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Histological indications of a progressive snorers disease in an upper airway muscle

American journal of respiratory and critical care medicine, 1998-02, Vol.157 (2), p.586-593

1998

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Muscular dystrophies: influence of physical conditioning on the disease evolution

Current opinion in clinical nutrition and metabolic care, 2003-07, Vol.6 (4), p.435-439

Ansved, Tor

2003

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Effects of hand-training in persons with myotonic dystrophy type 1 - a randomised controlled cross-over pilot study

Disability and rehabilitation, 2013-10, Vol.35 (21), p.1798-1807

2013

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A Mammalian Radial Spokehead-Like Gene, RSHL1, at the Myotonic Dystrophy-1 Locus

Biochemical and biophysical research communications, 2001-03, Vol.281 (4), p.835-841

2001

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Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1

Neuropathology and applied neurobiology, 2009-11, Vol.35 (6), p.603-613

2009

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Contractile properties of single muscle fibers in myotonic dystrophy

Muscle & nerve, 2000-04, Vol.23 (4), p.529-537

2000

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Effects of ageing on the motor unit

Progress in neurobiology, 1995-04, Vol.45 (5), p.397-458

1995

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Independent Regulation of the Myotonic Dystrophy 1 Locus Genes Postnatally and during Adult Skeletal Muscle Regeneration

The Journal of biological chemistry, 2000-06, Vol.275 (26), p.19964-19969

2000

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Impact of post-synaptic block of neuromuscular transmission, muscle unloading and mechanical ventilation on skeletal muscle protein and mRNA expression

Pflügers Archiv, 2006-10, Vol.453 (1), p.53-66

2006

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Electrophoretic determination of the myosin/actin ratio in the diagnosis of critical illness myopathy

Intensive care medicine, 2003-09, Vol.29 (9), p.1515-1527

2003

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Muscle fiber atrophy in leg muscles after botulinum toxin type A treatment of cervical dystonia

Neurology, 1997-05, Vol.48 (5), p.1440-1442

1997

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Effects of a hand training programme in five patients with myotonic dystrophy type 1

Occupational therapy international, 2005, Vol.12 (1), p.14-27

2005

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Decreased DMPK Transcript Levels in Myotonic Dystrophy 1 Type IIA Muscle Fibers

Biochemical and biophysical research communications, 2001-09, Vol.286 (5), p.1177-1182

2001

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Reliability of hand function testing instruments in patients with muscular dystrophies

International journal of therapy and rehabilitation, 2008-05, Vol.15 (5), p.211-219

2008

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Simultaneous Analysis of Expression of the Three Myotonic Dystrophy Locus Genes in Adult Skeletal Muscle Samples: The CTG Expansion Correlates Inversely with DMPK and 59 Expression Levels, but Not DMAHP Levels

Human molecular genetics, 1999-06, Vol.8 (6), p.1053-1060

1999

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Muscle biopsy, macro EMG, and clinical characteristics in patients with schizophrenia

Biological psychiatry (1969), 2000-06, Vol.47 (11), p.991-999

2000

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Effects of ageing on skeletal muscles and single motor units of the fast- and slow-twitch type

Ansved, Tor Gunnar

1990

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Larger CAG expansions in skeletal muscle compared with lymphocytes in Kennedy disease but not in Huntington disease

Neurology, 1998-11, Vol.51 (5), p.1442-1444

1998

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Charcot-Marie-Tooth disease – muscle biopsy findings in relation to neurophysiology

Neuromuscular disorders : NMD, 1998-05, Vol.8 (3), p.175-181

1998

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Effects of ageing on enzyme-histochemical, morphometrical and contractile properties of the soleus muscle in the rat

Journal of the neurological sciences, 1989-10, Vol.93 (1), p.105-124

1989

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CTG-repeat length in distal and proximal leg muscles of symptomatic and non-symptomatic patients with myotonic dystrophy: relation to muscle strength and degree of histopathological abnormalities

European journal of neurology, 1999-05, Vol.6 (3), p.341-346

1999

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Charcot-Marie-Tooth disease type 1 and 2-an immunohistochemical study of muscle fibre cytoskeletal proteins and a maker for muscle fibre cytoskeletal proteins and a marker for muscle fibre regeneration

European journal of neurology, 1998-11, Vol.5 (6), p.545-551

1998

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Quantitative and qualitative morphological properties of the soleus motor nerve and the L5 ventral root in young and old rats: Relation to the number of soleus muscle fibres

Journal of the neurological sciences, 1990-05, Vol.96 (2), p.269-282

1990

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Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but notDMAHP levels

Human molecular genetics, 1999-06, Vol.8 (6), p.1053

1999

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Charcot-Marie-Tooth disease type 1 and 2-an immunohistochemical study of muscle fibre cytoskeletal proteins and a marker for muscle fibre regeneration

European journal of neurology, 1998-11, Vol.5 (6), p.545-551

1998

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Histological indications of a progressive snorers disease in an upper airway muscle

Muscular dystrophies: influence of physical conditioning on the disease evolution

Effects of hand-training in persons with myotonic dystrophy type 1 - a randomised controlled cross-over pilot study

A Mammalian Radial Spokehead-Like Gene, RSHL1, at the Myotonic Dystrophy-1 Locus

Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1

Contractile properties of single muscle fibers in myotonic dystrophy

Effects of ageing on the motor unit

Independent Regulation of the Myotonic Dystrophy 1 Locus Genes Postnatally and during Adult Skeletal Muscle Regeneration

Impact of post-synaptic block of neuromuscular transmission, muscle unloading and mechanical ventilation on skeletal muscle protein and mRNA expression

Electrophoretic determination of the myosin/actin ratio in the diagnosis of critical illness myopathy

Muscle fiber atrophy in leg muscles after botulinum toxin type A treatment of cervical dystonia

Effects of a hand training programme in five patients with myotonic dystrophy type 1

Decreased DMPK Transcript Levels in Myotonic Dystrophy 1 Type IIA Muscle Fibers

Reliability of hand function testing instruments in patients with muscular dystrophies

Simultaneous Analysis of Expression of the Three Myotonic Dystrophy Locus Genes in Adult Skeletal Muscle Samples: The CTG Expansion Correlates Inversely with DMPK and 59 Expression Levels, but Not DMAHP Levels

Muscle biopsy, macro EMG, and clinical characteristics in patients with schizophrenia

Effects of ageing on skeletal muscles and single motor units of the fast- and slow-twitch type

Larger CAG expansions in skeletal muscle compared with lymphocytes in Kennedy disease but not in Huntington disease

Charcot-Marie-Tooth disease – muscle biopsy findings in relation to neurophysiology

Effects of ageing on enzyme-histochemical, morphometrical and contractile properties of the soleus muscle in the rat

CTG-repeat length in distal and proximal leg muscles of symptomatic and non-symptomatic patients with myotonic dystrophy: relation to muscle strength and degree of histopathological abnormalities

Charcot-Marie-Tooth disease type 1 and 2-an immunohistochemical study of muscle fibre cytoskeletal proteins and a maker for muscle fibre cytoskeletal proteins and a marker for muscle fibre regeneration

Quantitative and qualitative morphological properties of the soleus motor nerve and the L5 ventral root in young and old rats: Relation to the number of soleus muscle fibres

Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but notDMAHP levels

Charcot-Marie-Tooth disease type 1 and 2-an immunohistochemical study of muscle fibre cytoskeletal proteins and a marker for muscle fibre regeneration

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