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Bulbar weakness

Known as: Bulbar muscle weakness 
 
National Institutes of Health

Papers overview

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2019
2019
Spinal muscular atrophy (SMA) is a monogenetic motoneuron disease with onset in childhood or adolescence, clinically… Expand
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Review
2018
Review
2018
Myasthenia gravis with antibodies to the muscle‐specific tyrosine kinase (MuSK+ MG) is a rare disease with distinctive pathogenic… Expand
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2013
2013
We report clinical, neurophysiological and autoantibody profiles of 9 children presenting with fatigable weakness and MuSK… Expand
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2013
2013
ObjectiveMechanical insufflation-exsufflation (MI-E) is used to assist cough in patients with neuromuscular diseases. Clinically… Expand
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2012
2012
BACKGROUND Patients with Guillain-Barré syndrome (GBS) require assisted ventilation frequently. However, no single factor can… Expand
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Review
2004
Review
2004
Guillain-Barré Syndrome is the leading cause of nontraumatic acute paralysis in industrialized countries. About 30% of patients… Expand
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Review
2001
Review
2001
Bulbar dysfunction resulting from corticobulbar pathway or brainstem neuron degeneration is one of the most important clinical… Expand
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Highly Cited
1998
Highly Cited
1998
In vivo proton magnetic resonance spectroscopy (MRS) may be used to quantify brainstem neuronal degeneration in ALS because of… Expand
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Highly Cited
1997
Highly Cited
1997
Article abstract-Autoimmune serologic testing is indicated in the initial investigation of a patient believed to have myasthenia… Expand
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1992
1992
We report the cases of eight children with histologic findings in the muscle of congenital fiber-type disproportion myopathy… Expand
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