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Detecting dysphagia in inclusion body myositis

Journal of neurology, 2009-12, Vol.256 (12), p.2009-2013

2009

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Optimal Oral Anticoagulant Therapy in Patients with Mechanical Heart Valves

The New England journal of medicine, 1995-07, Vol.333 (1), p.11-17

1995

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Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families

Neurology, 2007-06, Vol.68 (24), p.2125

2007

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Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositis

Neurology, 2004-12, Vol.63 (12), p.2396

2004

Volltextzugriff (PDF)

Epidemiology of inclusion body myositis in the Netherlands: a nationwide study

Neurology, 2000-11, Vol.55 (9), p.1385

2000

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Difference in distribution of muscle weakness between myasthenia gravis and the Lambert–Eaton myasthenic syndrome

Journal of neurology, neurosurgery and psychiatry, 2002-12, Vol.73 (6), p.766-768

2002

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The epidemiology of the Lambert-Eaton myasthenic syndrome in the Netherlands

Neurology, 2004-07, Vol.63 (2), p.397

2004

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Necrotising myopathy, an unusual presentation of a steroid-responsive myopathy

Journal of neurology, 2003-04, Vol.250 (4), p.480-485

2003

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Magnetic resonance imaging of skeletal muscles in sporadic inclusion body myositis

Rheumatology (Oxford, England), 2011-06, Vol.50 (6), p.1153-1161

2011

Volltextzugriff (PDF)

Does modafinil enhance activity of patients with myotonic dystrophy? : a double-blind placebo-controlled crossover study

Journal of neurology, 2007, Vol.254 (1), p.26-28

2007

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Clinical fluctuations in MuSK myasthenia gravis are related to antigen-specific IgG4 instead of IgG1

Journal of neuroimmunology, 2008-03, Vol.195 (1), p.151-156

2008

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Neuropathy and IgM M-proteins: prognostic value of antibodies to MAG, SGPG, and sulfatide

Neurology, 2001-01, Vol.56 (2), p.228

2001

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Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset

Annals of neurology, 1998-04, Vol.43 (4), p.540-544

1998

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HLA and smoking in prediction and prognosis of small cell lung cancer in autoimmune Lambert–Eaton myasthenic syndrome

Journal of neuroimmunology, 2005-02, Vol.159 (1), p.230-237

2005

Volltextzugriff (PDF)

HLA class I and II in Lambert-Eaton myasthenic syndrome without associated tumor

Human immunology, 2001-08, Vol.62 (8), p.809-813

2001

Volltextzugriff (PDF)

The risk of intracerebral hemorrhage during oral anticoagulant treatment: A population study

Annals of neurology, 1984-11, Vol.16 (5), p.553-558

1984

Volltextzugriff (PDF)

The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands

Brain (London, England : 1878), 1996-10, Vol.119 (5), p.1471-1480

1996

Volltextzugriff (PDF)

Acquired neuromyotonia: Evidence for autoantibodies directed against K+ channels of peripheral nerves

Annals of neurology, 1995-11, Vol.38 (5), p.714-722

1995

Volltextzugriff (PDF)

Acquired slow-channel syndrome: A form of myasthenia gravis with prolonged open time of the acetylcholine receptor channel

Annals of neurology, 1998-10, Vol.44 (4), p.657-664

1998

Volltextzugriff (PDF)

Repetitive CMAPs: Mechanisms of neural and synaptic genesis

Muscle & nerve, 1996-09, Vol.19 (9), p.1127-1133

1996

Volltextzugriff (PDF)

Risk of stroke during long-term anticoagulant therapy in patients after myocardial infarction

Annals of neurology, 1996-03, Vol.39 (3), p.301-307

1996

Volltextzugriff (PDF)

Disruption of sleep-wake rhythmicity and daytime sleepiness in myotonic dystrophy

Journal of the neurological sciences, 1993, Vol.114 (1), p.68-75

1993

Volltextzugriff (PDF)

Reversible severe myopathy during treatment with finasteride

Muscle & nerve, 1997-04, Vol.20 (4), p.502-504

1997

Volltextzugriff (PDF)

The calcium channel blocker verapamil in hypokalemic periodic paralysis

Muscle & nerve, 1998-11, Vol.21 (11), p.1564-1565

1998

Volltextzugriff (PDF)

Dysphagia in inclusion body myositis

Journal of neurology, neurosurgery and psychiatry, 1988-12, Vol.51 (12), p.1542-1545

1988

Volltextzugriff (PDF)

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Detecting dysphagia in inclusion body myositis

Optimal Oral Anticoagulant Therapy in Patients with Mechanical Heart Valves

Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families

Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositis

Epidemiology of inclusion body myositis in the Netherlands: a nationwide study

Difference in distribution of muscle weakness between myasthenia gravis and the Lambert–Eaton myasthenic syndrome

The epidemiology of the Lambert-Eaton myasthenic syndrome in the Netherlands

Necrotising myopathy, an unusual presentation of a steroid-responsive myopathy

Magnetic resonance imaging of skeletal muscles in sporadic inclusion body myositis

Does modafinil enhance activity of patients with myotonic dystrophy? : a double-blind placebo-controlled crossover study

Clinical fluctuations in MuSK myasthenia gravis are related to antigen-specific IgG4 instead of IgG1

Neuropathy and IgM M-proteins: prognostic value of antibodies to MAG, SGPG, and sulfatide

Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset

HLA and smoking in prediction and prognosis of small cell lung cancer in autoimmune Lambert–Eaton myasthenic syndrome

HLA class I and II in Lambert-Eaton myasthenic syndrome without associated tumor

The risk of intracerebral hemorrhage during oral anticoagulant treatment: A population study

The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands

Acquired neuromyotonia: Evidence for autoantibodies directed against K+ channels of peripheral nerves

Acquired slow-channel syndrome: A form of myasthenia gravis with prolonged open time of the acetylcholine receptor channel

Repetitive CMAPs: Mechanisms of neural and synaptic genesis

Risk of stroke during long-term anticoagulant therapy in patients after myocardial infarction

Disruption of sleep-wake rhythmicity and daytime sleepiness in myotonic dystrophy

Reversible severe myopathy during treatment with finasteride

The calcium channel blocker verapamil in hypokalemic periodic paralysis

Dysphagia in inclusion body myositis

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