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Karlien Mul

Showing results (31-40 of 60) with videos related to

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Journal of Neurology|February 11, 2022
Long-term follow-up of respiratory function in facioscapulohumeral muscular dystrophySjan Teeselink, Sanne C C Vincenten, Nicol C Voermans, et al.
Disability and Rehabilitation|September 16, 2021
Experiences of patients with facioscapulohumeral dystrophy with facial weakness: a qualitative studySümeyye Sezer, Edith H C Cup, Lieve M Roets-Merken, et al.
Journal of Neuromuscular Diseases|May 24, 2021
Profiling Serum Antibodies Against Muscle Antigens in Facioscapulohumeral Muscular Dystrophy Finds No Disease-Specific AutoantibodiesAnna Greco, Kirsten R Straasheijm, Karlien Mul, et al.
Muscle & Nerve|September 19, 2024
The other face of facioscapulohumeral muscular dystrophy: Exploring orofacial weakness using muscle ultrasoundSanne C C Vincenten, Jeroen L M van Doorn, Sjan Teeselink, et al.
Disability and Rehabilitation|May 16, 2022
Development and validation of the patient-reported "Facial Function Scale" for facioscapulohumeral muscular dystrophyKarlien Mul, Feri Wijayanto, Tom G J Loonen, et al.
Neuromuscular Disorders : NMD|January 30, 2025
Muscle imaging in facioscapulohumeral muscular dystrophy research: A scoping review and expert recommendationsSanne C C Vincenten, Sjan Teeselink, Karlien Mul, et al.
Scientific Reports|January 27, 2022
Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkersAnita van den Heuvel, Saskia Lassche, Karlien Mul, 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.
Parkinsonism & Related Disorders|September 26, 2020
A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL geneKarlien Mul, Meyke I Schouten, Erica van der Looij, et al.
Clinical Genetics|September 14, 2018
Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1Karlien Mul, Nicol C Voermans, Richard J L F Lemmers, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Journal of Neurology|February 11, 2022
Long-term follow-up of respiratory function in facioscapulohumeral muscular dystrophySjan Teeselink, Sanne C C Vincenten, Nicol C Voermans, et al.
Disability and Rehabilitation|September 16, 2021
Experiences of patients with facioscapulohumeral dystrophy with facial weakness: a qualitative studySümeyye Sezer, Edith H C Cup, Lieve M Roets-Merken, et al.
Journal of Neuromuscular Diseases|May 24, 2021
Profiling Serum Antibodies Against Muscle Antigens in Facioscapulohumeral Muscular Dystrophy Finds No Disease-Specific AutoantibodiesAnna Greco, Kirsten R Straasheijm, Karlien Mul, et al.
Muscle & Nerve|September 19, 2024
The other face of facioscapulohumeral muscular dystrophy: Exploring orofacial weakness using muscle ultrasoundSanne C C Vincenten, Jeroen L M van Doorn, Sjan Teeselink, et al.
Disability and Rehabilitation|May 16, 2022
Development and validation of the patient-reported "Facial Function Scale" for facioscapulohumeral muscular dystrophyKarlien Mul, Feri Wijayanto, Tom G J Loonen, et al.
Neuromuscular Disorders : NMD|January 30, 2025
Muscle imaging in facioscapulohumeral muscular dystrophy research: A scoping review and expert recommendationsSanne C C Vincenten, Sjan Teeselink, Karlien Mul, et al.
Scientific Reports|January 27, 2022
Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkersAnita van den Heuvel, Saskia Lassche, Karlien Mul, 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.
Parkinsonism & Related Disorders|September 26, 2020
A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL geneKarlien Mul, Meyke I Schouten, Erica van der Looij, et al.
Clinical Genetics|September 14, 2018
Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1Karlien Mul, Nicol C Voermans, Richard J L F Lemmers, et al.
Pageof 6