Eva Kimber

Arthrogryposis multiplexa congenita: an epidemiologic study of nearly 9 million births in 24 EUROCAT registers

Prevalence of Muscular Dystrophies: A Systematic Literature Review

Piezos thrive under pressure: mechanically activated ion channels in health and disease

Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1

Arthrogryposis: A Review and Update

Piezo2 senses airway stretch and mediates lung inflation-induced apnoea

Myasthenia gravis: subgroup classification and therapeutic strategies

A family of distal arthrogryposis type 5 due to a novel PIEZO2 mutation

Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis

Diagnosis and etiology of congenital muscular dystrophy

Embryonic Myosin Heavy-Chain Mutations Cause Distal Arthrogryposis and Developmental Myosin Myopathy That Persists Postnatally

Distal arthrogryposis and muscle weakness associated with a β-tropomyosin mutation

Multiple congenital contractures: Birth prevalence, etiology, and outcome