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5‐Aminosalicylic acid‐induced pericarditis in pediatric Crohn’s disease

Pediatric investigation, 2022-01, Vol.64 (1), p.e14710-n/a

2022

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Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism

Fertility and sterility, 2014-10, Vol.102 (4), p.1130-1136.e3

2014

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Present status of prophylactic thyroidectomy in pediatric multiple endocrine neoplasia 2: a nationwide survey in Japan 1997-2017

Journal of pediatric endocrinology & metabolism : JPEM, 2019-06, Vol.32 (6), p.585

2019

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Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease

Brain & development (Tokyo. 1979), 2015-11, Vol.37 (10), p.960-966

2015

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Vitamin D deficiency rickets caused by improper lifestyle in Japanese children

Pediatrics international, 2005-04, Vol.47 (2), p.142-146

2005

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Utility of point-of-care Gram stain by physicians for urinary tract infection in children ≤36 months

Medicine (Baltimore), 2019-04, Vol.98 (14), p.e15101-e15101

2019

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Genotype–Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects

The journal of clinical endocrinology and metabolism, 2024-08, Vol.109 (9), p.2358-2365

2024

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Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene

Endocrine Journal, 2004, Vol.51(5), pp.473-477

2004

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Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects

The journal of clinical endocrinology and metabolism, 2024-02

2024

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Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene

ENDOCRINE JOURNAL, 2004, Vol.51 (5), p.473-477

2004

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A case of 3 months old Japanese boy with sporadic congenital none-autoimmune hyperthyroidism

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P98-P98, Article P98

2015

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The incidences of and risk factors for severe retinopathy requiring photocoagulation and albuminuria in Japanese patients with childhood-onset type 1 diabetes

Diabetology international, 2018-05, Vol.9 (2), p.121-128

2018

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Metabolic Syndrome and Risk of Developing Chronic Kidney Disease in Japanese Adults

Hypertension research, 2007-10, Vol.30 (10), p.937-943

2007

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Intact Long-Type dupA as a Marker for Gastroduodenal Diseases in Okinawan Subpopulation, Japan

Helicobacter (Cambridge, Mass.), 2013-02, Vol.18 (1), p.66-72

2013

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Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency

Nature communications, 2021-11, Vol.12 (1), p.6819-6819, Article 6819

2021

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Comparison of two screening tests for HIV-Associated Neurocognitive Disorder suspected Japanese patients with respect to cART usage

PloS one, 2018-06, Vol.13 (6), p.e0199106-e0199106

2018

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Axonal transport of Frizzled5 by Alcadein α-containing vesicles is associated with kinesin-1

Molecular biology of the cell, 2023-10, Vol.34 (11), p.ar110-ar110

2023

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Phosphorylation of multiple sites within an acidic region of Alcadein α is required for kinesin-1 association and Golgi exit of Alcadein α cargo

Molecular biology of the cell, 2017-12, Vol.28 (26), p.3844-3856

2017

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Four new resin glycosides, murasakimasarins I–IV, from the tuber of Ipomoea batatas

Journal of natural medicines, 2018-06, Vol.72 (3), p.784-792

2018

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Influence of Serum Albumin Levels during Opioid Rotation from Morphine or Oxycodone to Fentanyl for Cancer Pain

Biological and Pharmaceutical Bulletin, 2014/12/01, Vol.37(12), pp.1860-1865

2014

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The cytoplasmic region of the amyloid β‐protein precursor (APP) is necessary and sufficient for the enhanced fast velocity of APP transport by kinesin‐1

FEBS letters, 2018-08, Vol.592 (16), p.2716-2724

2018

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Phosphorylation of KLC1 modifies interaction with JIP1 and abolishes the enhanced fast velocity of APP transport by kinesin-1

Molecular biology of the cell, 2017-12, Vol.28 (26), p.3857-3869

2017

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Quantitative analysis of APP axonal transport in neurons: role of JIP1 in enhanced APP anterograde transport

Molecular biology of the cell, 2014-11, Vol.25 (22), p.3569-3580

2014

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Metabolic syndrome and risk of developing chronic kidney disease in Japanese adults

Hypertension research, 2007-10, Vol.30 (10), p.937-943

2007

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5‐Aminosalicylic acid‐induced pericarditis in pediatric Crohn’s disease

Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism

Present status of prophylactic thyroidectomy in pediatric multiple endocrine neoplasia 2: a nationwide survey in Japan 1997-2017

Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease

SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7

Vitamin D deficiency rickets caused by improper lifestyle in Japanese children

Utility of point-of-care Gram stain by physicians for urinary tract infection in children ≤36 months

Genotype–Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects

Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene

Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects

Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene

A case of 3 months old Japanese boy with sporadic congenital none-autoimmune hyperthyroidism

The incidences of and risk factors for severe retinopathy requiring photocoagulation and albuminuria in Japanese patients with childhood-onset type 1 diabetes

Metabolic Syndrome and Risk of Developing Chronic Kidney Disease in Japanese Adults

Intact Long-Type dupA as a Marker for Gastroduodenal Diseases in Okinawan Subpopulation, Japan

Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency

Comparison of two screening tests for HIV-Associated Neurocognitive Disorder suspected Japanese patients with respect to cART usage

Axonal transport of Frizzled5 by Alcadein α-containing vesicles is associated with kinesin-1

Phosphorylation of multiple sites within an acidic region of Alcadein α is required for kinesin-1 association and Golgi exit of Alcadein α cargo

Four new resin glycosides, murasakimasarins I–IV, from the tuber of Ipomoea batatas

Influence of Serum Albumin Levels during Opioid Rotation from Morphine or Oxycodone to Fentanyl for Cancer Pain

The cytoplasmic region of the amyloid β‐protein precursor (APP) is necessary and sufficient for the enhanced fast velocity of APP transport by kinesin‐1

Phosphorylation of KLC1 modifies interaction with JIP1 and abolishes the enhanced fast velocity of APP transport by kinesin-1

Quantitative analysis of APP axonal transport in neurons: role of JIP1 in enhanced APP anterograde transport

Metabolic syndrome and risk of developing chronic kidney disease in Japanese adults

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