alanine has been researched along with Amyloid Neuropathies, Familial in 7 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, Familial: Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 4 (57.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Muller, KR | 1 |
| Padbury, R | 1 |
| Jeffrey, GP | 1 |
| Poplawski, NK | 1 |
| Thompson, P | 1 |
| Tonkin, A | 1 |
| Harley, HA | 1 |
| 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 | 2 |
| Chiu, MJ | 1 |
| Liou, HH | 1 |
| Hsieh, ST | 1 |
| Liu, JY | 2 |
| Guo, YJ | 2 |
| Zhou, CK | 1 |
| Ye, YQ | 1 |
| Feng, JQ | 1 |
| Yin, F | 1 |
| Jiang, XM | 2 |
| Zhang, M | 1 |
| Sharma, P | 1 |
| Perri, RE | 1 |
| Sirven, JE | 1 |
| Zeldenrust, SR | 1 |
| Brandhagen, DJ | 1 |
| Rosen, CB | 1 |
| Douglas, DD | 1 |
| Mulligan, DC | 1 |
| Rakela, J | 1 |
| Wiesner, RH | 1 |
| Balan, V | 1 |
| Liu, YT | 1 |
| Lee, YC | 1 |
| Chen, ML | 1 |
| Lin, KP | 1 |
| Kotani, N | 1 |
| Hattori, T | 1 |
| Yamagata, S | 1 |
| Tokuda, T | 1 |
| Shirasawa, A | 1 |
| Yamaguchi, S | 1 |
| Kobayashi, S | 1 |
| Ikeda, S | 1 |
7 other studies available for alanine and Amyloid Neuropathies, Familial
| Article | Year |
|---|---|
Poor outcome after liver transplantation for transthyretin amyloid neuropathy in a family with an Ala36Pro transthyretin mutation: case report.
Topics: Adult; Alanine; Amyloid Neuropathies, Familial; Family Health; Fatal Outcome; Female; Genotype; Huma | 2010 |
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 |
Clinical and histopathological features of familial amyloidotic polyneuropathy with transthyretin Val30Ala in a Chinese family.
Topics: Adult; Alanine; Amyloid Neuropathies, Familial; Asian People; Fatal Outcome; Female; Humans; Male; P | 2011 |
Analysis of mitochondrial haplogroups associated with TTR Val30Ala familial amyloidotic polyneuropathy in Chinese patients.
Topics: Adult; Age of Onset; Aged; Alanine; Amyloid Neuropathies, Familial; Asian People; DNA, Mitochondrial | 2012 |
Outcome of liver transplantation for familial amyloidotic polyneuropathy.
Topics: Adult; Alanine; Amyloid Neuropathies, Familial; Diarrhea; Female; Glycine; Humans; Liver Transplanta | 2003 |
Transthyretin Ala97Ser in Chinese-Taiwanese patients with familial amyloid polyneuropathy: genetic studies and phenotype expression.
Topics: Aged; Alanine; Amino Acid Substitution; Amyloid Neuropathies, Familial; Asian People; Axons; DNA Mut | 2008 |
Transthyretin Thr60Ala Appalachian-type mutation in a Japanese family with familial amyloidotic polyneuropathy.
Topics: Aged; Alanine; Amino Acid Sequence; Amyloid Neuropathies, Familial; Base Sequence; DNA; Female; Huma | 2002 |