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Journal of Neurology
|
January 19, 2013
A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Sissel Løseth, Nicol C Voermans, Torberg Torbergsen, et al.
Neurology
|
December 21, 2018
Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophy
Rianne J M Goselink, Karlien Mul, Caroline R van Kernebeek, et al.
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association
|
May 22, 2018
Is fatigue a disease-specific or generic symptom in chronic medical conditions?
Juliane Menting, Cees J Tack, Gijs Bleijenberg, et al.
Connective Tissue Research
|
March 17, 2011
Mild muscular features in tenascin-X knockout mice, a model of Ehlers-danlos syndrome
N C Voermans, K Verrijp, L Eshuis, et al.
Journal of Neurology
|
July 26, 2014
Prior medical conditions and the risk of amyotrophic lateral sclerosis
Meinie Seelen, Perry T C van Doormaal, Anne E Visser, et al.
Neurology
|
January 21, 2021
Incidence, Prevalence, and Geographical Clustering of Motor Neuron Disease in the Netherlands
Adriaan D de Jongh, Ruben P A van Eijk, Susan M Peters, et al.
Journal of Virological Methods
|
December 5, 2021
Diminished amplification of SARS-CoV-2 ORF1ab in a commercial dual-target qRT-PCR diagnostic assay
Stephanie Popping, Richard Molenkamp, Joachim D Weigel, et al.
Clinical Chemistry
|
August 4, 2019
Cytidine Diphosphate-Ribitol Analysis for Diagnostics and Treatment Monitoring of Cytidine Diphosphate-l-Ribitol Pyrophosphorylase A Muscular Dystrophy
Walinka van Tol, Monique van Scherpenzeel, Mohammad Alsady, et al.
Neurology
|
November 8, 2014
Sporadic late-onset nemaline myopathy with MGUS: long-term follow-up after melphalan and SCT
Nicol C Voermans, Olivier Benveniste, Monique C Minnema, et al.
Journal of Neuropathology and Experimental Neurology
|
March 11, 2021
NEM6, KBTBD13-Related Congenital Myopathy: Myopathological Analysis in 18 Dutch Patients Reveals Ring Rods Fibers, Cores, Nuclear Clumps, and Granulo-Filamentous Protein Material
Karlijn Bouman, Benno Küsters, Josine M De Winter, et al.
Page
of 35
Search research articles
Search
Showing results (261-270 of 344) with videos related to
Sort By:
Page
of 35
Journal of Neurology
|
January 19, 2013
A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Sissel Løseth, Nicol C Voermans, Torberg Torbergsen, et al.
Neurology
|
December 21, 2018
Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophy
Rianne J M Goselink, Karlien Mul, Caroline R van Kernebeek, et al.
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association
|
May 22, 2018
Is fatigue a disease-specific or generic symptom in chronic medical conditions?
Juliane Menting, Cees J Tack, Gijs Bleijenberg, et al.
Connective Tissue Research
|
March 17, 2011
Mild muscular features in tenascin-X knockout mice, a model of Ehlers-danlos syndrome
N C Voermans, K Verrijp, L Eshuis, et al.
Journal of Neurology
|
July 26, 2014
Prior medical conditions and the risk of amyotrophic lateral sclerosis
Meinie Seelen, Perry T C van Doormaal, Anne E Visser, et al.
Neurology
|
January 21, 2021
Incidence, Prevalence, and Geographical Clustering of Motor Neuron Disease in the Netherlands
Adriaan D de Jongh, Ruben P A van Eijk, Susan M Peters, et al.
Journal of Virological Methods
|
December 5, 2021
Diminished amplification of SARS-CoV-2 ORF1ab in a commercial dual-target qRT-PCR diagnostic assay
Stephanie Popping, Richard Molenkamp, Joachim D Weigel, et al.
Clinical Chemistry
|
August 4, 2019
Cytidine Diphosphate-Ribitol Analysis for Diagnostics and Treatment Monitoring of Cytidine Diphosphate-l-Ribitol Pyrophosphorylase A Muscular Dystrophy
Walinka van Tol, Monique van Scherpenzeel, Mohammad Alsady, et al.
Neurology
|
November 8, 2014
Sporadic late-onset nemaline myopathy with MGUS: long-term follow-up after melphalan and SCT
Nicol C Voermans, Olivier Benveniste, Monique C Minnema, et al.
Journal of Neuropathology and Experimental Neurology
|
March 11, 2021
NEM6, KBTBD13-Related Congenital Myopathy: Myopathological Analysis in 18 Dutch Patients Reveals Ring Rods Fibers, Cores, Nuclear Clumps, and Granulo-Filamentous Protein Material
Karlijn Bouman, Benno Küsters, Josine M De Winter, et al.
Page
of 35