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.
Excerpt | Relevance | Reference |
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"In addition, genetic analysis for Dravet syndrome showed the presence of heterozygous disease-causing mutation SCN1A NM_001165963." | 1.42 | NMR-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." | 1.42 | Fibrillin-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) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (75.00) | 24.3611 |
2020's | 1 (25.00) | 2.80 |
Authors | Studies |
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Dobritzsch, D | 1 |
Meijer, J | 1 |
Meinsma, R | 1 |
Maurer, D | 1 |
Monavari, AA | 1 |
Gummesson, A | 1 |
Reims, A | 1 |
Cayuela, JA | 1 |
Kuklina, N | 1 |
Benoist, JF | 1 |
Perrin, L | 1 |
Assmann, B | 1 |
Hoffmann, GF | 1 |
Bierau, J | 1 |
Kaindl, AM | 1 |
van Kuilenburg, ABP | 1 |
Fang, Y | 1 |
Cai, C | 1 |
Wang, C | 1 |
Sun, B | 1 |
Zhang, X | 1 |
Fan, W | 1 |
Hu, W | 1 |
Meng, Y | 1 |
Lin, S | 1 |
Zhang, C | 1 |
Zhang, Y | 1 |
Shu, J | 1 |
Lam, CW | 1 |
Law, CY | 1 |
Leung, KF | 1 |
Lai, CK | 1 |
Pak-lam Chen, S | 1 |
Chan, B | 1 |
Chan, KY | 1 |
Yuen, YP | 1 |
Mak, CM | 1 |
Yan-wo Chan, A | 1 |
Van der Donckt, C | 1 |
Roth, L | 1 |
Vanhoutte, G | 1 |
Blockx, I | 1 |
Bink, DI | 1 |
Ritz, K | 1 |
Pintelon, I | 1 |
Timmermans, JP | 1 |
Bauters, D | 1 |
Martinet, W | 1 |
Daemen, MJ | 1 |
Verhoye, M | 1 |
De Meyer, GR | 1 |
4 other studies available for beta-alanine and Brain Diseases
Article | Year |
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β-Ureidopropionase deficiency due to novel and rare UPB1 mutations affecting pre-mRNA splicing and protein structural integrity and catalytic activity.
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.
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.
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.
Topics: Acrylamides; Animals; Apolipoproteins E; beta-Alanine; Blood-Brain Barrier; Brain; Brain Diseases; C | 2015 |