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Inappropriate Hemoglobin Alc Level, Interference or Bonus?

Internal Medicine, 1997, Vol.36(5), pp.321-321

OHBA, Yuzo

1997

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Ultraviolet Resonance Raman Studies of Quaternary Structure of Hemoglobin Using a Tryptophan β37 Mutant (∗)

The Journal of biological chemistry, 1995-01, Vol.270 (4), p.1636-1642

1995

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Unstable Hemoglobinemia, Hb Buenos Aires, Bryn Mawr, Followed Up for Eighteen Years

FUKUOKA ACTA MEDICA, 2004-11, Vol.95 (11), p.297-304

2004

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Sporadic case of hemoglobin Bushwick detected by chance in aplastic crisis

Pediatrics international, 2000-04, Vol.42 (2), p.160-163

2000

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In Memoriam: Professor Susumu Shibata

Hemoglobin, 1998, Vol.22 (1), p.iii-v

Ohba, Yuzo

1998

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Inappropriate hemoglobin A1c level, interference or bonus?

Internal medicine (Tokyo, 1992), 1997-05, Vol.36 (5), p.321-321

Ohba, Y

1997

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Aspirin acetylation of βLys-82 of human hemoglobin

Biochemical pharmacology, 2000-10, Vol.60 (7), p.917-922

2000

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Aspirin acetylation of βLys-82 of human hemoglobin: NMR study of acetylated hemoglobin tsurumai

Biochemical pharmacology, 2000-10, Vol.60 (7), p.917-922

2000

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Two-Dimensional Electrophoresis for the Determination of Isoenzyme Specficities of LDH-Binding Immunoglobulin in Serum

Japanese Journal of Clinical Chemistry, 1985/06/25, Vol.14(3), pp.208-212

1985

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β-THALASSEMIA IN THE KOREAN POPULATION

Hemoglobin, 2002-01, Vol.26 (2), p.135-145

2002

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Clinical Features and Biochemical Aspects of Red Blood Cells in Hb Hirosaki

The Tohoku Journal of Experimental Medicine, 1981, Vol.133(2), pp.187-196

1981

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Ultraviolet Resonance Raman Studies of Quaternary Structure of Hemoglobin Using a Tryptophan 37 Mutant

The Journal of biological chemistry, 1995-01, Vol.270 (4), p.1636

1995

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A Novel Globin Structural Mutant, Showa-Yakushiji (β110 Leu-Pro) Causing a β-Thalassemia Phenotype

Blood, 1987-11, Vol.70 (5), p.1688-1691

1987

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Abnormal haemoglobinopathy

Japanese Journal of Clinical Chemistry, 1977/11/25, Vol.5(4), pp.351-357

1977

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Amino Acid Substitution in Hemoglobin MAkita

Journal of biochemistry (Tokyo), 1968-02, Vol.63 (2), p.193-198

1968

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A possible example of gene conversion with a common beta-thalassemia mutation and Chi sequence present in the beta-globin gene

Human genetics, 1992-01, Vol.88 (3), p.357-358

1992

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THE THIRD INSTANCE OF Hb M SASKATOON DISEASE DISCOVERED IN JAPAN

KAWASAKI MEDICAL JOURNAL, 1976, Vol.2 (4), p.185-197

1976

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A possible example of gene conversion with a common ?-thalassemia mutation and Chi sequence present in the ?-globin gene

Human genetics, 1992-01, Vol.88 (3)

1992

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THREE-BASE DELETION IN EXON 3 OF THE β-GLOBIN GENE PRODUCED A NOVEL VARIANT (βGUNMA) WITH A THALASSEMIA-LIKE PHENOTYPE

Blood, 1990-11, Vol.76 (9), p.1894-1896

1990

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Source of elevated serum mitochondrial creatine kinase activity in patients with malignancy

Clinica chimica acta, 1987-11, Vol.169 (2), p.159-163

1987

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Molecular Analysis of Japanese δβ-Thalassemia

Blood, 1988-11, Vol.72 (5), p.1771-1776

1988

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A single nucleotide deletion in codon 123 of the β‐globin gene causes an inclusion body β‐thalassaemia trait: a novel elongated globin chain βMakabe

British journal of haematology, 1990-07, Vol.75 (3), p.393-399

1990

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A family case of beta-thalassemia minor and hemoglobin Queens: alpha 34 (B15) Leu-Arg

Journal of Korean medical science, 1992-12, Vol.7 (4), p.385-388

1992

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A case of juvenile erythroleukemia with uncoordinated expression of fetal red cell markers

Acta haematologica, 1983-01, Vol.69 (4), p.275

1983

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Hb Toyoake: β142 (H20) Ala → Pro. A New Unstable Hemoglobin With High Oxygen Affinity

Blood, 1981-04, Vol.57 (4), p.697-704

1981

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Inappropriate Hemoglobin Alc Level, Interference or Bonus?

Ultraviolet Resonance Raman Studies of Quaternary Structure of Hemoglobin Using a Tryptophan β37 Mutant (∗)

Unstable Hemoglobinemia, Hb Buenos Aires, Bryn Mawr, Followed Up for Eighteen Years

Sporadic case of hemoglobin Bushwick detected by chance in aplastic crisis

In Memoriam: Professor Susumu Shibata

Inappropriate hemoglobin A1c level, interference or bonus?

Aspirin acetylation of βLys-82 of human hemoglobin

Aspirin acetylation of βLys-82 of human hemoglobin: NMR study of acetylated hemoglobin tsurumai

Two-Dimensional Electrophoresis for the Determination of Isoenzyme Specficities of LDH-Binding Immunoglobulin in Serum

β-THALASSEMIA IN THE KOREAN POPULATION

Clinical Features and Biochemical Aspects of Red Blood Cells in Hb Hirosaki

Ultraviolet Resonance Raman Studies of Quaternary Structure of Hemoglobin Using a Tryptophan 37 Mutant

A Novel Globin Structural Mutant, Showa-Yakushiji (β110 Leu-Pro) Causing a β-Thalassemia Phenotype

Abnormal haemoglobinopathy

Amino Acid Substitution in Hemoglobin MAkita

A possible example of gene conversion with a common beta-thalassemia mutation and Chi sequence present in the beta-globin gene

THE THIRD INSTANCE OF Hb M SASKATOON DISEASE DISCOVERED IN JAPAN

A possible example of gene conversion with a common ?-thalassemia mutation and Chi sequence present in the ?-globin gene

THREE-BASE DELETION IN EXON 3 OF THE β-GLOBIN GENE PRODUCED A NOVEL VARIANT (βGUNMA) WITH A THALASSEMIA-LIKE PHENOTYPE

Source of elevated serum mitochondrial creatine kinase activity in patients with malignancy

Molecular Analysis of Japanese δβ-Thalassemia

A single nucleotide deletion in codon 123 of the β‐globin gene causes an inclusion body β‐thalassaemia trait: a novel elongated globin chain βMakabe

A family case of beta-thalassemia minor and hemoglobin Queens: alpha 34 (B15) Leu-Arg

A case of juvenile erythroleukemia with uncoordinated expression of fetal red cell markers

Hb Toyoake: β142 (H20) Ala → Pro. A New Unstable Hemoglobin With High Oxygen Affinity

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