Kleopas A. Kleopa
Neuroscience Laboratory
The Cyprus Institute of Neurology and Genetics
Nicosia
Cyprus
Name/email consistency: high
- Gap junction disorders of myelinating cells. Kleopa, K.A., Orthmann-Murphy, J., Sargiannidou, I. Rev. Neurosci (2010)
- Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X. Kleopa, K.A., Zamba-Papanicolaou, E., Alevra, X., Nicolaou, P., Georgiou, D.M., Hadjisavvas, A., Kyriakides, T., Christodoulou, K. Neurology (2006)
- Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations. Kleopa, K.A., Elman, L.B., Lang, B., Vincent, A., Scherer, S.S. Brain (2006)
- Molecular genetics of X-linked Charcot-Marie-Tooth disease. Kleopa, K.A., Scherer, S.S. Neuromolecular Med. (2006)
- A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypes. Kleopa, K.A., Georgiou, D.M., Nicolaou, P., Koutsou, P., Papathanasiou, E., Kyriakides, T., Christodoulou, K. Neurogenetics (2004)
- Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes. Kleopa, K.A., Orthmann, J.L., Enriquez, A., Paul, D.L., Scherer, S.S. Glia (2004)