Angelika F. Hahn - Concepedia

Author

Angelika F. Hahn

Also Known As

A F Hahn, A Hahn, A. F. HAHN, A. F. Hahn, A. Hahn, A.F. Hahn, ANGELIKA F. HAHN, Angelika F Hahn, Angelika F. Hahn, Richard J. Barohn

177

Publications

Citations

H-Index

Concepts

All Affiliations

Western University Victoria Hospital London Health Sciences Centre The University of Sydney University of Bergen

About

Angelika F. Hahn is an author at Western University specializing in medicine, neuropathology, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	24	1.8K
2	Allergy	5	5	283
3	Social Sciences	2	2	713
4	Health Sciences	1	1	15
5	Allergy Medicine	1	1	56

Angelika F. Hahn

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia Rita Shiang, Stephen G. Ryan, Yazhen Zhu, Nature Genetics Clinical Disordersα1 SubunitNeurobiology Of DiseaseNeurological DisorderInhibitory Glycine Receptor	1993	551
AN ACUTE AXONAL FORM OF GUILLAIN-BARRÉE POLYNEUROPATHY Thomas E. Feasby, J. J. Gilbert, William F. Brown, Brain	1986	532
Severe axonal degeneration in acute Guillain-Barré syndrome: Evidence of two different mechanisms? Thomas E. Feasby, Angelika F. Hahn, William F. Brown, Journal of the Neurological Sciences Different MechanismsNeurobiology Of DiseaseNeurological DisorderMedicineImmunology	1993	162
CMT1X phenotypes represent loss of <i>GJB1</i> gene function Michael E. Shy, Carly E. Siskind, E. R. Swan, Neurology	2007	155
X-LINKED DOMINANT HEREDITARY MOTOR AND SENSORY NEUROPATHY Angelika F. Hahn, William F. Brown, Wilma J. Koopman, Brain	1990	152
Clinical and electrophysiological parameters distinguishing acute‐onset chronic inflammatory demyelinating polyneuropathy from acute inflammatory demyelinating polyneuropathy Annie Dionne, Michael Nicolle, Angelika F. Hahn Muscle & Nerve	2009	128
Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia M. Zimoń, Jonathan Baets, Leonardo Almeida‐Souza, Nature Genetics Neurological DisorderAxonal NeuropathyNeurologyNeuroscienceMolecular Neurobiology	2012	127
Episodic ataxia type 1: clinical characterization, quality of life and genotype–phenotype correlation Tracey D. Graves, Yoon‐Hee Cha, Angelika F. Hahn, Brain GeneticsGenetic EpidemiologyDisease Gene IdentificationClinical GeneticsType 1	2014	97
Genotype/Phenotype Correlations in X‐Linked Dominant Charcot‐Marie‐Tooth Disease Angelika F. Hahn, Charles F. Bolton, Christopher M. White, Annals of the New York Academy of Sciences GeneticsGenetic EpidemiologyPathologyDisease Gene IdentificationPeripheral Nerves	1999	92
Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis Angelika F. Hahn, Peter Ainsworth, Charles F. Bolton, Acta Neuropathologica Gross AnatomyCharcot-marie-tooth DiseaseX-linked FormPathologyAnatomy	2001	90

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