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P. Reilich · SciRah

Researcher profile · Semantic Scholar

P. Reilich

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P. Reilich — researcher profile on SciRah

h-index: 27
Works: 73
Citations: 2,250

Most-cited papers

High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study
M. Walter, Hanns Lochmüller, M. Toepfer, B. Schlotter +4 more
2000Journal of Neurology236 citations
Semantic Scholar
Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study
M. Walter, Hanns Lochmüller, P. Reilich, T. Klopstock +5 more
2000Neurology158 citations
Semantic Scholar
Effects of tofersen treatment in patients with SOD1-ALS in a “real-world” setting – a 12-month multicenter cohort study from the German early access program
M. Wiesenfarth, J. Dorst, David A. Brenner, Z. Elmas +41 more
2024EClinicalMedicine113 citations Open access
Semantic Scholar
Disease burden of spinal muscular atrophy in Germany
C. Klug, O. Schreiber-Katz, S. Thiele, E. Schorling +4 more
2016Orphanet Journal of Rare Diseases103 citations Open access
Semantic Scholar
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial
M. Walter, P. Reilich, S. Thiele, J. Schessl +11 more
2013Orphanet Journal of Rare Diseases100 citations Open access
Semantic Scholar
The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene
P. Reilich, R. Horvath, S. Krause, N. Schramm +15 more
2011Journal of Neurology99 citations
Semantic Scholar
Muscle pathology in 57 patients with myotonic dystrophy type 2
B. Schoser, C. Schneider-Gold, W. Kress, H. Goebel +6 more
2004Muscle and Nerve92 citations
Semantic Scholar
Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P.
M. Walter, P. Reilich, A. Huebner, D. Fischer +10 more
2007Brain : a journal of neurology91 citations Open access
Semantic Scholar
The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy.
P. Reilich, B. Schoser, N. Schramm, S. Krause +5 more
2010Neuromuscular Disorders89 citations
Semantic Scholar
Muscle MRI findings in limb girdle muscular dystrophy type 2L.
A. Sarkozy, M. Deschauer, R. Carlier, B. Schrank +17 more
2012Neuromuscular Disorders86 citations Open access
Semantic Scholar
Comparative cost of illness analysis and assessment of health care burden of Duchenne and Becker muscular dystrophies in Germany
O. Schreiber-Katz, C. Klug, S. Thiele, E. Schorling +4 more
2014Orphanet Journal of Rare Diseases78 citations Open access
Semantic Scholar
Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weakness
Z. Lukács, Paulina Nieves Cobos, S. Wenninger, T. Willis +14 more
2016Neurology69 citations Open access
Semantic Scholar
Primary Headache in Children and Adolescents: Update on Pharmacotherapy of Migraine and Tension-Type Headache
M. Bonfert, A. Straube, A. Schroeder, P. Reilich +2 more
2013Neuropediatrics61 citations Open access
Semantic Scholar
An Integrated Diagnosis Strategy for Congenital Myopathies
J. Böhm, N. Vasli, E. Malfatti, S. Le Gras +15 more
2013PLoS ONE55 citations Open access
Semantic Scholar
Creatine monohydrate in myotonic dystrophy
M. Walter, P. Reilich, H. Lochmüller, R. Kohnen +5 more
2002Journal of Neurology54 citations
Semantic Scholar
Involvement patterns in myotilinopathy and desminopathy detected by a novel neuromuscular whole-body MRI protocol
N. Schramm, C. Born, S. Weckbach, P. Reilich +2 more
2008European Radiology47 citations
Semantic Scholar
Clinical, genetic, and cardiac magnetic resonance imaging findings in primary desminopathies.
K. Strach, T. Sommer, C. Grohé, C. Meyer +12 more
2008Neuromuscular Disorders43 citations Open access
Semantic Scholar
ALSFRS-R-SE: an adapted, annotated, and self-explanatory version of the revised amyotrophic lateral sclerosis functional rating scale
A. Maier, M. Boentert, P. Reilich, S. Witzel +14 more
2022Neurological Research and Practice41 citations Open access
Semantic Scholar
Creatine monohydrate in myotonic dystrophy: a double-blind, placebo-controlled clinical study.
M. Walter, P. Reilich, Hanns Lochmüller, R. Kohnen +5 more
2002Journal of Neurology41 citations
Semantic Scholar
Myofascial Trigger Points in Children With Tension-Type Headache: A New Diagnostic and Therapeutic Option
C. von Stülpnagel, P. Reilich, A. Straube, Jan Schäfer +6 more
2009Journal of Child Neurology40 citations
Semantic Scholar
Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis
W. Ruf, Matej Boros, A. Freischmidt, David A. Brenner +32 more
2023Brain Communications37 citations Open access
Semantic Scholar
Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy.
M. Walter, T. Witt, B. Weigel, P. Reilich +5 more
2005Neuromuscular Disorders36 citations
Semantic Scholar
Recent developments in Duchenne muscular dystrophy: facts and numbers
M. Walter, P. Reilich
2017Journal of Cachexia, Sarcopenia and Muscle33 citations Open access
Semantic Scholar
A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A)
P. Reilich, S. Krause, N. Schramm, U. Klutzny +6 more
2011Journal of Neurology31 citations
Semantic Scholar
Consensus statement: Botulinum toxin in myofacial pain
P. Reilich, K. Fheodoroff, U. Kern, S. Mense +3 more
2004Journal of Neurology30 citations
Semantic Scholar
Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein.
S. Krause, T. Göhringer, M. Walter, B. Schoser +7 more
2007Clinical Neuropathology28 citations Open access
Semantic Scholar
Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy.
J. Müller, Henriett Pikó, B. Schoser, B. Schlotter‐Weigel +7 more
2006Neuromuscular Disorders27 citations
Semantic Scholar
Methylation of the 4q35 D4Z4 repeat defines disease status in facioscapulohumeral muscular dystrophy.
Hannes Erdmann, Florentine Scharf, Stefanie Gehling, A. Benet-Pagès +18 more
2022Brain : a journal of neurology26 citations
Semantic Scholar
Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy
P. Reilich, N. Schramm, B. Schoser, P. Schneiderat +9 more
2010Journal of Neurology25 citations Open access
Semantic Scholar
Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations
M. Wiesenfarth, Kornelia Günther, Kathrin Müller, S. Witzel +24 more
2023Brain Communications24 citations Open access
Semantic Scholar
Cost of illness in Charcot-Marie-Tooth neuropathy
E. Schorling, S. Thiele, Laura Gumbert, S. Krause +5 more
2019Neurology24 citations
Semantic Scholar
Alterations in the trapezius muscle in young patients with migraine--a pilot case series with MRI.
M. Landgraf, B. Ertl-Wagner, I. Koerte, J. Thienel +6 more
2015European journal of paediatric neurology24 citations
Semantic Scholar
Ten-Year Follow-Up in a Case Series of Integrative Botulinum Toxin Intervention in Adolescents with Chronic Daily Headache and Associated Muscle Pain
A. Schroeder, K. Huss, A. Blaschek, I. Koerte +9 more
2012Neuropediatrics19 citations
Semantic Scholar
Respiratory insufficiency as a presenting symptom of LGMD2D in adulthood.
M. Walter, G. Dekomien, B. Schlotter‐Weigel, P. Reilich +5 more
2004Acta myologica18 citations
Semantic Scholar
Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patient.
Elena Ikenberg, I. Karin, B. Ertl-Wagner, A. Abicht +5 more
2017Neuromuscular Disorders16 citations
Semantic Scholar
Long-term efficiency of intravenously administered immunoglobulin in anti-Yo syndrome with paraneoplastic cerebellar degeneration
J. Schessl, M. Schuberth, P. Reilich, P. Schneiderat +4 more
2011Journal of Neurology14 citations
Semantic Scholar
Lower Limb Radiology of Distal Myopathy due to the S60F Myotilin Mutation
A. McNeill, D. Birchall, V. Straub, L. Goldfarb +5 more
2009European Neurology14 citations Open access
Semantic Scholar
Myelitis as a side effect of tofersen therapy in SOD1-associated ALS
P. Reilich, F. Schöberl, M. Hiebeler, M. Tonon +2 more
2023Journal of Neurology13 citations Open access
Semantic Scholar
Time to diagnosis of Duchenne muscular dystrophy in Austria and Germany
M. Hiebeler, S. Thiele, P. Reilich, G. Bernert +1 more
2023Scientific Reports13 citations Open access
Semantic Scholar
Sensory neuropathy due to RFC1 in a patient with ALS: more than a coincidence?
Florian Schöberl, A. Abicht, C. Kuepper, Stefan Voelk +8 more
2021Journal of Neurology12 citations Open access
Semantic Scholar
Charcot-Marie-Tooth disease type 2CC due to a frameshift mutation of the neurofilament heavy polypeptide gene in an Austrian family.
Elena Ikenberg, P. Reilich, A. Abicht, Corina Heller +2 more
2019Neuromuscular Disorders12 citations
Semantic Scholar
Measurement of structural integrity of the spinal cord in patients with amyotrophic lateral sclerosis using diffusion tensor magnetic resonance imaging
M. Patzig, K. Bochmann, J. Lutz, R. Stahl +4 more
2019PLoS ONE11 citations Open access
Semantic Scholar
An episode of geniospasm in sleep: Toward new insights into pathophysiology?
B. Kharraz, P. Reilich, S. Noachtar, A. Danek
2008Movement Disorders11 citations
Semantic Scholar
Closing the Gap - Detection of 5q-Spinal Muscular Atrophy by Short-Read Next-Generation Sequencing and Unexpected Results in a Diagnostic Patient Cohort
S. Kleinle, Veronika Scholz, A. Benet-Pagès, T. Wohlfrom +21 more
2023Journal of Neuromuscular Diseases7 citations Open access
Semantic Scholar
Consensus statement: botulinum toxin in myofascial [corrected] pain.
P. Reilich, K. Fheodoroff, U. Kern, S. Mense +3 more
2004Journal of Neurology7 citations
Semantic Scholar
Accuracy of botulinum toxin injections in myofascial pain. Response to Gobel et al. Pain 2006;125:82-8.
P. Reilich, B. Schoser
2007Pain5 citations
Semantic Scholar
LGMD 2I due to the common mutation 826C>A in the FKRP gene presenting as myopathy with vacuoles and paired-helical filaments.
P. Reilich, J. Petersen, S. Vielhaber, C. Mawrin +7 more
2006Acta myologica5 citations
Semantic Scholar
Congenital myopathy and epidermolysis bullosa due to PLEC variant.
Maggie C. Walter, P. Reilich, Sabine Krause, M. Hiebeler +4 more
2021Neuromuscular Disorders4 citations
Semantic Scholar
Health-related Quality of Life and Satisfaction with German Health Care Services in Patients with Charcot-Marie-Tooth Neuropathy
E. Schorling, Katja C. Senn, S. Thiele, Laura Gumbert +5 more
2021Journal of Neuromuscular Diseases4 citations
Semantic Scholar
Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option?
C. von Stülpnagel, P. Reilich, J. Schäfer, A. Blaschek +4 more
20064 citations Open access
Semantic Scholar

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Hanns Lochmüller×13
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