glycine has been researched along with Familial Hypokalemic Periodic Paralysis in 4 studies
| 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 Familial 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 |