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Keyword [Periodic paralysis]
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1. Genetic Research Of Disease-related Mutations And Clinical Study On Periodic Paralyses
2. Immunohistochemistry Study Of Hypokelamic Periodic Paralysis In Hyperthyroidism Of Graves Disease (HPPHGD) By Muscle Biopsies And The Association Between Polymorphism Of MICA And HPPHGD
3. Genetic Research Of Ion Channel Gene Mutations And Clinical Study On Primary Hypokalemic Periodic Paralysis
4. Fuctional Expression Of A Novel Mutation R675Q Identified In A Chinese Normakalemic Periodic Paralysis Family
5. Value Of Exercise Test In The Diagnosis Of Patients With Periodic Paralysis
6. Effect Of Ion Channels On Attack Of Hypokalemic Periodic Paralysis
7. Clinical Analysis On Hypokalemic Tendency Of Graves' Disease And Its Association With HLA-DQA1 Gene Polymorphism
8. Gene Analysis On Hypokalemic Periodic Paralysis
9. Analyse The 5' Flanking Of NKCC1 And Renin Gene In Patients With Thyrotoxic Periodic Paralysis
10. The Study Of Single Nucleotide Polymorphisms Of L-type Votage-gated Calcium Channel α1 Subunit Gene (CACNA1S) 11 Exon In Thyrotoxic Periodic Paralysis Patients Of Chinese
11. Molecular Scanning On 5' Flanking Region Nt-839 To Nt-358 Of CACNA1S Gene In Patients With Thyrotoxic Periodic Paralysis Of Chinese
12. Study On The Effectiveness Of Huangqi Injectio Used To Cure The Patients With Hypokalemic Periodic Paralysis Adjunctively
13. SCN4A Gene Mutations Analysis In Normokalemic Periodic Paralysis Patients
14. Clinical And Pathological Research Of Primary Hypokalemic Periodic Paralysis
15. Study Of Exercise Test In Hypokalemic Periodic Paralysis
16. The Clinical And Pathogenesis Characteristics Of Hypokalemic Periodic Paralysis
17. The Clinical And Genetic Features Of Thyrotoxic Periodic Paralysis
18. Analysis Of Mutation In Gene CACNA1S And SCN4A Of The Hypokalemic Periodic Paralysis Pedigree
19. The Study Of Clinical Features And Muscle Pathology In Patients With Hypokalemic Periodic Paralysis
20. Gene Sequence Analysis Of Hypokalemic Periodic Paralysis Patients In A Family
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