López-Laso E - Search Results

1

Mateos ME, López-Laso E, Pérez-Navero JL. Mateos ME, et al. Pediatr Blood Cancer. 2011 Oct;57(4):696. doi: 10.1002/pbc.23089. Epub 2011 Jun 30. Pediatr Blood Cancer. 2011. PMID: 21721106 No abstract available.

2

Successful response to cidofovir of adenovirus hepatitis during chemotherapy in a child with hepatoblastoma.

Mateos ME, López-Laso E, Pérez-Navero JL, Peña MJ, Velasco MJ. Mateos ME, et al. J Pediatr Hematol Oncol. 2012 Oct;34(7):e298-300. doi: 10.1097/MPH.0b013e318266ba72. J Pediatr Hematol Oncol. 2012. PMID: 22935664

3

Simpson-Golabi-Behmel syndrome type 1 and hepatoblastoma in a patient with a novel exon 2-4 duplication of the GPC3 gene.

Mateos ME, Beyer K, López-Laso E, Siles JL, Pérez-Navero JL, Peña MJ, Guzmán J, Matas J. Mateos ME, et al. Am J Med Genet A. 2013 May;161A(5):1091-5. doi: 10.1002/ajmg.a.35738. Epub 2013 Mar 5. Am J Med Genet A. 2013. PMID: 23463737

4

Response to nimotuzumab in a child with a progressive diffuse intrinsic pontine glioma.

Mateos ME, López-Laso E, Izquierdo L, Pérez-Navero JL, García S, Garzás C. Mateos ME, et al. Pediatr Int. 2011 Apr;53(2):261-3. doi: 10.1111/j.1442-200X.2010.03220.x. Pediatr Int. 2011. PMID: 21501315 No abstract available.

5

Dopa-responsive infantile hypokinetic rigid syndrome due to dominant guanosine triphosphate cyclohydrolase 1 deficiency.

López-Laso E, Camino R, Mateos ME, Pérez-Navero JL, Ochoa JJ, Lao-Villadóniga JI, Ormazabal A, Artuch R. López-Laso E, et al. J Neurol Sci. 2007 May 15;256(1-2):90-3. doi: 10.1016/j.jns.2007.02.007. Epub 2007 Mar 21. J Neurol Sci. 2007. PMID: 17368676

6

Reticulocyte hemoglobin content for the diagnosis of iron deficiency.

Mateos ME, De-la-Cruz J, López-Laso E, Valdés MD, Nogales A. Mateos ME, et al. J Pediatr Hematol Oncol. 2008 Jul;30(7):539-42. doi: 10.1097/MPH.0b013e31817580ca. J Pediatr Hematol Oncol. 2008. PMID: 18797202

7

Response to everolimus of a progressive plexiform neurofibroma in Neurofibromatosis type 1.

Mateos ME, López-Laso E, Vicente J, Ortega R, Vázquez F, Pérez-Navero JL. Mateos ME, et al. Pediatr Int. 2020 Jul;62(7):857-859. doi: 10.1111/ped.14183. Epub 2020 Jul 6. Pediatr Int. 2020. PMID: 32027426 No abstract available.

8

Segawa syndrome due to mutation Q89X in the GCH1 gene: a possible founder effect in Córdoba (southern Spain).

López-Laso E, Ochoa-Sepúlveda JJ, Ochoa-Amor JJ, Bescansa-Heredero E, Camino-León R, Gascón-Jiménez FJ, Mateos-González ME, Pérez-Navero JL, Lao-Villadóniga JI, Ormazabal A, Artuch R, Beyer K. López-Laso E, et al. J Neurol. 2009 Nov;256(11):1816-24. doi: 10.1007/s00415-009-5198-z. Epub 2009 Jun 16. J Neurol. 2009. PMID: 19533203

9

Oral phenylalanine loading test for the diagnosis of dominant guanosine triphosphate cyclohydrolase 1 deficiency.

López-Laso E, Ormazabal A, Camino R, Gascón FJ, Ochoa JJ, Mateos ME, Muñoz MJ, Pérez-Navero JL, Lao JI, Vilaseca MA, Artuch R. López-Laso E, et al. Clin Biochem. 2006 Sep;39(9):893-7. doi: 10.1016/j.clinbiochem.2006.03.002. Epub 2006 Apr 19. Clin Biochem. 2006. PMID: 16624273

10

Neuropsychiatric symptoms and intelligence quotient in autosomal dominant Segawa disease.

López-Laso E, Sánchez-Raya A, Moriana JA, Martínez-Gual E, Camino-León R, Mateos-González ME, Pérez-Navero JL, Ochoa-Sepúlveda JJ, Ormazabal A, Opladen T, Klein C, Lao-Villadóniga JI, Beyer K, Artuch R. López-Laso E, et al. J Neurol. 2011 Dec;258(12):2155-62. doi: 10.1007/s00415-011-6079-9. Epub 2011 May 10. J Neurol. 2011. PMID: 21556877

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