Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Karlien Mul

Showing results (1-10 of 60) with videos related to

Pageof 6
Sort By:
Continuum (Minneapolis, Minn.)|December 20, 2022
Facioscapulohumeral Muscular DystrophyKarlien Mul
European Journal of Neurology|November 25, 2025
Response to: Disentangling Facioscapulohumeral Muscular Dystrophy Disability From Age and Comorbidities: A Call for Refined StratificationSjan Teeselink, Karlien Mul
European Journal of Medical Genetics|March 1, 2015
Facioscapulohumeral muscular dystrophy as a genetic cause of pectus excavatumKarlien Mul, George W Padberg, Nicol C Voermans
Neuromuscular Disorders : NMD|June 20, 2017
225th ENMC international workshop:: A global FSHD registry framework, 18-20 November 2016, Heemskerk, The NetherlandsKarlien Mul, June Kinoshita, Hugh Dawkins, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 24, 2026
[The rise of genetic therapies: urgent moral and societal questions]Kris E Leeuwenberg, Karlien Mul, Bart P van de Warrenburg, et al.
The British Journal of Mathematical and Statistical Psychology|August 29, 2020
Semi-automated Rasch analysis using in-plus-out-of-questionnaire log likelihoodFeri Wijayanto, Karlien Mul, Perry Groot, et al.
Neuromuscular Disorders : NMD|July 26, 2024
Improving Heckmatt muscle ultrasound grading scale through Rasch analysisJuerd Wijntjes, Christiaan Saris, Jonne Doorduin, et al.
Muscle & Nerve|August 11, 2021
Variability in electrodiagnostic findings associated with neurogenic thoracic outlet syndromeKarlien Mul, Niels Pesser, Kimberly Vervaart, et al.
Neuromuscular Disorders : NMD|April 26, 2023
268th ENMC workshop - Genetic diagnosis, clinical classification, outcome measures, and biomarkers in Facioscapulohumeral Muscular Dystrophy (FSHD): Relevance for clinical trialsFederica Montagnese, Katy de Valle, Richard J L F Lemmers, et al.
Behavior Research Methods|September 7, 2022
Semi-automated Rasch analysis with differential item functioningFeri Wijayanto, Ioan Gabriel Bucur, Karlien Mul, et al.
Pageof 6

Showing results (1-10 of 60) with videos related to

Sort By:
Pageof 6
Continuum (Minneapolis, Minn.)|December 20, 2022
Facioscapulohumeral Muscular DystrophyKarlien Mul
European Journal of Neurology|November 25, 2025
Response to: Disentangling Facioscapulohumeral Muscular Dystrophy Disability From Age and Comorbidities: A Call for Refined StratificationSjan Teeselink, Karlien Mul
European Journal of Medical Genetics|March 1, 2015
Facioscapulohumeral muscular dystrophy as a genetic cause of pectus excavatumKarlien Mul, George W Padberg, Nicol C Voermans
Neuromuscular Disorders : NMD|June 20, 2017
225th ENMC international workshop:: A global FSHD registry framework, 18-20 November 2016, Heemskerk, The NetherlandsKarlien Mul, June Kinoshita, Hugh Dawkins, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 24, 2026
[The rise of genetic therapies: urgent moral and societal questions]Kris E Leeuwenberg, Karlien Mul, Bart P van de Warrenburg, et al.
The British Journal of Mathematical and Statistical Psychology|August 29, 2020
Semi-automated Rasch analysis using in-plus-out-of-questionnaire log likelihoodFeri Wijayanto, Karlien Mul, Perry Groot, et al.
Neuromuscular Disorders : NMD|July 26, 2024
Improving Heckmatt muscle ultrasound grading scale through Rasch analysisJuerd Wijntjes, Christiaan Saris, Jonne Doorduin, et al.
Muscle & Nerve|August 11, 2021
Variability in electrodiagnostic findings associated with neurogenic thoracic outlet syndromeKarlien Mul, Niels Pesser, Kimberly Vervaart, et al.
Neuromuscular Disorders : NMD|April 26, 2023
268th ENMC workshop - Genetic diagnosis, clinical classification, outcome measures, and biomarkers in Facioscapulohumeral Muscular Dystrophy (FSHD): Relevance for clinical trialsFederica Montagnese, Katy de Valle, Richard J L F Lemmers, et al.
Behavior Research Methods|September 7, 2022
Semi-automated Rasch analysis with differential item functioningFeri Wijayanto, Ioan Gabriel Bucur, Karlien Mul, et al.
Pageof 6