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Epidemiology of Huntington disease in Cyprus: A 20‐year retrospective study

Clinical genetics, 2018-03, Vol.93 (3), p.656-664

2018

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Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X

Neurology, 2006-02, Vol.66 (3), p.396-402

2006

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MuSK autoantibodies in myasthenia gravis detected by cell based assay — A multinational study

Journal of neuroimmunology, 2015-07, Vol.284, p.10-17

2015

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Genetic findings of Cypriot spinal muscular atrophy patients

Neurological sciences, 2015-10, Vol.36 (10), p.1829-1834

2015

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P34-3 A comparison between recordings obtained using reusable and disposable single fiber needle electrodes

Clinical neurophysiology, 2010, Vol.121, p.S305-S306

2010

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PO31-FR-18 Visual evoked potential interocular amplitude differences matter in the end

Journal of the neurological sciences, 2009, Vol.285, p.S325-S325

2009

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A correlative study of quantitative EMG and biopsy findings in 31 patients with myopathies

Acta myologica, 2011-06, Vol.30 (1), p.37-41

2011

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High frequency of Friedreich's ataxia carriers in the Paphos district of Cyprus

Acta myologica, 2009-07, Vol.28 (1), p.24-26

2009

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Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations

Brain (London, England : 1878), 2005-10, Vol.128 (10), p.2304-2314

2005

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A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis family

Neurology, 2009-01, Vol.72 (1), p.28-32

2009

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A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis

Journal of autoimmunity, 2014-08, Vol.52, p.139-145

2014

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Reversible inflammatory and vacuolar myopathy with vitamin E deficiency in celiac disease

Muscle & nerve, 2005-02, Vol.31 (2), p.260-265

2005

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Differential orbicularis oculi involvement in neuromuscular junction dysfunction

Journal of clinical neurophysiology, 2008-10, Vol.25 (5), p.293-298

2008

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Neurogenic vestibular evoked potentials using a tone pip auditory stimulus

Electromyography and clinical neurophysiology, 2004-04, Vol.44 (3), p.167

2004

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Hereditary Motor Neuronopathies

Revue neurologique, 2002-12, Vol.158 (12), p.1220-1224

2002

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Click evoked neurogenic vestibular potentials (NVESTEPs): a method of assessing the function of the vestibular system

Electromyography and clinical neurophysiology, 2003-10, Vol.43 (7), p.399

2003

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Titin antibodies in “seronegative” myasthenia gravis — A new role for an old antigen

Journal of neuroimmunology, 2016-03, Vol.292, p.108-115

2016

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Neurogenic vestibular evoked potentials in the diagnosis of multiple sclerosis

Electromyography and clinical neurophysiology, 2004-07, Vol.44 (5), p.313

2004

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Compressive lumbar myelopathy presenting as segmental motor neuron disease

Muscle & nerve, 2003-07, Vol.28 (1), p.69-73

2003

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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

Acta myologica, 2009-07, Vol.28 (1), p.42-42

2009

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Hereditary Motor Neuronopathies

Revue neurologique, 2002-12, Vol.158 (121), p.1220-1224

2002

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P-2. Friedreich’s ataxia carrier screening in the population originating from the Paphos district of Cyprus

Acta myologica, 2009-07, Vol.28 (1), p.44-44

2009

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P-3. Investigation of the spinocerebellar ataxia type 10 mutation in the Cypriot population

Acta myologica, 2009-07, Vol.28 (1), p.45-45

2009

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P-4. Investigation of Cypriot families with autosomal recessive spinocerebellar ataxia (arsca) by linkage analysis at known arsca genes/loci

Acta myologica, 2009-07, Vol.28 (1), p.45-45

2009

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P-8. Molecular genetic studies of Charcot-Marie-Tooth disease in the Cypriot population

Acta myologica, 2009-07, Vol.28 (1), p.47-47

2009

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Epidemiology of Huntington disease in Cyprus: A 20‐year retrospective study

Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X

MuSK autoantibodies in myasthenia gravis detected by cell based assay — A multinational study

Genetic findings of Cypriot spinal muscular atrophy patients

P34-3 A comparison between recordings obtained using reusable and disposable single fiber needle electrodes

PO31-FR-18 Visual evoked potential interocular amplitude differences matter in the end

A correlative study of quantitative EMG and biopsy findings in 31 patients with myopathies

High frequency of Friedreich's ataxia carriers in the Paphos district of Cyprus

Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations

A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis family

A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis

Reversible inflammatory and vacuolar myopathy with vitamin E deficiency in celiac disease

Differential orbicularis oculi involvement in neuromuscular junction dysfunction

Neurogenic vestibular evoked potentials using a tone pip auditory stimulus

Hereditary Motor Neuronopathies

Click evoked neurogenic vestibular potentials (NVESTEPs): a method of assessing the function of the vestibular system

Titin antibodies in “seronegative” myasthenia gravis — A new role for an old antigen

Neurogenic vestibular evoked potentials in the diagnosis of multiple sclerosis

Compressive lumbar myelopathy presenting as segmental motor neuron disease

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

Hereditary Motor Neuronopathies

P-2. Friedreich’s ataxia carrier screening in the population originating from the Paphos district of Cyprus

P-3. Investigation of the spinocerebellar ataxia type 10 mutation in the Cypriot population

P-4. Investigation of Cypriot families with autosomal recessive spinocerebellar ataxia (arsca) by linkage analysis at known arsca genes/loci

P-8. Molecular genetic studies of Charcot-Marie-Tooth disease in the Cypriot population

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