Skip Navigation
Skip to contents
Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

11 results
Display

A case of retinopathy with antirecoverinantibody preceding the diagnosis ofcancer

Lee DA, Park KM

CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Isolated abducens nerve palsy due tointernal carotid artery aneurysm

Kim BJ, Park KM

CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Insight into the prognostic factors ofchronic inflammatory demyelinatingpolyneuropathy

Baek SH

Chronic inflammatory demyelinating polyneuropathy (CIDP) is an immune-mediated neuropathy with heterogeneous features. Appropriate treatment will produce a favorable outcome, but a poor treatment response and severe disability have also been reported. The...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Ultrasonographic evaluation of commoncompression neuropathies in theupper limb

Seok JI

Neuromuscular ultrasonography has emerged over the last decade as a useful tool for diagnosing peripheral nerve disorders. It has been studied extensively with a particular focus on the assessment of compression neuropathies....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Febrile Hashimoto’s encephalopathymimicking infectious encephalitis

Lee JJ, Youn MS, Park JM, Kwon O, Lee WW, Kang K, Kim BK

Hashimoto’s encephalopathy (HE) is a heterogeneous encephalopathy with diverse clinical presentations. Here we report on a 69-year-old woman who presented with confusion, aphasia, fever, and focal ictal discharges. Cerebrospinal fluid analysis and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Electrognostic findings ofGuillain-Barré syndrome

Yoon BA, Bae JS, Kim JK

The electrodiagnostic findings in Guillain-Barré syndrome (GBS) play important roles in both understanding its pathophysiology and its diagnosis. Only demyelinating neuropathies were thought to be present when GBS patients were first diagnosed...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
LGMD2E with a novel nonsense variantin SGCB gene: a case of LGMD2E with anovel variant

La YK, Oh EK, Lyou HJ, Hong JM, Choi YC

Sarcoglycanopathies are a rare group of autosomal recessive limb-girdle muscular dystrophies (LGMDs) caused by genetic variants in α-, β-, γ-, or δ-sarcoglycan that maintain membrane integrity and contribute to molecular signal processing....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Likely pathogenic FIG4 related amyotrophiclateral sclerosis patient whocorrelated with clinical, imaging andneuropsychological studies

Ko PW, Min YS, Park JS

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder with numerous causes that include genetic factors. Efforts to reveal the genetics of ALS have identified several candidate genes that are associated with...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Neurolymphomatosis in patients withmantle cell lymphoma diagnosed byFDG PET-CT

Kim S, An H, Choi YS, Park KH, Sohn EH

Neurolymphomatosis (NL) is characterized by the infiltration of malignant lymphoma cells into peripheral nerves, nerve roots, plexuses, or cranial nerves. This is a very rare complication of mantle-cell lymphoma. Diagnosing NL is...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Steroid-resistant sarcoid myositis thatwas successfully treated with oralmethotrexate

Noh KH, Huh SY, Park YE, Shin JH, Kim DS

Acute sarcoid myositis is rarely complicated by sarcoidosis, and steroid therapy is considered the standard treatment. We experienced a patient with acute sarcoid myositis who did not respond to aggressive high-dose corticosteroid...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Immobilization-induced rhabdomyolysispatients with peripheral neuropathy:clinical, laboratory and imagingfindings

Seok JI, Lee IH, Ahn KS, Kang GW, Lee JW, Kwak S

Background: Peripheral nerve injury rarely occurs in patients with rhabdomyolysis. Based on our experience and previous reports, we consider prolonged immobilization a risk factor for the development of peripheral neuropathy in rhabdomyolysis...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr