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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 | 73 | 2000 |
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 | 66 | 2020 |
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 | 63 | 2006 |
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 | 53 | 2014 |
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 | 53 | 2009 |
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 | 50 | 2001 |
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 | 48 | 2009 |
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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 | 41 | 2008 |
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 | 40 | 2017 |
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 | 39 | 2013 |
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