Wolfgang N. Löscher

Author

Wolfgang N. Löscher

Also Known As

Fiona Zeiner, Jaqueline Lipka, Löscher Wolfgang N., Löscher, W.N., Löscher, Wolfgang, Paul Lingor, Vescei Laszlo, W Lscher, W Löscher, W N Loscher

231

Publications

5.9K

Citations

H-Index

132

Concepts

All Affiliations

Innsbruck Medical University Universität Innsbruck Medical University of Vienna Medical University of Graz Medizinische Hochschule Hannover

About

Wolfgang N. Löscher is an author at Innsbruck Medical University specializing in medicine, neuroscience, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	34	2.2K
2	Health Sciences	10	10	358
3	Social Sciences	7	7	166
4	Public Health	2	2	55
5	Natural Sciences	1	1	19

Wolfgang N. Löscher

Publications

4.8K

Citations

H-Index

Page 1

	Year	Citations
Safety and efficacy of eculizumab in anti-acetylcholine receptor antibody-positive refractory generalised myasthenia gravis (REGAIN): a phase 3, randomised, double-blind, placebo-controlled, multicentre study James F. Howard, Kimiaki Utsugisawa, Michael Benatar, The Lancet Neurology Multicentre StudyPharmacologyMedicineMyasthenia GravisNeuromuscular Blockade	2017	745
Carpal Tunnel Syndrome Assessment with US: Value of Additional Cross-sectional Area Measurements of the Median Nerve in Patients versus Healthy Volunteers Andrea Klauser, Ethan J. Halpern, Tobias De Zordo, Radiology	2008	378
Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I Annelies Rotthier, Michaela Auer‐Grumbach, Katrien Janssens, The American Journal of Human Genetics Molecular NeuroscienceMolecular PhysiologyAutonomic Neuropathy TypeGenetic DisorderMendelian Disorder	2010	186
Safety and Effectiveness of Long-term Intravenous Administration of Edaravone for Treatment of Patients With Amyotrophic Lateral Sclerosis Simon Witzel, André Maier, Robert Steinbach, JAMA Neurology	2022	176
Voxel‐based morphometry detects cortical atrophy in the Parkinson variant of multiple system atrophy Christian Brenneis, Klaus Seppi, Michael Schocke, Movement Disorders	2003	167
An X-Linked Myopathy with Postural Muscle Atrophy and Generalized Hypertrophy, Termed XMPMA, Is Caused by Mutations in FHL1 Christian Windpassinger, Benedikt Schoser, Volker Straub, The American Journal of Human Genetics Mitochondrial MyopathyMechanobiologyMuscle PathologyKinesiologyMendelian Disorder	2008	156
Excitatory drive to the alpha‐motoneuron pool during a fatiguing submaximal contraction in man. Wolfgang N. Löscher, Andrew G. Cresswell, Alf Thorstensson The Journal of Physiology	1996	147
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
Safety and efficacy of cipaglucosidase alfa plus miglustat versus alglucosidase alfa plus placebo in late-onset Pompe disease (PROPEL): an international, randomised, double-blind, parallel-group, phase 3 trial Benedikt Schoser, Mark Roberts, Barry J. Byrne, The Lancet Neurology Clinical TrialsCipaglucosidase AlfaPharmacotherapyMedicineLate-onset Pompe Disease	2021	124
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome Petri Luoma, Ningguang Luo, Wolfgang N. Löscher, Human Molecular Genetics	2005	110

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