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Neurology
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February 19, 2024
Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 Children
Jamie I Verhoeven, Jasper Kramer, Juergen Seeger, et al.
Neuromuscular Disorders : NMD
|
January 30, 2025
Muscle imaging in facioscapulohumeral muscular dystrophy research: A scoping review and expert recommendations
Sanne C C Vincenten, Sjan Teeselink, Karlien Mul, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
October 8, 2020
[Exertional heat stroke in athletes and soldiers]
Luuk R van den Bersselaar, Coen C W G Bongers, Thijs M H Eijsvogels, et al.
Journal of Neuromuscular Diseases
|
September 19, 2022
Perioperative Care for Patients with Neuromuscular Disorders in the Netherlands - A Questionnaire Study Among Anaesthesiologists, Neurologists and Clinical Geneticists
L R van den Bersselaar, M H M Gubbels, H Jungbluth, et al.
Neurology
|
October 4, 2022
Neuromuscular Features in XL-MTM Carriers: A Cross-sectional Study in an Unselected Cohort
Daniëlle K Franken, Karlijn Bouman, Stacha F I Reumers, et al.
Transfusion
|
April 5, 2025
Low rate of hepatitis Delta virus co-infection in first-time blood donors diagnosed with chronic hepatitis B virus infection in the Netherlands
Thijs J W van de Laar, Lesley A Patmore, Michel M Molier, et al.
Disability and Rehabilitation
|
May 16, 2022
Development and validation of the patient-reported "Facial Function Scale" for facioscapulohumeral muscular dystrophy
Karlien Mul, Feri Wijayanto, Tom G J Loonen, et al.
European Journal of Neurology
|
April 10, 2021
The facioscapulohumeral muscular dystrophy Rasch-built overall disability scale (FSHD-RODS)
Karlien Mul, Tatiana Hamadeh, Corinne G C Horlings, et al.
Neuromuscular Disorders : NMD
|
February 28, 2025
Obstetric and gynaecological features in females carrying variants in the skeletal muscle ryanodine receptor type 1 (RYR1) gene: a questionnaire study
Arti M Mistry, Georgia Saldanha, Luuk R van den Bersselaar, et al.
Biochemistry and Biophysics Reports
|
April 6, 2026
Sarco/endoplasmatic reticulum calcium ATPase activity in healthy muscle and Brody disease
J P Molenaar, M M Snoeck, S Treves, et al.
Page
of 35
Search research articles
Search
Showing results (211-220 of 344) with videos related to
Sort By:
Page
of 35
Neurology
|
February 19, 2024
Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 Children
Jamie I Verhoeven, Jasper Kramer, Juergen Seeger, et al.
Neuromuscular Disorders : NMD
|
January 30, 2025
Muscle imaging in facioscapulohumeral muscular dystrophy research: A scoping review and expert recommendations
Sanne C C Vincenten, Sjan Teeselink, Karlien Mul, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
October 8, 2020
[Exertional heat stroke in athletes and soldiers]
Luuk R van den Bersselaar, Coen C W G Bongers, Thijs M H Eijsvogels, et al.
Journal of Neuromuscular Diseases
|
September 19, 2022
Perioperative Care for Patients with Neuromuscular Disorders in the Netherlands - A Questionnaire Study Among Anaesthesiologists, Neurologists and Clinical Geneticists
L R van den Bersselaar, M H M Gubbels, H Jungbluth, et al.
Neurology
|
October 4, 2022
Neuromuscular Features in XL-MTM Carriers: A Cross-sectional Study in an Unselected Cohort
Daniëlle K Franken, Karlijn Bouman, Stacha F I Reumers, et al.
Transfusion
|
April 5, 2025
Low rate of hepatitis Delta virus co-infection in first-time blood donors diagnosed with chronic hepatitis B virus infection in the Netherlands
Thijs J W van de Laar, Lesley A Patmore, Michel M Molier, et al.
Disability and Rehabilitation
|
May 16, 2022
Development and validation of the patient-reported "Facial Function Scale" for facioscapulohumeral muscular dystrophy
Karlien Mul, Feri Wijayanto, Tom G J Loonen, et al.
European Journal of Neurology
|
April 10, 2021
The facioscapulohumeral muscular dystrophy Rasch-built overall disability scale (FSHD-RODS)
Karlien Mul, Tatiana Hamadeh, Corinne G C Horlings, et al.
Neuromuscular Disorders : NMD
|
February 28, 2025
Obstetric and gynaecological features in females carrying variants in the skeletal muscle ryanodine receptor type 1 (RYR1) gene: a questionnaire study
Arti M Mistry, Georgia Saldanha, Luuk R van den Bersselaar, et al.
Biochemistry and Biophysics Reports
|
April 6, 2026
Sarco/endoplasmatic reticulum calcium ATPase activity in healthy muscle and Brody disease
J P Molenaar, M M Snoeck, S Treves, et al.
Page
of 35