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A case of hemoglobin Hiroshima (β146 histidine to aspartic acid) with compensatory erythremia and undetectable HbA1c

International journal of hematology, 2012-06, Vol.95 (6), p.697-701

2012

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High incidence of α-thalassemia, hemoglobin e, and glucose-6-phosphate dehydrogenase deficiency in populations of malaria-endemic southern Shan State, myanmar

International journal of hematology, 2005-08, Vol.82 (2), p.119-123

2005

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A 6-year-old girl with hemoglobin H disease

Journal of Nippon Medical School = Nippon Ika Daigaku zasshi, 2011, Vol.78 (2), p.101-104

2011

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Hemoglobin Variant HbE Found in Two South Asian Diabetic Patients

Internal Medicine, 2009, Vol.48(16), pp.1397-1401

2009

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Normal glucose tolerance with high HbA1c levels observed in two cases of Hb variants

Diabetology international, 2010-12, Vol.1 (2), p.104-107

2010

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Simple and rapid analysis of beta-thalassemia mutation by sequence-specific amplification

Rinsho byori. The Japanese journal of clinical pathology, 2013-03, Vol.61 (3), p.217

2013

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Hb Nishinomiya [Leu-Gly-inserted between codons 69(E13) and 70(E14) of β]: A novel unstable hemoglobin with reduced oxygen affinity found in a patient with spherocytic hemolysis

International journal of hematology, 2002-08, Vol.76 (2), p.146-148

2002

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A family with hemoglobin Hirosaki

International journal of hematology, 2005-08, Vol.82 (2), p.124-126

2005

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The COL4A5 gene in Japanese Alport syndrome patients: Spectrum of mutations of all exons

Kidney international, 1996-03, Vol.49 (3), p.814-822

1996

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Two children with thalassemia identified during screening for anemia in junior high school

Journal of Nippon Medical School = Nippon Ika Daigaku zasshi, 2004-08, Vol.71 (4), p.297-300

2004

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Method-dependent HbA1c values in a family with hemoglobin Himeji

Clinica chimica acta, 2011-08, Vol.412 (17-18), p.1689-1692

2011

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Case of deletion type beta(0)-thalassemia found in an Asian (Malaysian) family living in Japan

Rinsho byori. The Japanese journal of clinical pathology, 2010-04, Vol.58 (4), p.325

2010

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A Study on Molecular Basis of Hypochromic Microcytic Anemia in Myanmar

KAWASAKI MEDICAL JOURNAL, 2005, Vol.31 (1/2), p.1-5

2005

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A Case With Falsely Elevated HbA1c Concentration Caused by Unknown Modified Hemoglobin

Journal of the Japan Diabetes Society, 2015/12/30, Vol.58(12), pp.915-922

2015

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A New Hemoglobin Variant, Hb Fukui [α139(HC1)Lys→Asn (AAA→AAC) (α2)]

Hemoglobin, 2003-01, Vol.27 (2), p.117-121

2003

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Application of an Automated Hemoglobin Analyzer, HLC-723G7, for Clinical Samples

KAWASAKI MEDICAL JOURNAL, 2004, Vol.30 (3/4), p.63-69

2004

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A case of hemoglobin Hiroshima ([beta]146 histidine to aspartic acid) with compensatory erythremia and undetectable HbA^sub 1c

International journal of hematology, 2012-06, Vol.95 (6), p.697

2012

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Hemoglobinopathies and Malaria Infection in Myanmar

KAWASAKI MEDICAL JOURNAL, 2002, Vol.28 (1), p.9-15

2002

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Hb Ube-2 in a Diabetic Case with an Abnormally Low HbA1C Value

Internal Medicine, 1999, Vol.38(10), pp.800-803

1999

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Hb Constant Spring [α142, Term→Gln (TAA>CAA in α2)] in the α-Thalassemia of Anemic Patients in Myanmar

Hemoglobin, 2008-01, Vol.32 (5), p.454-461

2008

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A Rare Super-Unstable Hemoglobin Variant, Hb Monroe [β30(B12)Arg-Thr], Found in Two Myanmar Children

KAWASAKI MEDICAL JOURNAL, 2001, Vol.27 (3/4), p.91-97

2001

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Hb Sallanches [α104(G11)Cys→Tyr, TGC→TAC (α2)]: An Unstable Hemoglobin Variant Found in an Indian Child

Hemoglobin, 2006, Vol.30 (3), p.393-396

2006

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Prevalence of Hemoglobin E Among the Children Taking Regular Blood Transfusion at the Day Care Room, Yangon Children Hospital, Myanmar

KAWASAKI MEDICAL JOURNAL, 2000, Vol.26 (4), p.149-154

2000

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Detection and Differentiation of Malaria Parasites in DNA Extracted from Blood Samples by the Polymerase Chain Reaction (PCR)

KAWASAKI MEDICAL JOURNAL, 2001, Vol.27 (3/4), p.83-89

2001

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Thalassemia Incidentally Found by Marked Erythrocytosis Due to an Ochre Mutation at Codon 35 in a Japanese Man

Internal Medicine, 1995, Vol.34(12), pp.1198-1200

1995

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A case of hemoglobin Hiroshima (β146 histidine to aspartic acid) with compensatory erythremia and undetectable HbA1c

High incidence of α-thalassemia, hemoglobin e, and glucose-6-phosphate dehydrogenase deficiency in populations of malaria-endemic southern Shan State, myanmar

A 6-year-old girl with hemoglobin H disease

Hemoglobin Variant HbE Found in Two South Asian Diabetic Patients

Normal glucose tolerance with high HbA1c levels observed in two cases of Hb variants

Simple and rapid analysis of beta-thalassemia mutation by sequence-specific amplification

Hb Nishinomiya [Leu-Gly-inserted between codons 69(E13) and 70(E14) of β]: A novel unstable hemoglobin with reduced oxygen affinity found in a patient with spherocytic hemolysis

A family with hemoglobin Hirosaki

The COL4A5 gene in Japanese Alport syndrome patients: Spectrum of mutations of all exons

Two children with thalassemia identified during screening for anemia in junior high school

Method-dependent HbA1c values in a family with hemoglobin Himeji

Case of deletion type beta(0)-thalassemia found in an Asian (Malaysian) family living in Japan

A Study on Molecular Basis of Hypochromic Microcytic Anemia in Myanmar

A Case With Falsely Elevated HbA1c Concentration Caused by Unknown Modified Hemoglobin

A New Hemoglobin Variant, Hb Fukui [α139(HC1)Lys→Asn (AAA→AAC) (α2)]

Application of an Automated Hemoglobin Analyzer, HLC-723G7, for Clinical Samples

A case of hemoglobin Hiroshima ([beta]146 histidine to aspartic acid) with compensatory erythremia and undetectable HbA^sub 1c

Hemoglobinopathies and Malaria Infection in Myanmar

Hb Ube-2 in a Diabetic Case with an Abnormally Low HbA1C Value

Hb Constant Spring [α142, Term→Gln (TAA>CAA in α2)] in the α-Thalassemia of Anemic Patients in Myanmar

A Rare Super-Unstable Hemoglobin Variant, Hb Monroe [β30(B12)Arg-Thr], Found in Two Myanmar Children

Hb Sallanches [α104(G11)Cys→Tyr, TGC→TAC (α2)]: An Unstable Hemoglobin Variant Found in an Indian Child

Prevalence of Hemoglobin E Among the Children Taking Regular Blood Transfusion at the Day Care Room, Yangon Children Hospital, Myanmar

Detection and Differentiation of Malaria Parasites in DNA Extracted from Blood Samples by the Polymerase Chain Reaction (PCR)

Thalassemia Incidentally Found by Marked Erythrocytosis Due to an Ochre Mutation at Codon 35 in a Japanese Man

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