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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....
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Stroke Recurrence in a Patient Twelve Years after Repair of a Secundum Atrial Septal Defect

Ok T, La YK, Cha HS, Cheon K, Choi BK, Yi GJ, Lee KY

BACKGROUND: Secundum atrial septal defect (ASD) is a common congenital heart defect in adults. Patients with ASDs at high risk of cardiovascular complications undergo either surgical repair or percutaneous device...
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Dural Arteriovenous Fistula Manifested as Rapid Progressive Dementia Successfully Treated by Endovascular Embolization Only

Hwang H, La YK, Baek MS, Baik K, Suh SH, Kim WJ

A 43-year-old male presented with daytime sleepiness at work and indifferent behavior like never before. Two weeks prior to hospital admission, he had episodic memory loss with well preserved remote...
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Isolated Leptomeningeal Neurosarcoidosis

La YK, Kim HI, Baek MS, Baik KW, Cha YJ, Kim WJ

No abstract available.
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Renal Subcapsular Hematoma after Intravenous Thrombolysis in a Patient with Acute Cerebral Infarction

La YK, Kim JH, Lee KY

A 74-year-old female with acute cerebral infarction was treated with intravenous recombinant tissue plasminogen activator. Subsequent percutaneous transfemoral angiography and mechanical thrombectomy were performed due to a right middle cerebral...
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