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Zamba E
Zamba E
Άγνωστη συνεργασία
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα cing.ac.cy
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A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis
P Zisimopoulou, P Evangelakou, J Tzartos, K Lazaridis, V Zouvelou, ...
Journal of autoimmunity 52, 139-145, 2014
3002014
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ...
Nature communications 10 (1), 3094, 2019
1832019
Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations
K Sivakumar, T Kyriakides, I Puls, GA Nicholson, B Funalot, A Antonellis, ...
Brain 128 (10), 2304-2314, 2005
1462005
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study
D Adams, M Polydefkis, A González-Duarte, J Wixner, AV Kristen, ...
The Lancet Neurology 20 (1), 49-59, 2021
1112021
MuSK autoantibodies in myasthenia gravis detected by cell based assay—a multinational study
AI Tsonis, P Zisimopoulou, K Lazaridis, J Tzartos, E Matsigkou, ...
Journal of neuroimmunology 284, 10-17, 2015
822015
Titin antibodies in “seronegative” myasthenia gravis—a new role for an old antigen
C Stergiou, K Lazaridis, V Zouvelou, J Tzartos, R Mantegazza, C Antozzi, ...
Journal of neuroimmunology 292, 108-115, 2016
732016
A novel form of distal hereditary motor neuronopathy maps to chromosome 9p21. 1–p12
K Christodoulou, E Zamba, M Tsingis, A Mubaidin, K Horani, S Abu‐Sheik, ...
Annals of neurology 48 (6), 877-884, 2000
722000
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation
V Chelban, MP Wilson, J Warman Chardon, J Vandrovcova, MN Zanetti, ...
Annals of Neurology 86 (2), 225-240, 2019
662019
Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X
KA Kleopa, E Zamba-Papanicolaou, X Alevra, P Nicolaou, DM Georgiou, ...
Neurology 66 (3), 396-402, 2006
602006
Risk factors for breast cancer brain metastases: a systematic review
L Koniali, A Hadjisavvas, A Constantinidou, K Christodoulou, Y Christou, ...
Oncotarget 11 (6), 650, 2020
582020
Epidemiological, clinical and genetic study of familial amyloidotic polyneuropathy in Cyprus
E Dardiotis, P Koutsou, EZ Papanicolaou, I Vonta, A Kladi, ...
Amyloid 16 (1), 32-37, 2009
532009
A Novel GBA2 Gene Missense Mutation in Spastic Ataxia
C Votsi, E Zamba‐Papanicolaou, LT Middleton, M Pantzaris, ...
Annals of human genetics 78 (1), 13-22, 2014
512014
Mapping of the second Friedreich's ataxia (FRDAff2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity
K Christodoulou, F Deymeer, P Serdaroğlu, C Özdemir, M Poda, ...
Neurogenetics 3, 127-132, 2001
512001
Reversible inflammatory and vacuolar myopathy with vitamin E deficiency in celiac disease
KA Kleopa, K Kyriacou, E Zamba‐Papanicolaou, T Kyriakides
Muscle & Nerve: Official Journal of the American Association of …, 2005
492005
Complement C1Q polymorphisms modulate onset in familial amyloidotic polyneuropathy TTR Val30Met
E Dardiotis, P Koutsou, E Zamba-Papanicolaou, I Vonta, M Hadjivassiliou, ...
Journal of the neurological sciences 284 (1-2), 158-162, 2009
472009
Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor ε-subunit gene
L Middleton, K Ohno, K Christodoulou, J Brengman, M Milone, ...
Neurology 53 (5), 1076-1076, 1999
421999
Identification of exosomal muscle-specific miRNAs in serum of myotonic dystrophy patients relating to muscle disease progress
A Koutsoulidou, M Photiades, TC Kyriakides, K Georgiou, M Prokopi, ...
Human molecular genetics 26 (17), 3285-3302, 2017
402017
A novel c. 5308_5311delGAGA mutation in Senataxin in a Cypriot family with an autosomal recessive cerebellar ataxia
P Nicolaou, A Georghiou, C Votsi, LT Middleton, E Zamba-Papanicolaou, ...
BMC Medical Genetics 9, 1-6, 2008
392008
A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease
P Nicolaou, C Cianchetti, A Minaidou, G Marrosu, E Zamba-Papanicolaou, ...
European Journal of Human Genetics 21 (2), 190-194, 2013
362013
Charcot-Marie-Tooth disease in Cyprus: epidemiological, clinical and genetic characteristics
P Nicolaou, E Zamba-Papanicolaou, P Koutsou, KA Kleopa, A Georghiou, ...
Neuroepidemiology 35 (3), 171-177, 2010
352010
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