V. Haug

Refining the phenotype of α‐1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly

H. Omran, G. Schuierer, K. Kutsche, 2008, Clinical genetics.

Late-onset autosomal dominant limb girdle muscular dystrophy and Paget's disease of bone unlinked to the VCP gene locus

R. Schwarzwald, W. Kress, S. Krause, 2010, Journal of the Neurological Sciences.

Intermittent dyspnea and cyanosis in a newborn caused by a hairy polyp.

W. Mann, B. Siegmund, E. Mildenberger, 2014, Pediatrics and neonatology.

Whole-body vibration training in children with Duchenne muscular dystrophy and spinal muscular atrophy.

E. Schönau, O. Semler, J. Kirschner, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency.

G. Dekomien, C. Anastasopoulos, S. Hoffjan, 2014, Molecular and cellular probes.

Comparison of three clinical rating scales in Friedreich ataxia (FRDA)

Dagmar Timmann, Sylvia Boesch, Thomas Klockgether, 2009, Movement disorders : official journal of the Movement Disorder Society.

Antidepressants Rescue Stress-Induced Disruption of Synaptic Plasticity via Serotonin Transporter–Independent Inhibition of L-Type Calcium Channels

J. Bischofberger, C. Normann, N. Klugbauer, 2017, Biological Psychiatry.

Unilateral Venous Thalamic Infarction in a Child Mimicking a Thalamic Tumor

I. Mader, V. Mall, R. Korinthenberg, 2009, Journal of child neurology.