arginine has been researched along with CADASIL in 14 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 6 (42.86) | 29.6817 |
| 2010's | 8 (57.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, S; Li, HF; Liu, HQ; Lu, C; Ni, W; Wang, N; Wu, L; Wu, ZY; Xu, YF; Yin, XZ; Zhang, L; Zhao, GX; Zheng, QJ | 1 |
| Ando, Y; Itoh, K; Kushimura, Y; Mizuno, T; Mizuta, I; Mukai, M; Nakashima, D; Noto, YI; Ohara, T; Ueda, A | 1 |
| Bermejo-Velasco, P; Calero, M; Serrano-Heranz, R; Zea-Sevilla, MA | 1 |
| Berbellini, A; Cozzolino, V; De Michele, G; Gobbato, R; Manca, A; Paci, C; Peluso, S; Pianese, L; Ragno, M; Sanguigni, S | 1 |
| Karlsson, WK; Kruuse, C; Sørensen, CG | 1 |
| Dichgans, M; Freilinger, T; Opherk, C; Peters, N; Pfefferkorn, T | 2 |
| Auteri, A; Blardi, P; Cevenini, G; De Lalla, A; De Stefano, N; Dotti, MT; Federico, A; Rufa, A; Zicari, E | 1 |
| Callaerts-Vegh, Z; Carmeliet, P; Collen, D; D'Hooge, R; Dewerchin, M; Lupu, F; Moons, L; Nuyens, D; Silasi-Mansat, R; Souffreau, J; Van Nuffelen, A; Wallays, G | 1 |
| Cacchiò, G; Caiazzo, AR; Di Marzio, F; Manca, A; Mirabella, M; Pianese, L; Ragno, M; Scarcella, M; Silvaggio, F; Silvestri, S; Tasca, G; Trojano, L | 1 |
| Mizuno, T; Nakagawa, M; Tanaka, M; Watanabe, Y; Watanabe-Hosomi, A | 1 |
| Juvonen, V; Kalimo, H; Lundkvist, J; Mykkänen, K; Penttinen, M; Pöyhönen, M; Savontaus, ML; Sistonen, P; Tuisku, S; Tuominen, S; Viitanen, M | 1 |
| Cacchiò, G; Fabrizi, GM; Ferrarini, M; Ragno, M; Scarcella, M; Selvaggio, F; Sirocchi, G; Taioli, F; Trojano, L | 1 |
| Babinet, C; Cohen-Tannoudji, M; Domenga, V; Gridley, T; Joutel, A; Langa, F; Lemaire, B; Monet, M; Souilhol, C; Tournier-Lasserve, E | 1 |
1 review(s) available for arginine and CADASIL
| Article | Year |
|---|---|
l-arginine and l-NMMA for assessing cerebral endothelial dysfunction in ischaemic cerebrovascular disease: A systematic review.
Topics: Arginine; CADASIL; Cerebrovascular Disorders; Clinical Trials as Topic; Endothelium, Vascular; Humans; omega-N-Methylarginine; Vasodilation | 2017 |
1 trial(s) available for arginine and CADASIL
| Article | Year |
|---|---|
Enhanced L-arginine-induced vasoreactivity suggests endothelial dysfunction in CADASIL.
Topics: Adult; Arginine; Blood Flow Velocity; Blood Pressure; CADASIL; Cerebrovascular Circulation; Endothelium; Female; Heart Rate; Humans; Male; Middle Aged; Middle Cerebral Artery; Receptor, Notch3; Receptors, Notch; Severity of Illness Index; Ultrasonography, Doppler, Transcranial; Vascular Diseases | 2008 |
12 other study(ies) available for arginine and CADASIL
| Article | Year |
|---|---|
Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective study.
Topics: Adult; Age of Onset; Arginine; Asian People; CADASIL; Cysteine; Exons; Female; Genetic Association Studies; Haplotypes; HEK293 Cells; Humans; Male; Middle Aged; Mutation; Receptor, Notch3; Retrospective Studies; Transfection | 2017 |
A Japanese CADASIL patient with homozygous NOTCH3 p.Arg544Cys mutation confirmed pathologically.
Topics: Arginine; Asian People; CADASIL; Cysteine; Humans; Magnetic Resonance Imaging; Male; Microscopy, Electron, Scanning; Middle Aged; Mutation; Receptor, Notch3; Skin | 2018 |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) associated with a novel C82R mutation in the NOTCH3 gene.
Topics: Aged; Arginine; Brain; CADASIL; Cysteine; Family Health; Female; Genetic Association Studies; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Receptor, Notch3; Receptors, Notch | 2015 |
Parkinsonism in a pair of monozygotic CADASIL twins sharing the R1006C mutation: a transcranial sonography study.
Topics: Aged; Arginine; CADASIL; Cysteine; Humans; Male; Mutation; Parkinson Disease; Receptor, Notch3; Twins, Monozygotic; Ultrasonography, Doppler, Transcranial | 2016 |
Plasma levels of asymmetric dimethylarginine in cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathy.
Topics: Adult; Antihypertensive Agents; Arginine; Biomarkers; Brain; CADASIL; Chromatography, High Pressure Liquid; Endothelium, Vascular; Female; Humans; Hypertension; Lipids; Magnetic Resonance Imaging; Male; Middle Aged; Receptor, Notch3; Receptors, Notch; Risk Factors | 2008 |
Notch3 Arg170Cys knock-in mice display pathologic and clinical features of the neurovascular disorder cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Topics: Animals; Arginine; Brain; CADASIL; Capillaries; Cystine; Disease Models, Animal; Fertility; Gene Knock-In Techniques; Mice; Motor Activity; Muscle, Smooth, Vascular; Mutation; Receptor, Notch3; Receptors, Notch | 2011 |
Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation.
Topics: Adult; Aged; Aged, 80 and over; Arginine; CADASIL; Cardiovascular Abnormalities; Cholesterol; Creatine Kinase; Cysteine; Disease Progression; Electromyography; Family Health; Female; Gene Frequency; Genotype; Humans; Italy; Magnetic Resonance Imaging; Male; Middle Aged; Muscle, Skeletal; Mutation; Neural Conduction; Neurophysiology; Neuropsychological Tests; Phenotype; Receptor, Notch3; Receptors, Notch; Tomography, X-Ray Computed | 2012 |
Transendocytosis is impaired in CADASIL-mutant NOTCH3.
Topics: Analysis of Variance; Arginine; Biotinylation; CADASIL; Calcium-Binding Proteins; Cell Line, Transformed; Coculture Techniques; Cysteine; Endocytosis; Gene Expression Regulation; Green Fluorescent Proteins; Humans; Intercellular Signaling Peptides and Proteins; Jagged-1 Protein; Ligands; Membrane Proteins; Mutation; Protein Transport; Receptor, Notch3; Receptors, Notch; Serrate-Jagged Proteins; Transfection | 2012 |
Detection of the founder effect in Finnish CADASIL families.
Topics: Amino Acid Substitution; Arginine; CADASIL; Chromosomes, Human, Pair 19; Cysteine; Female; Finland; Founder Effect; Gene Frequency; Haplotypes; Humans; Male; Microsatellite Repeats; Pedigree; Point Mutation; Proto-Oncogene Proteins; Receptor, Notch3; Receptors, Cell Surface; Receptors, Notch | 2004 |
Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene.
Topics: Aged; Arginine; CADASIL; Cysteine; DNA Mutational Analysis; Exons; Family Health; Female; Humans; Italy; Male; Middle Aged; Mutation; Neuropsychological Tests; Receptor, Notch3; Receptors, Notch | 2006 |
The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivo.
Topics: Aging; Animals; Arginine; CADASIL; Cerebral Arteries; Cysteine; Immunoglobulin J Recombination Signal Sequence-Binding Protein; Intracranial Arterial Diseases; Lac Operon; Mice; Mice, Knockout; Mutant Proteins; Mutation, Missense; Protein Structure, Tertiary; Receptor, Notch3; Receptors, Notch; Transgenes | 2007 |
Effects of short term atorvastatin treatment on cerebral hemodynamics in CADASIL.
Topics: Adult; Arginine; Atorvastatin; CADASIL; Carbon Dioxide; Cerebral Arteries; Cerebrovascular Circulation; Cohort Studies; Dose-Response Relationship, Drug; Drug Administration Schedule; Female; Heptanoic Acids; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hypercapnia; Hypoxia-Ischemia, Brain; Male; Middle Aged; Middle Cerebral Artery; Nitric Oxide; Pyrroles; Treatment Outcome; Ultrasonography, Doppler, Transcranial; Vasodilation | 2007 |