alanine has been researched along with Amyloid Neuropathies in 9 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
Amyloid Neuropathies: Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (11.11) | 18.2507 |
2000's | 6 (66.67) | 29.6817 |
2010's | 2 (22.22) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Yang, NC | 1 |
Lee, MJ | 1 |
Chao, CC | 1 |
Chuang, YT | 1 |
Lin, WM | 1 |
Chang, MF | 1 |
Hsieh, PC | 1 |
Kan, HW | 1 |
Lin, YH | 1 |
Yang, CC | 1 |
Chiu, MJ | 1 |
Liou, HH | 1 |
Hsieh, ST | 2 |
Magy, N | 1 |
Valleix, S | 1 |
Grateau, G | 1 |
Algros, MP | 1 |
Guillemain, R | 1 |
Kantelip, B | 1 |
Delpech, M | 1 |
Dupond, JL | 1 |
Mak, CM | 1 |
Lam, CW | 1 |
Fan, ST | 1 |
Liu, CL | 1 |
Tam, SC | 1 |
Yazaki, M | 1 |
Liepnieks, JJ | 1 |
Kincaid, JC | 1 |
Benson, MD | 1 |
Shimizu, Y | 1 |
Takeuchi, M | 1 |
Matsumura, M | 1 |
Tokuda, T | 1 |
Iwata, M | 1 |
Misrahi, AM | 1 |
Plante, V | 1 |
Lalu, T | 1 |
Serre, L | 1 |
Adams, D | 1 |
Lacroix, DC | 1 |
Saïd, G | 1 |
Lachmann, HJ | 1 |
Booth, DR | 1 |
Bybee, A | 1 |
Hawkins, PN | 1 |
Ramirez, P | 1 |
De Mingo, P | 1 |
Andreu, F | 1 |
Munar, M | 1 |
Hernández, Q | 1 |
Munítiz, V | 1 |
Robles, R | 1 |
Sanchez-Bueno, F | 1 |
Parrilla, P | 1 |
1 review available for alanine and Amyloid Neuropathies
Article | Year |
---|---|
Amyloid neuropathy with transthyretin mutations: overview and unique Ala97Ser in Taiwan.
Topics: Age of Onset; Alanine; Amyloid Neuropathies; Female; Genetic Predisposition to Disease; Humans; Male | 2011 |
8 other studies available for alanine and Amyloid Neuropathies
Article | Year |
---|---|
Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser.
Topics: Aged; Alanine; Amino Acid Substitution; Amyloid Neuropathies; Amyloid Neuropathies, Familial; Female | 2010 |
Transthyretin mutation (TTRGly47Ala) associated with familial amyloid polyneuropathy in a French family.
Topics: Adult; Alanine; Amyloid Neuropathies; Amyloidosis, Familial; Female; France; Glycine; Humans; Male; | 2002 |
Genetics of familial amyloidotic polyneuropathy in a Hong Kong Chinese kindred.
Topics: Adult; Alanine; Amyloid Neuropathies; Asian People; Female; Hong Kong; Humans; Mutation; Pedigree; P | 2003 |
Contribution of wild-type transthyretin to hereditary peripheral nerve amyloid.
Topics: Alanine; Amyloid; Amyloid Neuropathies; Blotting, Western; Dimerization; Electrophoresis, Polyacryla | 2003 |
A case of biopsy-proven leptomeningeal amyloidosis and intravenous Ig-responsive polyneuropathy associated with the Ala25Thr transthyretin gene mutation.
Topics: Alanine; Amino Acid Substitution; Amyloid Neuropathies; Amyloidosis; Brain; Brain Stem; Cerebellum; | 2006 |
New transthyretin variants SER 91 and SER 116 associated with familial amyloidotic polyneuropathy. Mutations in brief no. 151. Online.
Topics: Aged; Alanine; Amyloid Neuropathies; Humans; Male; Mutation; Prealbumin; Protein Isoforms; Serine; T | 1998 |
Transthyretin Ala97Ser is associated with familial amyloidotic polyneuropathy in a Chinese-Taiwanese family.
Topics: Alanine; Amino Acid Substitution; Amyloid Neuropathies; Codon, Nonsense; Humans; Male; Middle Aged; | 2000 |
Long-term results of liver transplantation in four siblings from the same family with familial amyloidotic polyneuropathy type I TTR Ala-71.
Topics: Adult; Alanine; Amyloid Neuropathies; Follow-Up Studies; Genetic Variation; Humans; Liver Transplant | 2000 |