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Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
January 31, 2009
The cognitive profile of amyotrophic lateral sclerosis: A meta-analysis
Joost Raaphorst, Marianne de Visser, Wim H J P Linssen, et al.
Neuromuscular Disorders : NMD
|
September 2, 2014
Comparing clinical data and muscle imaging of DYSF and ANO5 related muscular dystrophies
Leroy Ten Dam, Anneke J van der Kooi, Fleur Rövekamp, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 25, 2010
[Amyotrophic lateral sclerosis and frontotemporal dementia: overlapping characteristics]
Joost Raaphorst, Hepke F Grupstra, Wim H J P Linssen, et al.
Archives of Neurology
|
January 21, 2004
Polymyositis: an ongoing discussion about a disease entity
Irene M Bronner, Wim H J P Linssen, Marjon F G van der Meulen, et al.
Parkinsonism & Related Disorders
|
April 3, 2012
Paroxysmal kinesigenic dyskinesia: cortical or non-cortical origin
Teun W van Strien, Anne-Fleur van Rootselaar, Anthony A J Hilgevoord, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 22, 2010
Cognitive dysfunction in lower motor neuron disease: executive and memory deficits in progressive muscular atrophy
Joost Raaphorst, Marianne de Visser, Marie-José van Tol, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 13, 2007
Sumatriptan nasal spray in the acute treatment of migraine in adolescents and children
Petra M C Callenbach, Lise P M Pels, Paul G H Mulder, et al.
American Journal of Human Genetics
|
January 26, 2010
Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies
Véronique Bolduc, Gareth Marlow, Kym M Boycott, et al.
Neurology
|
September 14, 2012
The ALS-FTD-Q: a new screening tool for behavioral disturbances in ALS
Joost Raaphorst, Emma Beeldman, Ben Schmand, et al.
Clinical Genetics
|
March 29, 2019
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients
Leroy Ten Dam, Wendy S Frankhuizen, Wim H J P Linssen, et al.
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Search research articles
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Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
January 31, 2009
The cognitive profile of amyotrophic lateral sclerosis: A meta-analysis
Joost Raaphorst, Marianne de Visser, Wim H J P Linssen, et al.
Neuromuscular Disorders : NMD
|
September 2, 2014
Comparing clinical data and muscle imaging of DYSF and ANO5 related muscular dystrophies
Leroy Ten Dam, Anneke J van der Kooi, Fleur Rövekamp, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 25, 2010
[Amyotrophic lateral sclerosis and frontotemporal dementia: overlapping characteristics]
Joost Raaphorst, Hepke F Grupstra, Wim H J P Linssen, et al.
Archives of Neurology
|
January 21, 2004
Polymyositis: an ongoing discussion about a disease entity
Irene M Bronner, Wim H J P Linssen, Marjon F G van der Meulen, et al.
Parkinsonism & Related Disorders
|
April 3, 2012
Paroxysmal kinesigenic dyskinesia: cortical or non-cortical origin
Teun W van Strien, Anne-Fleur van Rootselaar, Anthony A J Hilgevoord, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 22, 2010
Cognitive dysfunction in lower motor neuron disease: executive and memory deficits in progressive muscular atrophy
Joost Raaphorst, Marianne de Visser, Marie-José van Tol, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 13, 2007
Sumatriptan nasal spray in the acute treatment of migraine in adolescents and children
Petra M C Callenbach, Lise P M Pels, Paul G H Mulder, et al.
American Journal of Human Genetics
|
January 26, 2010
Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies
Véronique Bolduc, Gareth Marlow, Kym M Boycott, et al.
Neurology
|
September 14, 2012
The ALS-FTD-Q: a new screening tool for behavioral disturbances in ALS
Joost Raaphorst, Emma Beeldman, Ben Schmand, et al.
Clinical Genetics
|
March 29, 2019
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients
Leroy Ten Dam, Wendy S Frankhuizen, Wim H J P Linssen, et al.
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of 2