Page last updated: 2024-11-08

alanine and Amyloid Neuropathies

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)

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (11.11)18.2507
2000's6 (66.67)29.6817
2010's2 (22.22)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Yang, NC1
Lee, MJ1
Chao, CC1
Chuang, YT1
Lin, WM1
Chang, MF1
Hsieh, PC1
Kan, HW1
Lin, YH1
Yang, CC1
Chiu, MJ1
Liou, HH1
Hsieh, ST2
Magy, N1
Valleix, S1
Grateau, G1
Algros, MP1
Guillemain, R1
Kantelip, B1
Delpech, M1
Dupond, JL1
Mak, CM1
Lam, CW1
Fan, ST1
Liu, CL1
Tam, SC1
Yazaki, M1
Liepnieks, JJ1
Kincaid, JC1
Benson, MD1
Shimizu, Y1
Takeuchi, M1
Matsumura, M1
Tokuda, T1
Iwata, M1
Misrahi, AM1
Plante, V1
Lalu, T1
Serre, L1
Adams, D1
Lacroix, DC1
Saïd, G1
Lachmann, HJ1
Booth, DR1
Bybee, A1
Hawkins, PN1
Ramirez, P1
De Mingo, P1
Andreu, F1
Munar, M1
Hernández, Q1
Munítiz, V1
Robles, R1
Sanchez-Bueno, F1
Parrilla, P1

Reviews

1 review available for alanine and Amyloid Neuropathies

ArticleYear
Amyloid neuropathy with transthyretin mutations: overview and unique Ala97Ser in Taiwan.
    Acta neurologica Taiwanica, 2011, Volume: 20, Issue:2

    Topics: Age of Onset; Alanine; Amyloid Neuropathies; Female; Genetic Predisposition to Disease; Humans; Male

2011

Other Studies

8 other studies available for alanine and Amyloid Neuropathies

ArticleYear
Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser.
    Neurology, 2010, Aug-10, Volume: 75, Issue:6

    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.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2002, Volume: 9, Issue:4

    Topics: Adult; Alanine; Amyloid Neuropathies; Amyloidosis, Familial; Female; France; Glycine; Humans; Male;

2002
Genetics of familial amyloidotic polyneuropathy in a Hong Kong Chinese kindred.
    Acta neurologica Scandinavica, 2003, Volume: 107, Issue:6

    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.
    Muscle & nerve, 2003, Volume: 28, Issue:4

    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.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2006, Volume: 13, Issue:1

    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.
    Human mutation, 1998, Volume: 12, Issue:1

    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.
    Human mutation, 2000, Volume: 16, Issue:2

    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.
    Transplant international : official journal of the European Society for Organ Transplantation, 2000, Volume: 13 Suppl 1

    Topics: Adult; Alanine; Amyloid Neuropathies; Follow-Up Studies; Genetic Variation; Humans; Liver Transplant

2000