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1. Full Text Two heads are better than one: benefits of joint models for ALS trials
by van Eijk, Ruben P A and Rooney, James and Hardiman, Orla and van den Berg, Leonard H
Journal of neurology, neurosurgery, and psychiatry, ISSN 0022-3050, 04/2019, Volume 90, Issue 9, p. jnnp-2019-320553
There are several methods to combine survival time and the ALSFRS-R.3 4 The Combined Assessment of Functional and Survival (CAFS) is a well-known composite... 
Clinical trials | Amyotrophic lateral sclerosis | Ostomy | Simulation | Patients
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2. Full Text P44-F Estimating number of trackable axons in excitability-testing using simulated CMAP scans
by Nassi, Thijs and Sleutjes, Boudewijn and Kovalchuk, Maria O and Buitenweg, Jan and van den Berg, Leonard H and Franssen, Hessel
Clinical Neurophysiology, ISSN 1388-2457, 07/2019, Volume 130, Issue 7, pp. e80 - e80
Excitability-testing enables assessment of treatment medication and provides insights into the underlying pathophysiology in neurodegenerative diseases.... 
Nervous system diseases | Analysis
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3. Full Text Evidence for a multimodal effect of riluzole in patients with ALS?
by de Jongh, Adriaan D and van Eijk, Ruben P A and van den Berg, Leonard H
Journal of neurology, neurosurgery, and psychiatry, ISSN 0022-3050, 03/2019, p. jnnp-2018-320211
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4. Full Text O-28 Simulated differential sensitivity of motor and sensory nerves for conduction block in immune-mediated neuropathies
by Sleutjes, Boudewijn T.H.M and Durmus, Naric and Kovalchuk, Maria O and van Putten, Michel J.A.M and van den Berg, Leonard H and Franssen, Hessel
Clinical Neurophysiology, ISSN 1388-2457, 07/2019, Volume 130, Issue 7, pp. e30 - e31
We extended our longitudinal axon model, which consisted of 41 nodes of Ranvier, with biophysical characteristics unique for human myelinated motor or sensory... 
Analysis | Neurophysiology
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5. Full Text Simulating perinodal changes observed in immune-mediated neuropathies - Impact on conduction in a model of myelinated motor and sensory axons
by Sleutjes, Boudewijn T.H.M and Kovalchuk, Maria O and Durmus, Naric and Buitenweg, Jan R and van Putten, Michel J.A.M and van den Berg, Leonard H and Franssen, Hessel
Journal of Neurophysiology, ISSN 0022-3077, 07/2019
Immune-mediated neuropathies affect myelinated axons, resulting in conduction slowing or block which may affect motor and sensory axons differently. The... 
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6. Full Text Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways
by Blokhuis, Anna M and Koppers, Max and Groen, Ewout J N and van den Heuvel, Dianne M A and Dini Modigliani, Stefano and Anink, Jasper J and Fumoto, Katsumi and van Diggelen, Femke and Snelting, Anne and Sodaar, Peter and Verheijen, Bert M and Demmers, Jeroen A A and Veldink, Jan H and Aronica, Eleonora and Bozzoni, Irene and den Hertog, Jeroen and van den Berg, Leonard H and Pasterkamp, R Jeroen
Acta neuropathologica, 08/2016, Volume 132, Issue 2, p. 175
Amyotrophic lateral sclerosis (ALS) is a devastating neurological disease with no effective treatment available. An increasing number of genetic causes of ALS... 
Adaptor Proteins, Vesicular Transport - genetics | Fragile X Mental Retardation Protein - metabolism | Adaptor Proteins, Vesicular Transport - metabolism | Motor Neurons - pathology | Ataxin-2 - genetics | DNA-Binding Proteins - metabolism | Ataxin-2 - metabolism | Guanine Nucleotide Exchange Factors - metabolism | C9orf72 Protein | Neurons - metabolism | Eye Proteins - genetics | Disease Models, Animal | Guanine Nucleotide Exchange Factors - genetics | Amyotrophic Lateral Sclerosis - genetics | Mice, Inbred C57BL | Mutant Proteins - genetics | RNA-Binding Protein FUS - genetics | Mutant Proteins - metabolism | Mitochondria - metabolism | RNA-Binding Protein FUS - metabolism | DNA-Binding Proteins - genetics | Motor Neurons - metabolism | Animals | Eye Proteins - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Fragile X Mental Retardation Protein - genetics
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7. Full Text Alzheimer's disease beyond APOE
by van den Berg, Leonard H and van Es, Michael A
Nature Genetics, ISSN 1061-4036, 10/2009, Volume 41, Issue 10, pp. 1047 - 1048
Two genome-wide association studies together report three new susceptibility loci for late-onset Alzheimer's disease. CLU, PICALM and CR1 may be involved in... 
ALLELE | GENE | GENETICS & HEREDITY | Genetic Predisposition to Disease | Genome-Wide Association Study | Clusterin - genetics | Monomeric Clathrin Assembly Proteins - genetics | Amyloid - metabolism | Apolipoproteins E - genetics | Humans | Alzheimer Disease - metabolism | Receptors, Complement 3b - genetics | Alzheimer Disease - genetics | Genome, Human | Proteins | Genetics | Alzheimers disease | Genes
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8. Full Text Brachial plexus magnetic resonance imaging differentiates between inflammatory neuropathies and does not predict disease course
by Jongbloed, BA and Bos, Jeroen W and Rutgers, Dirk|info:eu-repo/dai/nl/260608661 and van der Pol, WL|info:eu-repo/dai/nl/203721721 and van den Berg, Leonard H|info:eu-repo/dai/nl/288255216
Brain and Behavior, ISSN 2162-3279, 05/2017, Volume 7, Issue 5, pp. e00632 - n/a
OBJECTIVE: The main objective of this study was to evaluate the correlation between the distribution of brachial plexus magnetic resonance imaging (MRI)... 
inflammatory neuropathies | multifocal motor neuropathy | chronic inflammatory demyelinating polyradiculoneuropathy | Lewis‐Sumner syndrome | Brachial plexus | MRI | Brachial plexus MRI | Lewis-Sumner syndrome | INTRAVENOUS IMMUNOGLOBULIN | IVIG | BEHAVIORAL SCIENCES | NEUROSCIENCES | Diagnosis, Differential | Humans | Middle Aged | Magnetic Resonance Imaging - methods | Male | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - diagnosis | Netherlands | Polyneuropathies - diagnosis | Adult | Brachial Plexus - diagnostic imaging | Female | Aged | Retrospective Studies | Medicine, Experimental | Medical research | Magnetic resonance imaging | Epidemiology | Asymmetry | Neuromuscular diseases | Nuclear magnetic resonance--NMR | Index Medicus
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9. Full Text Patterns of symptom development in patients with motor neuron disease
by Walhout, Renée and Verstraete, Esther and van den Heuvel, Martijn P and Veldink, Jan H and van den Berg, Leonard H
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, 01/2018, Volume 19, Issue 1-2, pp. 21 - 28
Objective: To investigate whether symptom development in motor neuron disease (MND) is a random or organized process. Methods: Six hundred patients with... 
upper motor neuron | lower motor neuron | symptom development | amyotrophic lateral sclerosis | Motor neuron disease | FOCALITY | ALS | ADULT-ONSET | NEURODEGENERATION | MECHANISMS | AMYOTROPHIC-LATERAL-SCLEROSIS | NATURAL-HISTORY | CLINICAL NEUROLOGY | DEGENERATION | SPREADING PATTERNS | PROPAGATION | Index Medicus
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10. Full Text Mutational analysis of TARDBP in Parkinson's disease
by van Blitterswijk, Marka|van Es, Michael A.|Verbaan, Dagmar|van Hilten, Jacobus J.|Scheffer, Hans|van de Warrenburg, Bart P.|Veldink, Jan H.|van den Berg, Leonard H
Neurobiology of Aging, ISSN 0197-4580, 2013, Volume 34, Issue 5, pp. 1517.e1 - 1517.e3
Abstract Mutations in TAR DNA-binding protein ( TARDBP ) are associated with heterogenic phenotypes, including amyotrophic lateral sclerosis, frontotemporal... 
Neurology | Internal Medicine | Amyotrophic lateral sclerosis | Genetics | Parkinson's disease | Mutation | TARDBP | TDP-43 | NEUROSCIENCES | GERIATRICS & GERONTOLOGY | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Netherlands - epidemiology | Risk Factors | Male | Parkinson Disease - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Genetic Markers - genetics | Parkinson Disease - epidemiology | Polymorphism, Single Nucleotide - genetics | Female | Genetic Predisposition to Disease - epidemiology | Cohort Studies | Neurosciences | Genetic aspects | Binding proteins | Analysis | Index Medicus | DNA-binding protein | Missense mutation | Neurodegenerative diseases | Aging | Nervous system | Frontotemporal dementia | Movement disorders
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11. Full Text A replication study of genetic risk loci for ischemic stroke in a Dutch population : A case-control study
by Hauer, Allard J and Pulit, Sara L and Van Den Berg, Leonard H.|info:eu-repo/dai/nl/288255216 and De Bakker, Paul I.W.|info:eu-repo/dai/nl/342957082 and Veldink, Jan H.|info:eu-repo/dai/nl/266575722 and Ruigrok, Ynte M.|info:eu-repo/dai/nl/303621222 and Klijn, Catharina J.M.|info:eu-repo/dai/nl/227918681 and Algra, Ale|info:eu-repo/dai/nl/07483472X and Van Dijk, Ewoud J and Koudstaal, Peter J and Luijckx, Gert Jan and Nederkoorn, Paul J and Oostenbrugge, Robert J and Visser, Marieke C and Wermer, Marieke J H and Kappelle, L. Jaap
Scientific Reports, ISSN 2045-2322, 09/2017, Volume 7, Issue 1
We aimed to replicate reported associations of 10 SNPs at eight distinct loci with overall ischemic stroke (IS) and its subtypes in an independent cohort of... 
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12. Full Text Implications of spirometric reference values for amyotrophic lateral sclerosis
by van Eijk, Ruben P.A and Bakers, Jaap N.E and van Es, Michael A and Eijkemans, Marinus J.C and van den Berg, Leonard H
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, 07/2019, pp. 1 - 8
Objective: Spirometry is commonly used as screening tool for respiratory insufficiency in neuromuscular diseases. Despite the well-known effects of reference... 
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13. Full Text A case of ALS with posterior cortical atrophy
by Nijboer, Tanja C. W and Nitert, Bram and Westeneng, Henk-Jan and Van Den Berg, Leonard H and van Es, Michael A
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, 07/2019, pp. 1 - 5
Here, we provide a case-report of an amyotrophic lateral sclerosis (ALS) patient with cognitive deficits best defined as posterior cortical atrophy (PCA). This... 
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14. Full Text Amyotrophic lateral sclerosis as a multi-step process: an Australia population study
by Vucic, Steve and Westeneng, Henk-Jan and Al-Chalabi, Ammar and Van Den Berg, Leonard H and Talman, Paul and Kiernan, Matthew C
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, 07/2019, pp. 1 - 6
Objective: This study sought to investigate whether a multistep process was also evident in an Australian amyotrophic lateral sclerosis (ALS) population.... 
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15. Full Text The changing picture of amyotrophic lateral sclerosis: lessons from European registers
by Hardiman, Orla and Bulford, Samuel John and Al-Chalabi, Ammar and Singh, Surinder and Brayne, Carol and Beghi, Ettore and van den Berg, Leonard H and Chio, Adriano and Martin, Sarah and Logroscino, Giancarlo and Rooney, James
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 11/2012, Volume 88, Issue 7, p. 557
Prospective population based-registers of amyotrophic lateral sclerosis (ALS) have operated in Europe for over two decades, and have provided important... 
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16. Full Text Comment: Plateaus and reversals in ALS disease course or limitations of trial design?
by van Eijk, Ruben P.A and van den Berg, Leonard H
Neurology, ISSN 0028-3878, 03/2016, Volume 86, Issue 9, pp. 811 - 811
Amyotrophic lateral sclerosis (ALS) is a relentlessly progressive disease of motor neurons, resulting in worsening weakness of voluntary muscles until death... 
CLINICAL NEUROLOGY | Amyotrophic Lateral Sclerosis - diagnosis | Registries | Remission, Spontaneous | Clinical Trials as Topic - statistics & numerical data | Humans | Amyotrophic Lateral Sclerosis - epidemiology | Index Medicus | Abridged Index Medicus
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17. Full Text Participation restrictions in ambulatory amyotrophic lateral sclerosis patients: Physical and psychological factors
: Participation Restrictions in ALS
by Van Groenestijn, Annerieke C and Schröder, Carin D and Kruitwagen-Van Reenen, Esther T and Van Den Berg, Leonard H and Visser-Meily, Johanna M.A
Muscle & Nerve, ISSN 0148-639X, 11/2017, Volume 56, Issue 5, pp. 912 - 918
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18. Full Text The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public
by van der Spek, Rick A.A and van Rheenen, Wouter and Pulit, Sara L and Kenna, Kevin P and van den Berg, Leonard H and Veldink, Jan H and on behalf of the Project MinE ALS Sequencing Consortium
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, 07/2019, Volume 20, Issue 5-6, pp. 432 - 440
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive fatal neurodegenerative disease affecting one in 350 people. The aim of Project MinE is to... 
Databrowser | open-access | amyotrophic lateral sclerosis | whole-genome sequencing
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19. Full Text Caregiver burden in amyotrophic lateral sclerosis: A systematic review
by de Wit, Jessica and Bakker, Leonhard A and van Groenestijn, Annerieke C and van den Berg, Leonard H and Schröder, Carin D and Visser-Meily, Johanna M. A and Beelen, Anita
Palliative medicine, ISSN 0269-2163, 2017
Informal caregivers of patients with amyotrophic lateral sclerosis experience increased levels of caregiver burden as the disease progresses. Insight in the... 
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20. Full Text Whole-genome sequence variation, population structure and demographic history of the Dutch population
by Francioli, Laurent C and Menelaou, Anoniki and Pulit, Sara L and van Dijk, Freerk and Palamara, Pier Francesco and Elbers, Clara C and Neerincx, Pieter B. T and Ye, Kai and Guryev, Victor and Kloosterman, Wigard P and Deelen, Patrick and Abdellaoui, Abdel and van Leeuwen, Elisabeth M and van Oven, Mannis and Vermaat, Martijn and Li, Mingkun and Laros, Jeroen F. J and Karssen, Lennart C and Kanterakis, Alexanos and Amin, Najaf and Hottenga, Jouke Jan and Lameijer, Eric-Wubbo and Kattenberg, Mathijs and Dijkstra, Martijn and Byelas, Heorhiy and van Setten, Jessica and van Schaik, Barbera D. C and Bot, Jan and Nijman, Isaäc J and Renkens, Ivo and Marschall, Tobias and Schönhuth, Alexander and Hehir-Kwa, Jayne Y and Handsaker, Robert E and Polak, Paz and Sohail, Mashaal and Vuzman, Dana and Hormozdiari, Fereydoun and van Enckevort, David and Mei, Hailiang and Koval, Vyacheslav and Moed, Matthijs H and van der Velde, K. Joeri and Rivadeneira, Fernando and Estrada, Karol and Medina-Gomez, Carolina and Isaacs, Aaron and McCarroll, Steven A and Beekman, Marian and de Craen, Anton J. M and Suchiman, H. Eka D and Hofman, Albert and Oostra, Ben and Uitterlinden, Ané G and Willemsen, Gonneke and Platteel, Mathieu and Veldink, Jan H and van den Berg, Leonard H and Pitts, Steven J and Potluri, Shobha and Sundar, Purnima and Cox, David R and Sunyaev, Shamil R and den Dunnen, Johan T and Stoneking, Mark and de Knijff, Peter and Kayser, Manfred and Li, Qibin and Li, Yingrui and Du, Yuanping and Chen, Ruoyan and Cao, Hongzhi and Li, Ning and Cao, Sujie and Wang, Jun and Bovenberg, Jasper A and Pe'er, Itsik and Slagboom, P. Eline and van Duijn, Cornelia M and Boomsma, Dorret I and van Ommen, Gert-Jan B and de Bakker, Paul I. W and Swertz, Morris A and Wijmenga, Cisca and LifeLines Cohort Study and Genome Netherlands Consortium and Genome of the Netherlands Consortium and The Genome of the Netherlands Consortium
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 8, pp. 818 - 825
Whole-genome sequencing enables complete characterization of genetic variation, but geographic clustering of rare alleles demands many diverse populations be... 
GENETIC-VARIATION | IMPACT | HUMAN-DISEASE | EVOLUTION | DE-NOVO MUTATIONS | VARIANTS | RARE | EXOMES | HAPLOTYPE MAP | GENETICS & HEREDITY | COMMON | Haplotypes | European Continental Ancestry Group - genetics | Gene Frequency | Humans | Netherlands | Genetics, Population - methods | Gene Deletion | Alleles | Mutagenesis, Insertional | Polymorphism, Single Nucleotide | Genome, Human | Genome-Wide Association Study - methods | Sequence Analysis, DNA - methods | Usage | Single nucleotide polymorphisms | Research | Nucleotide sequencing | Methods | DNA sequencing | Studies | Industrial development | Genomics | Quality control | Genomes | Mitochondrial DNA | Deoxyribonucleic acid--DNA | Index Medicus
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