J. Zidar

发表

Analysis of electroencephalographic correlation during grip-force tracking

Gregorij Kurillo, T. Bajd, Janez Zidar, 2003, The IEEE Region 8 EUROCON 2003. Computer as a Tool..

B. Koritnik, J. Zidar, A. Belic, 2013, Respiratory Physiology & Neurobiology.

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Annelot M. Dekker, Raymond D. Schellevis, P. Visscher, 2016, Nature Genetics.

The electrophysiological correlates of the working memory subcomponents: evidence from high-density EEG and coherence analysis

G. Repovš, B. Koritnik, J. Zidar, 2015, Neurological Sciences.

Relation of CTG expansion and clinical variables to electrocardiogram conduction abnormalities and sudden death in patients with myotonic dystrophy

J. Zidar, B. Peterlin, M. Šabovič, 2003, Neuromuscular Disorders.

Decreased movement-related beta desynchronization and impaired post-movement beta rebound in amyotrophic lateral sclerosis

B. Koritnik, J. Zidar, N. Bizovičar, 2014, Clinical Neurophysiology.

Assessment of the haptic robot as a new tool for the study of the neural control of reaching

Marko Munih, Ales Belic, Blaz Koritnik, 2013, Neurological Sciences.

Quantitative EMG and muscle tension in painful muscles in fibromyalgia

J. Zidar, A. Bengtsson, K. Henriksson, 1990, Pain.

Genetic analysis of amyotrophic lateral sclerosis in the Slovenian population

C. Shaw, Bradley N Smith, C. Vance, 2015, Neurobiology of Aging.

CRITICAL ILLNESS MYOPATHY IN PATIENTS WITH CENTRAL NERVOUS SYSTEM DISORDERS

J. Zidar, T. Filipović, V. Svigelj, 2009 .

Beyond aphasia: Altered EEG connectivity in Broca’s patients during working memory task

G. Repovš, B. Koritnik, J. Zidar, 2016, Brain and Language.

Actigraphic assessment of sleep–wake rhythm during the first 6 months of life

J. Zidar, D. Neubauer, B. Gnidovec, 2002, Clinical Neurophysiology.

Inspiratory- and finger-flexion-related cortical potentials in patients with amyotrophic lateral sclerosis – An exploratory study

B. Koritnik, J. Zidar, N. Bizovičar, 2012, Clinical Neurology and Neurosurgery.

Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family

C. Broeckhoven, J. Zidar, V. Timmerman, 2000, Pflügers Archiv.

The N355K atlastin 1 mutation is associated with hereditary sensory neuropathy and pyramidal tract features

J. Zidar, M. Auer-Grumbach, L. Leonardis, 2012, European journal of neurology.

Auditory nerve is affected in one of two different point mutations of the neurofilament light gene

A. Starr, J. Zidar, K. Christodoulou, 2008, Clinical Neurophysiology.

Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred

A. Starr, J. Zidar, L. Kalaydjieva, 1999, Annals of neurology.

Genetic epidemiology of Duchenne and Becker muscular dystrophy in Slovenia

J. Zidar, B. Peterlin, N. Župančič, 1997, Clinical genetics.

Improvements in the multidisciplinary care are beneficial for survival in amyotrophic lateral sclerosis (ALS): experience from a tertiary ALS center

B. Koritnik, J. Zidar, L. Dolenc Grošelj, 2020, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Correlations between clinical, electrophysiological and genetic findings in hereditary motor and sensory neuropathy type I (HMSN I)

J. Zidar, B. Peterlin, L. Leonardis, 2006, Pflügers Archiv.

Diffuse large B cell lymphoma mimics myasthenia gravis

J. Zidar, Veronika Rutar Gorišek, A. Horvat Ledinek, 2019, Neurological Sciences.

Theme 8 Clinical imaging and electrophysiology

B. Koritnik, J. Zidar, L. Leonardis, 2019, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Ewout J. N. Groen, Annelot M. Dekker, Ross P. Byrne, 2021, Nature Genetics.

Differential Expression of Several miRNAs and the Host Genes AATK and DNM2 in Leukocytes of Sporadic ALS Patients

B. Koritnik, J. Zidar, D. Glavač, 2018, Front. Mol. Neurosci..

Differential expression of microRNAs and other small RNAs in muscle tissue of patients with ALS and healthy age-matched controls

Tomaž Curk, B. Koritnik, J. Zidar, 2018, Scientific Reports.

Pudendal nerve involvement in patients with hereditary motor and sensory neuropathy

J. Zidar, D. Vodušek, 1987, Acta neurologica Scandinavica.

Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP): reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRs.

J. Zidar, B. Rautenstrauss, P. Seeman, 2000, International journal of molecular medicine.

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Ewout J. N. Groen, Annelot M. Dekker, Ross P. Byrne, 2021, Nature Genetics.

Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I.

C. Blackstone, T. Strom, J. Zidar, 2011, American journal of human genetics.

A novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian family

J. Zidar, L. Middleton, K. Christodoulou, 2002, Neurogenetics.

Autosomal dominant Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: detection of the recombination in Slovene patients and exclusion of the potentially recessive Thr118Met PMP22 point mutation.

J. Zidar, A. Ekici, B. Peterlin, 1998, International journal of molecular medicine.

Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated allele

J. Zidar, C. Angelini, B. Peterlin, 2011, European journal of neurology.

Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy.

M. Zeviani, J. Zidar, E. Lamantea, 2005, Human molecular genetics.

Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family

C. Broeckhoven, J. Zidar, V. Timmerman, 2000, Pflugers Archiv : European journal of physiology.

Chromosome 10q-linked FSHD identifies DUX4 as principal disease gene

S. Tapscott, J. Zidar, D. Henderson, 2021, Journal of Medical Genetics.

Peripheral nerve ultrasonography in patients with transthyretin amyloidosis

J. Zidar, I. Tournev, S. Podnar, 2017, Clinical Neurophysiology.

Botulinum Toxin in the Treatment of Neurological Disorders

J. Zidar, D. Vodušek, Z. Pirtošek, 1994, Annals of the New York Academy of Sciences.

[Microelectromyography in the diagnosis of neuromuscular diseases].

J. Zidar, D. Vodušek, J. Trontelj, 1978, Neurologija.

CTG repeat analysis in lymphocytes, muscles and fibroblasts in patients with myotonic dystrophy

J. Zidar, B. Peterlin, N. Logar, 2006, Pflügers Archiv.

REMARKS ON NEUROCONTROL OF THE HAND AND SIGNIFICANCE OF AFFERENT INPUT

Janez Zidar, Nejc Sarabon, Milan R. Dimitrijevic, 2004 .

Sensitivity of motor unit potential analysis in facioscapulohumeral muscular dystrophy

J. Zidar, S. Podnar, 2006, Muscle & nerve.

Functional changes of the cortical motor system in hereditary spastic paraparesis

B. Koritnik, J. Zidar, J. Knific, 2009, Acta neurologica Scandinavica.

Amyotrophic lateral sclerosis patients show executive impairments on standard neuropsychological measures and an ecologically valid motor-free test of executive functions

G. Repovš, J. Zidar, S. Podnar, 2010, Journal of clinical and experimental neuropsychology.

ALS and FTLD: two faces of TDP‐43 proteinopathy

N. Cairns, L. Grinberg, J. Zidar, 2008, European journal of neurology.

Cognitive impairment in patients with amyotrophic lateral sclerosis: a neuropsychological perspective

G. Repovš, J. Zidar, V. Štukovnik, 2013 .

Percutaneous stimulation of human corticospinal tract: a single-fibre EMG study of individual motor unit responses

J. Zidar, J. Trontelj, M. Mihelin, 1987, Brain Research.

Facioscapulohumeral dystrophy: jitter in facial muscles.

J. Zidar, J. Trontelj, M. Mihelin, 1988, Journal of Neurology Neurosurgery & Psychiatry.

Functional organisation of the facial motor system in man.

J. Zidar, R. Liscic, 1998, Collegium antropologicum.

B. Koritnik, J. Zidar, N. Bizovičar, 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

I-3. Heterogeneity and atypical phenotypes in patients with facioscapulohumeral muscular dystrophy.

J. Zidar, 2009 .

Evidence of direct connection of corticobulbar fibers to orofacial muscles in man: Electromyographic study of individual motor unit responses

J. Zidar, M. Mihelin, R. Liscic, 1998, Muscle & nerve.

Separating the Idea from the Action: A sLORETA Study

Janez Zidar, Pierpaolo Busan, Piero Paolo Battaglini, 2018, Brain Topography.

Clinical neurophysiological assessment of spasticity

M. Dimitrijevic, J. Zidar, 1991 .

Using ANNs to predict a subject's response based on EEG traces

Drago Matko, Rihard Karba, Vito Logar, 2008, Neural Networks.

Lumbosacral evoked potentials (LSEPs) and cortical somatosensory evoked potentials (SEPs) in patients with lesions of the conus medullaris and cauda equina.

M. Dimitrijevic, L. Lehmkuhl, J. Zidar, 1988, Electroencephalography and clinical neurophysiology.

Using ANN on EEG signals to predict working memory task response

Drago Matko, Rihard Karba, Vito Logar, 2007 .

Shaky hands are a part of motor neuron disease phenotype: clinical and electrophysiological study of 77 patients

B. Koritnik, J. Zidar, T. Saifee, 2022, Journal of Neurology.

Differential expression of microRNAs and other small RNAs in muscle tissue of patients with ALS and healthy age-matched controls

Tomaž Curk, B. Koritnik, J. Zidar, 2018, Scientific Reports.

Cardiac Involvement in Emery‐Dreifuss Muscular Dystrophy: Role of a Diagnostic Pacemaker

J. Zidar, P. Rakovec, I. Zupan, 1995, Pacing and clinical electrophysiology : PACE.

The role of transcranial magnetic stimulation in evaluation of motor cortex excitability in Rett syndrome.

J. Zidar, N. Krajnc, 2016, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Gripping-force identification using EEG and phase-demodulation approach

I. Škrjanc, B. Koritnik, J. Zidar, 2008, Neuroscience Research.

Identification of the phase code in an EEG during gripping-force tasks: A possible alternative approach to the development of the brain-computer interfaces

Igor Skrjanc, Vito Logar, Ales Belic, 2008, Artif. Intell. Medicine.

The Project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

Naomi R. Wray, Mamede de Carvalho, Blaz Koritnik, 2018, bioRxiv.

Assessment of the haptic robot as a new tool for the study of the neural control of reaching

Piero Paolo Battaglni, M. Munih, B. Koritnik, 2013, Neurological Sciences.

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Annelot M. Dekker, Raymond D. Schellevis, Ashley R. Jones, 2016, Nature Genetics.