G. Kuhlenbaeumer

发表

Analysis of blood-based gene expression in idiopathic Parkinson disease

G. Deuschl, R. Shamir, I. Ulitsky, 2017, Neurology.

Polymorphisms and Noncardioembolic Stroke in Three Case-Control Studies

E. Ringelstein, J. Catanese, V. Garcia, 2011, Cerebrovascular Diseases.

Quantitative Vascular Pathology and Phenotyping Familial and Sporadic Cerebral Small Vessel Diseases

M. Viitanen, V. Deramecourt, J. Slade, 2013, Brain pathology.

Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c‐myb ET‐locus in two families with hereditary neuralgic amyotrophy (HNA)

C. Broeckhoven, J. Meuleman, V. Timmerman, 1998, Annals of human genetics.

Neurosonographical follow-up in patients with spontaneous cervical artery dissection

E. Ringelstein, D. Maintz, D. Nabavi, 2008, Neurological research.

Neurofilament light (NfL) as biomarker in serum and CSF in status epilepticus

W. Lieb, A. Franke, N. Margraf, 2023, Journal of Neurology.

Serum neuronal exosomes predict and differentiate Parkinson’s disease from atypical parkinsonism

Jason J. Davis, G. Deuschl, D. Berg, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

Identification of a novel risk variant in the FUS gene in essential tremor

G. Kuhlenbaeumer, 2014, Neurology.

Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases

M. Viitanen, V. Deramecourt, J. Slade, 2015, Neuropathology and applied neurobiology.

Genome-wide association study of autopsy-confirmed Multiple System Atrophy identifies common variants near ZIC1 and ZIC4

Alan J. Thomas, A. Peters, G. Schellenberg, 2021, medRxiv.

Genetic Variants in the C-Reactive Protein Gene Are Associated with Microangiopathic Ischemic Stroke

C. Kessler, E. Ringelstein, K. Berger, 2010, Cerebrovascular Diseases.