CMT1A current gene therapy approaches and promising biomarkers von Stavrou, Marina, Kleopa, Kleopas

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Emerging treatments for hereditary demyelinating neuropathies von Kleopa, Kleopas

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Gene therapy approaches targeting Schwann cells for demyelinating neuropathies von Sargiannidou, Irene, Kagiava, Alexia, Kleopa, Kleopas A.

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Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acq... von Irani, Sarosh R., Alexander, Sian, Waters, Patrick, Kleopa, Kleopas A., Pettingill, Philippa, Zuliani, Luigi, Peles, Elior, Buckley, Camilla, Lang, Bethan, Vincent, Angela

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Emerging Therapies for Charcot-Marie-Tooth Inherited Neuropathies von Stavrou, Marina, Sargiannidou, Irene, Georgiou, Elena, Kagiava, Alexia, Kleopa, Kleopas A

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Glial Cells as Key Regulators in Neuroinflammatory Mechanisms Associated with Multiple Sclerosis von Theophanous, Styliani, Sargiannidou, Irene, Kleopa, Kleopas A

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Morvan syndrome: Clinical and serological observations in 29 cases von Irani, Sarosh R., Pettingill, Philippa, Kleopa, Kleopas A., Schiza, Natasa, Waters, Patrick, Mazia, Claudio, Zuliani, Luigi, Watanabe, Osamu, Lang, Bethan, Buckley, Camilla, Vincent, Angela

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Novel de novo DNMT1 gene mutation associated with hereditary sensory and autonomic neuropathy 1E (HSAN1E) von Parissis, Dimitrios, Christodoulou, Kyproula, Kleopa, Kleopas A.

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Genetic mechanisms of peripheral nerve disease von Stavrou, Marina, Sargiannidou, Irene, Christofi, Theodoulakis, Kleopa, Kleopas A.

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How do mutations in GJB1 cause X-linked Charcot–Marie–Tooth disease? von Kleopa, Kleopas A, Abrams, Charles K, Scherer, Steven S

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A translatable RNAi-driven gene therapy silences PMP22/Pmp22 genes and improves neuropathy in CMT1A mice von Stavrou, Marina, Kagiava, Alexia, Choudury, Sarah G, Jennings, Matthew J, Wallace, Lindsay M, Fowler, Allison M, Heslegrave, Amanda, Richter, Jan, Tryfonos, Christina, Christodoulou, Christina, Zetterberg, Henrik, Horvath, Rita, Harper, Scott Q, Kleopa, Kleopas A

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The role of gap junctions in Charcot-Marie-Tooth disease von Kleopa, Kleopas A

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Charcot–Marie–Tooth neuropathies: Current gene therapy advances and the route toward translation von Stavrou, Marina, Kagiava, Alexia, Sargiannidou, Irene, Georgiou, Elena, Kleopa, Kleopas A.

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Adsorption of Cd(II), Cu(II), Ni(II) and Pb(II) onto natural bentonite: study in mono- and multi-metal systems von Anna, Bourliva, Kleopas, Michailidis, Constantine, Sikalidis, Anestis, Filippidis, Maria, Betsiou

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Highly Active Relapsing-Remitting Multiple Sclerosis with Neurofibromatosis Type 1: Radiological Aspects and Therapeutic Challenges – Case Report von Lemonaris, Marios, Kleopa, Kleopas A.

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Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy von Kagiava, Alexia, Sargiannidou, Irene, Theophilidis, George, Karaiskos, Christos, Richter, Jan, Bashiardes, Stavros, Schiza, Natasa, Nearchou, Marianna, Christodoulou, Christina, Scherer, Steven S., Kleopa, Kleopas A.

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Retrospective longitudinal study of ALS in Cyprus: Clinical characteristics, management and survival von Demetriou, Christiana A, Hadjivasiliou, Petros M, Kleopa, Kleopas A, Christou, Yiolanda P, Leonidou, Eleni, Kyriakides, Theodoros, Zamba-Papanicolaou, Eleni

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Editorial: Update on the Diagnosis and Management of CIDP Variants von Chroni, Elisabeth, Kleopa, Kleopas A.

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Dysregulation of Blood-Brain Barrier and Exacerbated Inflammatory Response in Cx47-Deficient Mice after Induction of EAE von Stavropoulos, Filippos, Georgiou, Elena, Sargiannidou, Irene, Kleopa, Kleopas A.

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Connexins, gap junctions and peripheral neuropathy von Kleopa, Kleopas A., Sargiannidou, Irene

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