glycine has been researched along with Pantothenate Kinase-Associated Neurodegeneration in 2 studies
Pantothenate Kinase-Associated Neurodegeneration: A rare autosomal recessive degenerative disorder which usually presents in late childhood or adolescence. Clinical manifestations include progressive MUSCLE SPASTICITY; hyperreflexia; MUSCLE RIGIDITY; DYSTONIA; DYSARTHRIA; and intellectual deterioration which progresses to severe dementia over several years. (From Adams et al., Principles of Neurology, 6th ed, p972; Davis & Robertson, Textbook of Neuropathology, 2nd ed, pp972-929)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Zhang, YH | 1 |
Tang, BS | 1 |
Zhao, AL | 1 |
Xia, K | 1 |
Long, ZG | 1 |
Guo, JF | 1 |
Westaway, SK | 1 |
Hayflick, SJ | 1 |
Kazek, B | 1 |
Jamroz, E | 1 |
Gencik, M | 1 |
Jezela Stanek, A | 1 |
Marszal, E | 1 |
Wojaczynska-Stanek, K | 1 |
2 other studies available for glycine and Pantothenate Kinase-Associated Neurodegeneration
Article | Year |
---|---|
Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration.
Topics: Adult; Asian People; Asparagine; Aspartic Acid; DNA Mutational Analysis; Exons; Glycine; Heterozygot | 2005 |
A novel PANK2 gene mutation: clinical and molecular characteristics of patients short communication.
Topics: Adolescent; Arginine; Child; Glycine; Humans; Male; Mutation; Pantothenate Kinase-Associated Neurode | 2007 |