Masashi Nagai - Publications

Safe administration of sotrovimab to a COVID-19 patient with acute phase type 1 diabetes mellitus.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: December 05, 2022

Mild progressive osseous heteroplasia overlap syndrome with PTH and TSH resistance appearing during adolescence and not early childhood.

Journal: Endocrine

Published: April 23, 2021

Genetic Analysis of UGT1A1 Polymorphisms Using Preserved Dried Umbilical Cord for Assessing the Potential of Neonatal Jaundice as a Risk Factor for Autism Spectrum Disorder in Children.

Journal: Journal of autism and developmental disorders

Published: February 16, 2021

The ACTN3 577XX Null Genotype Is Associated with Low Left Ventricular Dilation-Free Survival Rate in Patients with Duchenne Muscular Dystrophy.

Journal: Journal of cardiac failure

Published: October 23, 2019

Schwann cell-specific Dp116 is expressed in glioblastoma cells, revealing two novel DMD gene splicing patterns.

Journal: Biochemistry and biophysics reports

Published: May 09, 2019

Identification of the shortest splice variant of Dp71, together with five known variants, in glioblastoma cells.

Journal: Biochemical and biophysical research communications

Published: November 02, 2018

The prescription rates of glucagon for hypoglycemia by pediatricians and physicians are low in Japan.

Journal: Endocrine

Published: September 14, 2018

Preliminary Effectiveness and Safety of High Frequency Oscillation in Addition to Mechanical Insufflation and Exsufflation for Intratracheal Mucus Removal in Patients With Neuromuscular Disease: Protocol for a Prospective Study.

Journal: JMIR research protocols

Published: September 05, 2018

Detection of Dystrophin Dp71 in Human Skeletal Muscle Using an Automated Capillary Western Assay System.

Journal: International journal of molecular sciences

Published: April 26, 2018

Congenital Cytomegalovirus Infection in Children with Autism Spectrum Disorder: Systematic Review and Meta-Analysis.

Journal: Journal of autism and developmental disorders

Published: November 30, 2017

Diagnostic and clinical significance of the titin fragment in urine of Duchenne muscular dystrophy patients.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: September 02, 2017

Dystrophin Dp116: A yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene.

Journal: Genes

Published: August 11, 2017