Vilaseca MA - Search Results

1

Diagnostic approach to inborn errors of metabolism in an emergency unit.

Calvo M, Artuch R, Macià E, Luaces C, Vilaseca MA, Pou J, Pineda M. Calvo M, et al. Among authors: vilaseca ma. Pediatr Emerg Care. 2000 Dec;16(6):405-8. doi: 10.1097/00006565-200012000-00006. Pediatr Emerg Care. 2000. PMID: 11138882

2

Tocopherol in inborn errors of intermediary metabolism.

Moyano D, Vilaseca MA, Pineda M, Campistol J, Vernet A, Póo P, Artuch R, Sierra C. Moyano D, et al. Among authors: vilaseca ma. Clin Chim Acta. 1997 Jul 25;263(2):147-55. doi: 10.1016/s0009-8981(97)00061-2. Clin Chim Acta. 1997. PMID: 9246419

3

Assessment of the perimortem protocol in neonates for the diagnosis of inborn errors of metabolism.

Marín-Valencia I, Vilaseca MA, Thió M, García-Cazorla A, Artuch R, Campistol J. Marín-Valencia I, et al. Among authors: vilaseca ma. Eur J Paediatr Neurol. 2010 Mar;14(2):125-30. doi: 10.1016/j.ejpn.2009.05.001. Epub 2009 Jun 9. Eur J Paediatr Neurol. 2010. PMID: 19515591

4

[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.

5

[Aspects of neuropathy in mitochondrial diseases].

Colomer J, Iturriaga C, Bestué M, Artuch R, Briones P, Montoya J, Vilaseca MA, Pineda M. Colomer J, et al. Among authors: vilaseca ma. Rev Neurol. 2000 Jun 16-30;30(12):1117-21. Rev Neurol. 2000. PMID: 10935234 Spanish.

6

Personal experience with the application of carbohydrate-deficient transferrin (CDT) assays to the detection of congenital disorders of glycosylation.

Colomé C, Ferrer I, Artuch R, Vilaseca MA, Pineda M, Briones P. Colomé C, et al. Among authors: vilaseca ma. Clin Chem Lab Med. 2000 Oct;38(10):965-9. doi: 10.1515/CCLM.2000.143. Clin Chem Lab Med. 2000. PMID: 11140630

7

[Cerebral creatine transporter deficiency: an infradiagnosed neurometabolic disease].

Campistol J, Arias-Dimas A, Poo P, Pineda M, Hoffman M, Vilaseca MA, Artuch R, Ribes A. Campistol J, et al. Among authors: vilaseca ma. Rev Neurol. 2007 Mar 16-31;44(6):343-7. Rev Neurol. 2007. PMID: 17385170 Free article. Spanish.

8

Long-chain polyunsaturated fatty acid concentration in patients with inborn errors of metabolism.

Vilaseca MA, Gómez-López L, Lambruschini N, Gutiérrez A, García R, Meavilla S, Moreno J, Artuch R. Vilaseca MA, et al. Nutr Hosp. 2011 Jan-Feb;26(1):128-36. Nutr Hosp. 2011. PMID: 21519739

9

[Diagnosis of ornithine carbamoyl transferase deficiency and heterozygote detection with allopurinol loading test].

Pineda M, Vilaseca MA, Mas A, Fábrega C, Fernández Alvarez E. Pineda M, et al. Among authors: vilaseca ma. Med Clin (Barc). 1993 Oct 2;101(10):383-6. Med Clin (Barc). 1993. PMID: 8231346 Spanish.

10

Selective screening for hyperhomocysteinemia in pediatric patients.

Vilaseca MA, Moyano D, Artuch R, Ferrer I, Pineda M, Cardo E, Campistol J, Pavia C, Camacho JA. Vilaseca MA, et al. Clin Chem. 1998 Mar;44(3):662-4. Clin Chem. 1998. PMID: 9510877 No abstract available.

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