László Sztriha
Department of Pediatrics
Faculty of Medicine and Health Sciences
United Arab Emirates University
Name/email consistency: high
- Extreme microcephaly with agyria-pachygyria, partial agenesis of the corpus callosum, and pontocerebellar dysplasia. Sztriha, L., Johansen, J.G., Al-Gazali, L.I. J. Child Neurol. (2005)
- Spectrum of malformations of the hindbrain (cerebellum, pons, and medulla) in a cohort of children with high rate of parental consanguinity. Sztriha, L., Johansen, J.G. Am. J. Med. Genet. A (2005)
- Hippocampal dysgenesis associated with temporal lobe hypoplasia and arachnoid cyst of the middle cranial fossa. Sztriha, L., Gururaj, A. J. Child Neurol. (2005)
- Clinical, MRI, and pathological features of polymicrogyria in chromosome 22q11 deletion syndrome. Sztriha, L., Guerrini, R., Harding, B., Stewart, F., Chelloug, N., Johansen, J.G. Am. J. Med. Genet. A (2004)
- Microcephaly associated with abnormal gyral pattern. Sztriha, L., Dawodu, A., Gururaj, A., Johansen, J.G. Neuropediatrics (2004)
- Frameshift mutation of the zinc finger homeo box 1 B gene in syndromic corpus callosum agenesis (Mowat-Wilson syndrome). Sztriha, L., Espinosa-Parrilla, Y., Gururaj, A., Amiel, J., Lyonnet, S., Gerami, S., Johansen, J.G. Neuropediatrics (2003)
- Temporal lobe epilepsy in children: etiology in a cohort with new-onset seizures. Sztriha, L., Gururaj, A.K., Bener, A., Nork, M. Epilepsia (2002)
- Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus. Sztriha, L., Frossard, P., Hofstra, R.M., Verlind, E., Nork, M. J. Child Neurol. (2000)
- Abnormal myelin formation in rhizomelic chondrodysplasia punctata type 2 (DHAPAT-deficiency). Sztriha, L., Al-Gazali, L.I., Wanders, R.J., Ofman, R., Nork, M., Lestringant, G.G. Dev. Med. Child. Neurol (2000)
