Page last updated: 2024-11-08

aspartic acid and Pantothenate Kinase-Associated Neurodegeneration

aspartic acid has been researched along with Pantothenate Kinase-Associated Neurodegeneration in 3 studies

Aspartic Acid: One of the non-essential amino acids commonly occurring in the L-form. It is found in animals and plants, especially in sugar cane and sugar beets. It may be a neurotransmitter.
aspartic acid : An alpha-amino acid that consists of succinic acid bearing a single alpha-amino substituent
L-aspartic acid : The L-enantiomer of aspartic acid.

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)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Sener, RN1
Zhang, YH1
Tang, BS1
Zhao, AL1
Xia, K1
Long, ZG1
Guo, JF1
Westaway, SK1
Hayflick, SJ1
Kitis, O1
Tekgul, H1
Erdemir, G1
Polat, M1
Serdaroglu, G1
Tosun, A1
Coker, M1
Gokben, S1

Other Studies

3 other studies available for aspartic acid and Pantothenate Kinase-Associated Neurodegeneration

ArticleYear
Pantothenate kinase-associated neurodegeneration: MR imaging, proton MR spectroscopy, and diffusion MR imaging findings.
    AJNR. American journal of neuroradiology, 2003, Volume: 24, Issue:8

    Topics: Adolescent; Aspartic Acid; Brain; Cerebellar Nuclei; Choline; Creatine; Diagnosis, Differential; Dif

2003
Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration.
    Movement disorders : official journal of the Movement Disorder Society, 2005, Volume: 20, Issue:7

    Topics: Adult; Asian People; Asparagine; Aspartic Acid; DNA Mutational Analysis; Exons; Glycine; Heterozygot

2005
Identification of axonal involvement in Hallervorden-Spatz disease with magnetic resonance spectroscopy.
    Journal of neuroradiology = Journal de neuroradiologie, 2006, Volume: 33, Issue:2

    Topics: Aspartic Acid; Axons; Child; Creatinine; Humans; Inositol; Magnetic Resonance Spectroscopy; Male; Pa

2006