Page last updated: 2024-10-15

phosphoserine and Hereditary Sensory and Autonomic Neuropathies

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)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ernst, D1
Murphy, SM1
Sathiyanadan, K1
Wei, Y1
Othman, A1
LaurĂ¡, M1
Liu, YT1
Penno, A1
Blake, J1
Donaghy, M1
Houlden, H1
Reilly, MM1
Hornemann, T1

Other Studies

1 other study available for phosphoserine and Hereditary Sensory and Autonomic Neuropathies

ArticleYear
Novel HSAN1 mutation in serine palmitoyltransferase resides at a putative phosphorylation site that is involved in regulating substrate specificity.
    Neuromolecular medicine, 2015, Volume: 17, Issue:1

    Topics: Aged; Amino Acid Sequence; Amino Acid Substitution; Conserved Sequence; Electrophoresis, Gel, Two-Di

2015