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Bulbar weakness
Known as:
Bulbar muscle weakness
National Institutes of Health
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Related topics
Related topics
11 relations
AMYOTROPHIC LATERAL SCLEROSIS 21
Bulbo-Spinal Atrophy, X-Linked
Congenital Fiber Type Disproportion
Familial infantile myasthenia
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Letter to the editor: Need for a European network for enterovirus D68 surveillance after detections of EV-D68 of the new B3 lineage in Sweden and Italy, 2016
E. Pariani
,
L. Pellegrinelli
,
A. D. C. Merlone
,
A. Piralla
,
F. Baldanti
,
S. Binda
Euro surveillance : bulletin Europeen sur les…
2017
Corpus ID: 11541140
As the regional reference laboratory for acute flaccid paralysis (AFP) surveillance (Lombardy, northern Italy), a case of acute…
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2017
2017
Patient with statin‐associated immune‐mediated necrotizing myopathy presenting with subcutaneous edema, persistent bulbar weakness and absent anti‐HMGCR
S. G. Ong
,
H. Ding
International Journal of Rheumatic Diseases
2017
Corpus ID: 5347702
Dear Editor, Statin is commonly prescribed for treatment of dyslipidemia and prevention of cardiovascular disease…
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2015
2015
Myasthenic Crisis in an Elderly Patient with Positive Antibodies against Acetylcholine and Anti-MuSK, Successfully Treated with Noninvasive Mechanical Ventilation
J. Fernández
,
Antonio Fernández-Valiñas
,
D. Hernández
,
J. Orozco
,
A. Lugo
Case Reports in Critical Care
2015
Corpus ID: 14221566
Myasthenia gravis is an autoimmune disease characterized by muscle weakness. Subjects with antibodies against acetylcholine…
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2012
2012
Double trouble: Spinal muscular atrophy type II and seropositive myasthenia gravis in the same patient
M. Jokela
,
B. Udd
,
M. Päivärinta
Neuromuscular Disorders
2012
Corpus ID: 2010978
2012
2012
Chronic myeloid leukemia with an unusual paraneoplastic syndrome.
Namita Sharma
,
H. Dua
,
D. Rosha
Journal of Association of Physicians of India
2012
Corpus ID: 45161558
We report a 34 year old man who developed bilateral ptosis and predominantly respiratory, truncal and bulbar weakness, and a high…
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2010
2010
Evaluation of two different methods for per-oral gastrostomy tube placement in patients with motor neuron disease (MND): PIG versus PEG procedures
G. Chavada
,
A. El-Nayal
,
+6 authors
P. Shaw
Amyotrophic Lateral Sclerosis
2010
Corpus ID: 39316224
Abstract Placement of a gastrostomy tube remains the gold standard procedure to maintain nutrition in patients with motor neuron…
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2009
2009
PO8.3 Additional Diagnostic Value of Post-Exercise Exhaustion
Hyun-Jung Kim
,
Yoon-Ho Hong
,
Kwang‐Woo Lee
Clinical Neurophysiology
2009
Corpus ID: 53159760
2009
2009
PO8.2 Acquired Neuromyotonia with Myasthenia: A Case Report
Yoon-Ho Hong
Clinical Neurophysiology
2009
Corpus ID: 53145035
Review
2003
Review
2003
Pulmonary physical medicine interventions for elderly patients with muscular dysfunction.
R. Filart
,
J. Bach
Clinics in Geriatric Medicine
2003
Corpus ID: 32626035
1992
1992
Early predictors of poor outcome in congenital fiber-type disproportion myopathy.
C. Torres
,
R. Moxley
Archives of Neurology
1992
Corpus ID: 19283518
We report the cases of eight children with histologic findings in the muscle of congenital fiber-type disproportion myopathy…
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