Hendrik Rosewich

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

Hendrik Rosewich, Hölger Thiele, Andreas Ohlenbusch et al. · The Lancet Neurology · 2012 · 263 citations · Full text

Heterozygous De-novo Mutations, Mendelian Disorder, Genetic Disorder +7

The expanding clinical and genetic spectrum of ATP1A3-related disorders

Hendrik Rosewich, Andreas Ohlenbusch, Peter Huppke et al. · Neurology · 2014 · 113 citations

Clinical presentation of pediatric multiple sclerosis before puberty

Brenda Huppke, David Ellenberger, Hendrik Rosewich et al. · European Journal of Neurology · 2013 · 110 citations

Peroxisomal protein <scp>PEX</scp> 13 functions in selective autophagy

Ming Yeh Lee, Rhea Sumpter, Zhongju Zou et al. · EMBO Reports · 2016 · 69 citations · Full text

Research conference summary from the 2014 International Task Force on <i>ATP1A3</i> -Related Disorders

Hendrik Rosewich, Matthew Sweney, Suzanne D. DeBrosse et al. · Neurology Genetics · 2017 · 65 citations · Full text