Zamba E
Zamba E
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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
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
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
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
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
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 Ízdemir, M Poda, ...
Neurogenetics 3 (3), 127-132, 2001
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
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
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
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
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
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
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), 1-6, 2008
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
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
A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis family
N Mintchev, E Zamba-Papanicolaou, KA Kleopa, K Christodoulou
Neurology 72 (1), 28-32, 2009
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
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
Distal hereditary motor neuronopathy of the Jerash type
LT Middleton, K Christodoulou, A Mubaidin, E Zamba, M Tsingis, ...
Annals of the New York Academy of Sciences 883 (1), 65-68, 1999
Radial nerve F-waves: normative values with surface recording from the extensor indicis muscle
ES Papathanasiou, E Zamba, SS Papacostas
Clinical neurophysiology 112 (1), 145-152, 2001
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