glycine has been researched along with Amyloid Neuropathies in 4 studies
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 | 2 (50.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Magy, N | 1 |
| Valleix, S | 1 |
| Grateau, G | 1 |
| Algros, MP | 1 |
| Guillemain, R | 1 |
| Kantelip, B | 1 |
| Delpech, M | 1 |
| Dupond, JL | 1 |
| Skare, J | 1 |
| Jones, LA | 1 |
| Myles, N | 1 |
| Kane, K | 1 |
| Milunsky, A | 1 |
| Cohen, A | 1 |
| Skinner, M | 1 |
| Kishikawa, M | 1 |
| Nakanishi, T | 1 |
| Miyazaki, A | 1 |
| Hatanaka, M | 1 |
| Shimizu, A | 1 |
| Tamoto, S | 1 |
| Ohsawa, N | 1 |
| Hayashi, H | 1 |
| Kanai, M | 1 |
| Yamashita, T | 1 |
| Ando, Y | 1 |
| Bernt Suhr, O | 1 |
| Nakamura, M | 1 |
| Sakashita, N | 1 |
| Ohlsson, PI | 1 |
| Terazaki, H | 1 |
| Obayashi, K | 1 |
| Uchino, M | 1 |
| Ando, M | 1 |
4 other studies available for glycine and Amyloid Neuropathies
| Article | Year |
|---|---|
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 |
Two transthyretin mutations (glu42gly, his90asn) in an Italian family with amyloidosis.
Topics: Adult; Amyloid Neuropathies; Asparagine; Base Sequence; DNA Mutational Analysis; Female; Glutamic Ac | 1994 |
A new nonamyloid transthyretin variant, G101S, detected by electrospray ionization/mass spectrometry. Mutations in brief no. 201. Online.
Topics: Aged; Amyloid Neuropathies; Glycine; Humans; Male; Mass Spectrometry; Point Mutation; Prealbumin; Pr | 1998 |
A new diagnostic procedure to detect unknown transthyretin (TTR) mutations in familial amyloidotic polyneuropathy (FAP).
Topics: Amino Acid Substitution; Amyloid; Amyloid Neuropathies; Centrifugation; Coloring Agents; Congo Red; | 2000 |