phosphoserine has been researched along with Hereditary Sensory and Autonomic Neuropathies in 1 studies
Phosphoserine: The phosphoric acid ester of serine.
Hereditary Sensory and Autonomic Neuropathies: A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ernst, D | 1 |
Murphy, SM | 1 |
Sathiyanadan, K | 1 |
Wei, Y | 1 |
Othman, A | 1 |
LaurĂ¡, M | 1 |
Liu, YT | 1 |
Penno, A | 1 |
Blake, J | 1 |
Donaghy, M | 1 |
Houlden, H | 1 |
Reilly, MM | 1 |
Hornemann, T | 1 |
1 other study available for phosphoserine and Hereditary Sensory and Autonomic Neuropathies
Article | Year |
---|---|
Novel HSAN1 mutation in serine palmitoyltransferase resides at a putative phosphorylation site that is involved in regulating substrate specificity.
Topics: Aged; Amino Acid Sequence; Amino Acid Substitution; Conserved Sequence; Electrophoresis, Gel, Two-Di | 2015 |