Results 251 to 260 of about 20,177 (294)
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Journal of Clinical Neuroscience, 2019
Hypokalemic periodic paralysis secondary to distal renal tubular acidosis presenting with prominent bulbar symptoms is extremely rare. The exact pathophysiology by which hypokalemia causes weakness is yet to be elucidated though muscle and nerve membrane hyperpolarization have been hypothesized.
Katrina Hannah D, Ignacio +3 more
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Hypokalemic periodic paralysis secondary to distal renal tubular acidosis presenting with prominent bulbar symptoms is extremely rare. The exact pathophysiology by which hypokalemia causes weakness is yet to be elucidated though muscle and nerve membrane hyperpolarization have been hypothesized.
Katrina Hannah D, Ignacio +3 more
openaire +4 more sources
Improvement in bulbar weakness with guanoxan in type B botulism
The Lancet, 1990K.R. Neal, E.M. Dunbar
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2021
A 61-year-old man sought care for recurrent episodes of dysarthria for about 1 year. This symptom was more common after prolonged speaking. Six months before his evaluation he had significant slurring of his speech after talking for 3½ hours at work about a new project.
Jennifer A. Tracy, Vanda A. Lennon
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A 61-year-old man sought care for recurrent episodes of dysarthria for about 1 year. This symptom was more common after prolonged speaking. Six months before his evaluation he had significant slurring of his speech after talking for 3½ hours at work about a new project.
Jennifer A. Tracy, Vanda A. Lennon
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Vitamin E deficiency associated with vision loss and bulbar weakness
Annals of Neurology, 1985AbstractWe describe a 14‐year‐old boy who was severely debilitated by the neurological syndrome associated with vitamin E deficiency secondary to chronic cholestatic liver disease. In addition to the usual neurological deficits described with this deficiency, the patient had severe bulbar weakness and vision loss which we attribute to the degree and ...
P D, Larsen, D M, Mock, P S, O'Connor
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Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIa
Molecular Genetics and Metabolism, 2012Glycogen storage disorder type III (GSD III) is a rare autosomal recessive disorder resulting from a deficiency of glycogen debranching enzyme, critical in cytosolic glycogen degradation. GSD IIIa, the most common form of GSD III, primarily affects the liver, cardiac muscle, and skeletal muscle.
Horvath, Jeffrey J +7 more
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Indian Journal of Emergency Medicine, 2022
A 20 years old female came to ED with c/o giddiness since 4 days, headache since 3 days with diplopia with slurring of speech, lower limb weakness, difficulty in swallowing, and dropping of left eyelid since 1 day. Patient had no any pre-existing comorbidity and not on any regular medication. Last menstrual period was on 5 days back.
Ritul Srivastava +2 more
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A 20 years old female came to ED with c/o giddiness since 4 days, headache since 3 days with diplopia with slurring of speech, lower limb weakness, difficulty in swallowing, and dropping of left eyelid since 1 day. Patient had no any pre-existing comorbidity and not on any regular medication. Last menstrual period was on 5 days back.
Ritul Srivastava +2 more
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Neurology, 2012
Objective: To report a case of chronic inflammatory demyelinating polyneuropathy in a patient presenting with recurrent bouts of ataxia, bulbar weakness, and respiratory dysfunction. Background Chronic inflammatory demyelinating polyneuropathy (CIDP) can have a variable presentation leading to delay in diagnosis and treatment.
R. Malka, E. Muntean
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Objective: To report a case of chronic inflammatory demyelinating polyneuropathy in a patient presenting with recurrent bouts of ataxia, bulbar weakness, and respiratory dysfunction. Background Chronic inflammatory demyelinating polyneuropathy (CIDP) can have a variable presentation leading to delay in diagnosis and treatment.
R. Malka, E. Muntean
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Neurological Sciences, 2009
Bilateral facial palsy is a common sign of autoimmune myasthenia gravis (MG). However, facial muscle weakness without clinical signs of extraocular muscle (EOM) involvement is extremely rare. We describe a late onset generalized MG presenting with facial weakness and bulbar signs without EOM deficits.
L. Cucurachi +3 more
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Bilateral facial palsy is a common sign of autoimmune myasthenia gravis (MG). However, facial muscle weakness without clinical signs of extraocular muscle (EOM) involvement is extremely rare. We describe a late onset generalized MG presenting with facial weakness and bulbar signs without EOM deficits.
L. Cucurachi +3 more
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Periodic weakness of the diaphragm as the sole manifestation of bulbar onset myasthenia.
The Medical journal of Malaysia, 2020No abstract provided.
J, Finsterer +3 more
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Muscle & Nerve, 2015
ABSTRACTIntroduction: Acute bulbar, neck, and limb weakness carries several potential differential diagnoses. Although a diagnosis can often be established clinically, investigations such as electrodiagnostic and antibody testing can provide support for the clinical diagnosis and may aid in understanding the pathogenesis.
Nidhi, Garg +4 more
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ABSTRACTIntroduction: Acute bulbar, neck, and limb weakness carries several potential differential diagnoses. Although a diagnosis can often be established clinically, investigations such as electrodiagnostic and antibody testing can provide support for the clinical diagnosis and may aid in understanding the pathogenesis.
Nidhi, Garg +4 more
openaire +2 more sources