glycine has been researched along with Amyloid Neuropathies, Familial in 11 studies
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 | 9 (81.82) | 29.6817 |
| 2010's | 2 (18.18) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Schänzer, A | 1 |
| Kimmich, C | 1 |
| Röcken, C | 1 |
| Haverkamp, T | 1 |
| Weidner, I | 1 |
| Acker, T | 1 |
| Krämer, HH | 1 |
| Roe, RH | 2 |
| Cunningham, ET | 2 |
| Hammarström, P | 1 |
| Sekijima, Y | 1 |
| White, JT | 1 |
| Wiseman, RL | 1 |
| Lim, A | 1 |
| Costello, CE | 1 |
| Altland, K | 1 |
| Garzuly, F | 1 |
| Budka, H | 1 |
| Kelly, JW | 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 |
| Haagsma, EB | 1 |
| Hawkins, PN | 1 |
| Benson, MD | 1 |
| Lachmann, HJ | 1 |
| Bybee, A | 1 |
| Hazenberg, BP | 1 |
| Kim, HS | 1 |
| Kim, SM | 1 |
| Kang, SW | 1 |
| Jung, SC | 1 |
| Lee, KS | 1 |
| Kim, TS | 1 |
| Choi, YC | 1 |
| Rosenzweig, M | 1 |
| Skinner, M | 1 |
| Prokaeva, T | 1 |
| Théberge, R | 1 |
| Costello, C | 1 |
| Drachman, BM | 1 |
| Connors, LH | 1 |
| O'Hearn, TM | 1 |
| Fawzi, A | 1 |
| He, S | 1 |
| Rao, NA | 1 |
| Lim, JI | 1 |
| Kansoul, HA | 1 |
| Axelsson, R | 1 |
| Yamamoto, S | 1 |
| Savicheva, I | 1 |
| Aspelin, P | 1 |
| Ericzon, BG | 1 |
| Gjertsen, H | 1 |
| Fisher, Y | 1 |
| Eagle, RC | 1 |
| Fine, HF | 1 |
| Pelo, E | 1 |
| Da Prato, L | 1 |
| Ciaccheri, M | 1 |
| Castelli, G | 1 |
| Gori, F | 1 |
| Pizzi, A | 1 |
| Torricelli, F | 1 |
| Marconi, G | 1 |
11 other studies available for glycine and Amyloid Neuropathies, Familial
| Article | Year |
|---|---|
A woman with a rare p.Glu74Gly transthyretin mutation presenting exclusively with a rapidly progressive neuropathy: a case report.
Topics: Adult; Amyloid Neuropathies, Familial; Benzoxazoles; Disease Progression; Fatal Outcome; Female; Gen | 2014 |
Considering amyloidosis in patients with clinically unresponsive vitreous inflammation (Oculoleptomeningeal amyloidosis in 3 individuals with transthyretin variant Tyr69His. Vol. 44[3]).
Topics: Adrenal Cortex Hormones; Amyloid Neuropathies, Familial; Drug Resistance; Eye Diseases; Genetic Vari | 2010 |
D18G transthyretin is monomeric, aggregation prone, and not detectable in plasma and cerebrospinal fluid: a prescription for central nervous system amyloidosis?
Topics: Amino Acid Sequence; Amyloid Neuropathies, Familial; Aspartic Acid; Blood-Brain Barrier; Central Ner | 2003 |
Outcome of liver transplantation for familial amyloidotic polyneuropathy.
Topics: Adult; Alanine; Amyloid Neuropathies, Familial; Diarrhea; Female; Glycine; Humans; Liver Transplanta | 2003 |
Familial amyloidotic polyneuropathy with severe renal involvement in association with transthyretin Gly47Glu in Dutch, British and American-Finnish families.
Topics: Aged; Amino Acid Substitution; Amyloid Neuropathies, Familial; Family; Female; Glutamic Acid; Glycin | 2004 |
An aggressive form of familial amyloid polyneuropathy caused by a Glu54Gly mutation in the transthyretin gene.
Topics: Amyloid Neuropathies, Familial; DNA Mutational Analysis; Family Health; Female; Glutamic Acid; Glyci | 2005 |
A new transthyretin variant (Glu61Gly) associated with cardiomyopathy.
Topics: Amino Acid Substitution; Amyloid Neuropathies, Familial; Base Sequence; Cardiomyopathies; DNA Mutati | 2007 |
Early onset vitreous amyloidosis in familial amyloidotic polyneuropathy with a transthyretin Glu54Gly mutation is associated with elevated vitreous VEGF.
Topics: Adult; Age of Onset; Amyloid Neuropathies, Familial; Asian People; Eye Diseases, Hereditary; Fluores | 2007 |
Parameters obtained by hepatobiliary scintigraphy have significant correlation with biochemical factors early after liver transplantation.
Topics: Adolescent; Adult; Aged; Alanine Transaminase; Amyloid Neuropathies, Familial; Aniline Compounds; As | 2007 |
Oculoleptomeningeal amyloidosis in a patient with a TTR Val30Gly mutation in the transthyretin gene.
Topics: Adult; Amyloid; Amyloid Neuropathies, Familial; DNA Mutational Analysis; Eye Diseases; Glycine; Huma | 2007 |
Familial amyloid polyneuropathy with genetic anticipation associated to a gly47glu transthyretin variant in an Italian kindred.
Topics: Adult; Amino Acid Sequence; Amyloid Neuropathies, Familial; Base Sequence; DNA; Female; Glutamic Aci | 2002 |