Neigung zur thyreotoxischen periodischen Paralyse 1
Die Neigung zu thyreotoxischer periodischer Paralyse Typ 1 wird bestimmt durch Variationen im CACNA1S-Gen.
Gliederung
Hyperthyreose
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Basedow-Krankheit
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Familiäre Schwangerschaftshyperthyreose
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McCune-Albright-Syndrom
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Neigung zur thyreotoxischen periodischen Paralyse 1
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CACNA1S
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Nicht-autoimmunbedingte Hyperthyreose
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Referenzen:
| 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. |
Kusakabe T et. al. (1976) Thyrotoxic periodic paralysis: a peculiar case with unusual dystonic behavior and variable relations of paralysis to serum potassium levels. [^] |
| 3. |
None (1985) Familial "hashitoxic' periodic paralysis. [^] |
| 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. [^] |
