Skip Navigation, or press ALT and K together and then press enter.Welcome to the OMC website. This site has been developed for both the visually impaired and non visually impaired. If you would like to use the visually impaired version of this site please go to omc.gov.ie/viewtxt.asp, or press ALT and I together and then press enter

Irish Child Health Database - Peer Reviewed Papers

Database Search


Irish Child Health Database » » A » autosomal dominant inheritance

autosomal dominant inheritance

Your search returns 2 documents

  • 1.   Hereditary cerebral cavernous angiomas: Presentation as idiopathic familial epilepsy

    This case report discusses a cause of familial epilepsy that also emphasises the importance of MRI as the modality of choice in investigating seizures in children - Hereditary cerebral cavernous angiomas

    Irish Medical Journal, Vol: 95 Page: 56-58 2002
    D. Coghlan; B. Lynch; D. Allcutt

    [Preview] [Read]

  • 2.   REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31

    The aim of this study was to examine REEP1 mutation spectrum and genotype/phenotype correlation for hereditary spastic paraplegia type 31

    Brain, Vol: 131 Page: 1078-1086 2008
    C. Beetz; R. Schule; T. Deconinck; K. N. Tran-Viet; H. Zhu; B. P. H. Kremer; S. G. M. Frints; W. A. G. Van Zelst-Stams; P. Byrne; S. Otto; A. O. H. Nygren; J. Baets; K. Smets; B. Ceulemans; B. Dan; N. Nagan; J. Kassubek; S. Klimpe; T. Klopstock; H. Stolze; H. J. M. Smeets; C. T. R. M. Schrander-Stumpel; M. Hutchinson; B. P. Van De Warrenburg; C. Braastad; T. Deufel; M. Pericak-Vance; L. Schols; P. De Jonghe; S. Zuchner

    [Preview] [Read]