J Dullinger

Breakpoint Cloning and Haplotype Analysis Indicate a Single Origin of the Common Inv(10)(p11.2q21.2) Mutation among Northern Europeans

Mette Gilling, J Dullinger, Stefan Gesk et al. · The American Journal of Human Genetics · 2006 · 96 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Spastin related hereditary spastic paraplegia with dysplastic corpus callosum

Burkhard Alber, Magdalena Pernauer, Annemarie Schwan et al. · Journal of the Neurological Sciences · 2005 · 26 citations

Medicine, Neurology, Neuroscience +9

Progressive muscle atrophy with hypokalemic periodic paralysis and calcium channel mutation

Thomas Meyer, Karin Jurkat‐Rott, Angela Huebner et al. · Muscle & Nerve · 2007 · 14 citations

Life Sciences, Genetics, Neurology +17

Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy

K. Haug, Joachim Kremerskothen, Kerstin Hallmann et al. · Molecular and Cellular Probes · 2000 · 12 citations

Life Sciences, Genetics, Molecular Genetics +12

Influence of Sedation Level and Ventilation Status on the Diagnostic Validity of Delirium Screening Tools in the ICU—An International, Prospective, Bi-Center Observational Study (IDeAS)

Flávio E. Nácul, Nicolas Paul, Claudia Spies et al. · Medicina · 2020 · 10 citations · Full text

Medicine, Critical Care Nursing, Neurocritical Care +15