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High efficacy of rituximab for myasthenia gravis: a comprehensive nationwide study in Austria

Journal of neurology, 2019-03, Vol.266 (3), p.699-706

2019

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Myasthenic crisis following SARS-CoV-2 infection and delayed virus clearance in a patient treated with rituximab: clinical course and 6-month follow-up

Journal of neurology, 2021-08, Vol.268 (8), p.2700-2702

2021

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Bioenergetics of the calf muscle in Friedreich ataxia patients measured by 31P-MRS before and after treatment with recombinant human erythropoietin

PloS one, 2013-07, Vol.8 (7), p.e69229-e69229

2013

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Multifocal motor neuropathy in Austria: a nationwide survey of clinical features and response to treatment

Journal of neurology, 2018-12, Vol.265 (12), p.2834-2840

2018

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Involvement of Peripheral Nerves in the Transgenic PLP-α-Syn Model of Multiple System Atrophy: Extending the Phenotype

PloS one, 2015-10, Vol.10 (10), p.e0136575-e0136575

2015

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Successful treatment of CANOMAD with IVIg and rituximab

Journal of neurology, 2013-04, Vol.260 (4), p.1168-1170

2013

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Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositis

Neuromuscular disorders : NMD, 2013-01, Vol.23 (1), p.75-83

2013

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Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance

Journal of the neurological sciences, 2012-07, Vol.318 (1), p.1-18

2012

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Endothelial and Myogenic Differentiation of Hematopoietic Progenitor Cells in Inflammatory Myopathies

Journal of neuropathology and experimental neurology, 2008-07, Vol.67 (7), p.711-719

2008

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Acute motor and sensory axonal neuropathy in Burkitt-like lymphoma

Muscle & nerve, 2006-10, Vol.34 (4), p.494-498

2006

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Autonomic function testing in Friedreich’s ataxia

Journal of neurology, 2018-09, Vol.265 (9), p.2015-2022

2018

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The prion protein in human neuromuscular diseases

The Journal of pathology, 2004-11, Vol.204 (3), p.241-247

2004

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Peripheral nerve function in patients with excessive fragmentary myoclonus during sleep

Sleep medicine, 2016-06, Vol.22, p.61-64

2016

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Autonomic function testing in spinocerebellar ataxia type 2

Clinical autonomic research, 2018-06, Vol.28 (3), p.341-346

2018

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Skeletal Muscle Involvement in Friedreich Ataxia and Potential Effects of Recombinant Human Erythropoietin Administration on Muscle Regeneration and Neovascularization

Journal of neuropathology and experimental neurology, 2012-08, Vol.71 (8), p.708-715

2012

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Correlation of frataxin content in blood and skeletal muscle endorses frataxin as a biomarker in Friedreich ataxia

Movement disorders, 2011-08, Vol.26 (10), p.1935-1938

2011

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Associations between co-medications and survival in ALS—a cohort study from Austria

Journal of neurology, 2015-07, Vol.262 (7), p.1698-1705

2015

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Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome

Human molecular genetics, 2005-07, Vol.14 (14), p.1907-1920

2005

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Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene

Archives of neurology (Chicago), 2007-07, Vol.64 (7), p.966

2007

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Coexistence of Alzheimer-type neuropathology in Creutzfeldt-Jakob disease

Acta neuropathologica, 1998-08, Vol.96 (2), p.116-122

1998

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Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations

European journal of human genetics : EJHG, 2009-09, Vol.17 (9), p.1154-1159

2009

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Intrathecal anti-αB-crystallin IgG antibody responses: Potential inflammatory markers in Guillain-Barré syndrome

Journal of neurology, 2008-06, Vol.255 (6), p.917-924

2008

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Selective neuronal vulnerability in human prion diseases : Fatal familial insomnia differs from other types of prion diseases

The American journal of pathology, 1999-11, Vol.155 (5), p.1453-1457

1999

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Intrathecal anti-[alpha]B-crystallin IgG antibody responses: Potential inflammatory markers in Guillain-Barre syndrome

Journal of neurology, 2008-06, Vol.255 (6), p.917

2008

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Alteration of the serotonergic nervous system in fatal familial insomnia

Annals of neurology, 2000-11, Vol.48 (5), p.788-791

2000

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High efficacy of rituximab for myasthenia gravis: a comprehensive nationwide study in Austria

Myasthenic crisis following SARS-CoV-2 infection and delayed virus clearance in a patient treated with rituximab: clinical course and 6-month follow-up

Bioenergetics of the calf muscle in Friedreich ataxia patients measured by 31P-MRS before and after treatment with recombinant human erythropoietin

Multifocal motor neuropathy in Austria: a nationwide survey of clinical features and response to treatment

Involvement of Peripheral Nerves in the Transgenic PLP-α-Syn Model of Multiple System Atrophy: Extending the Phenotype

Successful treatment of CANOMAD with IVIg and rituximab

Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositis

Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance

Endothelial and Myogenic Differentiation of Hematopoietic Progenitor Cells in Inflammatory Myopathies

Acute motor and sensory axonal neuropathy in Burkitt-like lymphoma

Autonomic function testing in Friedreich’s ataxia

The prion protein in human neuromuscular diseases

Peripheral nerve function in patients with excessive fragmentary myoclonus during sleep

Autonomic function testing in spinocerebellar ataxia type 2

Skeletal Muscle Involvement in Friedreich Ataxia and Potential Effects of Recombinant Human Erythropoietin Administration on Muscle Regeneration and Neovascularization

Correlation of frataxin content in blood and skeletal muscle endorses frataxin as a biomarker in Friedreich ataxia

Associations between co-medications and survival in ALS—a cohort study from Austria

Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome

Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene

Coexistence of Alzheimer-type neuropathology in Creutzfeldt-Jakob disease

Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations

Intrathecal anti-αB-crystallin IgG antibody responses: Potential inflammatory markers in Guillain-Barré syndrome

Selective neuronal vulnerability in human prion diseases : Fatal familial insomnia differs from other types of prion diseases

Intrathecal anti-[alpha]B-crystallin IgG antibody responses: Potential inflammatory markers in Guillain-Barre syndrome

Alteration of the serotonergic nervous system in fatal familial insomnia

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