Page last updated: 2024-10-16

beta-alanine and Brain Diseases

beta-alanine has been researched along with Brain Diseases in 4 studies

Brain Diseases: Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM.

Research Excerpts

ExcerptRelevanceReference
"In addition, genetic analysis for Dravet syndrome showed the presence of heterozygous disease-causing mutation SCN1A NM_001165963."1.42NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndrome. ( Chan, B; Chan, KY; Lai, CK; Lam, CW; Law, CY; Leung, KF; Mak, CM; Pak-lam Chen, S; Yan-wo Chan, A; Yuen, YP, 2015)
"Xanthomas were mainly located in fibrillin-1-rich regions, such as the choroid plexus and the neocortex."1.42Fibrillin-1 impairment enhances blood-brain barrier permeability and xanthoma formation in brains of apolipoprotein E-deficient mice. ( Bauters, D; Bink, DI; Blockx, I; Daemen, MJ; De Meyer, GR; Martinet, W; Pintelon, I; Ritz, K; Roth, L; Timmermans, JP; Van der Donckt, C; Vanhoutte, G; Verhoye, M, 2015)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (75.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Dobritzsch, D1
Meijer, J1
Meinsma, R1
Maurer, D1
Monavari, AA1
Gummesson, A1
Reims, A1
Cayuela, JA1
Kuklina, N1
Benoist, JF1
Perrin, L1
Assmann, B1
Hoffmann, GF1
Bierau, J1
Kaindl, AM1
van Kuilenburg, ABP1
Fang, Y1
Cai, C1
Wang, C1
Sun, B1
Zhang, X1
Fan, W1
Hu, W1
Meng, Y1
Lin, S1
Zhang, C1
Zhang, Y1
Shu, J1
Lam, CW1
Law, CY1
Leung, KF1
Lai, CK1
Pak-lam Chen, S1
Chan, B1
Chan, KY1
Yuen, YP1
Mak, CM1
Yan-wo Chan, A1
Van der Donckt, C1
Roth, L1
Vanhoutte, G1
Blockx, I1
Bink, DI1
Ritz, K1
Pintelon, I1
Timmermans, JP1
Bauters, D1
Martinet, W1
Daemen, MJ1
Verhoye, M1
De Meyer, GR1

Other Studies

4 other studies available for beta-alanine and Brain Diseases

ArticleYear
β-Ureidopropionase deficiency due to novel and rare UPB1 mutations affecting pre-mRNA splicing and protein structural integrity and catalytic activity.
    Molecular genetics and metabolism, 2022, Volume: 136, Issue:3

    Topics: Abnormalities, Multiple; Amidohydrolases; Animals; beta-Alanine; Brain Diseases; Humans; Mammals; Mo

2022
Clinical and genetic analysis of 7 Chinese patients with β-ureidopropionase deficiency.
    Medicine, 2019, Volume: 98, Issue:1

    Topics: Abnormalities, Multiple; Amidohydrolases; Aminoisobutyric Acids; Asian People; beta-Alanine; Brain D

2019
NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndrome.
    Clinica chimica acta; international journal of clinical chemistry, 2015, Feb-02, Volume: 440

    Topics: Abnormalities, Multiple; Amidohydrolases; beta-Alanine; Brain Diseases; Epilepsies, Myoclonic; Gas C

2015
Fibrillin-1 impairment enhances blood-brain barrier permeability and xanthoma formation in brains of apolipoprotein E-deficient mice.
    Neuroscience, 2015, Jun-04, Volume: 295

    Topics: Acrylamides; Animals; Apolipoproteins E; beta-Alanine; Blood-Brain Barrier; Brain; Brain Diseases; C

2015