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Karlien Mul

Radboud University Nijmegen

39

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274

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Exploring the influence of smoking and alcohol consumption on clinical severity in patients with facioscapulohumeral muscular dystrophy.

2021 Neuromuscular Disorders
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The FacioScapuloHumeral muscular Dystrophy Rasch-built Overall Disability Scale (FSHD-RODS).

2021 European Journal of Neurology
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Profiling Serum Antibodies Against Muscle Antigens in Facioscapulohumeral Muscular Dystrophy Finds No Disease-Specific Autoantibodies

2021 Journal of neuromuscular diseases
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Facioscapulohumeral muscular dystrophy-Reproductive counseling, pregnancy, and delivery in a complex multigenetic disease.

2021 Clinical Genetics
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A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene.

2020 Parkinsonism & Related Disorders
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Deep phenotyping of Facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging.

2020 European Journal of Neurology
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Evaluation of blood gene expression levels in facioscapulohumeral muscular dystrophy patients.

2020 Scientific Reports
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Muscle ultrasound is a responsive biomarker in facioscapulohumeral dystrophy

2020 Neurology
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P.306Multicentric MRI study in a cohort of FSHD2 patients: pattern definition and differences between FSHD1 and FSHD2

2019 Neuromuscular Disorders
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Chronische polyneuropathie en dunnevezelneuropathie: diagnostiek en behandeling

2019 Bijblijven
- Karlien Mul
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