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Significance of End-Diastolic Forward Flow in Patients With Repaired Tetralogy of Fallot　― Its Interaction With the Left Ventricular Property and End Organ Damage

Circulation Journal, 2023/12/25, Vol.88(1), pp.73-80

2023

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Impact of nitrogen metabolism-associated culture pH changes on regulation of Fusarium trichothecene biosynthesis: revision of roles of polyamine agmatine and transcription factor AreA

Current genetics, 2020-12, Vol.66 (6), p.1179-1190

2020

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Acute encephalopathy in children with tuberous sclerosis complex

Orphanet journal of rare diseases, 2021-01, Vol.16 (1), p.5-5, Article 5

2021

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Characteristic proton magnetic resonance spectroscopy in glucose transporter type 1 deficiency syndrome

Pediatrics international, 2018-10, Vol.60 (10), p.978-979

2018

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Chronological T‐wave alternation before and after the onset of arrhythmogenic right ventricular cardiomyopathy

Annals of noninvasive electrocardiology, 2022-11, Vol.27 (6), p.e12965-n/a

2022

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A female with obstructive hemivagina and ipsilateral renal anomaly syndrome diagnosed early from unilateral renal urinary tract abnormality during fetal life and vulvar mass increased by abdominal pressure

Journal of Japan Society of Perinatal and Neonatal Medicine, 2022, Vol.58(3), pp.579-582

2022

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Identification of amino acids negatively affecting Fusarium trichothecene biosynthesis

Antonie van Leeuwenhoek, 2019-03, Vol.112 (3), p.471-478

2019

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GNAO1 mutation-related severe involuntary movements treated with gabapentin

Brain & development (Tokyo. 1979), 2021-04, Vol.43 (4), p.576-579

2021

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Long-term outcome of a group of Japanese children with myelin-oligodendrocyte glycoprotein encephalomyelitis without preventive immunosuppressive therapy

Brain & development (Tokyo. 1979), 2019-10, Vol.41 (9), p.790-795

2019

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Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy

Genetics in medicine, 2022-12, Vol.24 (12), p.2453-2463

2022

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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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Clinical and genetic features of acute encephalopathy in children taking theophylline

Brain & development (Tokyo. 1979), 2015-05, Vol.37 (5), p.463-470

2015

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Case report: Cerebellar swelling and hydrocephalus in familial hemophagocytic lymphohistiocytosis

Frontiers in pediatrics, 2022-12, Vol.10, p.1051623

2022

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Intellectual outcomes of extremely preterm infants at school age

Pediatrics international, 2017-05, Vol.59 (5), p.570-577

2017

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A case of amniotic band syndrome with extensive acrania

Journal of Japan Society of Perinatal and Neonatal Medicine, 2023, Vol.59(1), pp.62-66

2023

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Successful endoscopic sclerotherapy with bile duct stenting for a vascular malformation neighboring the duodenal papilla in blue rubber bleb nevus syndrome

DEN open, 2022-04, Vol.2 (1), p.n/a

2022

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Temporal brain metabolite changes in preterm infants with normal development

Brain & development (Tokyo. 1979), 2017-03, Vol.39 (3), p.196-202

2017

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Reduction in peripheral regulatory T cell population in childhood ocular type myasthenia gravis

Brain & development (Tokyo. 1979), 2015-09, Vol.37 (8), p.808-816

2015

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Efficacy and safety of fosphenytoin for acute encephalopathy in children

Brain & development (Tokyo. 1979), 2015-04, Vol.37 (4), p.418-422

2015

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Lactulose: A treatment for hyperammonemia in a lysinuric protein–intolerant patient with dynamic blood amino acid concentrations

Molecular genetics and metabolism reports, 2022-09, Vol.32, p.100898-100898, Article 100898

2022

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Survey of death cases in neonatal intensive care unit, Iwate Medical University Hospital General Perinatal Maternal and Child Medical Center

Journal of Japan Society of Perinatal and Neonatal Medicine, 2022, Vol.58(3), pp.479-485

2022

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Assessing Temporal Brain Metabolite Changes in Preterm Infants Using Multivoxel Magnetic Resonance Spectroscopy

Magnetic Resonance in Medical Sciences, 2016, Vol.15(2), pp.187-192

2016

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Hypofibrinogenemia caused by adrenocorticotropic hormone for infantile spasms: A case report

Brain & development (Tokyo. 1979), 2015-01, Vol.37 (1), p.137-139

2015

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Aicardi–Goutières syndrome with systemic lupus erythematosus and hypothyroidism

Brain & development (Tokyo. 1979), 2013-01, Vol.35 (1), p.87-90

2013

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Proton Magnetic Resonance Spectroscopic Images in Preterm Infants with Bilirubin Encephalopathy

The Journal of pediatrics, 2012-02, Vol.160 (2), p.342-344

2012

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Significance of End-Diastolic Forward Flow in Patients With Repaired Tetralogy of Fallot　― Its Interaction With the Left Ventricular Property and End Organ Damage

Impact of nitrogen metabolism-associated culture pH changes on regulation of Fusarium trichothecene biosynthesis: revision of roles of polyamine agmatine and transcription factor AreA

Acute encephalopathy in children with tuberous sclerosis complex

Characteristic proton magnetic resonance spectroscopy in glucose transporter type 1 deficiency syndrome

Chronological T‐wave alternation before and after the onset of arrhythmogenic right ventricular cardiomyopathy

A female with obstructive hemivagina and ipsilateral renal anomaly syndrome diagnosed early from unilateral renal urinary tract abnormality during fetal life and vulvar mass increased by abdominal pressure

Identification of amino acids negatively affecting Fusarium trichothecene biosynthesis

GNAO1 mutation-related severe involuntary movements treated with gabapentin

Long-term outcome of a group of Japanese children with myelin-oligodendrocyte glycoprotein encephalomyelitis without preventive immunosuppressive therapy

Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy

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

Clinical and genetic features of acute encephalopathy in children taking theophylline

Case report: Cerebellar swelling and hydrocephalus in familial hemophagocytic lymphohistiocytosis

Intellectual outcomes of extremely preterm infants at school age

A case of amniotic band syndrome with extensive acrania

Successful endoscopic sclerotherapy with bile duct stenting for a vascular malformation neighboring the duodenal papilla in blue rubber bleb nevus syndrome

Temporal brain metabolite changes in preterm infants with normal development

Reduction in peripheral regulatory T cell population in childhood ocular type myasthenia gravis

Efficacy and safety of fosphenytoin for acute encephalopathy in children

Lactulose: A treatment for hyperammonemia in a lysinuric protein–intolerant patient with dynamic blood amino acid concentrations

Survey of death cases in neonatal intensive care unit, Iwate Medical University Hospital General Perinatal Maternal and Child Medical Center

Assessing Temporal Brain Metabolite Changes in Preterm Infants Using Multivoxel Magnetic Resonance Spectroscopy

Hypofibrinogenemia caused by adrenocorticotropic hormone for infantile spasms: A case report

Aicardi–Goutières syndrome with systemic lupus erythematosus and hypothyroidism

Proton Magnetic Resonance Spectroscopic Images in Preterm Infants with Bilirubin Encephalopathy

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