Search Results - "Gabis, L.V."

  • Showing 1 - 2 results of 2
Refine Results
  1. 1

    Creatine transporter deficiency: Novel mutations and functional studies by Ardon, O., Procter, M., Mao, R., Longo, N., Landau, Y.E., Shilon-Hadass, A., Gabis, L.V., Hoffmann, C., Tzadok, M., Heimer, G., Sada, S., Ben-Zeev, B., Anikster, Y.

    Published in Molecular genetics and metabolism reports (01-09-2016)
    “…X-linked cerebral creatine deficiency (MIM 300036) is caused by deficiency of the creatine transporter encoded by the SLC6A8 gene. Here we report three…”
    Get full text
    Journal Article
  2. 2

    Prediction of participation and sensory modulation of late preterm infants at 12 months: A prospective study by Bart, O., Shayevits, S., Gabis, L.V., Morag, I.

    Published in Research in developmental disabilities (01-11-2011)
    “…► At age of 1 year, children born as late preterm are at increased risk of developing sensory modulation disorder. ► At age of 1 year, children born as late…”
    Get full text
    Journal Article