Publications by authors named "Frank Hanisch"

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Complex Repetitive Discharges: A Sign of Motor Axonal Reinnervation?
Andreas Posa, Izabela Niśkiewicz, Alexander Emmer, Frank Hanisch, Malte E Kornhuber

Brain Sci· June 2020

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The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy.
Angela Rosenbohm, Susanne Hirsch, Alexander E Volk, Torsten Grehl, Julian Grosskreutz, Frank Hanisch

J Neurol· May 2018

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The concept and diagnostic criteria of primary lateral sclerosis.
Verena Wais, Angela Rosenbohm, Susanne Petri, Katja Kollewe, Andreas Hermann, Frank Hanisch

Acta Neurol Scand· September 2017

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Reduced hnRNPA3 increases C9orf72 repeat RNA levels and dipeptide-repeat protein deposition.
Kohji Mori, Yoshihiro Nihei, Thomas Arzberger, Qihui Zhou, Ian R Mackenzie, Frank Hanisch

EMBO Rep· September 2016

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Clinical features and differential diagnosis of flail arm syndrome.
Annemarie Hübers, Viviane Hildebrandt, Susanne Petri, Katja Kollewe, Andreas Hermann, Frank Hanisch

J Neurol· February 2016

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Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study.
Johannes Dorst, Luc Dupuis, Susanne Petri, Katja Kollewe, Susanne Abdulla, Frank Hanisch

J Neurol· January 2016

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SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions.
Frank Hanisch, Malte Kornhuber, Charlotte L Alston, Robert W Taylor, Marcus Deschauer

J Neurol Neurosurg Psychiatry· June 2015

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Impairment of respiratory function in late-onset distal myopathy due to MATR3 Mutation.
Torsten Kraya, Bernd Schmidt, Tobias Müller, Frank Hanisch

Muscle Nerve· June 2015

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Characteristics of pain in amyotrophic lateral sclerosis.
Frank Hanisch, Anika Skudlarek, Janine Berndt, Malte E Kornhuber

Brain Behav· March 2015

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Long-term observation of incremental response and antibodies to voltage-gated calcium channels in patients with Lambert-Eaton myasthenic syndrome: two case reports.
Ilka Schneider, Malte E Kornhuber, Frank Hanisch

J Med Case Rep· March 2015

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Phenotype of matrin-3-related distal myopathy in 16 German patients.
Tobias J Müller, Torsten Kraya, Gisela Stoltenburg-Didinger, Frank Hanisch, Malte Kornhuber

Ann Neurol· November 2014

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Urge incontinence and gastrointestinal symptoms in adult patients with pompe disease: a cross-sectional survey.
Nesrin Karabul, Anika Skudlarek, Janine Berndt, Cornelia Kornblum, Rudolf A Kley, Frank Hanisch

JIMD Rep· November 2014

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Functional relevance of mitochondrial abnormalities in sporadic inclusion body myositis.
Pushpa Raj Joshi, Mirjam Vetterke, Anja Hauburger, Pawel Tacik, Gisela Stoltenburg, Frank Hanisch

J Clin Neurosci· November 2014

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Sialylation and muscle performance: sialic acid is a marker of muscle ageing.
Frank Hanisch, Wenke Weidemann, Mona Großmann, Pushpa Raj Joshi, Hans-Jürgen Holzhausen

PLoS One· September 2014

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Pregnancy and delivery in women with Pompe disease.
Nesrin Karabul, Janine Berndt, Cornelia Kornblum, Rudolf A Kley, S Wenninger, Frank Hanisch

Mol Genet Metab· June 2014

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Mitochondrial abnormalities in myofibrillar myopathies.
Pushpa R Joshi, Anja Hauburger, Rudolf Kley, Kristl G Claeys, Ilka Schneider, Frank Hanisch

Clin Neuropathol· May 2014

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Limb girdle muscular dystrophy type 2L presenting as necrotizing myopathy.
Ilka Schneider, Gisela Stoltenburg, Marcus Deschauer, Martin Winterholler, Frank Hanisch

Acta Myol· May 2014

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Glycogenosome accumulation in the arrector pili muscle in Pompe disease.
Istvan Katona, Joachim Weis, Frank Hanisch

Orphanet J Rare Dis· February 2014

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Pseudo-Popeye syndrome: extramedullary plasmacytoma manifesting in skeletal muscle.
Ilka Schneider, Tobias Müller, Gisela Stoltenburg, Hans-Jürgen Holzhausen, Christian Mawrin, Frank Hanisch

Neurology· February 2014

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Eosinophils in hereditary and inflammatory myopathies.
Thomas Schröder, Johann Fuchss, Ilka Schneider, Gisela Stoltenburg-Didinger, Frank Hanisch

Acta Myol· December 2013

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Diagnostic impact of myotonic discharges in myofibrillar myopathies.
Frank Hanisch, Torsten Kraya, Malte Kornhuber, Stephan Zierz

Muscle Nerve· June 2013

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Respiratory function in late-onset Pompe disease patients receiving long-term enzyme replacement therapy for more than 48 months.
Ilka Schneider, Frank Hanisch, Tobias Müller, Bernd Schmidt, Stephan Zierz

Wien Med Wochenschr· January 2013

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36 months observational clinical study of 38 adult Pompe disease patients under alglucosidase alfa enzyme replacement therapy.
Caroline Regnery, Cornelia Kornblum, Frank Hanisch, Stefan Vielhaber, Nicola Strigl-Pill

J Inherit Metab Dis· September 2012

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Frequency of the FKRP mutation c.826C>A in isolated hyperCKemia and in limb girdle muscular dystrophy type 2 in German patients.
Frank Hanisch, Dörte Grimm, Stephan Zierz, Marcus Deschauer

J Neurol· February 2010

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AMP deaminase deficiency in skeletal muscle is unlikely to be of clinical relevance.
Frank Hanisch, Pushpa Joshi, Stephan Zierz

J Neurol· March 2008

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