Angelika F. Hahn
Publications by Year
Research Areas
Hereditary Neurological Disorders, Peripheral Neuropathies and Disorders, Genetic Neurodegenerative Diseases, Neurological diseases and metabolism, Mitochondrial Function and Pathology
Most-Cited Works
- → Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia(1993)551 cited
- → AN ACUTE AXONAL FORM OF GUILLAIN-BARRÉE POLYNEUROPATHY(1986)535 cited
- → Guillain-Barré syndrome(1998)393 cited
- → Severe axonal degeneration in acute Guillain-Barré syndrome: Evidence of two different mechanisms?(1993)162 cited
- → CMT1X phenotypes represent loss of GJB1 gene function(2007)155 cited
- → X-LINKED DOMINANT HEREDITARY MOTOR AND SENSORY NEUROPATHY(1990)152 cited
- → Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia(2012)129 cited
- → Clinical and electrophysiological parameters distinguishing acute‐onset chronic inflammatory demyelinating polyneuropathy from acute inflammatory demyelinating polyneuropathy(2009)128 cited
- → Episodic ataxia type 1: clinical characterization, quality of life and genotype–phenotype correlation(2014)97 cited
- → Genotype/Phenotype Correlations in X‐Linked Dominant Charcot‐Marie‐Tooth Disease(1999)92 cited