Jamiyan Purevsuren
Izumo, Japan
Last Updated: 09/26/2026
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Found 15 publications
Overview of Telemedicine Services in Mongolia.
Journal: Current pediatrics reports
Published: June 29, 2021
Assessment of Spinal Muscular Atrophy Carrier Status by Determining SMN1 Copy Number Using Dried Blood Spots.
Journal: International journal of neonatal screening
Published: April 28, 2020
Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening.
Journal: Molecular genetics and metabolism reports
Published: March 31, 2018
The first Mongolian cases of phenylketonuria in selective screening of inborn errors of metabolism.
Journal: Molecular genetics and metabolism reports
Published: September 30, 2016
Efficacy of bezafibrate on fibroblasts of glutaric acidemia type II patients evaluated using an in vitro probe acylcarnitine assay.
Journal: Brain & development
Published: December 28, 2015
Internal Tandem Duplication in FLT3 Attenuates Proliferation and Regulates Resistance to the FLT3 Inhibitor AC220 by Modulating p21Cdkn1a and Pbx1 in Hematopoietic Cells.
Journal: PloS one
Published: November 24, 2015
Clinical Features of Carnitine Deficiency Secondary to Pivalate-Conjugated Antibiotic Therapy.
Journal: The Journal of pediatrics
Published: October 20, 2015
Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases.
Journal: Brain & development
Published: July 22, 2015
Mutations in HADHB, which encodes the β-subunit of mitochondrial trifunctional protein, cause infantile onset hypoparathyroidism and peripheral polyneuropathy.
Journal: American journal of medical genetics. Part A
Published: July 18, 2013
Clinical study of organic acidemias and fatty acid oxidation disorders detected in adults
Journal: Rinsho shinkeigaku = Clinical neurology
Published: March 26, 2013
Intracellular in vitro probe acylcarnitine assay for identifying deficiencies of carnitine transporter and carnitine palmitoyltransferase-1.
Journal: Analytical and bioanalytical chemistry
Published: July 24, 2012
Clinical and molecular aspects of Japanese children with medium chain acyl-CoA dehydrogenase deficiency.
Journal: Molecular genetics and metabolism
Published: June 18, 2012
Last Updated: 09/26/2026