Kornelia Günther

发表

A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations

A. Ludolph, J. Dorst, D. Fan, 2021, Translational Neurodegeneration.

Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.

H. Braak, T. Meitinger, P. Andersen, 2019, Brain : a journal of neurology.

Hot-spot KIF5A mutations cause familial ALS

H. Braak, T. Meitinger, T. Strom, 2018, Brain : a journal of neurology.

Comprehensive analysis of the mutation spectrum in 301 German ALS families

S. Klebe, T. Meitinger, T. Strom, 2018, Journal of Neurology, Neurosurgery, and Psychiatry.

Safety and Effectiveness of Long-term Intravenous Administration of Edaravone for Treatment of Patients With Amyotrophic Lateral Sclerosis.

S. Petri, A. Ludolph, J. Grosskreutz, 2022, JAMA neurology.

Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations

D. Lulé, S. Petri, J. Grosskreutz, 2023, Brain communications.

DNA Methylation Analysis in Monozygotic Twins Discordant for ALS in Blood Cells

O. Ammerpohl, K. Danzer, Volkan Yazar, 2023, Epigenetics insights.

Metabolic alterations precede neurofilament changes in presymptomatic ALS gene carriers

P. Andersen, J. Kassubek, Joachim Schuster, 2023, EBioMedicine.

Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cells

J. Mill, A. Ludolph, O. Ammerpohl, 2022, Neurobiology of Aging.