serine has been researched along with Spastic Paraplegia, Hereditary in 3 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
Spastic Paraplegia, Hereditary: A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64(1):61-6; Curr Opin Neurol 1997 Aug;10(4):313-8)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Svenson, IK | 1 |
| Kloos, MT | 1 |
| Gaskell, PC | 1 |
| Nance, MA | 1 |
| Garbern, JY | 1 |
| Hisanaga, S | 1 |
| Pericak-Vance, MA | 1 |
| Ashley-Koch, AE | 1 |
| Marchuk, DA | 1 |
| McDermott, CJ | 1 |
| Burness, CE | 1 |
| Kirby, J | 1 |
| Cox, LE | 1 |
| Rao, DG | 1 |
| Hewamadduma, C | 1 |
| Sharrack, B | 1 |
| Hadjivassiliou, M | 1 |
| Chinnery, PF | 1 |
| Dalton, A | 1 |
| Shaw, PJ | 1 |
| Cho, HJ | 1 |
| Sung, DH | 1 |
| Ki, CS | 1 |
3 other studies available for serine and Spastic Paraplegia, Hereditary
| Article | Year |
|---|---|
Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations.
Topics: Adenosine Triphosphatases; Adolescent; Alternative Splicing; CDC2 Protein Kinase; Child; Child, Pres | 2004 |
Clinical features of hereditary spastic paraplegia due to spastin mutation.
Topics: Adenosine Triphosphatases; Adult; Aged; Cohort Studies; DNA Mutational Analysis; Exons; Female; Gene | 2006 |
Identification of de novo BSCL2 Ser90Leu mutation in a Korean family with Silver syndrome and distal hereditary motor neuropathy.
Topics: Adolescent; Adult; Amino Acid Substitution; DNA Mutational Analysis; Female; GTP-Binding Protein gam | 2007 |