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Molecular Genetic Dissection and Neonatal/Infantile Intrahepatic Cholestasis Using Targeted Next-Generation Sequencing

The Journal of pediatrics, 2016-04, Vol.171, p.171-177.e4

2016

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Clinical, Pathologic, and Genetic Features of Neonatal Dubin-Johnson Syndrome: A Multicenter Study in Japan

The Journal of pediatrics, 2018-05, Vol.196, p.161-167.e1

2018

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Antiviral therapy for hepatitis B virus during second pregnancies

The journal of obstetrics and gynaecology research, 2018-03, Vol.44 (3), p.566-569

2018

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Real-life Progression of the Use of a Genetic Panel in to Diagnose Neonatal Cholestasis

JPGN reports, 2022-05, Vol.3 (2), p.e196-e196

2022

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Standardization of phototherapy for neonatal hyperbilirubinemia using multiple-wavelength irradiance integration

Pediatrics and neonatology, 2020-02, Vol.61 (1), p.100-105

2020

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Neurodevelopmental outcomes at 3 years old for infants with birth weights under 500 g

Pediatrics and neonatology, 2018-06, Vol.59 (3), p.274-280

2018

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Case Report: Management of Cholestasis Associated With Congenital Syphilis

Frontiers in pediatrics, 2020-12, Vol.8, p.607506

2020

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Prenatal findings of holoprosencephaly

Congenital anomalies, 2015-08, Vol.55 (3), p.161-163

2015

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Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state

Brain & development (Tokyo. 1979), 2015-10, Vol.37 (9), p.887-890

2015

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Effects of tolvaptan on congestive heart failure complicated with chylothorax in a neonate

Pediatrics international, 2015-10, Vol.57 (5), p.1020-1022

2015

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Effects of 4‐phenylbutyrate therapy in a preterm infant with cholestasis and liver fibrosis

Pediatrics international, 2016-06, Vol.58 (6), p.506-509

2016

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Combination of Miller–Dieker syndrome and VACTERL association causes extremely severe clinical presentation

European journal of pediatrics, 2014-11, Vol.173 (11), p.1541-1544

2014

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Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants

Pediatrics international, 2016-06, Vol.58 (6), p.461-466

2016

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Neurodevelopmental Outcomes at 18 Months’ Corrected Age of Infants Born at 22 Weeks of Gestation

Neonatology (Basel, Switzerland), 2011-01, Vol.100 (3), p.228-232

2011

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Effects of exchange transfusion on cytokine profiles in necrotizing enterocolitis

Pediatrics international, 2012-12, Vol.54 (6), p.931-933

2012

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Detection of Pivaloylcarnitine in Pediatric Patients with Hypocarnitinemia after Long-Term Administration of Pivalate-Containing Antibiotics

The Tohoku Journal of Experimental Medicine, 2010, Vol.221(4), pp.309-313

2010

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Efficacy of pegylated interferon-α2a monotherapy in Japanese children with chronic hepatitis C

Hepatology research, 2011-05, Vol.41 (5), p.399-404

2011

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Hypothermia attenuates the severity of oxidative stress development in asphyxiated newborns

Journal of critical care, 2012-10, Vol.27 (5), p.469-473

2012

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Periventricular Leukomalacia is Decreasing in Japan

Pediatric neurology, 2012-07, Vol.47 (1), p.35-39

2012

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Efficacy of antiviral therapy for the prevention of mother-to-child transmission of hepatitis B virus and the risk of postpartum hepatitis flare after discontinuation of antiviral therapy

Hepatology research, 2024-04

2024

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Hepatitis C Virus Clearance after Discontinuation of Pegylated Interferon Alpha-2a Monotherapy in a Child

Case Reports in Medicine, 2012-01, Vol.2012, p.597348-4

2012

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Effects of cyclosporine A in hyperzincaemia and hypercalprotectinaemia

Acta pædiatrica (Oslo), 2006-07, Vol.95 (7), p.857-860

2006

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Recurrent Cholangitis with Congenital Hepatic Fibrosis and Pancreaticobiliary Maljunction after Roux-en-Y Reconstruction

European journal of pediatric surgery reports, 2013-06, Vol.1 (1), p.043-045

2013

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Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome

Acta Paediatrica, 2017-11, Vol.106 (11), p.1817-1824

2017

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Polymorphisms of the Factor VII Gene Associated with the Low Activities of Vitamin K-Dependent Coagulation Factors in One-Month-Old Infants

The Tohoku Journal of Experimental Medicine, 2007, Vol.211(1), pp.1-8

2007

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Molecular Genetic Dissection and Neonatal/Infantile Intrahepatic Cholestasis Using Targeted Next-Generation Sequencing

Clinical, Pathologic, and Genetic Features of Neonatal Dubin-Johnson Syndrome: A Multicenter Study in Japan

Antiviral therapy for hepatitis B virus during second pregnancies

Real-life Progression of the Use of a Genetic Panel in to Diagnose Neonatal Cholestasis

Standardization of phototherapy for neonatal hyperbilirubinemia using multiple-wavelength irradiance integration

Neurodevelopmental outcomes at 3 years old for infants with birth weights under 500 g

Case Report: Management of Cholestasis Associated With Congenital Syphilis

Prenatal findings of holoprosencephaly

Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state

Effects of tolvaptan on congestive heart failure complicated with chylothorax in a neonate

Effects of 4‐phenylbutyrate therapy in a preterm infant with cholestasis and liver fibrosis

Combination of Miller–Dieker syndrome and VACTERL association causes extremely severe clinical presentation

Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants

Neurodevelopmental Outcomes at 18 Months’ Corrected Age of Infants Born at 22 Weeks of Gestation

Effects of exchange transfusion on cytokine profiles in necrotizing enterocolitis

Detection of Pivaloylcarnitine in Pediatric Patients with Hypocarnitinemia after Long-Term Administration of Pivalate-Containing Antibiotics

Efficacy of pegylated interferon-α2a monotherapy in Japanese children with chronic hepatitis C

Hypothermia attenuates the severity of oxidative stress development in asphyxiated newborns

Periventricular Leukomalacia is Decreasing in Japan

Efficacy of antiviral therapy for the prevention of mother-to-child transmission of hepatitis B virus and the risk of postpartum hepatitis flare after discontinuation of antiviral therapy

Hepatitis C Virus Clearance after Discontinuation of Pegylated Interferon Alpha-2a Monotherapy in a Child

Effects of cyclosporine A in hyperzincaemia and hypercalprotectinaemia

Recurrent Cholangitis with Congenital Hepatic Fibrosis and Pancreaticobiliary Maljunction after Roux-en-Y Reconstruction

Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome

Polymorphisms of the Factor VII Gene Associated with the Low Activities of Vitamin K-Dependent Coagulation Factors in One-Month-Old Infants

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