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Practical Neurology
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February 11, 2016
What's in a name? The clinical features of facioscapulohumeral muscular dystrophy
Karlien Mul, Saskia Lassche, Nicol C Voermans, et al.
Neuromuscular Disorders : NMD
|
February 4, 2018
Specific muscle strength is reduced in facioscapulohumeral dystrophy: An MRI based musculoskeletal analysis
Marco A Marra, Linda Heskamp, Karlien Mul, et al.
Amino Acids
|
July 13, 2016
Monitoring creatine and phosphocreatine by (13)C MR spectroscopic imaging during and after (13)C4 creatine loading: a feasibility study
Barbara H Janssen, Saskia Lassche, Maria T Hopman, et al.
Ultrasound in Medicine & Biology
|
August 3, 2017
Ultrasound Imaging of Muscle Contraction of the Tibialis Anterior in Patients with Facioscapulohumeral Dystrophy
Kaj Gijsbertse, Rianne Goselink, Saskia Lassche, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
November 11, 2018
Computer-aided detection of fasciculations and other movements in muscle with ultrasound: Development and clinical application
Kaj Gijsbertse, Max Bakker, André Sprengers, et al.
Muscle & Nerve
|
September 22, 2020
Reduced specific force in patients with mild and severe facioscapulohumeral muscular dystrophy
Saskia Lassche, Nicol C Voermans, Tim Schreuder, et al.
Journal of Neuromuscular Diseases
|
September 14, 2020
Correlation Between Quantitative MRI and Muscle Histopathology in Muscle Biopsies from Healthy Controls and Patients with IBM, FSHD and OPMD
Saskia Lassche, Benno Küsters, Arend Heerschap, et al.
Journal of Neuromuscular Diseases
|
August 15, 2018
MRI-Guided Biopsy as a Tool for Diagnosis and Research of Muscle Disorders
Saskia Lassche, Barbara H Janssen, Ties IJzermans, et al.
Neuromuscular Disorders : NMD
|
May 19, 2019
Muscle fiber dysfunction contributes to weakness in inclusion body myositis
Saskia Lassche, Anke Rietveld, Arend Heerschap, et al.
Muscle & Nerve
|
March 19, 2014
A novel KCNA1 mutation causing episodic ataxia type I
Saskia Lassche, Sergio Lainez, Bastiaan R Bloem, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Practical Neurology
|
February 11, 2016
What's in a name? The clinical features of facioscapulohumeral muscular dystrophy
Karlien Mul, Saskia Lassche, Nicol C Voermans, et al.
Neuromuscular Disorders : NMD
|
February 4, 2018
Specific muscle strength is reduced in facioscapulohumeral dystrophy: An MRI based musculoskeletal analysis
Marco A Marra, Linda Heskamp, Karlien Mul, et al.
Amino Acids
|
July 13, 2016
Monitoring creatine and phosphocreatine by (13)C MR spectroscopic imaging during and after (13)C4 creatine loading: a feasibility study
Barbara H Janssen, Saskia Lassche, Maria T Hopman, et al.
Ultrasound in Medicine & Biology
|
August 3, 2017
Ultrasound Imaging of Muscle Contraction of the Tibialis Anterior in Patients with Facioscapulohumeral Dystrophy
Kaj Gijsbertse, Rianne Goselink, Saskia Lassche, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
November 11, 2018
Computer-aided detection of fasciculations and other movements in muscle with ultrasound: Development and clinical application
Kaj Gijsbertse, Max Bakker, André Sprengers, et al.
Muscle & Nerve
|
September 22, 2020
Reduced specific force in patients with mild and severe facioscapulohumeral muscular dystrophy
Saskia Lassche, Nicol C Voermans, Tim Schreuder, et al.
Journal of Neuromuscular Diseases
|
September 14, 2020
Correlation Between Quantitative MRI and Muscle Histopathology in Muscle Biopsies from Healthy Controls and Patients with IBM, FSHD and OPMD
Saskia Lassche, Benno Küsters, Arend Heerschap, et al.
Journal of Neuromuscular Diseases
|
August 15, 2018
MRI-Guided Biopsy as a Tool for Diagnosis and Research of Muscle Disorders
Saskia Lassche, Barbara H Janssen, Ties IJzermans, et al.
Neuromuscular Disorders : NMD
|
May 19, 2019
Muscle fiber dysfunction contributes to weakness in inclusion body myositis
Saskia Lassche, Anke Rietveld, Arend Heerschap, et al.
Muscle & Nerve
|
March 19, 2014
A novel KCNA1 mutation causing episodic ataxia type I
Saskia Lassche, Sergio Lainez, Bastiaan R Bloem, et al.
Page
of 3