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The Major Bactericidal Activity of Human Seminal Plasma Is Zinc-Dependent and Derived from Fragmentation of the Semenogelins

The Journal of immunology (1950), 2008-09, Vol.181 (5), p.3413-3421

2008

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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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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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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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β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and pH-dependent mechanism

PLoS pathogens, 2012-04, Vol.8 (4), p.e1002625-e1002625

2012

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534-P: Evaluating the Impact of a Simulation Module on Empathy Development in Nursing Students

Diabetes (New York, N.Y.), 2023-06, Vol.72 (Supplement_1), p.1

EDSTROM, GRETCHEN L.

2023

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G.O.1 Welander distal myopathy is caused by a mutated RNA binding protein

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.873-873

2012

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G.P.35 Identical TTN gene A-band mutation causing HMERF occurs in different European populations

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.818-819

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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Motoneuron activity and muscle fibre type composition in hemiparesis

Journal of rehabilitation medicine, 2020-05, Vol.24 (3), p.115-119

2020

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Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy

Human molecular genetics, 1993-09, Vol.2 (9), p.1397-1400

1993

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Changes in diaphragm structure following prolonged mechanical ventilation in piglets

Acta anaesthesiologica Scandinavica, 2004-04, Vol.48 (4), p.430-437

2004

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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

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Sarcoplasmic body myopathy - a rare hereditary myopathy with characteristic inclusions

Acta neurologica Scandinavica, 2005-10, Vol.112 (4), p.223-227

2005

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Effects of age on physiological, immunohistochemical and biochemical properties of fast-twitch single motor units in the rat

The Journal of physiology, 1991-11, Vol.443 (1), p.257-275

1991

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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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Effects of age on contractile and enzyme-histochemical properties of fast- and slow-twitch single motor units in the rat

The Journal of physiology, 1987-11, Vol.392 (1), p.129-145

1987

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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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MHC composition and enzyme-histochemical and physiological properties of a novel fast-twitch motor unit type

American Journal of Physiology: Cell Physiology, 1991-07, Vol.261 (1), p.C93-C101

1991

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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

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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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Fibre-type composition, structure and cytoskeletal protein location of fibres in anterior tibial muscle. Comparison between young adults and physically active aged humans

Acta neuropathologica, 1990-01, Vol.80 (5), p.459-468

1990

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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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Welander distal myopathy – an overview

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

1998

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The Major Bactericidal Activity of Human Seminal Plasma Is Zinc-Dependent and Derived from Fragmentation of the Semenogelins

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

Huntington Disease Phenocopy Is a Familial Prion Disease

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

β-Microseminoprotein endows post coital seminal plasma with potent candidacidal activity by a calcium- and pH-dependent mechanism

534-P: Evaluating the Impact of a Simulation Module on Empathy Development in Nursing Students

G.O.1 Welander distal myopathy is caused by a mutated RNA binding protein

G.P.35 Identical TTN gene A-band mutation causing HMERF occurs in different European populations

Hereditary myopathy with early respiratory failure: occurrence in various populations

Motoneuron activity and muscle fibre type composition in hemiparesis

Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy

Changes in diaphragm structure following prolonged mechanical ventilation in piglets

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

Sarcoplasmic body myopathy - a rare hereditary myopathy with characteristic inclusions

Effects of age on physiological, immunohistochemical and biochemical properties of fast-twitch single motor units in the rat

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

Effects of age on contractile and enzyme-histochemical properties of fast- and slow-twitch single motor units in the rat

Genetic linkage of Welander distal myopathy to chromosome 2p13

MHC composition and enzyme-histochemical and physiological properties of a novel fast-twitch motor unit type

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

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

Fibre-type composition, structure and cytoskeletal protein location of fibres in anterior tibial muscle. Comparison between young adults and physically active aged humans

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

Welander distal myopathy – an overview

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