Knut Brockmann

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.

Succinate in dystrophic white matter: A proton magnetic resonance spectroscopy finding characteristic for complex II deficiency

Jens Frahm, Peter Dechent, P. Dechent, 2002, Annals of 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.

tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia

Ingeborg Krägeloh-Mann, Francesco Muntoni, Peter Nürnberg, 2008, Nature Genetics.

A mosaic activating mutation in AKT1 associated with the Proteus syndrome.

Jamie K Teer, Shlomo Wientroub, Leslie G Biesecker, 2011, The New England journal of medicine.

A novel ATP1A3 mutation with unique clinical presentation

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

Regional Age Dependence of Human Brain Metabolites from Infancy to Adulthood as Detected by Quantitative Localized Proton MRS

Jens Frahm, Markus Wick, Bernd Kruse, 1999, Pediatric Research.