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Urine Desmosine as a Novel Biomarker for Bronchopulmonary Dysplasia and Postprematurity Respiratory Disease in Extremely Preterm or Low Birth Weight Infants

American journal of perinatology, 2024-05, Vol.41 (S 01), p.e1030-e1036

2024

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Our challenges for the Intact Survival of Newborn Babies

Perinatology (Online), 2017-03, Vol.28 (1), p.1

Wada, Kazuko

2017

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4-Phenylbutyrate ameliorates apoptotic neural cell death in Down syndrome by reducing protein aggregates

Scientific reports, 2020-08, Vol.10 (1), p.14047-14047, Article 14047

2020

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Laryngeal atresia, esophageal atresia, and total anomalous pulmonary venous return in a monochorionic twin

Pediatrics international, 2022-01, Vol.64 (1), p.e14986-n/a

2022

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Socioeconomic inequity in survival for deliveries at 22–24 weeks of gestation

Archives of disease in childhood. Fetal and neonatal edition, 2018-05, Vol.103 (3), p.F202-F207

2018

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Feasibility of portable capnometer for mechanically ventilated preterm infants in the delivery room

European journal of pediatrics, 2022-02, Vol.181 (2), p.629-636

2022

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Postneonatal mortality of severely small for gestational age extremely low birth weight infants

Pediatrics and neonatology, 2024-03, Vol.65 (2), p.165-169

2024

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Effect of fluctuation of oxygenation on the development of severe retinopathy of prematurity in extremely preterm infants

Journal of perinatology, 2020-03, Vol.40 (3), p.515-521

2020

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Availability of portable capnometers in children with tracheostomy

Pediatrics international, 2021-07, Vol.63 (7), p.833-837

2021

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Systematic Cellular Disease Models Reveal Synergistic Interaction of Trisomy 21 and GATA1 Mutations in Hematopoietic Abnormalities

Cell reports (Cambridge), 2016-05, Vol.15 (6), p.1228-1241

2016

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MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene

Human genome variation, 2020, Vol.7 (1), p.4-4, Article 4

2020

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Elimination of protein aggregates prevents premature senescence in human trisomy 21 fibroblasts

PloS one, 2019-07, Vol.14 (7), p.e0219592

2019

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Mortality and morbidity of extremely low birth weight infants in Japan, 2015

Pediatrics international, 2023-01, Vol.65 (1), p.e15493-n/a

2023

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Pregnancy outcomes after preterm premature rupture of membranes: The Japan Environment and Children's Study

The journal of obstetrics and gynaecology research, 2022-11, Vol.48 (11), p.2756-2765

2022

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Early ileostomy in a 419 g infant and long‐term follow up: A case report

Pediatrics international, 2020-01, Vol.62 (1), p.94-95

2020

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Umbilical cord prolapse after preterm premature rupture of membranes

Taiwanese journal of obstetrics & gynecology, 2022-05, Vol.61 (3), p.489-493

2022

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Acquired uniparental disomy of chromosome 7 in a patient with MIRAGE syndrome that veiled a pathogenic SAMD9 variant

Clinical Pediatric Endocrinology, 2021, Vol.30(4), pp.163-169

2021

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Medical care of newborns born to mothers with confirmed or suspected severe acute respiratory syndrome coronavirus 2 infections in Japan

Pediatrics international, 2022-01, Vol.64 (1), p.e14855-n/a

2022

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Multiplex Real-Time PCR-Based Newborn Screening for Severe Primary Immunodeficiency and Spinal Muscular Atrophy in Osaka, Japan: Our Results after 3 Years

Genes, 2024-02, Vol.15 (3), p.314

2024

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Surgical treatment of traction retinal detachment associated with compound heterozygous congenital protein C deficiency

American journal of ophthalmology case reports, 2023-06, Vol.30, p.101854, Article 101854

2023

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A Pair of Maternal Chromosomes Derived from Meiotic Nondisjunction in Trisomy 21 Affects Nuclear Architecture and Transcriptional Regulation

Scientific reports, 2017-04, Vol.7 (1), p.764-14, Article 764

2017

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Inhaled nitric oxide for preterm infants with persistent pulmonary hypertension

Annals of Clinical Epidemiology, 2019, Vol.1(1), pp.18-27

2019

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Nationwide survey of neonatal transportation practices in Japan

Pediatrics international, 2016-04, Vol.58 (4), p.311-313

2016

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A novel de novo SLC26A3 mutation causing congenital chloride diarrhea in a Japanese neonate

Molecular genetics & genomic medicine, 2020-11, Vol.8 (11), p.e1505-n/a

2020

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Feeding interval and use of donor breast milk for very low birthweight infants: A nationwide survey in Japan

Pediatrics and neonatology, 2019-06, Vol.60 (3), p.245-251

2019

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Urine Desmosine as a Novel Biomarker for Bronchopulmonary Dysplasia and Postprematurity Respiratory Disease in Extremely Preterm or Low Birth Weight Infants

Our challenges for the Intact Survival of Newborn Babies

4-Phenylbutyrate ameliorates apoptotic neural cell death in Down syndrome by reducing protein aggregates

Laryngeal atresia, esophageal atresia, and total anomalous pulmonary venous return in a monochorionic twin

Socioeconomic inequity in survival for deliveries at 22–24 weeks of gestation

Feasibility of portable capnometer for mechanically ventilated preterm infants in the delivery room

Postneonatal mortality of severely small for gestational age extremely low birth weight infants

Effect of fluctuation of oxygenation on the development of severe retinopathy of prematurity in extremely preterm infants

Availability of portable capnometers in children with tracheostomy

Systematic Cellular Disease Models Reveal Synergistic Interaction of Trisomy 21 and GATA1 Mutations in Hematopoietic Abnormalities

MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene

Elimination of protein aggregates prevents premature senescence in human trisomy 21 fibroblasts

Mortality and morbidity of extremely low birth weight infants in Japan, 2015

Pregnancy outcomes after preterm premature rupture of membranes: The Japan Environment and Children's Study

Early ileostomy in a 419 g infant and long‐term follow up: A case report

Umbilical cord prolapse after preterm premature rupture of membranes

Acquired uniparental disomy of chromosome 7 in a patient with MIRAGE syndrome that veiled a pathogenic SAMD9 variant

Medical care of newborns born to mothers with confirmed or suspected severe acute respiratory syndrome coronavirus 2 infections in Japan

Multiplex Real-Time PCR-Based Newborn Screening for Severe Primary Immunodeficiency and Spinal Muscular Atrophy in Osaka, Japan: Our Results after 3 Years

Surgical treatment of traction retinal detachment associated with compound heterozygous congenital protein C deficiency

A Pair of Maternal Chromosomes Derived from Meiotic Nondisjunction in Trisomy 21 Affects Nuclear Architecture and Transcriptional Regulation

Inhaled nitric oxide for preterm infants with persistent pulmonary hypertension

Nationwide survey of neonatal transportation practices in Japan

A novel de novo SLC26A3 mutation causing congenital chloride diarrhea in a Japanese neonate

Feeding interval and use of donor breast milk for very low birthweight infants: A nationwide survey in Japan

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