Auditory dysfunction in chronic inflammatory demyelinating polyradiculoneuropathyHENGSTMAN, Gerald J. D; SCHELHAAS, Helenius J; ZWARTS, Machiel J et al.Neurology. 2004, Vol 62, Num 8, pp 1446-1448, issn 0028-3878, 3 p.Article

CSF neurofilament protein analysis in the differential diagnosis of ALSREIJN, Thierry S; ABDO, Wilson F; SCHELHAAS, Helenius J et al.Journal of neurology. 2009, Vol 256, Num 4, pp 615-619, issn 0340-5354, 5 p.Article

EFFECT OF SMALL MOTOR UNIT POTENTIALS ON THE MOTOR UNIT NUMBER ESTIMATEVAN DIJK, Johannes P; ZWARTS, Machiel J; SCHELHAAS, Helenius J et al.Muscle & nerve. 2008, Vol 38, Num 1, pp 887-892, issn 0148-639X, 6 p.Article

Firing pattern of fasciculations in ALS : Evidence for axonal and neuronal originKLEINE, Bert U; STEGEMAN, Dick F; SCHELHAAS, Helenius J et al.Neurology. 2008, Vol 70, Num 5, pp 353-359, issn 0028-3878, 7 p.Article

Evidence for an oligogenic basis of amyotrophic lateral sclerosisBLITTERSWIJK, Marka Van; ES, Michael A. Van; DE BAKKER, Paul I. W et al.Human molecular genetics (Print). 2012, Vol 21, Num 17, pp 3776-3784, issn 0964-6906, 9 p.Article

Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosisHERDEWYN, Sarah; HUI ZHAO; ROBBERECHT, Wim et al.Human molecular genetics (Print). 2012, Vol 21, Num 11, pp 2412-2419, issn 0964-6906, 8 p.Article

MONITORING DISEASE PROGRESSION USING HIGH-DENSITY MOTOR UNIT NUMBER ESTIMATION IN AMYOTROPHIC LATERAL SCLEROSISVAN DIJK, Johannes P; SCHELHAAS, Helenius J; VAN SCHAIK, Ivo N et al.Muscle & nerve. 2010, Vol 42, Num 2, pp 239-244, issn 0148-639X, 6 p.Article

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosisVAN ES, Michael A; VELDINK, Jan H; VAN DER KOOI, Anneke J et al.Nature genetics. 2009, Vol 41, Num 10, pp 1083-1087, issn 1061-4036, 5 p.Article

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansionsSIMON-SANCHEZ, Javier; DOPPER, Elise G. P; SMITS, Marion et al.Brain. 2012, Vol 135, pp 723-735, issn 0006-8950, 13 p., 3Article

Mutations in Potassium Channel KCND3 Cause Spinocerebellar Ataxia Type 19DUARRI, Anna; JEZIERSKA, Justyna; KUSTERS, Benno et al.Annals of neurology. 2012, Vol 72, Num 6, pp 870-880, issn 0364-5134, 11 p.Article

Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2CAUER-GRUMBACH, Michaela; OLSCHEWSKI, Andrea; STROHMAIER, Heimo et al.Nature genetics. 2010, Vol 42, Num 2, pp 160-164, issn 1061-4036, 5 p.Article

Peripheral nerve involvement in spinocerebellar ataxiasVAN DE WARRENBURG, Bart P. C; NOTERMANS, Nicolette C; SCHELHAAS, Helenius J et al.Archives of neurology (Chicago). 2004, Vol 61, Num 2, pp 257-261, issn 0003-9942, 5 p.Article

Hexanucleotide repeat expansions in C90RF72 in the spectrum of motor neuron diseasesVAN RHEENEN, Wouter; VAN BLITTERSWIJK, Marka; RAAPHORST, Joost et al.Neurology. 2012, Vol 79, Num 9, pp 878-882, issn 0028-3878, 5 p.Article

Motor unit number index (MUNIX) versus motor unit number estimation (MUNE): A direct comparison in a longitudinal study of ALS patientsBOEKESTEIN, Werner A; SCHELHAAS, Helenius J; PUTTEN, Michel J. A. M. Van et al.Clinical neurophysiology. 2012, Vol 123, Num 8, pp 1644-1649, issn 1388-2457, 6 p.Article

Smoking, Alcohol Consumption, and the Risk of Amyotrophic Lateral Sclerosis: A Population-based StudyDE JONG, Sonja W; HUISMAN, Mark H. B; SUTEDJA, Nadia A et al.American journal of epidemiology. 2012, Vol 176, Num 3, pp 233-239, issn 0002-9262, 7 p.Article

Angiogenin Variants in Parkinson Disease and Amyotrophic Lateral SclerosisVAN ES, Michael A; SCHELHAAS, Helenius J; FUMOTO, Katsumi et al.Annals of neurology. 2011, Vol 70, Num 6, pp 964-973, issn 0364-5134, 10 p.Article

FUS Mutations in Familial Amyotrophic Lateral Sclerosis in the NetherlandsGROEN, Ewout J. N; VAN ES, Michael A; PASTERKAMP, R. Jeroen et al.Archives of neurology (Chicago). 2010, Vol 67, Num 2, pp 224-230, issn 0003-9942, 7 p.Article

Microglial Upregulation of Progranulin as a Marker of Motor Neuron DegenerationPHILIPS, Thomas; DE MUYNCK, Louis; SCIOT, Raf et al.Journal of neuropathology and experimental neurology. 2010, Vol 69, Num 12, pp 1191-1200, issn 0022-3069, 10 p.Article

Survival Profiles of Patients With Frontotemporal Dementia and Motor Neuron DiseaseHU, William T; SEELAAR, Harro; KUESTERS, Benno et al.Archives of neurology (Chicago). 2009, Vol 66, Num 11, pp 1359-1364, issn 0003-9942, 6 p.Article

ARSACS in the Dutch population : a frequent cause of early-onset cerebellar ataxiaVERMEER, Sascha; MEIJER, Rowdy P. P; KREMER, Berry et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 3, pp 207-214, issn 1364-6745, 8 p.Article

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosisVAN ES, Michael A; VAN VUGHT, Paul Wj; LEMMENS, Robin et al.Nature genetics. 2008, Vol 40, Num 1, pp 29-31, issn 1061-4036, 3 p.Article