glycine has been researched along with Congenital Stiff-Man Syndrome in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (12.50) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 5 (62.50) | 24.3611 |
| 2020's | 1 (12.50) | 2.80 |
| Authors | Studies |
|---|---|
| Chia, NH | 1 |
| McKeon, A | 1 |
| Dalakas, MC | 1 |
| Flanagan, EP | 1 |
| Bower, JH | 1 |
| Klassen, BT | 1 |
| Dubey, D | 1 |
| Zalewski, NL | 1 |
| Duffy, D | 1 |
| Pittock, SJ | 1 |
| Zekeridou, A | 1 |
| Schaefer, N | 1 |
| Langlhofer, G | 1 |
| Kluck, CJ | 1 |
| Villmann, C | 1 |
| Arribas-González, E | 1 |
| de Juan-Sanz, J | 1 |
| Aragón, C | 1 |
| López-Corcuera, B | 1 |
| Chau, A | 1 |
| Roitfarb, M | 1 |
| Carabuena, JM | 1 |
| Camann, W | 1 |
| Ehmsen, JT | 1 |
| Liu, Y | 1 |
| Wang, Y | 1 |
| Paladugu, N | 1 |
| Johnson, AE | 1 |
| Rothstein, JD | 1 |
| du Lac, S | 1 |
| Mattson, MP | 1 |
| Höke, A | 1 |
| Lape, R | 1 |
| Plested, AJ | 1 |
| Moroni, M | 1 |
| Colquhoun, D | 1 |
| Sivilotti, LG | 1 |
| Breitinger, HG | 1 |
| Lanig, H | 1 |
| Vohwinkel, C | 1 |
| Grewer, C | 1 |
| Breitinger, U | 1 |
| Clark, T | 1 |
| Becker, CM | 1 |
| Floeter, MK | 1 |
| Valls-Solé, J | 1 |
| Toro, C | 1 |
| Jacobowitz, D | 1 |
| Hallett, M | 1 |
1 review available for glycine and Congenital Stiff-Man Syndrome
| Article | Year |
|---|---|
Glycine receptor mouse mutants: model systems for human hyperekplexia.
Topics: Animals; Disease Models, Animal; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glycine | 2013 |
7 other studies available for glycine and Congenital Stiff-Man Syndrome
| Article | Year |
|---|---|
Stiff person spectrum disorder diagnosis, misdiagnosis, and suggested diagnostic criteria.
Topics: Autoantibodies; Diagnostic Errors; Glycine; Humans; Immunoglobulin G; Receptors, Glycine; Retrospect | 2023 |
Molecular basis of the dominant negative effect of a glycine transporter 2 mutation associated with hyperekplexia.
Topics: Animals; Biotinylation; Calnexin; Cerebral Cortex; Chlorocebus aethiops; COS Cells; Densitometry; Do | 2015 |
Anesthetic management of a parturient with hyperekplexia.
Topics: Adult; Anesthesia, Epidural; Anesthesia, Obstetrical; Female; Glycine; Humans; Infant, Newborn; Muta | 2015 |
The astrocytic transporter SLC7A10 (Asc-1) mediates glycinergic inhibition of spinal cord motor neurons.
Topics: Amino Acid Transport System y+; Animals; Astrocytes; Autoantigens; Brain; Cells, Cultured; Female; G | 2016 |
The α1K276E startle disease mutation reveals multiple intermediate states in the gating of glycine receptors.
Topics: Animals; Glycine; HEK293 Cells; Humans; Ion Channel Gating; Mutation; Rats; Receptors, Glycine; Refl | 2012 |
Molecular dynamics simulation links conformation of a pore-flanking region to hyperekplexia-related dysfunction of the inhibitory glycine receptor.
Topics: Cell Line; Computer Simulation; Dose-Response Relationship, Drug; Glycine; Helix-Turn-Helix Motifs; | 2004 |
Physiologic studies of spinal inhibitory circuits in patients with stiff-person syndrome.
Topics: Adult; Aged; Electromyography; Femoral Nerve; gamma-Aminobutyric Acid; Glycine; H-Reflex; Humans; In | 1998 |