glycine has been researched along with Demyelinating Diseases in 3 studies
Demyelinating Diseases: Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ammar, N | 1 |
| Nelis, E | 1 |
| Merlini, L | 1 |
| Barisić, N | 1 |
| Amouri, R | 1 |
| Ceuterick, C | 1 |
| Martin, JJ | 1 |
| Timmerman, V | 1 |
| Hentati, F | 1 |
| De Jonghe, P | 1 |
| Shuman, RM | 1 |
| Leech, RW | 1 |
| Scott, CR | 1 |
| Kolkmann, W | 1 |
3 other studies available for glycine and Demyelinating Diseases
| Article | Year |
|---|---|
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease.
Topics: Alleles; Arginine; Charcot-Marie-Tooth Disease; Cysteine; Demyelinating Diseases; DNA Mutational Ana | 2003 |
The neuropathology of the nonketotic and ketotic hyperglycinemias: three cases.
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Corpus Callosum; Demyelinating Diseases; Fem | 1978 |
[Findings concerning the glia in diffuse and focally disseminated types of infantile spongy neurodystrophy].
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases; Demyelinating Diseases; Glycine; Humans; Infan | 1968 |