Pineda M - 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: pineda m. 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: pineda m. 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

[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. Med Clin (Barc). 1993 Oct 2;101(10):383-6. Med Clin (Barc). 1993. PMID: 8231346 Spanish.

4

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. Among authors: pineda m. Clin Chem. 1998 Mar;44(3):662-4. Clin Chem. 1998. PMID: 9510877 No abstract available.

5

[Respiratory chain and pyruvate metabolism deficiencies in pediatric patients: evaluation of biochemical tests for selective screening].

Artuch R, Pineda M, Vilaseca MA, Briones P, Ribes A, Colomer J, Vernet A, Campistol J. Artuch R, et al. Among authors: pineda m. Rev Neurol. 1998 Jan;26(149):38-42. Rev Neurol. 1998. PMID: 9533203 Spanish.

6

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. 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.

7

[Risk factors in cerebrovascular disease in childhood].

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

8

[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: pineda m. Rev Neurol. 2000 Jun 16-30;30(12):1117-21. Rev Neurol. 2000. PMID: 10935234 Spanish.

9

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: pineda m. Clin Chem Lab Med. 2000 Oct;38(10):965-9. doi: 10.1515/CCLM.2000.143. Clin Chem Lab Med. 2000. PMID: 11140630

10

[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: pineda m. Rev Neurol. 2007 Mar 16-31;44(6):343-7. Rev Neurol. 2007. PMID: 17385170 Free article. Spanish.

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