Kohei Kashima
Narita, Japan
Last Updated: 09/26/2026
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Found 28 publications
Severe Unilateral Hand Reduction Defect With a Central Cleft in a Child With Megalencephaly-Capillary Malformation Syndrome.
Journal: Congenital anomalies
Published: May 12, 2026
Outcomes of early-phase ampicillin plus aminoglycosides versus ampicillin plus cefotaxime for preterm infants.
Journal: Pediatric research
Published: November 15, 2025
Helios expression in naive CD4+ T cells decreases from neonates to older adults.
Journal: Clinical and experimental immunology
Published: August 20, 2025
Author Correction: Host-derived protein profiles of human neonatal meconium across gestational ages.
Author Correction: Host-derived protein profiles of human neonatal meconium across gestational ages.
Journal: Nature communications
Published: June 25, 2025
Urinary prostaglandin E major urinary metabolite in neonates: Gestational age at birth-dependent dynamics and clinical implications.
Journal: Pediatrics and neonatology
Published: June 04, 2025
Ischemic placental disease as a risk factor for bronchopulmonary dysplasia in extremely preterm infants.
Journal: The journal of obstetrics and gynaecology research
Published: December 25, 2024
Association between early-phase opioid use and outcomes in extremely preterm infants: A nationwide study.
Journal: Pediatric research
Published: October 10, 2024
Factors associated with extrauterine growth restriction in very-low-birth-weight infants: A retrospective study in Japan.
Journal: Pediatrics and neonatology
Published: October 09, 2024
Rate of vertical transmission of coronavirus disease 2019 and effect of maternal vaccination: A prospective cohort study.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: June 18, 2024
Neurological outcomes and associated perinatal factors in infants born between 22 and 25 weeks with active care.
Journal: Journal of perinatology : official journal of the California Perinatal Association
Published: June 09, 2024
A case of inherited glycosylphosphatidylinositol deficiency caused by PGAP3 variant with uniparental isodisomy on chromosome 17.
Journal: Molecular genetics & genomic medicine
Published: January 27, 2024
Last Updated: 09/26/2026