A Mutation in the KCNE3 Potassium Channel Gene Is Associated with Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis

Cited by (114)

Items 101–114 of 114

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2. Thyrotoxic Periodic Paralysis: A Review and Suggestions for Treatment
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3. Muscle channelopathies: periodic paralyses and nondystrophic myotonias
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4. Thyroid Disorders
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5. Channelopathies
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6. Thyroid emergencies
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7. 第13回臨床内分泌代謝:Update Proceeding 1
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8. Muscle Channelopathies
   Jeffrey W. Ralph, Louis J. Ptáček · 2014 · Elsevier eBooks
9. Exercise Induced Paralysis in Two Young Ghanaian Men
   Braimah Baba Abubakari, Patrick Adjei, Foster Osei‐Poku, Kodwo Nkromah, Albert Kwaku Akpalu · 2022 · Postgraduate Medical Journal of Ghana
10. 10.1016/b978-1-4160-2911-3.50013-3
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11. KCNE gene family: From basic functions to diseases
    Junshen Xiao, Cheng Xu, D H Huang, Shichao Wei, Zhaoyang Hu · 2025 · Genes & Diseases
12. Thyroid emergencies
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13. Extrarenal potassium metabolism
    Shubhada N. Ahya, Aleksandra Gmurczyk, Robert M. Rosa · 2026 · Elsevier eBooks
14. Inherited Channelopathies of Muscle: Implications for Therapy
    Theodore Cummins, Robert Louis Ruff · 2005 · Elsevier eBooks