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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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N van Alfen

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Clinical Genetics|August 8, 2009

Neuromuscular features in Marfan syndromeN c Voermans, J Timmermans, N van Alfen, et al.

Neuropediatrics|November 7, 2007

Neuromuscular abnormalities in ataxia telangiectasia: a clinical, electrophysiological and muscle ultrasound studyM M M Verhagen, N van Alfen, S Pillen, et al.

Neuromuscular Disorders : NMD|May 8, 2012

Congenital myopathy caused by a novel missense mutation in the CFL2 geneC W Ockeloen, H J Gilhuis, R Pfundt, et al.

Neuromuscular Disorders : NMD|January 14, 2017

The yield of diagnostic work-up of patients presenting with myalgia, exercise intolerance, or fatigue: A prospective observational studyM G E Te Riele, T H A Schreuder, N van Alfen, et al.

Pain Practice : the Official Journal of World Institute of Pain|March 27, 2025

The clinical value of EMG and SSEP in diagnosing chronic pelvic pain syndrome; a systematic reviewM C Wissing, S E I van der Wal, S Bongarts, et al.

BMC Neurology|October 24, 2024

A 5-year natural history study in LAMA2-related muscular dystrophy and SELENON-related myopathy: the Extended LAST STRONG studyE C M de Laat, S L S Houwen-van Opstal, K Bouman, et al.

Pageof 4

Search research articles

Showing results (31-40 of 36) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 36 results.

Clinical Genetics|August 8, 2009

Neuromuscular features in Marfan syndromeN c Voermans, J Timmermans, N van Alfen, et al.

Neuropediatrics|November 7, 2007

Neuromuscular abnormalities in ataxia telangiectasia: a clinical, electrophysiological and muscle ultrasound studyM M M Verhagen, N van Alfen, S Pillen, et al.

Neuromuscular Disorders : NMD|May 8, 2012

Congenital myopathy caused by a novel missense mutation in the CFL2 geneC W Ockeloen, H J Gilhuis, R Pfundt, et al.

Neuromuscular Disorders : NMD|January 14, 2017

The yield of diagnostic work-up of patients presenting with myalgia, exercise intolerance, or fatigue: A prospective observational studyM G E Te Riele, T H A Schreuder, N van Alfen, et al.

Pain Practice : the Official Journal of World Institute of Pain|March 27, 2025

The clinical value of EMG and SSEP in diagnosing chronic pelvic pain syndrome; a systematic reviewM C Wissing, S E I van der Wal, S Bongarts, et al.

BMC Neurology|October 24, 2024

A 5-year natural history study in LAMA2-related muscular dystrophy and SELENON-related myopathy: the Extended LAST STRONG studyE C M de Laat, S L S Houwen-van Opstal, K Bouman, et al.

Pageof 4