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Journal of Neuromuscular Diseases
|
August 2, 2021
Behavioural Impairment and Frontotemporal Dementia in Oculopharyngeal Muscular Dystrophy
Maurits Tankink, Corinne G C Horlings, Nicol Voermans, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 21, 2004
Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity
B M van der Sluijs, H J ter Laak, H Scheffer, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
October 7, 2004
Diminished central activation during maximal voluntary contraction in chronic fatigue syndrome
M L Schillings, J S Kalkman, S P van der Werf, 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.
Tijdschrift Voor Psychiatrie
|
April 14, 2022
[The association between religious coping styles and psychopathological symptomatology within a Christian population]
A L Oudijn-van Engelen, N Jacobs, J Lataster, et al.
Iscience
|
June 6, 2024
Transcriptomic gene signatures measure satellite cell activity in muscular dystrophies
Elise N Engquist, Anna Greco, Leo A B Joosten, et al.
NAM Journal
|
June 29, 2026
Including genetic susceptibility towards Parkinson's disease in NAM-based hazard and risk assessment of pesticides: a semi-systematic review
Julia J Meerman, Véronique M P de Bruijn, Thomas Luechtefeld, et al.
NPJ Primary Care Respiratory Medicine
|
September 24, 2020
The experience of general practitioners with Very Brief Advice in the treatment of tobacco addiction
Onno C P van Schayck, Lynn Bindels, Ancka Nijs, et al.
International Journal of Cardiology
|
March 9, 2020
22q11.2 deletion syndrome is associated with increased mortality in adults with tetralogy of Fallot and pulmonary atresia with ventricular septal defect
Dirkjan Kauw, Odilia I Woudstra, Klaartje van Engelen, et al.
Journal of Neurology
|
September 8, 2018
Quantitative muscle MRI and ultrasound for facioscapulohumeral muscular dystrophy: complementary imaging biomarkers
Karlien Mul, Corinne G C Horlings, Sanne C C Vincenten, et al.
Page
of 84
Search research articles
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Showing results (321-330 of 831) with videos related to
Sort By:
Page
of 84
Journal of Neuromuscular Diseases
|
August 2, 2021
Behavioural Impairment and Frontotemporal Dementia in Oculopharyngeal Muscular Dystrophy
Maurits Tankink, Corinne G C Horlings, Nicol Voermans, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 21, 2004
Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity
B M van der Sluijs, H J ter Laak, H Scheffer, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
October 7, 2004
Diminished central activation during maximal voluntary contraction in chronic fatigue syndrome
M L Schillings, J S Kalkman, S P van der Werf, 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.
Tijdschrift Voor Psychiatrie
|
April 14, 2022
[The association between religious coping styles and psychopathological symptomatology within a Christian population]
A L Oudijn-van Engelen, N Jacobs, J Lataster, et al.
Iscience
|
June 6, 2024
Transcriptomic gene signatures measure satellite cell activity in muscular dystrophies
Elise N Engquist, Anna Greco, Leo A B Joosten, et al.
NAM Journal
|
June 29, 2026
Including genetic susceptibility towards Parkinson's disease in NAM-based hazard and risk assessment of pesticides: a semi-systematic review
Julia J Meerman, Véronique M P de Bruijn, Thomas Luechtefeld, et al.
NPJ Primary Care Respiratory Medicine
|
September 24, 2020
The experience of general practitioners with Very Brief Advice in the treatment of tobacco addiction
Onno C P van Schayck, Lynn Bindels, Ancka Nijs, et al.
International Journal of Cardiology
|
March 9, 2020
22q11.2 deletion syndrome is associated with increased mortality in adults with tetralogy of Fallot and pulmonary atresia with ventricular septal defect
Dirkjan Kauw, Odilia I Woudstra, Klaartje van Engelen, et al.
Journal of Neurology
|
September 8, 2018
Quantitative muscle MRI and ultrasound for facioscapulohumeral muscular dystrophy: complementary imaging biomarkers
Karlien Mul, Corinne G C Horlings, Sanne C C Vincenten, et al.
Page
of 84