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Wolfgang Mueller‐Felber

Observed names: Mueller-Felber, W, Mueller-Felber, Wolfgang, W Mueller-Felber, W Müeller-Felber, W. Mueller-Felber, W. Mueller‐Felber, W. Mueller–Felber, W. Müeller-Felber, Wolfgang Mueller-Felber, Wolfgang Mueller-felber
OpenAlex ID: A5109102678
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
2011 · Monika B. Hartig, Arcangela Iuso, et al. · The American Journal of Human Genetics · 264
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Consensus Statement on Standard of Care for Congenital Muscular Dystrophies
2010 · Ching H. Wang, Carsten G. Bonnemann, et al. · Journal of Child Neurology · 221
A randomized placebo-controlled phase 3 trial of an antisense oligonucleotide, drisapersen, in Duchenne muscular dystrophy
2017 · Nathalie Goemans, Eugenio Mercuri, et al. · Neuromuscular Disorders · 135
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Myogenic changes of the levator ani muscle in premenopausal women: The impact of vaginal delivery and age
1998 · Th. Dimpfl, Ch. Jaeger, et al. · Neurourology and Urodynamics · 112
A phase 3 randomized placebo-controlled trial of tadalafil for Duchenne muscular dystrophy
2017 · Ronald G. Victor, H. Lee Sweeney, et al. · Neurology · 78
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244th ENMC international workshop: Newborn screening in spinal muscular atrophy May 10–12, 2019, Hoofdorp, The Netherlands
2019 · Tamara Dangouloff, Arthur Burghes, et al. · Neuromuscular Disorders · 73
Fish oil supplementation improves visual evoked potentials in children with phenylketonuria
2001 · S. Beblo, H. Reinhardt, et al. · Neurology · 67
5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2
2024 · Katharina Vill, Moritz Tacke, et al. · Journal of Neurology · 22
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Chronic Progressive External Ophthalmoplegia: MR Spectroscopy and MR Diffusion Studies in the Brain
2006 · Jens O. Heidenreich, Thomas Klopstock, et al. · American Journal of Roentgenology · 22
Serum Levels of Matrix Metalloproteinases-2 and -9 and Their Tissue Inhibitors in Inflammatory Neuromuscular Disorders
2006 · S. Hurnaus, W. Mueller-Felber, et al. · European Neurology · 20
Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndrome
1995 · Dimitrios I. Zafeiriou, Berthold Koletzko, et al. · Brain and Development · 20
Pattern of myogenesis and vascular repair in early and advanced lesions of juvenile dermatomyositis
2018 · Matthias Baumann, Christiane Gumpold, et al. · Neuromuscular Disorders · 18
Return to Participation – Significant Improvement after Bilateral Pallidal Stimulation in Rapidly ProgressiveDYT-1Dystonia
2008 · I. Borggraefe, K. Boetzel, et al. · Neuropediatrics · 13
Inflammatory myopathy in POEMS syndrome
2000 · N. Goebels, E.U. Walther, et al. · Neurology · 9
B.06 Safety and efficacy of nusinersen in infants/children with spinal muscular atrophy (SMA): part 1 of the phase 2 EMBRACE study
2018 · PB Shieh, G Acsadi, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 6
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Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosis
2010 · A Blaschek, P Lohse, et al. · Multiple Sclerosis Journal · 5
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Identification of a second major locus for neurodegeneration with brain iron accumulation
2011 · MB Hartig, A Iuso, et al. · Neuropediatrics · 4
The Pompe Registry: tracking Pompe disease symptoms in a broad patient population
2008 · B Byrne, PS Kishnani, et al. · Pediatric Rheumatology · 3
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O0068 Visual Evoked Potentials in Infants After Dietary Supply of Docosahexaenoic Acid and 5-methyl-tetrahydrofolate During Pregnancy
2004 · I. Broekaert, C. Campoy, et al. · Journal of Pediatric Gastroenterology and Nutrition · 3
A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathy
2022 · Ingrid Bader, M. Freilinger, et al. · Orphanet Journal of Rare Diseases · 2
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Newborn infant screening for spinal muscular atrophy: Chances and challenges
2022 · Wolfgang Mueller‐Felber · Developmental Medicine & Child Neurology · 2
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Safety and Efficacy of Nusinersen in Infants/Children with Spinal Muscular Atrophy (SMA): Part 1 of the Phase 2 EMBRACE Study (P2.324)
2018 · Perry B. Shieh, Gyula Acsadi, et al. · Neurology · 2
Unilateral Tongue Fasciculation Associated with Genetic Paraganglioma Syndrome
2017 · Wolfgang Mueller-Felber, Irene Schmid, et al. · Neuropediatrics · 2
Safety and efficacy of nusinersen in infants/children with spinal muscular atrophy (SMA): part 1 of the phase 2 EMBRACE study
2017 · G. Acsadi, P. Shieh, et al. · Neuromuscular Disorders · 2
G.P.1 02 The Pompe registry: centralized data collection to outline the natural course of Pompe disease
2006 · A. van der Ploeg, W. Mueller-Felber, et al. · Neuromuscular Disorders · 1
Works count: 38
Citation count: 1,108
H-index: 13
I10-index: 13
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