Verdú A - Search Results

1

Respiratory chain complex I deficiency in an infant with infantile spasms.

Verdú A, Alonso LA, Arenas J. Verdú A, et al. J Neurol Neurosurg Psychiatry. 1996 Mar;60(3):349. doi: 10.1136/jnnp.60.3.349. J Neurol Neurosurg Psychiatry. 1996. PMID: 8609522 Free PMC article. No abstract available.

2

Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient.

Blázquez A, Gil-Borlado MC, Morán M, Verdú A, Cazorla-Calleja MR, Martín MA, Arenas J, Ugalde C. Blázquez A, et al. Among authors: verdu a. Neuromuscul Disord. 2009 Feb;19(2):143-6. doi: 10.1016/j.nmd.2008.11.016. Epub 2009 Jan 21. Neuromuscul Disord. 2009. PMID: 19162478

3

Dandy-Walker malformation in an infant with tetrasomy 9p.

Cazorla Calleja MR, Verdú A, Félix V. Cazorla Calleja MR, et al. Among authors: verdu a. Brain Dev. 2003 Apr;25(3):220-3. doi: 10.1016/s0387-7604(02)00211-5. Brain Dev. 2003. PMID: 12689705

4

Uniparental disomy as a cause of spinal muscular atrophy and progressive myoclonic epilepsy: phenotypic homogeneity due to the homozygous c.125C>T mutation in ASAH1.

Giráldez BG, Guerrero-López R, Ortega-Moreno L, Verdú A, Carrascosa-Romero MC, García-Campos Ó, García-Muñozguren S, Pardal-Fernández JM, Serratosa JM. Giráldez BG, et al. Among authors: verdu a. Neuromuscul Disord. 2015 Mar;25(3):222-4. doi: 10.1016/j.nmd.2014.11.007. Epub 2014 Nov 22. Neuromuscul Disord. 2015. PMID: 25578555

5

Novel mutation in STXBP1 gene in a patient with non-lesional Ohtahara syndrome.

Ortega-Moreno L, Giráldez BG, Verdú A, García-Campos O, Sánchez-Martín G, Serratosa JM, Guerrero-López R. Ortega-Moreno L, et al. Among authors: verdu a. Neurologia. 2016 Oct;31(8):523-7. doi: 10.1016/j.nrl.2014.10.017. Epub 2015 Jan 24. Neurologia. 2016. PMID: 25631041 Free article. English, Spanish.

6

Prenatal stroke in a neonate heterozygous for factor V Leiden mutation.

Verdu A, Cazorla MR, Moreno JC, Casado LF. Verdu A, et al. Brain Dev. 2005 Sep;27(6):451-4. doi: 10.1016/j.braindev.2004.10.004. Epub 2004 Dec 18. Brain Dev. 2005. PMID: 16122636

7

Early infantile epileptic encephalopathy with unusual favourable outcome.

Cazorla MR, Verdú A, Montes C, Ayuga F. Cazorla MR, et al. Among authors: verdu a. Brain Dev. 2010 Sep;32(8):673-6. doi: 10.1016/j.braindev.2009.08.007. Epub 2009 Sep 19. Brain Dev. 2010. PMID: 19767162

8

Neuroimage findings in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency.

Cazorla MR, Verdú A, Pérez-Cerdá C, Ribes A. Cazorla MR, et al. Among authors: verdu a. Pediatr Neurol. 2007 Apr;36(4):264-7. doi: 10.1016/j.pediatrneurol.2006.11.014. Pediatr Neurol. 2007. PMID: 17437913

9

Basilar artery thrombosis in a child heterozygous for factor V Leiden mutation.

Verdú A, Cazorla MR, Granados MA, Alonso JA, Casado LF. Verdú A, et al. Pediatr Neurol. 2001 Jan;24(1):69-71. doi: 10.1016/s0887-8994(00)00228-9. Pediatr Neurol. 2001. PMID: 11182285

10

Intramedullary dermoid of the cervical spinal cord in a child.

Verdu A, de la Cruz M, Pascual-Castroviejo I, Villarejo F. Verdu A, et al. J Neurol Neurosurg Psychiatry. 1986 Apr;49(4):462-3. doi: 10.1136/jnnp.49.4.462. J Neurol Neurosurg Psychiatry. 1986. PMID: 3701362 Free PMC article. No abstract available.

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