Wolfgang Müller‐Felber

Author

Ludwig-Maximilians-Universität München ORCID

Also Known As

Declan O’Rourke, J Dowling, Muller-Felber, W., Müller-Felber, W., Müller-Felber, Wolfgang, Petra Müller, Robert Dalla Pozza, W Müller-Felber, W. Muller-Felber, W. Müller-Felber

269

Publications

6.4K

Citations

H-Index

179

Concepts

All Affiliations

Ludwig-Maximilians-Universität München Friedrich Baur Stiftung University Hospital Münster Genetikum RWTH Aachen University

About

Wolfgang Müller‐Felber is an author at Ludwig-Maximilians-Universität München specializing in medicine, genetics, and health sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	45	2.7K
2	Health Sciences	11	13	438
3	Engineering	3	3	199
4	Education	2	2	57
5	Natural Sciences	1	1	16

Wolfgang Müller‐Felber

Publications

5.4K

Citations

H-Index

Page 1

	Year	Citations
Enzyme replacement therapy with alglucosidase alfa in 44 patients with late-onset glycogen storage disease type 2: 12-month results of an observational clinical trial S. Strothotte, N. Strigl‐Pill, Birgit Grunert, Journal of Neurology Observational Clinical TrialEnzyme Replacement TherapyInherited Metabolic DiseaseGlycobiologyAlglucosidase Alfa	2009	249
Late onset Pompe disease: Clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients Wolfgang Müller‐Felber, Rita Horváth, Klaus Gempel, Neuromuscular Disorders NeurologyNeurophysiological SpectrumMedicineLong-term Follow-upNeuropathology	2007	236
High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study Maggie C. Walter, Hanns Lochmüller, M. Toepfer, Journal of Neurology High-dose Immunoglobulin TherapyAutoimmune DiseaseImmunodeficienciesImmunologyImmunohaematology	2000	233
Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy Jan Senderek, Carsten Bergmann, Claudia Stendel, The American Journal of Human Genetics Neurodegenerative DiseasesMolecular NeuroscienceMendelian DisorderGenetic DisorderGenetics	2003	210
One Year of Newborn Screening for SMA – Results of a German Pilot Project Katharina Vill, Heike Kölbel, Oliver Schwartz, Journal of Neuromuscular Diseases	2019	176
Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study M. C. Walter, Hanns Lochmüller, Peter Reilich, Neurology	2000	167
Newborn screening for spinal muscular atrophy in Germany: clinical results after 2 years Katharina Vill, Oliver Schwartz, Astrid Blaschek, Orphanet Journal of Rare Diseases	2021	158
Methods for a prompt and reliable laboratory diagnosis of Pompe disease: Report from an international consensus meeting Bryan Winchester, Deeksha Bali, Olaf A. Bodamer, Molecular Genetics and Metabolism Medical DiagnosticsPompe DiseaseInternational Consensus MeetingEngineeringMedicine	2007	155
Pompe disease: Design, methodology, and early findings from the Pompe Registry Barry J. Byrne, Priya S. Kishnani, Laura E. Case, Molecular Genetics and Metabolism Pompe DiseasePompe RegistryDiagnosisPathologyEarly Findings	2011	148
LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood Caroline Michot, Laurence Hubert, Michèle Brivet, Human Mutation	2010	130

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