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Secondary myopathy due to systemic diseases

Acta neurologica Scandinavica, 2016-12, Vol.134 (6), p.388-402

2016

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Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin‐related familial amyloidosis, and Pompe's disease

Acta neurologica Scandinavica, 2017-12, Vol.136 (6), p.558-569

2017

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Pompe disease in Austria: clinical, genetic and epidemiological aspects

Journal of neurology, 2018-01, Vol.265 (1), p.159-164

2018

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Consequences of mutations within the C terminus of the FHL1 gene

Neurology, 2009-08, Vol.73 (7), p.543-551

2009

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The frequency of occurrence of atypical lymphocytes in peripheral blood smears of natalizumab‐treated patients with multiple sclerosis

International journal of laboratory hematology, 2017-10, Vol.39 (5), p.469-474

2017

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The chemotherapeutic oxaliplatin alters voltage-gated Na + channel kinetics on rat sensory neurons

European journal of pharmacology, 2000-10, Vol.406 (1), p.25-32

2000

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AB1036 Ultrasound in Carpal Tunnel Syndrome: Predictive Value of Baseline B-Mode and Power Doppler Assessment for Long-Term Functional Outcome

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.1244-1245

2015

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Iatrogenic lesions of peripheral nerves

Acta neurologica Scandinavica, 2015-11, Vol.132 (5), p.291-303

2015

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Der deutsche Wortschatz nach Sachgruppen

2020

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Chemotherapy-induced peripheral neuropathy

Journal of neurology, 2002, Vol.249 (1), p.9-17

2002

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Calcium potentials and tetrodotoxin-resistant sodium potentials in unmyelinated C fibres of biopsied human sural nerve

Neuroscience, 1995-12, Vol.69 (3), p.955-965

1995

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Effects of pressure block on sinusoidal current perception and sensory thresholds

Clinical neurophysiology, 2007-05, Vol.118 (5), p.e154-e154

2007

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A mechanosensitive K + channel with fast-gating kinetics on human axons blocked by gadolinium ions

Neuroscience letters, 1994-03, Vol.169 (1), p.39-42

Quasthoff, S.

1994

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X-linked dominant Charcot–Marie–Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations

Journal of the neurological sciences, 1999-08, Vol.167 (2), p.90-101

1999

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Clinical aspects and molecular basis of oxaliplatin neurotoxicity: Current management and development of preventive measures

Seminars in oncology, 2002-10, Vol.29 (5), p.21-33, Article asonc02905p0021

2002

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An X-Linked Myopathy with Postural Muscle Atrophy and Generalized Hypertrophy, Termed XMPMA, Is Caused by Mutations in FHL1

American journal of human genetics, 2008-01, Vol.82 (1), p.88-99

2008

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X-linked dominant Charcot-Marie-Tooth disease : nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln)

Acta neuropathologica, 1998-05, Vol.95 (5), p.443-449

1998

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Capsaicin blocks tetrodotoxin-resistant sodium potentials and calcium potentials in unmyelinated C fibres of biopsied human sural nerve in vitro

Neuroscience letters, 1996-04, Vol.208 (1), p.49-52

1996

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P2612Elevated cardiac troponin T but not troponin I in patients with skeletal muscle disease

European heart journal, 2017-08, Vol.38 (suppl_1)

2017

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Energy Efficient Non-Road Hybrid Electric Vehicles: Advanced Modeling and Control

1st ed. 2016, 2016

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No blocking effects of the pentapeptide QYNAD on Na+ channel subtypes expressed in Xenopus oocytes or action potential conduction in isolated rat sural nerve

Neuroscience letters, 2003-09

Quasthoff, S

2003

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Hyperglycaemic hypoxia alters after-potential and fast K+ conductance of rat axons by cytoplasmic acidification

The Journal of physiology, 1993-06, Vol.465 (1), p.679-697

1993

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Schmerz ist nicht gleich Schmerz: Nozizeptiver versus neuropathischer Schmerz, Teil I

Psychopraxis neuropraxis, 2014-06, Vol.17 (3), p.22-27

Quasthoff, S.

2014

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Neuralgic Amyotrophy: A Rare Disease in Adolescence

Neuropediatrics, 2015, Vol.46 (S 01)

2015

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Aspects of Oral Communication

Quasthoff, Uta M

Reprint 2011., 2011

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Secondary myopathy due to systemic diseases

Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin‐related familial amyloidosis, and Pompe's disease

Pompe disease in Austria: clinical, genetic and epidemiological aspects

Consequences of mutations within the C terminus of the FHL1 gene

The frequency of occurrence of atypical lymphocytes in peripheral blood smears of natalizumab‐treated patients with multiple sclerosis

The chemotherapeutic oxaliplatin alters voltage-gated Na + channel kinetics on rat sensory neurons

AB1036 Ultrasound in Carpal Tunnel Syndrome: Predictive Value of Baseline B-Mode and Power Doppler Assessment for Long-Term Functional Outcome

Iatrogenic lesions of peripheral nerves

Der deutsche Wortschatz nach Sachgruppen

Chemotherapy-induced peripheral neuropathy

Calcium potentials and tetrodotoxin-resistant sodium potentials in unmyelinated C fibres of biopsied human sural nerve

Effects of pressure block on sinusoidal current perception and sensory thresholds

A mechanosensitive K + channel with fast-gating kinetics on human axons blocked by gadolinium ions

X-linked dominant Charcot–Marie–Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations

Clinical aspects and molecular basis of oxaliplatin neurotoxicity: Current management and development of preventive measures

An X-Linked Myopathy with Postural Muscle Atrophy and Generalized Hypertrophy, Termed XMPMA, Is Caused by Mutations in FHL1

X-linked dominant Charcot-Marie-Tooth disease : nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln)

Capsaicin blocks tetrodotoxin-resistant sodium potentials and calcium potentials in unmyelinated C fibres of biopsied human sural nerve in vitro

P2612Elevated cardiac troponin T but not troponin I in patients with skeletal muscle disease

Energy Efficient Non-Road Hybrid Electric Vehicles: Advanced Modeling and Control

No blocking effects of the pentapeptide QYNAD on Na+ channel subtypes expressed in Xenopus oocytes or action potential conduction in isolated rat sural nerve

Hyperglycaemic hypoxia alters after-potential and fast K+ conductance of rat axons by cytoplasmic acidification

Schmerz ist nicht gleich Schmerz: Nozizeptiver versus neuropathischer Schmerz, Teil I

Neuralgic Amyotrophy: A Rare Disease in Adolescence

Aspects of Oral Communication

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