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Developmental outcome of electroencephalographic findings in SYNGAP1 encephalopathy.
Front Cell Dev Biol. 2024 Mar 5;12:1321282. doi: 10.3389/fcell.2024.1321282. eCollection 2024.
Front Cell Dev Biol. 2024.
PMID: 38505260
Free PMC article.
Early infantile epileptic encephalopathy with unusual favourable outcome.
Cazorla MR, Verdú A, Montes C, Ayuga F.
Cazorla MR, et al.
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
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Neuroimage findings in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency.
Cazorla MR, Verdú A, Pérez-Cerdá C, Ribes A.
Cazorla MR, et al.
Pediatr Neurol. 2007 Apr;36(4):264-7. doi: 10.1016/j.pediatrneurol.2006.11.014.
Pediatr Neurol. 2007.
PMID: 17437913
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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. Among authors: cazorla mr.
Pediatr Neurol. 2001 Jan;24(1):69-71. doi: 10.1016/s0887-8994(00)00228-9.
Pediatr Neurol. 2001.
PMID: 11182285
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Prenatal stroke in a neonate heterozygous for factor V Leiden mutation.
Verdu A, Cazorla MR, Moreno JC, Casado LF.
Verdu A, et al. Among authors: cazorla mr.
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
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