glycine has been researched along with Hypokalemic Periodic Paralysis in 4 studies
Hypokalemic Periodic Paralysis: An autosomal dominant familial disorder characterized by recurrent episodes of skeletal muscle weakness associated with falls in serum potassium levels. The condition usually presents in the first or second decade of life with attacks of trunk and leg paresis during sleep or shortly after awakening. Symptoms may persist for hours to days and generally are precipitated by exercise or a meal high in carbohydrates. (Adams et al., Principles of Neurology, 6th ed, p1483)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Hypokalemic periodic paralysis (HOKPP) is a rare disorder characterized by episodic muscle weakness with hypokalemia." | 1.36 | Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis. ( Kil, TH; Kim, JB, 2010) |
| "The clinical features of TPP resemble familial hypokalemic periodic paralysis (hypoKPP), which has been linked to two mutations in the gene encoding the skeletal muscle calcium channel alpha-1 subunit (CACN1AS; Arg528His and Arg1239His) and to the sodium channel alpha-subunit (SCN4A; Arg672His)." | 1.32 | Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis. ( Cheah, JS; Lui, KF; Ng, WY; Thai, AC, 2004) |
| "Hypokalaemic periodic paralysis (hypoPP) is a dominantly inherited muscle disorder characterized by episodes of flaccid weakness." | 1.31 | Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type II. ( Hang, C; Jurkat-Rott, K; Kuzmenkin, A; Lehmann-Horn, F; Lerche, H; Mitrovic, N; Muncan, V, 2002) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kil, TH | 1 |
| Kim, JB | 2 |
| Ng, WY | 1 |
| Lui, KF | 1 |
| Thai, AC | 1 |
| Cheah, JS | 1 |
| Lee, KY | 1 |
| Hur, JK | 1 |
| Kuzmenkin, A | 1 |
| Muncan, V | 1 |
| Jurkat-Rott, K | 1 |
| Hang, C | 1 |
| Lerche, H | 1 |
| Lehmann-Horn, F | 1 |
| Mitrovic, N | 1 |
4 other studies available for glycine and Hypokalemic Periodic Paralysis
| Article | Year |
|---|---|
Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis.
Topics: Adolescent; Amiloride; Amino Acid Substitution; Arginine; Calcium Channels; Calcium Channels, L-Type | 2010 |
Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis.
Topics: Adult; Arginine; Calcium Channels; Calcium Channels, L-Type; Case-Control Studies; Female; Glycine; | 2004 |
A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G).
Topics: Acetazolamide; Adolescent; Arginine; Calcium Channels; Calcium Channels, L-Type; Codon; Exons; Famil | 2005 |
Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type II.
Topics: Arginine; Cells, Cultured; Glycine; Histidine; Humans; Hydrogen-Ion Concentration; Hypokalemic Perio | 2002 |