H. J. Schelhaas

发表

Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis

N. Brown, S. Köhler, D. Horn, 2017, bioRxiv.

Diagnostic yield of muscle fibre conduction velocity in myopathies

D. Stegeman, M. Zwarts, B. Engelen, 2011, Journal of the Neurological Sciences.

Early diagnosis of ALS: The search for signs of denervation in clinically normal muscles

M. Zwarts, B. Engelen, H. J. Schelhaas, 2007, Journal of the Neurological Sciences.

Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders.

D F Stegeman, M J Zwarts, D. Stegeman, 2006, Journal of applied physiology.

Prognostic value of decreased tongue strength on survival time in patients with amyotrophic lateral sclerosis

A. Geurts, H. J. Schelhaas, J. Hendriks, 2012, Journal of Neurology.

Hereditary spastic paraplegia caused by a mutation in the VCP gene.

H. J. Schelhaas, S. de Bot, B. P. Van de Warrenburg, 2012, Brain : a journal of neurology.

Survival profiles of patients with frontotemporal dementia and motor neuron disease.

William T. Hu, R. Petersen, J. Trojanowski, 2009, Archives of neurology.

A new screening tool for behavioral disturbances in ALS

Y. Pijnenburg, H. J. Schelhaas, B. Schmand, 2012 .

The ALS-FTD-Q

Ben Schmand, Leonard H van den Berg, Y. Pijnenburg, 2012, Neurology.

Defining the phenotypic spectrum of SLC6A1 mutations

G. Carvill, H. Mefford, P. Striano, 2018, Epilepsia.

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.

Klaus Lehnert, Holger Lerche, Annapurna Poduri, 2018, American journal of human genetics.

Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients

J. Veldink, H. J. Schelhaas, M. V. Es, 2012, Neurobiology of Aging.

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

Ewout J N Groen, Machiel J Zwarts, Fernando Rivadeneira, 2009, Nature Genetics.

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

Frank Baas, Cisca Wijmenga, Lude Franke, 2008, Nature Genetics.

Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia

R. Sinke, H. J. Schelhaas, G. Hageman, 2001, Journal of Neurology.

SCA19 and SCA22: evidence for one locus with a worldwide distribution.

R. Sinke, H. J. Schelhaas, B. P. Van de Warrenburg, 2004, Brain : a journal of neurology.

Tau Rather than TDP-43 Proteins are Potential Cerebrospinal Fluid Biomarkers for Frontotemporal Lobar Degeneration Subtypes: A Pilot Study.

Y. Pijnenburg, H. J. Schelhaas, M. Verbeek, 2016, Journal of Alzheimer's Disease.

ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia

J. Cruysberg, J. Timmermans, H. J. Schelhaas, 2008, neurogenetics.

TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations.

W. Kamphorst, H. J. Schelhaas, J. V. van Swieten, 2007, Brain : a journal of neurology.

Quantitative muscle ultrasonography in amyotrophic lateral sclerosis.

S. Pillen, M. Zwarts, S. Overeem, 2008, Ultrasound in medicine & biology.

Ultrasonographic Detection of Fasciculations Markedly Increases Diagnostic Sensitivity of ALS

M. Zwarts, H. J. Schelhaas, J. P. van Dijk, 2012, Neurology.

Inhibition of cortical excitability by retigabine: Measurement of intracortical inhibition using transcranial magnetic stimulation

D. Stegeman, M. Zwarts, H. J. Schelhaas, 2013, Neurophysiologie Clinique/Clinical Neurophysiology.

Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability

R. Pfundt, J. Verhoeven, H. Brunner, 2018, Epilepsia.

ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia

J. Cruysberg, J. Timmermans, H. J. Schelhaas, 2008, neurogenetics.

Human KCNQ5 de novo Mutations Underlie Epilepsy and Intellectual Disability.

J. Ramirez, T. Zwingman, J. Verhoeven, 2022, Journal of neurophysiology.

Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C

Andrea Olschewski, Zoltán Bálint, Eleonore Fröhlich, 2009, Nature Genetics.

Mutations in the TRPV4 gene are not associated with sporadic progressive muscular atrophy.

L. H. van den Berg, P. V. van Vught, H. J. Schelhaas, 2012, Archives of neurology.

Electrodiagnostic criteria for ALS: Time to STARD

M. Zwarts, H. J. Schelhaas, B. Kleine, 2008, Clinical Neurophysiology.

Acute deterioration of bulbar function after botulinum toxin treatment for sialorrhoea in amyotrophic lateral sclerosis.

A. Geurts, M. Zwarts, H. J. Schelhaas, 2008, American journal of physical medicine & rehabilitation.

VCP mutations in familial and sporadic amyotrophic lateral sclerosis

Ewout J. N. Groen, P. V. van Vught, J. Veldink, 2012, Neurobiology of Aging.

H. J. Schelhaas, G. Hageman, F. Beemer, 2000, European journal of neurology.

Epilepsy and Sleep in the ATR-X Syndrome

S. Pillen, H. J. Schelhaas, H. Braakman, 2021, Neuropediatrics.

Early onset cerebellar ataxia with retained tendon reflexes: foot deformity in a first grade family member

H. J. Schelhaas, G. Hageman, M. Hulst, 1999, Clinical Neurology and Neurosurgery.

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

Y. Pijnenburg, L. H. van den Berg, P. Heutink, 2012, Brain : a journal of neurology.

Genetic Overlap between Apparently Sporadic Motor Neuron Diseases

L. H. van den Berg, M. V. van Es, J. Veldink, 2012, PloS one.

TDP-43 plasma levels are higher in amyotrophic lateral sclerosis

L. H. van den Berg, J. Veldink, H. J. Schelhaas, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19

C. Wijmenga, M. Swertz, R. Sinke, 2012, Annals of neurology.

Clinical, psychological, and genetic characteristics of spinocerebellar ataxia type 19 (SCA19)

H. J. Schelhaas, B. P. Warrenburg, B. Warrenburg, 2008, The Cerebellum.

Increased plasma amyloid-β42 protein in sporadic inclusion body myositis

W. F. Abdo, H. J. Schelhaas, M. Verbeek, 2009, Acta Neuropathologica.

Smoking, alcohol consumption, and the risk of amyotrophic lateral sclerosis: a population-based study.

L. H. van den Berg, J. Veldink, H. J. Schelhaas, 2012, American journal of epidemiology.

Demyelinating polyneuropathy in Leber hereditary optic neuropathy

J. Cruysberg, M. Zwarts, H. J. Schelhaas, 2006, Neuromuscular Disorders.

Transient cerebral white matter lesions in a patient with connexin 32 missense mutation

M. Zwarts, H. J. Schelhaas, G. Hageman, 2002, Neurology.

BSCL2 mutations in two Dutch families with overlapping Silver syndrome-distal hereditary motor neuropathy

M. Zwarts, B. Engelen, H. J. Schelhaas, 2006, Neuromuscular Disorders.

A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy.

F. Baas, H. J. Schelhaas, B. V. van Engelen, 2012, Human molecular genetics.

Family history of neurodegenerative and vascular diseases in ALS

L. H. van den Berg, J. Veldink, H. J. Schelhaas, 2011, Neurology.

Sensitivity and specificity of the ‘Awaji’ electrodiagnostic criteria for amyotrophic lateral sclerosis: Retrospective comparison of the Awaji and revised El Escorial criteria for ALS

M. Zwarts, H. J. Schelhaas, B. Kleine, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.

Ewout J. N. Groen, R. Ophoff, E. Cuppen, 2010, Archives of neurology.

UNC13A is a modifier of survival in amyotrophic lateral sclerosis

P. Andersen, F. Diekstra, W. Robberecht, 2012, Neurobiology of Aging.

A CASE OF ALS-FTD IN A LARGE FALS PEDIGREE WITH A K17I ANG MUTATION

R. Ophoff, F. Baas, F. Diekstra, 2009, Neurology.

Effect of Presymptomatic Body Mass Index and Consumption of Fat and Alcohol on Amyotrophic Lateral Sclerosis.

L. H. van den Berg, J. Veldink, H. J. Schelhaas, 2015, JAMA neurology.

Effect of Presymptomatic BodyMass Index and Consumption of Fat and Alcohol on Amyotrophic Lateral Sclerosis

J. Veldink, H. J. Schelhaas, J. Vries, 2015 .

Parental age and the risk of amyotrophic lateral sclerosis

L. H. van den Berg, J. Veldink, H. J. Schelhaas, 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases

Sterling C. Johnson, Nick C Fox, Keith A. Johnson, 2012, Neurology.

Muscle ultrasonography: A diagnostic tool for amyotrophic lateral sclerosis

S. Pillen, M. Zwarts, S. Overeem, 2012, Clinical Neurophysiology.

Contribution Smoking , Alcohol Consumption , and the Risk of Amyotrophic Lateral Sclerosis : A Population-based Study

J. Veldink, H. J. Schelhaas, N. Sutedja, 2012 .

CSF neurofilament protein analysis in the differential diagnosis of ALS

W. F. Abdo, H. J. Schelhaas, M. Verbeek, 2009, Journal of Neurology.

CSF hypocretin-1 levels are normal in patients with amyotrophic lateral sclerosis

S. Overeem, H. J. Schelhaas, M. Verbeek, 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

A case of neuromuscular mimicry

M. Zwarts, B. Engelen, S. Overeem, 2006, Neuromuscular Disorders.

Case report A case of neuromuscular mimicry

M. Zwarts, S. Overeem, H. J. Schelhaas, 2006 .

Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients

J. Veldink, H. J. Schelhaas, M. V. Es, 2012, Neurobiology of Aging.

Rapidly deteriorating course in Dutch hereditary spastic paraplegia type 11 patients

H. J. Schelhaas, B. P. Warrenburg, M. Knaap, 2013, European Journal of Human Genetics.

Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?

S. Dimauro, H. J. Schelhaas, R. Wevers, 2008, Neurology.

The “split hand” phenomenon

M. Zwarts, H. J. Schelhaas, B. P. Van de Warrenburg, 2003, Neurology.

Evaluation of perampanel in patients with intellectual disability and epilepsy

H. J. Schelhaas, M. Majoie, F. Snoeijen-Schouwenaars, 2017, Epilepsy & Behavior.

University of Groningen Mutations in Potassium Channel KCND 3 Cause Spinocerebellar Ataxia Type 19

C. Wijmenga, M. Swertz, R. Sinke, 2012 .

A LRSAM1 mutation links Charcot–Marie–Tooth type 2 to Parkinson's disease

F. Baas, B. Bloem, H. J. Schelhaas, 2015, Annals of clinical and translational neurology.

Auditory dysfunction in chronic inflammatory demyelinating polyradiculoneuropathy

M. Zwarts, H. J. Schelhaas, G. Hengstman, 2004, Neurology.

Muscle changes in amyotrophic lateral sclerosis: A longitudinal ultrasonography study

S. Pillen, M. Zwarts, S. Overeem, 2011, Clinical Neurophysiology.

MRI locates a posterior fossa aneurysm in the fourth ventricle

H. J. Schelhaas, P. Brouwers, R. Prevo, 1998, Clinical Neurology and Neurosurgery.

Intramuscular fibrous tissue determines muscle echo intensity in amyotrophic lateral sclerosis

J. A. van der Laak, S. Pillen, M. Zwarts, 2012, Muscle & nerve.

Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations

H. J. Schelhaas, B. P. Van de Warrenburg, H. Scheffer, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation

M. Zwarts, S. Overeem, J. Timmermans, 2007, Neuromuscular Disorders.

Mood, anxiety, and perceived quality of life in adults with epilepsy and intellectual disability

H. J. Schelhaas, A. Aldenkamp, J. Hendriksen, 2019, Acta neurologica Scandinavica.

Serum angiogenin levels are elevated in ALS, but not Parkinson's disease

B. Bloem, L. H. van den Berg, M. V. van Es, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

SPORADIC LATE-ONSET NEMALINE MYOPATHY EFFECTIVELY TREATED BY MELPHALAN AND STEM CELL TRANSPLANT

H. J. Schelhaas, B. V. van Engelen, N. Voermans, 2008, Neurology.

SCN1A-deficient hiPSC-derived excitatory neuronal networks display mutation-specific phenotypes

D. Schubert, J. Verhoeven, H. J. Schelhaas, 2023, bioRxiv.

Botulinum toxin‐A injections vs radiotherapy for drooling in ALS

H. J. Schelhaas, J. Kalf, J. Weikamp, 2016, Acta neurologica Scandinavica.

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

I. Scheffer, H. Mefford, M. Mackay, 2020, Genetics in Medicine.

Population based epidemiology of amyotrophic lateral sclerosis using capture–recapture methodology

Leonard H van den Berg, L. H. van den Berg, J. Veldink, 2011, Journal of Neurology, Neurosurgery & Psychiatry.

Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis

L. H. van den Berg, J. Veldink, H. J. Schelhaas, 2009, Annals of neurology.

Evidence for an oligogenic basis of amyotrophic lateral sclerosis.

Leonard H van den Berg, P. D. de Bakker, L. H. van den Berg, 2012, Human molecular genetics.

Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis

A. Goris, D. Lambrechts, W. Robberecht, 2012, Human molecular genetics.

Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C 9 orf 72 as cause of amyotrophic lateral sclerosis

A. Goris, D. Lambrechts, W. Robberecht, 2012 .

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

F. Baas, D. Troost, A. Al-Chalabi, 2006, Brain : a journal of neurology.

People with epilepsy and intellectual disability: More than a sum of two conditions

H. J. Schelhaas, R. Shankar, F. Snoeijen-Schouwenaars, 2021, Epilepsy & Behavior.

European perspective of perampanel response in people with Intellectual Disability.

W. Henley, H. J. Schelhaas, R. Shankar, 2020, Acta neurologica Scandinavica.

Efficacy and tolerability of brivaracetam in patients with intellectual disability and epilepsy

H. J. Schelhaas, M. Majoie, D. Festen, 2020, Acta Neurologica Belgica.

Efficacy and tolerability of brivaracetam in patients with intellectual disability and epilepsy

H. J. Schelhaas, M. Majoie, D. Festen, 2020, Acta Neurologica Belgica.

A systematic review of neuropsychiatric comorbidities in patients with both epilepsy and intellectual disability

Albert P. Aldenkamp, H. J. Schelhaas, A. Aldenkamp, 2016, Epilepsy & Behavior.

Vagus Nerve Stimulation in children: A focus on intellectual disability.

L. Lagae, A. Kessels, H. J. Schelhaas, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Psychogenic nonepileptic seizures in adults with epilepsy and intellectual disability: A neglected area

H. J. Schelhaas, A. Aldenkamp, J. Hendriksen, 2018, Seizure.

Classification of intellectual disability according to domains of adaptive functioning and between‐domains discrepancy in adults with epilepsy

H. J. Schelhaas, A. Aldenkamp, J. Hendriksen, 2018, Journal of intellectual disability research : JIDR.

Letter: Evaluating the care of a multidisciplinary clinic by using the White Paper “Listening for a change: Medical and social needs of people with intellectual disability who have epilepsy”

H. J. Schelhaas, M. Majoie, I. Tan, 2015, Epilepsia.

The Lambert–Eaton myasthenic syndrome 1988–2008: A clinical picture in 97 patients

H. J. Schelhaas, J. Verschuuren, J. Kuks, 2008, Journal of Neuroimmunology.

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

R. Ophoff, C. Wijmenga, F. Baas, 2007, The Lancet Neurology.

Autoantibodies to cytosolic 5′‐nucleotidase 1A in inclusion body myositis

B. Engelen, H. J. Schelhaas, M. Verbeek, 2013, Annals of neurology.

Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites

L. Schöls, H. J. Schelhaas, W. D. den Dunnen, 2009, Neuropathology and applied neurobiology.

Mutations in BICD2, which encodes a golgin and important motor adaptor, cause congenital autosomal-dominant spinal muscular atrophy.

J. Veltman, B. Wirth, R. Sinke, 2013, American journal of human genetics.

VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient

J. Veldink, H. J. Schelhaas, W. V. Rheenen, 2012, Neurobiology of Aging.

Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes.

W. Robberecht, L. H. van den Berg, J. Veldink, 2009, Archives of neurology.

TDP-43 accumulation is common in myopathies with rimmed vacuoles

Martin Lammens, Benno Küsters, B. Engelen, 2009, Acta Neuropathologica.

Phenytoin as a last‐resort treatment in SCN8A encephalopathy

J. Verhoeven, H. J. Schelhaas, C. Haaxma, 2017, Epilepsia open.

Carbamazepine and oxcarbazepine in adult patients with Dravet syndrome: Friend or foe?

H. J. Schelhaas, B. Kleine, A. Louw, 2015, Seizure.

Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis

Edwin Cuppen, Christine Klein, Dagmar Verbaan, 2011, Annals of neurology.

Lifetime physical activity and the risk of amyotrophic lateral sclerosis

L. H. van den Berg, J. Veldink, H. J. Schelhaas, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes

H. J. Schelhaas, B. P. Warrenburg, H. Scheffer, 2009, Journal of Neurology.

Monitoring disease progression using high‐density motor unit number estimation in amyotrophic lateral sclerosis

Dick F Stegeman, Machiel J Zwarts, D. Stegeman, 2010, Muscle & nerve.

Normal values for quantitative muscle ultrasonography in adults

Sebastiaan Overeem, S. Pillen, M. Zwarts, 2010, Muscle & nerve.

Dissociated small hand muscle atrophy in aging: the ‘senile hand’ is a split hand

H. J. Schelhaas, M. Munneke, N. Voermans, 2006, European journal of neurology.

Effect of small motor unit potentials on the motor unit number estimate

D. Stegeman, M. Zwarts, H. J. Schelhaas, 2008, Muscle & nerve.

Motor unit number index (MUNIX) versus motor unit number estimation (MUNE): A direct comparison in a longitudinal study of ALS patients

Dick F. Stegeman, Johannes P. van Dijk, D. Stegeman, 2012, Clinical Neurophysiology.

The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder

Michelle K. Lupton, T. Hortobágyi, Robert H. Brown, 2012, European Journal of Human Genetics.

Peripheral nerve involvement in spinocerebellar ataxias.

N. van Alfen, M. Zwarts, R. Sinke, 2004, Archives of neurology.

Firing pattern of fasciculations in ALS Evidence for axonal and neuronal origin

D. Stegeman, M. Zwarts, H. J. Schelhaas, 2019 .

Euthanasia and physician-assisted suicide in amyotrophic lateral sclerosis: a prospective study

J. Veldink, B. Onwuteaka-Philipsen, H. J. Schelhaas, 2014, Journal of Neurology.

Lithium lacks effect on survival in amyotrophic lateral sclerosis: a phase IIb randomised sequential trial

L. H. van den Berg, J. Veldink, H. J. Schelhaas, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

Firing pattern of fasciculations in ALS

Dick F. Stegeman, Bert U. Kleine, D. Stegeman, 2008, Neurology.

Prevalence and distribution of fasciculations in healthy adults: Effect of age, caffeine consumption and exercise

M. Zwarts, S. Overeem, H. J. Schelhaas, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype

M. Zwarts, H. J. Schelhaas, B. V. van Engelen, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Cognitive impairment in SCA-19.

H. J. Schelhaas, B. Kremer, G. Hageman, 2003, Acta neurologica Belgica.

Muscle ultrasonography to predict survival in amyotrophic lateral sclerosis

S. Pillen, M. Zwarts, S. Overeem, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Fasciculations and their F-response revisited: High-density surface EMG in ALS and benign fasciculations

Dick F. Stegeman, Bert U. Kleine, D. Stegeman, 2012, Clinical Neurophysiology.

Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis

R. Ophoff, D. Lambrechts, P. Andersen, 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Autism and behavior in adult patients with Dravet syndrome (DS)

H. J. Schelhaas, A. Aldenkamp, M. Willemsen, 2015, Epilepsy & Behavior.

Structural MRI reveals cortical thinning in amyotrophic lateral sclerosis

M. P. van den Heuvel, L. H. van den Berg, J. Veldink, 2011, Journal of Neurology, Neurosurgery & Psychiatry.

Is the Frontal Assessment Battery reliable in ALS patients?

L. H. van den Berg, R. D. de Haan, H. J. Schelhaas, 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Prospective, blind study of the triple stimulation technique in the diagnosis of ALS

D. Stegeman, M. Zwarts, H. J. Schelhaas, 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Amyotrofische laterale sclerose

J. Veldink, H. J. Schelhaas, J. Weikamp, 2010 .

Primary respiratory failure in inclusion body myositis

M. Zwarts, H. J. Schelhaas, N. Voermans, 2004, Neurology.

Microglial Upregulation of Progranulin as a Marker of Motor Neuron Degeneration

D. Lambrechts, K. Sleegers, C. van Broeckhoven, 2010, Journal of neuropathology and experimental neurology.

TDP-43 plasma levels do not differentiate sporadic inclusion body myositis from other inflammatory myopathies

W. F. Abdo, B. Engelen, H. J. Schelhaas, 2010, Acta Neuropathologica.

Superficial Siderosis, Traumatic Tap, and Xanthochromia

H. J. Schelhaas, L. V. D. Berg, M. Visser, 2016 .

Letter: Recruitment of patients with both epilepsy and intellectual disability

H. J. Schelhaas, B. Kleine, M. Willemsen, 2015, Epilepsia.

H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis

A. Al-Chalabi, C. Shaw, P. Andersen, 2013, Neurobiology of Aging.

Breath analysis in detecting epilepsy

K. Kho, H. J. Schelhaas, A. Colon, 2020, Journal of breath research.

Cumulative effect of 5 daily sessions of theta burst stimulation on corticospinal excitability in amyotrophic lateral sclerosis

Sebastiaan Overeem, Dick F Stegeman, Machiel J Zwarts, 2013, Muscle & nerve.

Accuracy of WISC-III and WAIS-IV short forms in patients with neurological disorders

H. J. Schelhaas, A. Aldenkamp, J. Hendriksen, 2018, Developmental neurorehabilitation.

Neurodegenerative phenotypes in an A 53 T a-synuclein transgenic mouse model are independent of LRRK 2

A. Goris, W. Robberecht, H. J. Schelhaas, 2012 .

Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis

Peter N. Robinson, N. Brown, S. Köhler, 2017, Genome Medicine.

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.

I. Scheffer, H. Mefford, E. Haan, 2019, American Journal of Human Genetics.

Source (or Part of the following Source): Type Article Title Population Based Epidemiology of Amyotrophic Lateral Sclerosis Using Capture-recapture Methodology Author(s) Population Based Epidemiology of Amyotrophic Lateral Sclerosis Using Captureerecapture Methodology

L. H. van den Berg, J. Veldink, H. J. Schelhaas, 2022 .

Neuromuscular transmission in SCA6

M. Zwarts, H. J. Schelhaas, H. Kremer, 2004, Annals of neurology.

Transcranial direct current stimulation does not modulate motor cortex excitability in patients with amyotrophic lateral sclerosis

Dick F Stegeman, Machiel J Zwarts, D. Stegeman, 2011, Muscle & nerve.

Normal values for quantitative muscle ultrasonography in adults

S. Pillen, M. Zwarts, S. Overeem, 2010, Muscle & nerve.

[Amyotrophic lateral sclerosis].

L. H. van den Berg, J. Veldink, H. J. Schelhaas, 2010, Nederlands tijdschrift voor tandheelkunde.

Neurophysiologic Studies in Early-Onset Cerebellar Ataxia

M. Zwarts, H. J. Schelhaas, B. Kremer, 2006, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.