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The efficacy and safety of intravenous immunoglobulin infusion in 12 h for the initial treatment of Kawasaki disease

Pediatrics and neonatology, 2024-09, Vol.65 (5), p.441-444

2024

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High-dose thiamine prevents brain lesions and prolongs survival of Slc19a3-deficient mice

PloS one, 2017-06, Vol.12 (6), p.e0180279-e0180279

2017

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Lateral neck pain as a symptom of severe sinusitis: A case report

Pediatrics international, 2021-05, Vol.63 (5), p.589-590

2021

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Lipidomics analysis revealed the phospholipid compositional changes in muscle by chronic exercise and high-fat diet

Scientific reports, 2013-11, Vol.3 (1), p.3267-3267, Article 3267

2013

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Isozyme-Specific Role of SAD-A in Neuronal Migration During Development of Cerebral Cortex

Cerebral cortex (New York, N.Y. 1991), 2019-08, Vol.29 (9), p.3738-3751

2019

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The effect of rapamycin, NVP-BEZ235, aspirin, and metformin on PI3K/AKT/mTOR signaling pathway of PIK3CA-related overgrowth spectrum (PROS)

Oncotarget, 2017-07, Vol.8 (28), p.45470-45483

2017

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Identification of B.1.346 Lineage of SARS-CoV-2 in Japan: Genomic Evidence of Re-entry of Clade 20C

The Keio Journal of Medicine, 2021, Vol.70(2), pp.44-50

2021

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Identification and characterization of splicing variants of PLEKHA5 (Plekha5) during brain development

Gene, 2012-01, Vol.492 (1), p.270-275

2012

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A wide spectrum of clinical and brain MRI findings in patients with SLC19A3 mutations

BMC medical genetics, 2010-12, Vol.11 (1), p.171-171

2010

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Analysis of Effective Field Gradient in Microwave-Assisted Magnetic Recording

IEEE transactions on magnetics, 2014-11, Vol.50 (11), p.1-4

2014

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The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations

American journal of medical genetics. Part A, 2014-08, Vol.164A (8), p.1899-1908

2014

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Mutations in SIP1 , encoding Smad interacting protein-1, cause a form of Hirschsprung disease

Nature genetics, 2001-04, Vol.27 (4), p.369-370

2001

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MBTPS2 mutation causes BRESEK/BRESHECK syndrome

American journal of medical genetics. Part A, 2012-01, Vol.158A (1), p.97-102

2012

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Ultra-narrow interval angular control signal for holographic data storage system

Optical review (Tokyo, Japan), 2016-10, Vol.23 (5), p.848-858

2016

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Chronic exercise enhances insulin secretion ability of pancreatic islets without change in insulin content in non-diabetic rats

Biochemical and biophysical research communications, 2013-01, Vol.430 (2), p.676-682

2013

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The first case of recurrent ultra late onset group B streptococcal sepsis in a 3-year-old child

IDCases, 2017-01, Vol.7 (C), p.16-18

2017

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Clinical and biochemical characterization of 3-hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency that causes Leigh-like disease and ketoacidosis

Molecular genetics and metabolism reports, 2014-01, Vol.1 (C), p.455-460

2014

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Microwave assisted magnetic Recording: Physics and application to hard disk drives

Journal of magnetism and magnetic materials, 2022-12, Vol.563, p.169859, Article 169859

2022

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Magnetization switching of a perpendicular nanomagnet induced by vertical nonlocal injection of pure spin current

Scientific reports, 2019-12, Vol.9 (1), p.19543-9, Article 19543

2019

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Magnetoresistance Ratio and Resistance Area Design of CPP-MR Film for 2-5 \hbox^ Read Sensors

IEEE transactions on magnetics, 2010-06, Vol.46 (6), p.2086-2089

2010

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Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion

Journal of medical genetics, 2015-10, Vol.52 (10), p.691-698

2015

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Clinical and molecular genetic characterization of two female patients harboring the Xq27.3q28 deletion with different ratios of X chromosome inactivation

Human mutation, 2020-08, Vol.41 (8), p.1447-1460

2020

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Clinical and genetic characterization of a patient with SOX5 haploinsufficiency caused by a de novo balanced reciprocal translocation

Gene, 2018-05, Vol.655, p.65-70

2018

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Pathogenicity evaluation of variants of uncertain significance at exon-intron junction by splicing assay in patients with Mowat-Wilson syndrome

European journal of medical genetics, 2023-12, Vol.66 (12), p.104882-104882, Article 104882

2023

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Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy

Brain (London, England : 1878), 2018-06, Vol.141 (6), p.1622-1636

2018

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The efficacy and safety of intravenous immunoglobulin infusion in 12 h for the initial treatment of Kawasaki disease

High-dose thiamine prevents brain lesions and prolongs survival of Slc19a3-deficient mice

Lateral neck pain as a symptom of severe sinusitis: A case report

Lipidomics analysis revealed the phospholipid compositional changes in muscle by chronic exercise and high-fat diet

Isozyme-Specific Role of SAD-A in Neuronal Migration During Development of Cerebral Cortex

The effect of rapamycin, NVP-BEZ235, aspirin, and metformin on PI3K/AKT/mTOR signaling pathway of PIK3CA-related overgrowth spectrum (PROS)

Identification of B.1.346 Lineage of SARS-CoV-2 in Japan: Genomic Evidence of Re-entry of Clade 20C

Identification and characterization of splicing variants of PLEKHA5 (Plekha5) during brain development

A wide spectrum of clinical and brain MRI findings in patients with SLC19A3 mutations

Analysis of Effective Field Gradient in Microwave-Assisted Magnetic Recording

The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations

Mutations in SIP1 , encoding Smad interacting protein-1, cause a form of Hirschsprung disease

MBTPS2 mutation causes BRESEK/BRESHECK syndrome

Ultra-narrow interval angular control signal for holographic data storage system

Chronic exercise enhances insulin secretion ability of pancreatic islets without change in insulin content in non-diabetic rats

The first case of recurrent ultra late onset group B streptococcal sepsis in a 3-year-old child

Clinical and biochemical characterization of 3-hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency that causes Leigh-like disease and ketoacidosis

Microwave assisted magnetic Recording: Physics and application to hard disk drives

Magnetization switching of a perpendicular nanomagnet induced by vertical nonlocal injection of pure spin current

Magnetoresistance Ratio and Resistance Area Design of CPP-MR Film for 2-5 \hbox^ Read Sensors

Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion

Clinical and molecular genetic characterization of two female patients harboring the Xq27.3q28 deletion with different ratios of X chromosome inactivation

Clinical and genetic characterization of a patient with SOX5 haploinsufficiency caused by a de novo balanced reciprocal translocation

Pathogenicity evaluation of variants of uncertain significance at exon-intron junction by splicing assay in patients with Mowat-Wilson syndrome

Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy

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