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Effectiveness of rotavirus vaccines against hospitalisations in Japan

BMC pediatrics, 2017-07, Vol.17 (1), p.156-156, Article 156

2017

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Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families

PloS one, 2016-05, Vol.11 (5), p.e0154827-e0154827

2016

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Neonatal transient eosinophilic colitis with single bubble sign

Pediatrics international, 2018-12, Vol.60 (12), p.1092-1093

2018

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Familial episodic limb pain in kindreds with novel Nav1.9 mutations

PloS one, 2018-12, Vol.13 (12), p.e0208516-e0208516

2018

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A Retrospective, Hospital-Based Study to Determine the Incidence of Rotavirus Hospitalizations among Children Less than 5 Years of Age over a 10-Year Period (2001–2011) in Akita Prefecture, Japan

Japanese Journal of Infectious Diseases, 2014, Vol.67(6), pp.464-468

2014

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Clinical and genetic features of lysinuric protein intolerance in Japan

Pediatrics international, 2016-10, Vol.58 (10), p.979-983

2016

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Novel mutation in the TMPRSS6 gene with iron‐refractory iron deficiency anemia

Pediatrics international, 2014-08, Vol.56 (4), p.e41-e44

2014

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Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: Few clinical features suggestive of Beckwith-Wiedemann syndrome

Endocrine Journal, 2013, Vol.60(4), pp.403-408

2013

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Fatigue and quality of life in citrin deficiency during adaptation and compensation stage

Molecular genetics and metabolism, 2013-05, Vol.109 (1), p.9-13

2013

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Elevation of Serum Acid Sphingomyelinase Activity in Acute Kawasaki Disease

The Tohoku Journal of Experimental Medicine, 2015, Vol.237(2), pp.133-140

2015

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Phenotypical variety of insulin resistance in a family with a novel mutation of the insulin receptor gene

Endocrine Journal, 2010, Vol.57(6), pp.509-516

2010

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Niemann-Pick Disease Type C: Cataplexy and Hypocretin in Cerebrospinal Fluid

The Tohoku Journal of Experimental Medicine, 2006, Vol.209(3), pp.263-267

2006

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Biopsy‐proven acute interstitial nephritis due to fosfomycin in a child

Nephrology (Carlton, Vic.), 2018-09, Vol.23 (9), p.890-890

2018

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MELAS: A nationwide prospective cohort study of 96 patients in Japan

Biochimica et biophysica acta, 2012-05, Vol.1820 (5), p.619-624

2012

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Pathological fracture of the femur in Alagille syndrome that was treated with low-intensity pulsed ultrasound stimulation and an Ilizarov ring fixator: a case report

BMC musculoskeletal disorders, 2014-07, Vol.15 (1), p.225-225, Article 225

2014

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The useful preliminary diagnosis of Niemann-Pick disease type C by filipin test in blood smear

Molecular genetics and metabolism, 2013-11, Vol.110 (3), p.401-404

2013

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Chylothorax in a polysplenia infant with cor triatriatum, pulmonary stenosis and sick sinus syndrome

Heart and vessels, 1997-01, Vol.12 (5), p.247-249

1997

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Five novel SLC7A7 variants and y+L gene-expression pattern in cultured lymphoblasts from Japanese patients with lysinuric protein intolerance

Human mutation, 2002-11, Vol.20 (5), p.375-381

2002

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SLC7A7 genomic structure and novel variants in three Japanese lysinuric protein intolerance families

Human mutation, 2000-04, Vol.15 (4), p.367-372

2000

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Functional hearing loss in children

International journal of pediatric otorhinolaryngology, 1989-07, Vol.17 (3), p.287-295

1989

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Transcriptome analysis of umbilical cord mesenchymal stem cells revealed fetal programming due to chorioamnionitis

Scientific reports, 2022-04, Vol.12 (1), p.6537-6537, Article 6537

2022

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Effects of undernutrition and low energy availability on reproductive functions and their underlying neuroendocrine mechanisms

Endocrine Journal, 2022, Vol.69(12), pp.1363-1372

2022

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Changes in Serum Oxytocin Levels under Physiological and Supraphysiological Gonadal Steroid Hormone Conditions in Women of Reproductive Age: A Preliminary Study

Nutrients, 2022-12, Vol.14 (24), p.5350

2022

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Age-Dependent Changes in the Effects of Androgens on Female Metabolic and Body Weight Regulation Systems in Humans and Laboratory Animals

International journal of molecular sciences, 2023-12, Vol.24 (23), p.16567

2023

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Effectiveness of rotavirus vaccines against hospitalisations in Japan

Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families

Neonatal transient eosinophilic colitis with single bubble sign

Familial episodic limb pain in kindreds with novel Nav1.9 mutations

Newborn screening for carnitine palmitoyltransferase II deficiency using (C16+C18:1)/C2: Evaluation of additional indices for adequate sensitivity and lower false-positivity

A Retrospective, Hospital-Based Study to Determine the Incidence of Rotavirus Hospitalizations among Children Less than 5 Years of Age over a 10-Year Period (2001–2011) in Akita Prefecture, Japan

Clinical and genetic features of lysinuric protein intolerance in Japan

Novel mutation in the TMPRSS6 gene with iron‐refractory iron deficiency anemia

Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: Few clinical features suggestive of Beckwith-Wiedemann syndrome

Fatigue and quality of life in citrin deficiency during adaptation and compensation stage

Elevation of Serum Acid Sphingomyelinase Activity in Acute Kawasaki Disease

Phenotypical variety of insulin resistance in a family with a novel mutation of the insulin receptor gene

Niemann-Pick Disease Type C: Cataplexy and Hypocretin in Cerebrospinal Fluid

Biopsy‐proven acute interstitial nephritis due to fosfomycin in a child

MELAS: A nationwide prospective cohort study of 96 patients in Japan

Pathological fracture of the femur in Alagille syndrome that was treated with low-intensity pulsed ultrasound stimulation and an Ilizarov ring fixator: a case report

The useful preliminary diagnosis of Niemann-Pick disease type C by filipin test in blood smear

Chylothorax in a polysplenia infant with cor triatriatum, pulmonary stenosis and sick sinus syndrome

Five novel SLC7A7 variants and y+L gene-expression pattern in cultured lymphoblasts from Japanese patients with lysinuric protein intolerance

SLC7A7 genomic structure and novel variants in three Japanese lysinuric protein intolerance families

Functional hearing loss in children

Transcriptome analysis of umbilical cord mesenchymal stem cells revealed fetal programming due to chorioamnionitis

Effects of undernutrition and low energy availability on reproductive functions and their underlying neuroendocrine mechanisms

Changes in Serum Oxytocin Levels under Physiological and Supraphysiological Gonadal Steroid Hormone Conditions in Women of Reproductive Age: A Preliminary Study

Age-Dependent Changes in the Effects of Androgens on Female Metabolic and Body Weight Regulation Systems in Humans and Laboratory Animals

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