K. Reinhardt

Novel CLN8 mutations confirm the clinical and ethnic diversity of late infantile neuronal ceroid lipofuscinosis

W. Brück, J. Gärtner, R. Steinfeld, 2010, Clinical genetics.

Cathepsin D deficiency is associated with a human neurodegenerative disorder.

P. Saftig, W. Bruck, Kathrin Schreiber, 2006, American journal of human genetics.

Unilateral Dilation of Virchow-Robin Spaces in Early Childhood

P. Dechent, J. Gärtner, K. Brockmann, 2009, Neuropediatrics.

Neuromyelitis optica and NMO-IgG in European pediatric patients

P. Huppke, J. Gärtner, B. Huppke, 2010, Neurology.

Polymicrogyria in fetal alcohol syndrome.

J. Gärtner, A. Mohr, K. Brockmann, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Multiple sclerosis in children and adolescents: incidence and clinical picture – new insights from the nationwide German surveillance (2009–2011)

J. Rosenbauer, J. Gärtner, K. Reinhardt, 2014, European journal of neurology.

Polymicrogyria in fetal alcohol syndrome.

J. Gärtner, A. Mohr, K. Brockmann, 2009, Birth defects research. Part A, Clinical and molecular teratology.