J. Pineda M, et al. Among authors: vilaseca ma. Dev Med Child Neurol. 2000 Sep;42(9):629-33. doi: 10.1017/s0012162200001171. Dev Med Child Neurol. 2000. PMID: 11034457 Free article.

2

Glutaric aciduria type I with high residual glutaryl-CoA dehydrogenase activity.

Pineda M, Ribes A, Busquets C, Vilaseca MA, Aracil A, Christensen E. Pineda M, et al. Among authors: vilaseca ma. Dev Med Child Neurol. 1998 Dec;40(12):840-2. doi: 10.1111/j.1469-8749.1998.tb12362.x. Dev Med Child Neurol. 1998. PMID: 9881681 Free article.

3

Children with stroke: polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin status.

Cardo E, Monrós E, Colomé C, Artuch R, Campistol J, Pineda M, Vilaseca MA. Cardo E, et al. Among authors: vilaseca ma. J Child Neurol. 2000 May;15(5):295-8. doi: 10.1177/088307380001500505. J Child Neurol. 2000. PMID: 10830195

4

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: vilaseca ma. Neurology. 2006 Apr 11;66(7):1074-8. doi: 10.1212/01.wnl.0000204415.39853.4a. Neurology. 2006. PMID: 16606920

5

Long-term evolution of eight Spanish patients with CDG type Ia: typical and atypical manifestations.

Pérez-Dueñas B, García-Cazorla A, Pineda M, Poo P, Campistol J, Cusí V, Schollen E, Matthijs G, Grunewald S, Briones P, Pérez-Cerdá C, Artuch R, Vilaseca MA. Pérez-Dueñas B, et al. Among authors: vilaseca ma. Eur J Paediatr Neurol. 2009 Sep;13(5):444-51. doi: 10.1016/j.ejpn.2008.09.002. Epub 2008 Oct 22. Eur J Paediatr Neurol. 2009. PMID: 18948042

6

Normal pubertal development in a female with carbohydrate deficient glycoprotein syndrome.

Pineda M, Pavia C, Vilaseca MA, Ferrer I, Temudo T, Chabas A, Stibler H, Jaeken J. Pineda M, et al. Among authors: vilaseca ma. Arch Dis Child. 1996 Mar;74(3):242-3. doi: 10.1136/adc.74.3.242. Arch Dis Child. 1996. PMID: 8787432 Free PMC article.

7

Biochemical monitoring of the treatment in paediatric patients with mitochondrial disease.

Artuch R, Vilaseca MA, Pineda M. Artuch R, et al. Among authors: vilaseca ma. J Inherit Metab Dis. 1998 Dec;21(8):837-45. doi: 10.1023/a:1005470702369. J Inherit Metab Dis. 1998. PMID: 9870209

8

Evaluation of hyperhomocysteinaemia in children with stroke.

Cardo E, Vilaseca MA, Campistol J, Artuch R, Colomé C, Pineda M. Cardo E, et al. Among authors: vilaseca ma. Eur J Paediatr Neurol. 1999;3(3):113-7. doi: 10.1016/s1090-3798(99)90098-3. Eur J Paediatr Neurol. 1999. PMID: 10461566

9

[Ubiquinone: metabolism and functions. Ubiquinone deficiency and its implication in mitochondrial encephalopathies. Treatment with ubiquinone].

Artuch R, Colomé C, Vilaseca MA, Pineda M, Campistol J. Artuch R, et al. Among authors: vilaseca ma. Rev Neurol. 1999 Jul 1-15;29(1):59-63. Rev Neurol. 1999. PMID: 10528314 Review. Spanish.

10

[Risk factors in cerebrovascular disease in childhood].

Cardo E, Pineda M, Vilaseca MA, Artuch R, Campistol J. Cardo E, et al. Among authors: vilaseca ma. Rev Neurol. 2000 Jan 1-15;30(1):21-7. Rev Neurol. 2000. PMID: 10742991 Spanish.

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