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First breeding record of the Daurian Redstart at Zao Onsen, Yamagata Prefecture, Japan.
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- Bird Research, 2022, v. 18, p. S5
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- Article
Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy.
- Published in:
- 2018
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- Publication type:
- journal article
The application of shotgun metagenomics to the diagnosis of granulomatous amoebic encephalitis due to Balamuthia mandrillaris: a case report.
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- 2021
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- Publication type:
- journal article
Prevalence of Fragile X-Associated Tremor/Ataxia Syndrome in Patients with Cerebellar Ataxia in Japan.
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- Cerebellum, 2022, v. 21, n. 5, p. 851, doi. 10.1007/s12311-021-01323-x
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- Publication type:
- Article
An MFN2-related Charcot-Marie-Tooth Disease Patient with Optic Nerve Atrophy, Neurogenic Bladder Dysfunction, and Diaphragmatic Weakness.
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- Internal Medicine, 2022, v. 61, n. 11, p. 1743, doi. 10.2169/internalmedicine.6487-20
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- Article
HYPERINSULINAEMIA INCREASES THE GENE EXPRESSION OF ENDOTHELIAL NITRIC OXIDE SYNTHASE AND THE PHOSPHATIDYLINOSITOL 3-KINASE/AKT PATHWAY IN RAT AORTA.
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- Clinical & Experimental Pharmacology & Physiology, 2006, v. 33, n. 5/6, p. 440, doi. 10.1111/j.1440-1681.2006.04385.x
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- Article
Muscle pathology of hereditary motor and sensory neuropathy with proximal dominant involvement with TFG mutation.
- Published in:
- 2019
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- Publication type:
- journal article
Calcium Channel Blockers Reduce Angiotensin II-Induced Superoxide Generation and Inhibit Lectin-Like Oxidized Low-Density Lipoprotein Receptor-1 Expression in Endothelial Cells.
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- Hypertension Research, 2006, v. 29, n. 2, p. 105, doi. 10.1291/hypres.29.105
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- Publication type:
- Article
Calcium Channel Blockades Exhibit Anti-Inflammatory and Antioxidative Effects by Augmentation of Endothelial Nitric Oxide Synthase and the Inhibition of Angiotensin Converting Enzyme in the N<sup>G</sup>-Nitro-L-Arginine Methyl Ester-Induced Hypertensive Rat Aorta: Vasoprotective Effects beyond the Blood Pressure-Lowering Effects of Amlodipine and Manidipine
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- Hypertension Research, 2005, v. 28, n. 8, p. 689, doi. 10.1291/hypres.28.689
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- Publication type:
- Article
Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP).
- Published in:
- 2015
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- Publication type:
- Case Study
Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP).
- Published in:
- 2015
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- Publication type:
- journal article
Effectiveness of drug safety measures for reducing the incidence of adverse drug reactions: Post-hoc analysis of data from all-case surveillance of iguratimod using generalized estimating equations.
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- PLoS ONE, 2021, v. 16, n. 7, p. 1, doi. 10.1371/journal.pone.0253513
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- Publication type:
- Article
Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications.
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- Acta Neuropathologica Communications, 2024, v. 12, n. 1, p. 1, doi. 10.1186/s40478-024-01847-3
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- Publication type:
- Article
Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications.
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- Acta Neuropathologica Communications, 2023, v. 12, n. 1, p. 1, doi. 10.1186/s40478-024-01847-3
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- Publication type:
- Article
Recurrence of Left Ventricular Outflow Tract Obstruction Requiring Alcohol Septal Ablation after Transcatheter Aortic Valve Implantation.
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- Case Reports in Cardiology, 2018, p. 1, doi. 10.1155/2018/5026190
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- Publication type:
- Article
Modeling the spread of pine wilt disease caused by nematodes with pine sawyers as vector.
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- Ecology, 1999, v. 80, n. 5, p. 1691, doi. 10.1890/0012-9658(1999)080[1691:MTSOPW]2.0.CO;2
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- Publication type:
- Article
Peripheral neuropathy in a case with CADASIL: a case report.
- Published in:
- 2018
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- Publication type:
- journal article
Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan.
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- Annals of Clinical & Translational Neurology, 2024, v. 11, n. 1, p. 96, doi. 10.1002/acn3.51936
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- Publication type:
- Article
Novel heterozygous variants of SLC12A6 in Japanese families with Charcot–Marie–Tooth disease.
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- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 7, p. 902, doi. 10.1002/acn3.51603
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- Publication type:
- Article
Novel de novo POLR3B mutations responsible for demyelinating Charcot–Marie–Tooth disease in Japan.
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- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 5, p. 747, doi. 10.1002/acn3.51555
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- Publication type:
- Article
Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation.
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- Frontiers in Neurology, 2023, p. 01, doi. 10.3389/fneur.2023.1241678
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- Publication type:
- Article
Gene panel analysis of 119 index patients with suspected periodic paralysis in Japan.
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- Frontiers in Neurology, 2023, v. 14, p. 01, doi. 10.3389/fneur.2023.1078195
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- Publication type:
- Article
Multi-type RFC1 repeat expansions as the most common cause of hereditary sensory and autonomic neuropathy.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.986504
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- Publication type:
- Article
Genetic and clinical features of cerebellar ataxia with RFC1 biallelic repeat expansions in Japan.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.952493
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- Article
Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan.
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- Clinical Genetics, 2021, v. 99, n. 3, p. 359, doi. 10.1111/cge.13881
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- Publication type:
- Article
Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2.
- Published in:
- 2016
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- Publication type:
- journal article
Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum.
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- Journal of Neurology, 2024, v. 271, n. 1, p. 419, doi. 10.1007/s00415-023-11998-3
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- Publication type:
- Article
Genetic spectrum and founder effect of non-dystrophic myotonia: a Japanese case series study.
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- Journal of Neurology, 2022, v. 269, n. 12, p. 6406, doi. 10.1007/s00415-022-11305-6
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- Publication type:
- Article
Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes.
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- Journal of Neurology, 2022, v. 269, n. 8, p. 4129, doi. 10.1007/s00415-022-11026-w
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- Publication type:
- Article
Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible.
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- Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071546
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- Article
Pulmonary Hypertension in Rats 2.
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- International Archives of Allergy & Immunology, 1995, v. 108, n. 3, p. 287, doi. 10.1159/000237166
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- Article
Pulmonary Hypertension in Rats 1.
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- International Archives of Allergy & Immunology, 1995, v. 108, n. 3, p. 281, doi. 10.1159/000237165
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- Publication type:
- Article
Factors influencing physician decisions to discontinue treatment after onset of liver dysfunction: Post-hoc analysis of an all-case post-marketing surveillance study of iguratimod.
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- Modern Rheumatology, 2020, v. 30, n. 4, p. 633, doi. 10.1080/14397595.2019.1649229
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- Publication type:
- Article
Investigation of the predictors of the response to Iguratimod therapy: A post-hoc analysis of post-marketing surveillance study.
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- Modern Rheumatology, 2020, v. 30, n. 4, p. 626, doi. 10.1080/14397595.2019.1649110
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- Publication type:
- Article
Geographic characteristics of HTLV-1 molecular subgroups and genetic substitutions in East Asia: Insights from complete genome sequencing of HTLV-1 strains isolated in Taiwan and Japan.
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- PLoS Neglected Tropical Diseases, 2024, v. 18, n. 2, p. 1, doi. 10.1371/journal.pntd.0011928
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- Publication type:
- Article
A novel homozygous HPDL variant in Japanese siblings with autosomal recessive hereditary spastic paraplegia: case report and literature review.
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- Neurogenetics, 2024, v. 25, n. 2, p. 149, doi. 10.1007/s10048-024-00746-y
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- Publication type:
- Article
Late-onset Charcot-Marie-Tooth disease 4F caused by periaxin gene mutation.
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- Neurogenetics, 2012, v. 13, n. 4, p. 359, doi. 10.1007/s10048-012-0338-5
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- Article
Genetic, electrophysiological, and pathological studies on patients with SCN9A‐related pain disorders.
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- Journal of the Peripheral Nervous System, 2023, v. 28, n. 4, p. 597, doi. 10.1111/jns.12590
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- Article
Clinical features of inherited neuropathy with BSCL2 mutations in Japan.
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- Journal of the Peripheral Nervous System, 2020, v. 25, n. 2, p. 125, doi. 10.1111/jns.12369
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- Article
Clinical and genetic features of Charcot‐Marie‐Tooth disease 2F and hereditary motor neuropathy 2B in Japan.
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- Journal of the Peripheral Nervous System, 2018, v. 23, n. 1, p. 40, doi. 10.1111/jns.12252
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- Publication type:
- Article
Clinical and genetic diversities of Charcot-Marie-Tooth disease with MFN2 mutations in a large case study.
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- Journal of the Peripheral Nervous System, 2017, v. 22, n. 3, p. 191, doi. 10.1111/jns.12228
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- Publication type:
- Article
Neurofilament light mutation causes hereditary motor and sensory neuropathy with pyramidal signs.
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- Journal of the Peripheral Nervous System, 2014, v. 19, n. 4, p. 311, doi. 10.1111/jns.12102
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- Publication type:
- Article
Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IE.
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- Journal of the Peripheral Nervous System, 2013, v. 18, n. 1, p. 89, doi. 10.1111/jns5.12012
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- Publication type:
- Article