Hendrik Rosewich

Research conference summary from the 2014 International Task Force on ATP1A3-Related Disorders

Frederick Andermann, Masayuki Sasaki, Allison Brashear, 2017, Neurology: Genetics.

Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study

Birgit Zirn, Peter Nürnberg, Peter Frommolt, 2012, The Lancet Neurology.

The expanding clinical and genetic spectrum of ATP1A3-related disorders

Robert Steinfeld, Hendrik Rosewich, P. Huppke, 2014, Neurology.

Phenotypic overlap of alternating hemiplegia of childhood and CAPOS syndrome

Hendrik Rosewich, J. Gärtner, K. Brockmann, 2014, Neurology.

A novel ATP1A3 mutation with unique clinical presentation

Hendrik Rosewich, J. Gärtner, K. Brockmann, 2014, Journal of the Neurological Sciences.

Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype

Pier D Lambiase, Henry Houlden, Josemir W Sander, 2015, Brain : a journal of neurology.