Yukio Hattori

Ube, Japan

Last Updated: 09/26/2026

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Found 12 publications

Unstable hemoglobin Bicêtre, NM_000518.4(HBB):C.191A>C (p.His64Pro), with slightly decreased P50 and no polycythemia after splenectomy.

Unstable hemoglobin Bicêtre, NM_000518.4(HBB):C.191A>C (p.His64Pro), with slightly decreased P50 and no polycythemia after splenectomy.

Journal: Pediatric blood & cancer

Published: November 21, 2021

A new Krüppel-like factor 1 mutation (c.947G > A or p.C316Y) in humans causes β-thalassemia minor.

A new Krüppel-like factor 1 mutation (c.947G > A or p.C316Y) in humans causes β-thalassemia minor.

Journal: Hemoglobin

Published: February 19, 2015

The interference by HbF on HbA1c (BM Test HbA1c) measurement in enzymatic method.

The interference by HbF on HbA1c (BM Test HbA1c) measurement in enzymatic method.

Journal: Annals of clinical biochemistry

Published: December 21, 2014

Analysis of the Xmn1-(G) γ polymorphism in β-thalassemia/hemoglobin E (HbE) and homozygous HbE patients with low and high levels of HbF.

Analysis of the Xmn1-(G) γ polymorphism in β-thalassemia/hemoglobin E (HbE) and homozygous HbE patients with low and high levels of HbF.

Journal: International journal of laboratory hematology

Published: July 22, 2014

Oxidation status of β-thalassemia minor and Hb H disease, and its association with glycerol lysis time (GLT50).

Oxidation status of β-thalassemia minor and Hb H disease, and its association with glycerol lysis time (GLT50).

Journal: Hemoglobin

Published: March 12, 2014

Detection of beta-thalassemia/hemoglobin E disease in samples which initially were diagnosed as homozygous hemoglobin E.

Detection of beta-thalassemia/hemoglobin E disease in samples which initially were diagnosed as homozygous hemoglobin E.

Journal: Clinical laboratory

Published: July 20, 2013

A new β(0)-thalassemia mutation (codon 102, AAC>ATCAC) in coexistence with a heterozygous P4.2 Nippon gene.

A new β(0)-thalassemia mutation (codon 102, AAC>ATCAC) in coexistence with a heterozygous P4.2 Nippon gene.

Journal: Hemoglobin

Published: April 23, 2013

Establishment of multiplex hybri-probe method--analysis using the polymorphism of UGT1A1 gene

Establishment of multiplex hybri-probe method--analysis using the polymorphism of UGT1A1 gene

Journal: Rinsho byori. The Japanese journal of clinical pathology

Published: August 14, 2012

A 25-year observation of a Japanese female patient with Hb Nottingham who has two children with the same disorder.

A 25-year observation of a Japanese female patient with Hb Nottingham who has two children with the same disorder.

Journal: Hemoglobin

Published: July 17, 2012

The +1,506 (A>C) mutation in the 3' untranslated region affects β-globin expression.

The +1,506 (A>C) mutation in the 3' untranslated region affects β-globin expression.

Journal: Hemoglobin

Published: June 28, 2012

Identification of a novel mutation in the β-globin gene 3' untranslated region [+1,506 (A>C)] in a Japanese male with a heterozygous β-thalassemia phenotype.

Identification of a novel mutation in the β-globin gene 3' untranslated region [+1,506 (A>C)] in a Japanese male with a heterozygous β-thalassemia phenotype.

Journal: Hemoglobin

Published: January 06, 2012

Improved hybridization probe method for genetic analysis of beta-thalassemia

Improved hybridization probe method for genetic analysis of beta-thalassemia

Journal: Rinsho byori. The Japanese journal of clinical pathology

Published: November 25, 2011

Showing 1-12 of 12

Last Updated: 09/26/2026