Epidemiology of Huntington disease in Cyprus: A 20‐year retrospective study von Demetriou, C.A., Heraclides, A., Salafori, C., Tanteles, G.A., Christodoulou, K., Christou, Y., Zamba‐Papanicolaou, E.

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Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X von KLEOPA, K. A, ZAMBA-PAPANICOLAOU, E, ALEVRA, X, NICOLAOU, P, GEORGIOU, D.-M, HADJISAVVAS, A, KYRIAKIDES, T, CHRISTODOULOU, K

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MuSK autoantibodies in myasthenia gravis detected by cell based assay — A multinational study von Tsonis, A.I, Zisimopoulou, P, Lazaridis, K, Tzartos, J, Matsigkou, E, Zouvelou, V, Mantegazza, R, Antozzi, C, Andreetta, F, Evoli, A, Deymeer, F, Saruhan-Direskeneli, G, Durmus, H, Brenner, T, Vaknin, A, Berrih-Aknin, S, Behin, A, Sharshar, T, De Baets, M, Losen, M, Martinez-Martinez, P, Kleopa, K.A, Zamba-Papanicolaou, E, Kyriakides, T, Kostera-Pruszczyk, A, Szczudlik, P, Szyluk, B, Lavrnic, D, Basta, I, Peric, S, Tallaksen, C, Maniaol, A, Casasnovas Pons, C, Pitha, J, Jakubíkova, M, Hanisch, F, Tzartos, S.J

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Genetic findings of Cypriot spinal muscular atrophy patients von Theodorou, L., Nicolaou, P., Koutsou, P., Georghiou, A., Anastasiadou, V., Tanteles, G., Kyriakides, T., Zamba-Papanicolaou, E., Christodoulou, K.

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P34-3 A comparison between recordings obtained using reusable and disposable single fiber needle electrodes von Papathanasiou, E.S, Zamba-Papanicolaou, E

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PO31-FR-18 Visual evoked potential interocular amplitude differences matter in the end von Myrianthopoulou, P, Papathanasiou, E.S, Pantzaris, M, Kyriakides, T, Zamba-Papanicolaou, E, Galganski-Cleanthous, M.E, Papacostas, S.S

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A correlative study of quantitative EMG and biopsy findings in 31 patients with myopathies von Dardiotis, E, Papathanasiou, E, Vonta, I, Hadjigeorgiou, G, Zamba-Papanicolaou, E, Kyriakides, T

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High frequency of Friedreich's ataxia carriers in the Paphos district of Cyprus von Zamba-Papanicolaou, E, Koutsou, P, Daiou, C, Gaglia, E, Georghiou, A, Christodoulou, K

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Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations von Sivakumar, Kumaraswamy, Kyriakides, Theodoros, Puls, Imke, Nicholson, Garth A., Funalot, Benoît, Antonellis, Anthony, Sambuughin, Nyamkhishig, Christodoulou, Kyproula, Beggs, John L., Zamba-Papanicolaou, Eleni, Ionasescu, Victor, Dalakas, Marinos C., Green, Eric D., Fischbeck, Kenneth H., Goldfarb, Lev G.

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A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis family von MINTCHEV, Nikolay, ZAMBA-PAPANICOLAOU, Eleni, KLEOPA, Kleopas A, CHRISTODOULOU, Kyproula

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A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis von Zisimopoulou, P, Evangelakou, P, Tzartos, J, Lazaridis, K, Zouvelou, V, Mantegazza, R, Antozzi, C, Andreetta, F, Evoli, A, Deymeer, F, Saruhan-Direskeneli, G, Durmus, H, Brenner, T, Vaknin, A, Berrih-Aknin, S, Frenkian Cuvelier, M, Stojkovic, T, DeBaets, M, Losen, M, Martinez-Martinez, P, Kleopa, K.A, Zamba-Papanicolaou, E, Kyriakides, T, Kostera-Pruszczyk, A, Szczudlik, P, Szyluk, B, Lavrnic, D, Basta, I, Peric, S, Tallaksen, C, Maniaol, A, Tzartos, S.J

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Reversible inflammatory and vacuolar myopathy with vitamin E deficiency in celiac disease von Kleopa, Kleopas A., Kyriacou, Kyriacos, Zamba-Papanicolaou, Eleni, Kyriakides, Theodoros

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Differential Orbicularis Oculi Involvement in Neuromuscular Junction Dysfunction von Papathanasiou, Eleftherios S, Zamba-Papanicolaou, Eleni

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Titin antibodies in “seronegative” myasthenia gravis — A new role for an old antigen von Stergiou, C, Lazaridis, K, Zouvelou, V, Tzartos, J, Mantegazza, R, Antozzi, C, Andreetta, F, Evoli, A, Deymeer, F, Saruhan-Direskeneli, G, Durmus, H, Brenner, T, Vaknin, A, Berrih-Aknin, S, Behin, A, Sharshar, T, De Baets, M, Losen, M, Martinez-Martinez, P, Kleopa, K.A, Zamba-Papanicolaou, E, Kyriakides, T, Kostera-Pruszczyk, A, Szczudlik, P, Szyluk, B, Lavrnic, D, Basta, I, Peric, S, Tallaksen, C, Maniaol, A, Gilhus, N.E, Casasnovas Pons, C, Pitha, J, Jakubíkova, M, Hanisch, F, Bogomolovas, J, Labeit, D, Labeit, S, Tzartos, S.J

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Distal hereditary motor neuronopathy of the Jerash type is caused by a novel SIGMAR1 c.500A>T missense mutation von Ververis, A, Dajani, R, Koutsou, P, Aloqaily, A, Nelson-Williams, C, Loring, E, Arafat, A, Mubaidin, AF, Horany, K, Bader, MB, Al-Baho, Y, Ali, B, Muhtaseb, A, DeSpenza, T, Al-Qudah, AA, Middleton, LT, Zamba-Papanicolaou, E, Lifton, R, Christodoulou, K

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Compressive lumbar myelopathy presenting as segmental motor neuron disease von Kleopa, Kleopas A., Zamba-Papanicolaou, Eleni, Kyriakides, Theodoros

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O-7. Examining the lower orbicularis oculi muscle reduces the number of false negative results with respect to myasthenia gravis diagnosis: a Stimulated Single fiber EMG study von Papathanasiou, ES, Zamba-Papanicolaou, E

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P-2. Friedreich’s ataxia carrier screening in the population originating from the Paphos district of Cyprus von Koutsou, P, Daiou, C, Georghiou, A, Gaglia, E, Zamba-Papanicolaou, E, Christodoulou, K

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P-4. Investigation of Cypriot families with autosomal recessive spinocerebellar ataxia (arsca) by linkage analysis at known arsca genes/loci von Votsi, C, Zamba-Papanicolaou, E, Pantzaris, M, Papacostas, S, Kyriakides, T, Christodoulou, K

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P-3. Investigation of the spinocerebellar ataxia type 10 mutation in the Cypriot population von Votsi, C, Georghiou, A, Kyriakides, T, Pantzaris, M, Papacostas, S, Zamba-Papanicolaou, E, Christodoulou, K

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