Kumiko Ohkubo
Fukuoka, Japan
Last Updated: 09/26/2026
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Found 8 publications
Analysis of the diagnostic capabilities of urinary neutrophil gelatinase-associated lipocalin and serum procalcitonin for acute kidney injury at the early stage of critical care intensive care unit admission.
Journal: Journal of clinical laboratory analysis
Published: March 11, 2021
Definitive diagnosis of mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome caused by a recurrent de novo mutation in the POLD1 gene.
Journal: Endocrine journal
Published: December 05, 2017
Analysis of Hepatitis B Virus Reactivation in Fukuoka University Hospital
Journal: Rinsho byori. The Japanese journal of clinical pathology
Published: June 01, 2016
Novel subtype of congenital partial lipodystrophy with mandibular hypoplasia, sensorineural deafness and short stature of unknown genetic origin.
Journal: Journal of diabetes investigation
Published: January 18, 2016
A Hospital-Based Analysis in the Department of Clinical Chemistry for the Patients with HBV Reactivation after Anti-Cancer or Immunosuppressive Therapy.
Journal: Rinsho byori. The Japanese journal of clinical pathology
Published: November 04, 2015
A novel mutation of CLCNKB in a Japanese patient of Gitelman-like phenotype with diuretic insensitivity to thiazide administration.
Journal: Meta gene
Published: December 24, 2013
Influence of pre-analytical storage conditions on four plasma coagulation molecular markers measured using a STACIA automatic coagulation analyzer
Journal: Rinsho byori. The Japanese journal of clinical pathology
Published: February 23, 2013
Clinical application of the different cross-reactivities of anti-insulin antibodies to insulin lispro to evaluate endogenous insulin secretion.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: August 02, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026