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Publications by Bjarne Udd

Actininopathy – A New Muscular Dystrophy Caused by ACTN2 Dominant Mutations

Annals of Neurology
Neurology
2019English

Autosomal Dominant Late-Onset Spinal Motor Neuronopathy Is Linked to a New Locus on Chromosome 22q11.2-Q13.2

European Journal of Human Genetics
Genetics
2012English

Dominantly Inherited Distal Nemaline/Cap Myopathy Caused by a Large Deletion in the Nebulin Gene

Neuromuscular Disorders
Child HealthNeurologyPediatricsPerinatologyGenetics
2019English

1st ENMC European Meeting: THE EURO-NMD Pathology Working Group Recommended Standards for Muscle Pathology 7 December 2018, Amsterdam, the Netherlands

Neuromuscular Disorders
Child HealthNeurologyPediatricsPerinatologyGenetics
2019English

Consensus-Based Care Recommendations for Adults With Myotonic Dystrophy Type 2

Neurology: Clinical Practice
Neurology
2019English

Lamin a/C Mutation Affecting Primarily the Right Side of the Heart

Cardiogenetics
2013English

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