M. Panas

发表

Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot-Marie-Tooth disease.

N. Wood, H. Houlden, G. Koutsis, 2012, Brain : a journal of neurology.

Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia

N. Wood, H. Houlden, M. Sweeney, 2012, Journal of the Neurological Sciences.

Pseudodominant Friedreich's ataxia with phenotypic heterogeneity

M. Panas, D. Vassilopoulos, N. Kalfakis, 2007, Acta neurologica Scandinavica.

Prevalence of interatrial block in patients with Friedreich's ataxia.

C. Stefanadis, G. Siasos, M. Panas, 2010, International journal of cardiology.

Crescendo Transient Ischemic Attacks due to Middle Cerebral Artery Stenosis

M. Panas, G. Tsivgoulis, K. Vemmos, 2003, Cerebrovascular Diseases.

Erratum to: Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation

H. Houlden, G. Koutsis, M. Panas, 2015, Journal of Neurology.

APOE genotypes in Greek multiple sclerosis patients: no effect on the MS Severity Score

G. Koutsis, M. Panas, G. Karadima, 2007, Journal of Neurology.

Relapsing Remitting Multiple Sclerosis in X-Linked Charcot-Marie-Tooth Disease with Central Nervous System Involvement

G. Koutsis, M. Panas, G. Karadima, 2015, Case reports in neurological medicine.

Effect of CAG repeat length on psychiatric disorders in Huntington's disease.

E. Vassos, M. Panas, D. Vassilopoulos, 2008, Journal of psychiatric research.

The Byzantine Empress Zoe Porphyrogenita and the quest for eternal youth

M. Panas, D. Vassilopoulos, E. Poulakou-Rebelakou, 2012, Journal of cosmetic dermatology.

Association of genetically proven Huntington’s disease and sporadic amyotrophic lateral sclerosis in a 72-year-old woman

E. Vassos, M. Panas, S. Papageorgiou, 2006, Journal of Neurology.

Mutational analysis of Greek patients with suspected hereditary neuropathy with liability to pressure palsies (HNPP): a 15‐year experience

G. Koutsis, M. Panas, G. Karadima, 2015, Journal of the peripheral nervous system : JPNS.

Low plasma total cholesterol in patients with Huntington's disease and first-degree relatives.

M. Panas, N. Kalfakis, D. Vassilopoulos, 2008, Molecular genetics and metabolism.

C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population

G. Koutsis, M. Panas, G. Karadima, 2015, Neurobiology of Aging.

Replication study of GWAS risk loci in Greek multiple sclerosis patients

G. Koutsis, M. Panas, G. Karadima, 2018, Neurological Sciences.

Phenotypic discordance in a pair of monozygotic twins with Huntington’s disease

M. Panas, G. Karadima, D. Vassilopoulos, 2008, Clinical genetics.

From Mild Ataxia to Huntington Disease Phenocopy: The Multiple Faces of Spinocerebellar Ataxia 17

G. Koutsis, M. Panas, G. Karadima, 2014, Case reports in neurological medicine.

Genotyping of presenilin-1 polymorphism in amyotrophic lateral sclerosis

M. Panas, G. Karadima, M. Petersen, 2000, Journal of Neurology.

New mutation of the MPZ gene in a family with the Dejerine–Sottas disease phenotype

M. Panas, G. Karadima, D. Vassilopoulos, 2007, Muscle & nerve.

Apolipoprotein E polymorphism in the Greek population

M. Panas, G. Karadima, D. Vassilopoulos, 1996, Clinical genetics.

Human CCS gene: genomic organization and exclusion as a candidate for amyotrophic lateral sclerosis (ALS)

A. Silahtaroglu, Z. Tümer, N. Tommerup, 2002, BMC Genetics.

Mutational analysis of PMP22, GJB1 and MPZ in Greek Charcot–Marie–Tooth type 1 neuropathy patients

G. Koutsis, M. Panas, G. Karadima, 2011, Clinical genetics.

Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population

H. Houlden, G. Koutsis, M. Panas, 2022, Journal of the Neurological Sciences.

Platelet monoamine oxidase activity in subjects tested for Huntington’s disease gene mutation

M. Panas, D. Vassilopoulos, N. Kalfakis, 2004, Journal of Neural Transmission.

Presymptomatic neuromuscular disorders disclosed following statin treatment.

M. Panas, G. Tsivgoulis, N. Karandreas, 2006, Archives of internal medicine.

Central motor and sensory pathway involvement in an X-linked Charcot-Marie-Tooth family.

M. Panas, G. Karadima, E. Kararizou, 2008, Acta neurologica Belgica.

Four novel connexin 32 mutations in X-linked Charcot–Marie–Tooth disease. Phenotypic variability and central nervous system involvement

G. Koutsis, M. Panas, G. Karadima, 2014, Journal of the Neurological Sciences.

Four novel connexin 32 mutations in X–linked Charcot–Marie–Tooth disease with phenotypic variability

M. Panas, G. Karadima, D. Vassilopoulos, 2006, Journal of Neurology.

A V38A mutation in X-linked Charcot-Marie-Tooth neuropathy with unusual clinical features

M. Panas, G. Karadima, D. Vassilopoulos, 2004, Journal of Neurology.

Hereditary neuropathy with liability to pressure palsies emerging during vincristine treatment

M. Panas, G. Karadima, D. Vassilopoulos, 2002, Neurology.

Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene

M. Panas, D. Vassilopoulos, N. Kalfakis, 2001, Neurology.

Plasma testosterone, dehydroepiandrosterone sulfate, and cortisol in female patients with Huntington's disease.

M. Panas, D. Vassilopoulos, M. Markianos, 2007, Neuro endocrinology letters.

The risk of cancer in relatives of patients with brain neoplasm

D. Sakas, M. Panas, P. Carvounis, 1994, Acta Neurochirurgica.

Late-onset Huntington's disease: diagnostic and prognostic considerations.

G. Koutsis, M. Panas, G. Karadima, 2014, Parkinsonism & related disorders.

Parkinsonism and Related Disorders

G. Koutsis, M. Panas, G. Karadima, 2014 .

Huntington's disease in Greece: the experience of 14 years

E. Vassos, M. Panas, G. Karadima, 2011, Clinical genetics.

Plasma testosterone in male patients with Huntington's disease: Relations to severity of illness and dementia

M. Panas, D. Vassilopoulos, Dimitrios Vassilopoulos, 2005, Annals of neurology.

Higher Levels of Extroverted Hostility Detected in Gene Carriers at Risk for Huntington’s Disease

E. Vassos, M. Panas, D. Vassilopoulos, 2007, Biological Psychiatry.

X linked Charcot-Marie-Tooth disease and multiple sclerosis: emerging evidence for an association

M. Anagnostouli, G. Koutsis, M. Panas, 2018, Journal of Neurology, Neurosurgery, and Psychiatry.

[Superficial siderosis of the CNS. Case report and literature review].

G. Koutsis, M. Panas, G. Tsivgoulis, 2004, Der Nervenarzt.

Superficial Siderosis of the Brain as a Late Complication of Subarachnoid Haemorrhage

M. Panas, K. Vemmos, K. Spengos, 2003, Cerebrovascular Diseases.

Neck flexion-induced finger tremor: A novel observation in Hirayama disease

G. Koutsis, M. Panas, E. Karavasilis, 2016, Journal of the Neurological Sciences.

An APOA1 promoter polymorphism is associated with cognitive performance in patients with multiple sclerosis

G. Koutsis, M. Panas, G. Karadima, 2009, Multiple sclerosis.

Friedreich's ataxia mimicking hereditary motor and sensory neuropathy

M. Panas, G. Karadima, D. Vassilopoulos, 2002, Journal of Neurology.

Charcot-Marie-Tooth disease type 1A with central nervous system involvement in two generations

M. Panas, G. Karadima, D. Vassilopoulos, 2004, Journal of Neurology.

Reevaluation of the CMT1A duplication frequency in Greek Charcot‐Marie‐Tooth type 1 patients

G. Koutsis, M. Panas, G. Karadima, 2014, Clinical genetics.

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases

P. Holmans, S. Tabrizi, A. Durr, 2016, Annals of neurology.

Assessment of Parkinson's disease risk loci in Greece

Hannah A. Pliner, D. Hernandez, M. Nalls, 2014, Neurobiology of Aging.

Genetic screening of Greek patients with Huntington's disease phenocopies identifies an SCA8 expansion

N. Wood, H. Houlden, M. Sweeney, 2012, Journal of Neurology.

The challenge of juvenile Huntington disease

G. Koutsis, M. Panas, G. Karadima, 2013, Neurology.

G. Koutsis, M. Panas, G. Karadima, 2021, Journal of the peripheral nervous system : JPNS.

Central nervous system involvement in four patients with Charcot-Marie-Tooth disease with connexin 32 extracellular mutations

D. Avramopoulos, M. Panas, D. Vassilopoulos, 1998, Journal of neurology, neurosurgery, and psychiatry.

Acute Painful Sensory Neuropathy with Subclinical Autonomic Dysfunction as a Presenting Feature of Hodgkin’s Disease

G. Koutsis, M. Panas, C. Sfagos, 2005, European Neurology.

Inner ear dysfunction in myotonic dystrophy type 1

D. Felekis, M. Panas, J. Xenellis, 2013, Acta neurologica Scandinavica.

Evidence for Cognitive Deficits in X-Linked Charcot-Marie-Tooth Disease

G. Koutsis, M. Panas, G. Karadima, 2020, Journal of the International Neuropsychological Society.

APOE ε4 is associated with impaired verbal learning in patients with MS

G. Koutsis, M. Panas, G. Karadima, 2007, Neurology.

Hereditary Spastic Paraplegia in Greece: Characterisation of a previously unexplored population using next generation sequencing

H. Houlden, G. Koutsis, M. Panas, 2015, European Journal of Human Genetics.

A Greek National Cross-Sectional Study on Myotonic Dystrophies

V. Kimiskidis, G. Koutsis, M. Panas, 2022, International journal of molecular sciences.

High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients

H. Houlden, G. Koutsis, J. Polke, 2012, Neurobiology of Aging.

Co-segregation of Huntington Disease and Hereditary Spastic Paraplegia in 4 Generations

M. Panas, G. Karadima, D. Vassilopoulos, 2011, The neurologist.

Migraine With Aura: Segregation Analysis and Heritability Estimation

M. Panas, N. Kalfakis, D. Vassilopoulos, 1996, Headache.

Apolipoprotein E and presenilin-1 genotypes in Huntington’s disease

D. Avramopoulos, M. Panas, G. Karadima, 1999, Journal of Neurology.

A novel ABCD1 mutation detected by next generation sequencing in presumed hereditary spastic paraplegia: A 30-year diagnostic delay caused by misleading biochemical findings

G. Koutsis, M. Panas, G. Karadima, 2015, Journal of the Neurological Sciences.

Screening for the FMR1 premutation in Greek patients with late-onset movement disorders.

G. Koutsis, M. Panas, G. Karadima, 2022, Parkinsonism & related disorders.

The different faces of the p. A53T alpha-synuclein mutation: A screening of Greek patients with parkinsonism and/or dementia

G. Koutsis, M. Panas, G. Karadima, 2017, Neuroscience Letters.

Spinobulbar muscular atrophy (Kennedy's disease): A rare diagnosis in the Greek population

G. Koutsis, M. Panas, G. Karadima, 2015, Journal of the Neurological Sciences.

Screening for the C9ORF72 repeat expansion in a greek frontotemporal dementia cohort

G. Koutsis, M. Panas, G. Karadima, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Friedreich's ataxia and other hereditary ataxias in Greece: An 18-year perspective

N. Wood, H. Houlden, G. Koutsis, 2014, Journal of the Neurological Sciences.

Elevated Serum α-Synuclein Levels in Huntington’s Disease Patients

G. Koutsis, M. Panas, G. Karadima, 2020, Neuroscience.

The rs10492972 KIF1B polymorphism and disease progression in Greek patients with multiple sclerosis

G. Koutsis, M. Panas, G. Karadima, 2011, Journal of Neurology.

Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot–Marie–Tooth type 1 patients

H. Houlden, G. Koutsis, A. Pandraud, 2012, Clinical genetics.

Mutational screening of the SH3TC2 gene in Greek patients with suspected demyelinating recessive Charcot‐Marie‐Tooth disease reveals a varied and unusual phenotypic spectrum

G. Koutsis, M. Panas, G. Karadima, 2019, Journal of the peripheral nervous system : JPNS.

APOE epsilon4 is associated with impaired verbal learning in patients with MS.

G. Koutsis, M. Panas, G. Karadima, 2007, Neurology.

Variant transthyretin amyloidosis (ATTRv) polyneuropathy in Greece: a broad overview with a focus on non-endemic unexplored regions of the country

M. Dimopoulos, E. Oikonomou, K. Kleopa, 2021, Neuromuscular Disorders.

Plasma Homovanillic Acid and Prolactin in Huntington’s Disease

M. Panas, D. Vassilopoulos, M. Markianos, 2009, Neurochemical Research.

Screening for spinocerebellar ataxia type 36 (SCA36) in the Greek population

M. Panas, G. Karadima, G. Koutsis, 2019, Journal of the Neurological Sciences.

C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population

G. Koutsis, M. Panas, G. Karadima, 2015, Neurobiology of Aging.

Mutational screening of Greek patients with axonal Charcot‐Marie‐Tooth disease using targeted next‐generation sequencing: Clinical and molecular spectrum delineation

G. Koutsis, M. Panas, G. Karadima, 2023, Journal of the peripheral nervous system : JPNS.

Age at onset in Huntington's disease: replication study on the association of HAP1.

G. Koutsis, M. Panas, G. Karadima, 2012, Parkinsonism & related disorders.

Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene

M. Panas, E. Dardiotis, G. Hadjigeorgiou, 2010, Neurological Sciences.