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Tolerability and efficacy of switching anti-fibrotic treatment from nintedanib to pirfenidone for idiopathic pulmonary fibrosis.
- Published in:
- PLoS ONE, 2024, v. 19, n. 6, p. 1, doi. 10.1371/journal.pone.0305429
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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.
- Published in:
- Neurogenetics, 2024, v. 25, n. 2, p. 149, doi. 10.1007/s10048-024-00746-y
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- Publication type:
- Article
Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan.
- Published in:
- Annals of Clinical & Translational Neurology, 2024, v. 11, n. 1, p. 96, doi. 10.1002/acn3.51936
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- Publication type:
- Article
Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum.
- Published in:
- 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, 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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- Publication type:
- Article
CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-45011-8
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- Publication type:
- Article
A case of severe paraneoplastic glutamic acid decarboxylase antibody‐spectrum disorder with improvement through prior immunotherapy before surgical intervention.
- Published in:
- Clinical & Experimental Neuroimmunology, 2023, v. 14, n. 4, p. 202, doi. 10.1111/cen3.12764
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- Publication type:
- Article
CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-45011-8
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- Publication type:
- Article
CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-45011-8
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- Publication type:
- Article
Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation.
- Published in:
- Frontiers in Neurology, 2023, p. 01, doi. 10.3389/fneur.2023.1241678
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- Publication type:
- Article
Siblings with Cockayne Syndrome B Type III Presenting with Slowly Progressive Cerebellar Ataxia.
- Published in:
- Internal Medicine, 2023, v. 62, n. 15, p. 2253, doi. 10.2169/internalmedicine.0061-22
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- Publication type:
- Article
68‐1: Invited Paper: A Waveguide‐type Retinal Scan AR Display with Pupil Expansion System.
- Published in:
- SID Symposium Digest of Technical Papers, 2023, v. 54, n. 1, p. 962, doi. 10.1002/sdtp.16727
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- Publication type:
- Article
White spot syndrome virus (WSSV) modulates lipid metabolism in white shrimp.
- Published in:
- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-04924-w
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- Publication type:
- Article
Successful baricitinib treatment of refractory anti‐synthetase syndrome associated with interstitial lung disease.
- Published in:
- 2023
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- Publication type:
- Case Study
Anti-ganglionic acetylcholine receptor antibodies in functional neurological symptom disorder/conversion disorder.
- Published in:
- Frontiers in Neurology, 2023, v. 14, p. 1, doi. 10.3389/fneur.2023.1137958
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- Publication type:
- Article
Efficacy of l‐Arginine treatment in patients with HTLV‐1‐associated neurological disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2023, v. 10, n. 2, p. 237, doi. 10.1002/acn3.51715
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- Publication type:
- Article
Pleuroparenchymal fibroelastosis in mycobacterium avium complex lung disease.
- Published in:
- 2023
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- Publication type:
- Case Study
Gene panel analysis of 119 index patients with suspected periodic paralysis in Japan.
- Published in:
- Frontiers in Neurology, 2023, v. 14, p. 01, doi. 10.3389/fneur.2023.1078195
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- Publication type:
- Article
Mycelial differentiation linked avermectin production in Streptomyces avermitilis studied with Raman imaging.
- Published in:
- Applied Microbiology & Biotechnology, 2023, v. 107, n. 1, p. 369, doi. 10.1007/s00253-022-12314-1
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- Publication type:
- Article
Direct imaging of intracellular RNA, DNA, and liquid–liquid phase separated membraneless organelles with Raman microspectroscopy.
- Published in:
- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-04342-4
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- Publication type:
- Article
Genetic spectrum and founder effect of non-dystrophic myotonia: a Japanese case series study.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 12, p. 6406, doi. 10.1007/s00415-022-11305-6
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- Publication type:
- Article
Coronavirus disease 2019 vaccination‐induced acute exacerbation in idiopathic pulmonary fibrosis.
- Published in:
- 2022
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- Publication type:
- Case Study
Prevalence of Fragile X-Associated Tremor/Ataxia Syndrome in Patients with Cerebellar Ataxia in Japan.
- Published in:
- Cerebellum, 2022, v. 21, n. 5, p. 851, doi. 10.1007/s12311-021-01323-x
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- Publication type:
- Article
Japanese case of Charcot–Marie–Tooth disease type 2Z with severe retinitis pigmentosa.
- Published in:
- Neurology & Clinical Neuroscience, 2022, v. 10, n. 5, p. 266, doi. 10.1111/ncn3.12660
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- Publication type:
- Article
Oral administration of Blautia wexlerae ameliorates obesity and type 2 diabetes via metabolic remodeling of the gut microbiota.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32015-7
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- Publication type:
- Article
Multi-type RFC1 repeat expansions as the most common cause of hereditary sensory and autonomic neuropathy.
- Published in:
- 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.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.952493
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- Publication type:
- Article
Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 8, p. 4129, doi. 10.1007/s00415-022-11026-w
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- Publication type:
- Article
Novel heterozygous variants of SLC12A6 in Japanese families with Charcot–Marie–Tooth disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 7, p. 902, doi. 10.1002/acn3.51603
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- Publication type:
- Article
Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible.
- Published in:
- Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071546
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- Publication type:
- Article
Multiple endotracheal metastases of combined small cell lung carcinoma.
- Published in:
- 2022
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- Publication type:
- Case Study
Raman Microspectroscopy Imaging Analysis of Extracellular Vesicles Biogenesis by Filamentous Fungus Penicilium chrysogenum.
- Published in:
- Advanced Biology, 2022, v. 6, n. 6, p. 1, doi. 10.1002/adbi.202101322
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- Publication type:
- Article
Raman Microspectroscopy Imaging Analysis of Extracellular Vesicles Biogenesis by Filamentous Fungus Penicilium chrysogenum (Adv. Biology 6/2022).
- Published in:
- Advanced Biology, 2022, v. 6, n. 6, p. 1, doi. 10.1002/adbi.202270063
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- Publication type:
- Article
Novel de novo POLR3B mutations responsible for demyelinating Charcot–Marie–Tooth disease in Japan.
- Published in:
- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 5, p. 747, doi. 10.1002/acn3.51555
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- Publication type:
- Article
The first case of infantile-onset multisystem neurologic, endocrine, and pancreatic disease caused by novel PTRH2 mutation in Japan.
- Published in:
- 2022
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- Publication type:
- Letter
Efficacy of early antifibrotic treatment for idiopathic pulmonary fibrosis.
- Published in:
- 2021
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- Publication type:
- journal article
Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan.
- Published in:
- Clinical Genetics, 2021, v. 99, n. 3, p. 359, doi. 10.1111/cge.13881
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- Publication type:
- Article
Molecular profiling of lipid droplets inside HuH7 cells with Raman micro-spectroscopy.
- Published in:
- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-1100-4
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- Publication type:
- Article
Miliary opacities in pulmonary sarcoidosis.
- Published in:
- Respirology Case Reports, 2020, v. 8, n. 5, p. 1, doi. 10.1002/rcr2.563
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- Publication type:
- Article
Bevacizumab plus chemotherapy in nonsquamous non‐small cell lung cancer patients with malignant pleural effusion uncontrolled by tube drainage or pleurodesis: A phase II study North East Japan Study group trial NEJ013B.
- Published in:
- Thoracic Cancer, 2020, v. 11, n. 7, p. 1876, doi. 10.1111/1759-7714.13472
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- Publication type:
- Article
Organelle specific simultaneous Raman/green fluorescence protein microspectroscopy for living cell physicochemical studies.
- Published in:
- Journal of Biophotonics, 2020, v. 13, n. 4, p. 1, doi. 10.1002/jbio.201960163
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- Article
Cover Image.
- Published in:
- Journal of Raman Spectroscopy, 2019, v. 50, n. 8, p. i, doi. 10.1002/jrs.5647
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- Publication type:
- Article
Universal detection of body fluid traces in situ with Raman hyperspectroscopy for forensic purposes: Evaluation of a new detection algorithm (HAMAND) using semen samples.
- Published in:
- Journal of Raman Spectroscopy, 2019, v. 50, n. 8, p. 1147, doi. 10.1002/jrs.5621
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- Publication type:
- Article
Autoimmune pulmonary alveolar proteinosis presenting peripheral ground‐glass opacities.
- Published in:
- 2019
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- Publication type:
- Case Study
Peripheral neuropathy in a case with CADASIL: a case report.
- Published in:
- 2018
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- Publication type:
- journal article
Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Resolution of Infliximab-Refractory Nivolumab- Induced Acute Severe Enterocolitis After Cyclosporine Treatment in a Patient with Non-Small Cell Lung Cancer.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Analysis of root surface properties by fluorescence/Raman intensity ratio.
- Published in:
- 2017
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- Publication type:
- journal article
Clinical and genetic diversities of Charcot-Marie-Tooth disease with MFN2 mutations in a large case study.
- Published in:
- 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
On-site Direct Detection of Astaxanthin from Salmon Fillet Using Raman Spectroscopy.
- Published in:
- Marine Biotechnology, 2017, v. 19, n. 2, p. 157, doi. 10.1007/s10126-017-9739-7
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- Publication type:
- Article