Angelika F. Hahn

Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

Rita Shiang, Stephen G. Ryan, Yazhen Zhu et al. · Nature Genetics · 1993 · 551 citations

Clinical Disorders, α1 Subunit, Neurobiology Of Disease +12

AN ACUTE AXONAL FORM OF GUILLAIN-BARRÉE POLYNEUROPATHY

Thomas E. Feasby, J. J. Gilbert, William F. Brown et al. · Brain · 1986 · 532 citations

Severe axonal degeneration in acute Guillain-Barré syndrome: Evidence of two different mechanisms?

Thomas E. Feasby, Angelika F. Hahn, William F. Brown et al. · Journal of the Neurological Sciences · 1993 · 162 citations

Different Mechanisms, Neurobiology Of Disease, Neurological Disorder +12

CMT1X phenotypes represent loss of <i>GJB1</i> gene function

Michael E. Shy, Carly E. Siskind, E. R. Swan et al. · Neurology · 2007 · 155 citations

X-LINKED DOMINANT HEREDITARY MOTOR AND SENSORY NEUROPATHY

Angelika F. Hahn, William F. Brown, Wilma J. Koopman et al. · Brain · 1990 · 152 citations