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Kinase Domain of Titin Controls Muscle Gene Expression and Protein Turnover

Science (American Association for the Advancement of Science), 2005-06, Vol.308 (5728), p.1599-1603

2005

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Welander distal myopathy is caused by a mutation in the RNA-binding protein TIA1

Annals of neurology, 2013-04, Vol.73 (4), p.500-509

2013

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Altered autophagy gene expression and persistent atrophy suggest impaired remodeling in chronic hemiplegic human skeletal muscle

Muscle & nerve, 2012-11, Vol.46 (5), p.785-792

2012

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Hereditary myopathy with early respiratory failure: occurrence in various populations

Journal of neurology, neurosurgery and psychiatry, 2014-03, Vol.85 (3), p.345-353

2014

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Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

Nature communications, 2019-03, Vol.10 (1), p.1396-14, Article 1396

2019

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Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2

Acta neuropathologica, 2010-04, Vol.119 (4), p.465-479

2010

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Huntington Disease Phenocopy Is a Familial Prion Disease

American journal of human genetics, 2001-12, Vol.69 (6), p.1385-1388

2001

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Mice expressing L345P mutant desmin exhibit morphological and functional changes of skeletal and cardiac mitochondria

Journal of muscle research and cell motility, 2008, Vol.29 (1), p.25-36

2008

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Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain

Brain (London, England : 1878), 2014-06, Vol.137 (Pt 6), p.e279-e279

2014

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Feasibility and effects of a physical exercise programme in adults with myotonic dystrophy type 1: a randomized controlled pilot study

Journal of rehabilitation medicine, 2011-07, Vol.43 (8), p.695-702

2011

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Properly formed but improperly localized synaptic specializations in the absence of laminin α4

Nature neuroscience, 2001-06, Vol.4 (6), p.597-604

2001

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Acute quadriplegia and loss of muscle myosin in patients treated with nondepolarizing neuromuscular blocking agents and corticosteroids : Mechanisms at the cellular and molecular levels

Critical care medicine, 2000, Vol.28 (1), p.34-45

2000

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Influence of Isoflurane Concentration and Hypoxia on Functional Magnetic Resonance Imaging for the Detection of Bicuculline-Induced Neuronal Activation

Neuro-Signals, 2004-01, Vol.13 (3), p.144-149

2004

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Myofibers from Duchenne/Becker Muscular Dystrophy and Myositis Express the Intermediate Filament Nestin

Journal of neuropathology and experimental neurology, 1994-07, Vol.53 (4), p.416-423

1994

Volltextzugriff (PDF)

Effects of excessive use of remaining muscle fibers in prior polio and LV lesion

Muscle & nerve, 1988-12, Vol.11 (12), p.1219-1230

1988

Volltextzugriff (PDF)

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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Neurogenic effects on the palatopharyngeal muscle in patients with obstructive sleep apnoea: a muscle biopsy study

Journal of neurology, neurosurgery and psychiatry, 1992-10, Vol.55 (10), p.916-920

1992

Volltextzugriff (PDF)

Genetic linkage of Welander distal myopathy to chromosome 2p13

Annals of neurology, 1999-09, Vol.46 (3), p.399-404

1999

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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

Volltextzugriff (PDF)

Autosomal Dominant Myopathy with Proximal Weakness and Early Respiratory Muscle Involvement Maps to Chromosome 2q

American journal of human genetics, 1999-03, Vol.64 (3), p.788-792

1999

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A Huntington Disease–Like Neurodegenerative Disorder Maps to Chromosome 20p

American journal of human genetics, 1998-11, Vol.63 (5), p.1431-1438

1998

Volltextzugriff (PDF)

Welander distal myopathy outside the Swedish population: phenotype and genotype

Neuromuscular disorders : NMD, 2002-08, Vol.12 (6), p.544-547

2002

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Properly formed but improperly localized synaptic specializations in the absence of laminin [alpha]4

Nature neuroscience, 2001-06, Vol.4 (6), p.597

2001

Volltextzugriff (PDF)

Welander distal myopathy – an overview

Neuromuscular disorders : NMD, 1998-04, Vol.8 (2), p.115-118

1998

Volltextzugriff (PDF)

A Scandinavian perspective on aid to education

Prospects (Paris), 1974-06, Vol.4 (2), p.229-237

Edström, Lars-Olof

1974

Volltextzugriff (PDF)

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Kinase Domain of Titin Controls Muscle Gene Expression and Protein Turnover

Welander distal myopathy is caused by a mutation in the RNA-binding protein TIA1

Altered autophagy gene expression and persistent atrophy suggest impaired remodeling in chronic hemiplegic human skeletal muscle

Hereditary myopathy with early respiratory failure: occurrence in various populations

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2

Huntington Disease Phenocopy Is a Familial Prion Disease

Mice expressing L345P mutant desmin exhibit morphological and functional changes of skeletal and cardiac mitochondria

Reply: Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain

Feasibility and effects of a physical exercise programme in adults with myotonic dystrophy type 1: a randomized controlled pilot study

Properly formed but improperly localized synaptic specializations in the absence of laminin α4

Acute quadriplegia and loss of muscle myosin in patients treated with nondepolarizing neuromuscular blocking agents and corticosteroids : Mechanisms at the cellular and molecular levels

Influence of Isoflurane Concentration and Hypoxia on Functional Magnetic Resonance Imaging for the Detection of Bicuculline-Induced Neuronal Activation

Myofibers from Duchenne/Becker Muscular Dystrophy and Myositis Express the Intermediate Filament Nestin

Effects of excessive use of remaining muscle fibers in prior polio and LV lesion

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

Neurogenic effects on the palatopharyngeal muscle in patients with obstructive sleep apnoea: a muscle biopsy study

Genetic linkage of Welander distal myopathy to chromosome 2p13

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

Autosomal Dominant Myopathy with Proximal Weakness and Early Respiratory Muscle Involvement Maps to Chromosome 2q

A Huntington Disease–Like Neurodegenerative Disorder Maps to Chromosome 20p

Welander distal myopathy outside the Swedish population: phenotype and genotype

Properly formed but improperly localized synaptic specializations in the absence of laminin [alpha]4

Welander distal myopathy – an overview

A Scandinavian perspective on aid to education

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