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Results: 1-8 |
Results: 8
MR and other imaging methods in the investigation of mycetomas
Authors: Czechowski, J Nork, M Haas, D Lestringant, G Ekelund, L
Citation: J. Czechowski et al., MR and other imaging methods in the investigation of mycetomas, ACT RADIOL, 42(1), 2001, pp. 24-26
Bilateral frontoparietal polymicrogyria and epilepsy
Authors: Sztriha, L Nork, M
Citation: L. Sztriha et M. Nork, Bilateral frontoparietal polymicrogyria and epilepsy, PED NEUROL, 22(3), 2000, pp. 240-243
Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus
Authors: Sztriha, L Frossard, P Hofstra, RMW Verlind, E Nork, M
Citation: L. Sztriha et al., Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus, J CHILD NEU, 15(4), 2000, pp. 239-243
Sturge-Weber syndrome without facial nevus: a case report and review of the literature
Authors: Gururaj, AK Sztriha, L Johansen, J Nork, M
Citation: Ak. Gururaj et al., Sturge-Weber syndrome without facial nevus: a case report and review of the literature, ACT PAEDIAT, 89(6), 2000, pp. 740-743
Abnormal myelin formation in rhizomelic chondrodysplasia punctata type 2 (DHAPAT-deficiency)
Authors: Sztriha, L Al-Gazali, LI Wanders, RJA Ofman, R Nork, M Lestringant, GG
Citation: L. Sztriha et al., Abnormal myelin formation in rhizomelic chondrodysplasia punctata type 2 (DHAPAT-deficiency), DEVELOP MED, 42(7), 2000, pp. 492-495
Joubert's syndrome: New cases and review of clinicopathologic correlation
Authors: Sztriha, L Al-Gazali, LI Aithala, GR Nork, M
Citation: L. Sztriha et al., Joubert's syndrome: New cases and review of clinicopathologic correlation, PED NEUROL, 20(4), 1999, pp. 274-281
Autosomal recessive micrencephaly with simplified gyral pattern, abnormal myelination and arthrogryposis
Authors: Sztriha, L Al-Gazali, LI Varady, E Goebel, HH Nork, M
Citation: L. Sztriha et al., Autosomal recessive micrencephaly with simplified gyral pattern, abnormal myelination and arthrogryposis, NEUROPEDIAT, 30(3), 1999, pp. 141-145
Absent pituitary gland and hypoplasia of the cerebellar vermis associated with partial ophthalmoplegia and postaxial polydactyly: a variant of orofaciodigital syndrome VI or a new syndrome?
Authors: Al-Gazali, LI Sztriha, L Punnose, J Shather, W Nork, M
Citation: Li. Al-gazali et al., Absent pituitary gland and hypoplasia of the cerebellar vermis associated with partial ophthalmoplegia and postaxial polydactyly: a variant of orofaciodigital syndrome VI or a new syndrome?, J MED GENET, 36(2), 1999, pp. 161-166
Risultati: 1-8 |