Works by Tsuji, Shoji
Results: 335
The incidence and risk factors of asymptomatic primary spontaneous pneumothorax detected during health check-ups.
- Published in:
- 2017
- By:
- Publication type:
- journal article
In-frame deletion variant of ABCD1 in a sporadic case of adrenoleukodystrophy.
- Published in:
- Human Genome Variation, 2025, v. 12, n. 1, p. 1, doi. 10.1038/s41439-025-00309-z
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- Publication type:
- Article
Accuracy of diagnosing acute kidney injury by assessing urine output within the first week of life in extremely preterm infants.
- Published in:
- Clinical & Experimental Nephrology, 2022, v. 26, n. 7, p. 709, doi. 10.1007/s10157-022-02206-z
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- Publication type:
- Article
Optimal bacterial colony counts for the diagnosis of upper urinary tract infections in infants.
- Published in:
- Clinical & Experimental Nephrology, 2020, v. 24, n. 3, p. 253, doi. 10.1007/s10157-019-01812-8
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- Publication type:
- Article
Risk factors for sodium valproate-induced renal tubular dysfunction.
- Published in:
- Clinical & Experimental Nephrology, 2018, v. 22, n. 2, p. 420, doi. 10.1007/s10157-017-1472-z
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- Publication type:
- Article
Prediction of urine volume soon after birth using serum cystatin C.
- Published in:
- Clinical & Experimental Nephrology, 2016, v. 20, n. 5, p. 764, doi. 10.1007/s10157-015-1215-y
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- Publication type:
- Article
Serum albumin level accurately reflects antioxidant potentials in idiopathic nephrotic syndrome.
- Published in:
- Clinical & Experimental Nephrology, 2012, v. 16, n. 3, p. 411, doi. 10.1007/s10157-011-0578-y
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- Publication type:
- Article
Hereditary Spastic Paraplegia Type 43 ( SPG43) is Caused by Mutation in C19orf12.
- Published in:
- Human Mutation, 2013, v. 34, n. 10, p. 1357, doi. 10.1002/humu.22378
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- Publication type:
- Article
Reduced interhemispheric inhibition in mild cognitive impairment.
- Published in:
- Experimental Brain Research, 2012, v. 218, n. 1, p. 21, doi. 10.1007/s00221-011-2997-0
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- Publication type:
- Article
An immigrant family with Kii amyotrophic lateral sclerosis/parkinsonism-dementia complex.
- Published in:
- 2022
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- Publication type:
- journal article
JASPAC: Japan Spastic Paraplegia Research Consortium.
- Published in:
- Brain Sciences (2076-3425), 2018, v. 8, n. 8, p. 153, doi. 10.3390/brainsci8080153
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- Publication type:
- Article
HTLV-I-like sequence in MS.
- Published in:
- Acta Neurologica Scandinavica, 1995, v. 91, n. 6, p. 516, doi. 10.1111/j.1600-0404.1995.tb00457.x
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- Publication type:
- Article
Construction of an Equalized cDNA Library from Human Brain by Semi-Solid Self-Hybridization System.
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- DNA Research, 1994, v. 1, n. 2, p. 91
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- Publication type:
- Article
Mercury chloride decreases the water permeability of aquaporin-4-reconstituted proteoliposomes.
- Published in:
- Biology of the Cell (Wiley-Blackwell), 2008, v. 100, n. 6, p. 355, doi. 10.1042/BC20070132
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- Publication type:
- Article
Molecular clearance of ataxin-3 is regulated by a mammalian E4.
- Published in:
- EMBO Journal, 2004, v. 23, n. 3, p. 659, doi. 10.1038/sj.emboj.7600081
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- Publication type:
- Article
SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data.
- Published in:
- BMC Bioinformatics, 2009, v. 10, p. 1, doi. 10.1186/1471-2105-10-121
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- Publication type:
- Article
Cerebellar dysfunction in progressive supranuclear palsy: A transcranial magnetic stimulation study.
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- Movement Disorders, 2010, v. 25, n. 14, p. 2413, doi. 10.1002/mds.23298
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- Publication type:
- Article
Postural tremor in X-linked spinal and bulbar muscular atrophy.
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- Movement Disorders, 2009, v. 24, n. 14, p. 2063, doi. 10.1002/mds.22566
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- Publication type:
- Article
A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype-phenotype correlations.
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- Movement Disorders, 2009, v. 24, n. 3, p. 441, doi. 10.1002/mds.22435
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- Publication type:
- Article
Severe hypokinesis caused by paraneoplastic anti-Ma2 encephalitis associated with bilateral intratubular germ-cell neoplasm of the testes.
- Published in:
- 2007
- By:
- Publication type:
- journal article
An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene.
- Published in:
- 2000
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- Publication type:
- journal article
Stereotyped hand clasping: An unusual tardive movement disorder.
- Published in:
- Movement Disorders, 1993, v. 8, n. 2, p. 230, doi. 10.1002/mds.870080224
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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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- Publication type:
- Article
VPS13D‐related disorders presenting as a pure and complicated form of hereditary spastic paraplegia.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 3, p. 1, doi. 10.1002/mgg3.1108
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- Publication type:
- Article
Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes.
- Published in:
- JAMA Neurology, 2021, v. 78, n. 7, p. 853, doi. 10.1001/jamaneurol.2021.1509
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- Publication type:
- Article
Parietal dysgraphia: Characterization of abnormal writing stroke sequences, character formation and character recall.
- Published in:
- Behavioural Neurology, 2007, v. 18, n. 2, p. 99, doi. 10.1155/2007/906417
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- Publication type:
- Article
Neuron-specific analysis of histone modifications with post-mortem brains.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-60775-z
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- Publication type:
- Article
Chronic cerebral hypoperfusion shifts the equilibrium of amyloid β oligomers to aggregation-prone species with higher molecular weight.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-39494-7
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- Publication type:
- Article
Does the Clock Tick Slower or Faster in Parkinson’s Disease? – Insights Gained From the Synchronized Tapping Task.
- Published in:
- Frontiers in Psychology, 2018, p. N.PAG, doi. 10.3389/fpsyg.2018.01178
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- Publication type:
- Article
Cephalic tetanus presenting as acute vertigo with bilateral vestibulopathy.
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- Acta Oto-Laryngologica, 2011, v. 131, n. 3, p. 334, doi. 10.3109/00016489.2010.526144
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- Publication type:
- Article
Novel Use of Rituximab for Steroid-Dependent Nephrotic Syndrome in Children.
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- American Journal of Nephrology, 2014, v. 38, n. 6, p. 483, doi. 10.1159/000356439
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- Publication type:
- Article
A Novel Nuclear Factor κB Inhibitor, Dehydroxymethylepoxyquinomicin, Ameliorates Puromycin Aminonucleoside-Induced Nephrosis in Mice.
- Published in:
- American Journal of Nephrology, 2013, v. 37, n. 4, p. 302, doi. 10.1159/000348803
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- Publication type:
- Article
A Novel Nuclear Factor [kappa]B Inhibitor, Dehydroxymethylepoxyquinomicin, Ameliorates Puromycin Aminonucleoside-Induced Nephrosis in Mice.
- Published in:
- 2013
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- Publication type:
- Journal Article
Earthquakes and neurological care.
- Published in:
- European Journal of Neurology, 2012, v. 19, n. 2, p. 185, doi. 10.1111/j.1468-1331.2011.03446.x
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- Publication type:
- Article
Dysbiosis of the gut microbiota in children with severe motor and intellectual disabilities receiving enteral nutrition: A pilot study.
- Published in:
- JPEN Journal of Parenteral & Enteral Nutrition, 2023, v. 47, n. 1, p. 67, doi. 10.1002/jpen.2435
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- Publication type:
- Article
Superiority of Cystatin Cover Creatinine for Early Diagnosis of Acute Kidney Injury in Pediatric Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma.
- Published in:
- Tohoku Journal of Experimental Medicine, 2021, v. 254, n. 3, p. 163, doi. 10.1620/tjem.254.163
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- Publication type:
- Article
Elective Cesarean Section at 37 Weeks Is Associated with the Higher Risk of Neonatal Complications.
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- Tohoku Journal of Experimental Medicine, 2014, v. 233, n. 4, p. 243, doi. 10.1620/tjem.233.243
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- Publication type:
- Article
Voiding Cystourethrography Is Mandatory in Infants with Febrile Urinary Tract Infection.
- Published in:
- Tohoku Journal of Experimental Medicine, 2013, v. 231, n. 2, p. 251, doi. 10.1620/tjem.231.251
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- Publication type:
- Article
Production of Nitric Oxide Is Lower in Shiga Toxin-Stimulated Neutrophils of Infants Compared to Those of Children or Adults.
- Published in:
- Tohoku Journal of Experimental Medicine, 2012, v. 228, n. 3, p. 247, doi. 10.1620/tjem.228.247
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- Publication type:
- Article
Intravenous Immunoglobulin Counteracts Oxidative Stress in Kawasaki Disease.
- Published in:
- Pediatric Cardiology, 2012, v. 33, n. 7, p. 1086, doi. 10.1007/s00246-012-0229-4
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- Publication type:
- Article
Prediction of the Risk of Coronary Arterial Lesions in Kawasaki Disease by Brain Natriuretic Peptide.
- Published in:
- Pediatric Cardiology, 2011, v. 32, n. 8, p. 1106, doi. 10.1007/s00246-011-9986-8
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- Publication type:
- Article
A mutation database for amyotrophic lateral sclerosis.
- Published in:
- 2010
- By:
- Publication type:
- Other
Partial deletions of putative adrenoleukodystrophy (ALD) gene in Japanese ALD patients.
- Published in:
- Human Mutation, 1995, v. 6, n. 3, p. 263, doi. 10.1002/humu.1380060314
- By:
- Publication type:
- Article
Host MICA Polymorphism as a Potential Predictive Marker in Response to Chemotherapy for Colorectal Liver Metastases.
- Published in:
- Digestive Diseases, 2018, v. 36, n. 6, p. 437, doi. 10.1159/000490411
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- Publication type:
- Article
AgIn: measuring the landscape of CpG methylation of individual repetitive elements.
- Published in:
- Bioinformatics, 2016, v. 32, n. 19, p. 2911, doi. 10.1093/bioinformatics/btw360
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- Publication type:
- Article
Clinical features of a family with late‐onset distal hereditary motor neuropathy harboring p.Pro39Leu variant of HSPB1.
- Published in:
- Journal of the Peripheral Nervous System, 2023, v. 28, n. 3, p. 518, doi. 10.1111/jns.12567
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- Publication type:
- Article
Noncanonical splice‐site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies.
- Published in:
- Journal of the Peripheral Nervous System, 2023, v. 28, n. 3, p. 513, doi. 10.1111/jns.12558
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- Publication type:
- Article
Clinical features of inherited neuropathy with BSCL2 mutations in Japan.
- Published in:
- Journal of the Peripheral Nervous System, 2020, v. 25, n. 2, p. 125, doi. 10.1111/jns.12369
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- Publication type:
- Article
Comparison of the characteristics and factors influencing hospital visits among children with nocturnal enuresis in Japan: The Hirakata–Urayasu population‐based cohort study.
- Published in:
- International Journal of Urology, 2023, v. 30, n. 4, p. 408, doi. 10.1111/iju.15148
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- Publication type:
- Article
Desmopressin response in nocturnal enuresis without nocturnal polyuria in Japanese children.
- Published in:
- International Journal of Urology, 2021, v. 28, n. 9, p. 964, doi. 10.1111/iju.14615
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- Publication type:
- Article