glycine has been researched along with Hypermyotonia in 6 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Hyperekplexia is characterised by neonatal hypertonia and an exaggerated startle reflex in response to acoustic or tactile stimuli." | 2.44 | The genetics of hyperekplexia: more than startle! ( Harvey, K; Harvey, RJ; Rees, MI; Topf, M, 2008) |
| "VWMD is a rare autosomal recessive leukoencephalopathy which typically begins during infancy or early childhood with a chronic progressive neurological deterioration with cerebellar ataxia and spasticity." | 1.38 | [Case of adult onset vanishing white matter disease developed after minor head trauma]. ( Kanai, K; Koga, S; Kuwabara, S; Mutoh, M; Sekiguchi, Y, 2012) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Harvey, RJ | 1 |
| Topf, M | 1 |
| Harvey, K | 1 |
| Rees, MI | 1 |
| Frizzo, JK | 1 |
| Cardoso, MP | 1 |
| de Assis, AM | 1 |
| Perry, ML | 1 |
| Volonté, C | 1 |
| Frizzo, ME | 1 |
| Koga, S | 1 |
| Sekiguchi, Y | 1 |
| Kanai, K | 1 |
| Mutoh, M | 1 |
| Kuwabara, S | 1 |
| Kimura, M | 1 |
| Taketani, T | 1 |
| Horie, A | 1 |
| Isumi, H | 1 |
| Sejima, H | 1 |
| Yamaguchi, S | 1 |
| Tuchman, M | 1 |
| Berry, SA | 1 |
| Thuy, LP | 1 |
| Nyhan, WL | 1 |
| Crone, C | 1 |
| Nielsen, J | 1 |
| Petersen, N | 1 |
| Tijssen, MA | 1 |
| van Dijk, JG | 1 |
1 review available for glycine and Hypermyotonia
| Article | Year |
|---|---|
The genetics of hyperekplexia: more than startle!
Topics: Animals; Genetic Testing; Glycine; Health; Humans; Muscle Hypertonia; Receptors, Glycine; Reflex, St | 2008 |
5 other studies available for glycine and Hypermyotonia
| Article | Year |
|---|---|
Effects of acute perinatal asphyxia in the rat hippocampus.
Topics: Acute Disease; Animals; Animals, Newborn; Asphyxia; Biological Transport; Cell Survival; Female; Glu | 2010 |
[Case of adult onset vanishing white matter disease developed after minor head trauma].
Topics: Adult; Biomarkers; Consciousness Disorders; Craniocerebral Trauma; Diagnosis, Differential; Glycine; | 2012 |
Two Japanese families with hyperekplexia who have a Arg271Gln mutation in the glycine receptor alpha 1 subunit gene.
Topics: Child, Preschool; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glycine; Hip D | 2006 |
Partial methylcrotonyl-coenzyme A carboxylase deficiency in an infant with failure to thrive, gastrointestinal dysfunction, and hypertonia.
Topics: Biotin; Carbon-Carbon Ligases; Failure to Thrive; Gastrointestinal Diseases; Glycine; Humans; Infant | 1993 |
Patients with the major and minor form of hyperekplexia differ with regards to disynaptic reciprocal inhibition between ankle flexor and extensor muscles.
Topics: Adult; Ankle Joint; Electromyography; Glycine; H-Reflex; Humans; Middle Aged; Movement Disorders; Mu | 2001 |