Hendrika B. Ginjaar
Leiden, ZH, Netherlands
Last Updated: 09/26/2026
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Found 10 publications
Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands.
Journal: Neuromuscular disorders : NMD
Published: November 19, 2017
Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samples.
Journal: Muscle & nerve
Published: April 14, 2015
Validation of genetic modifiers for Duchenne muscular dystrophy: a multicentre study assessing SPP1 and LTBP4 variants.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: April 24, 2014
Forty-Five Years of Duchenne Muscular Dystrophy in The Netherlands.
Journal: Journal of neuromuscular diseases
Published: January 01, 2014
Prolonged Ambulation in Duchenne Patients with a Mutation Amenable to Exon 44 Skipping.
Journal: Journal of neuromuscular diseases
Published: January 01, 2014
Dystrophin levels and clinical severity in Becker muscular dystrophy patients.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: December 03, 2013
Clinical characterisation of Becker muscular dystrophy patients predicts favourable outcome in exon-skipping therapy.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: May 14, 2013
Hypomorphic NOTCH3 alleles do not cause CADASIL in humans.
Journal: Human mutation
Published: April 22, 2013
Long-term follow-up study on patients with Miyoshi phenotype of distal muscular dystrophy.
Journal: European journal of neurology
Published: October 31, 2012
An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophy.
Journal: European journal of human genetics : EJHG
Published: June 07, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026