Susceptibility to thyrotoxic periodic paralysis type 1 is defined by variations in the calcium channel gene CACNA1S.
|
|
|
|||
|
|
|
|||
|
|
|
|||
|
|
|
|||
|
|
|
|||
|
|
|
|
||
| 1. |
Kung AW et al. (2004) Association of novel single nucleotide polymorphisms in the calcium channel alpha 1 subunit gene (Ca(v)1.1) and thyrotoxic periodic paralysis.
|
| 2. |
None (1985) Familial "hashitoxic' periodic paralysis.
|
| 3. |
Kusakabe T et al. (1976) Thyrotoxic periodic paralysis: a peculiar case with unusual dystonic behavior and variable relations of paralysis to serum potassium levels.
|
| 4. |
Au KS et al. (1972) Thyrotoxic periodic paralysis. Periodic variation in the muscle calcium pump activity.
|
| 5. |
Yeung RT et al. (1974) Thyrotoxic periodic paralysis. Effect of propranolol.
|
| 6. |
Layzer RB et al. (1974) Periodic paralysis caused by abuse of thyroid hormone.
|
| 7. |
Bernard JD et al. (1972) Thyrotoxic periodic paralysis in Californians of Mexican and Filipino ancestry.
|
| 8. |
McFadzean AJ et al. (1967) Periodic paralysis complicating thyrotoxicosis in Chinese.
|
| 9. |
Kilpatrick RE et al. (1994) Thyrotoxic hypokalemic periodic paralysis: report of four cases in black American males.
|
| 10. |
Sternberg D et al. (2003) Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis.
|
| 11. |
Jurkat-Rott K et al. (2004) Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation.
|
| 12. |
None (2006) Clinical review: Thyrotoxic periodic paralysis: a diagnostic challenge.
|
| 13. |
Shah N et al. (1979) Familial periodic paralysis and hyperthyroidism.
|
| 14. |
None (1975) Letter: fibre content of bread.
|
| 15. |
Dias Da Silva MR et al. (2002) A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis.
|
| 16. |
OMIM.ORG article Omim 188580
|