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Hemoglobin-specific antibody in a multiply transfused patient with sickle cell disease

Blood, 1997-03, Vol.89 (6), p.2155-2158

1997

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Juvenile myelomonocytic leukemia (JMML) with the hematologic phenotype of severe β thalassemia

American journal of hematology, 1998-05, Vol.58 (1), p.67-71

1998

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Hemoglobin Warsaw (Phe beta 42(CD1)----Val), an unstable variant with decreased oxygen affinity. Characterization of its synthesis, functional properties, and structure

The Journal of biological chemistry, 1990-01, Vol.265 (1), p.126-132

1990

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Fetal hemoglobin expression in transplant recipients of placental blood hematopoietic progenitor cells

Pediatric research, 1995-04, Vol.37 (4), p.432-436

1995

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Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia

The Journal of clinical investigation, 1984-06, Vol.73 (6), p.1740-1749

1984

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Hemoglobin Lincoln Park: a betadelta fusion (anti-Lepore) variant with an amino acid deletion in the delta chain-derived segment

Proceedings of the National Academy of Sciences - PNAS, 1978-03, Vol.75 (3), p.1475-1479

1978

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Similarities of the Erythrocytes in Juvenile Chronic Myelogenous Leukemia to Fetal Erythrocytes

Blood, 1972-06, Vol.39 (6), p.778-784

1972

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Hb South milwaukee [β105 (G7) leu → Phe]: A newly‐identified hemoglobin variant with high oxygen affinity

American journal of hematology, 1990-07, Vol.34 (3), p.199-203

1990

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Hb Warsaw (β42 Phe → Val): An unstable hemoglobin with decreased oxygen affinity. I. Hematologic and clinical expression

American journal of hematology, 1989-09, Vol.32 (1), p.36-41

1989

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Two New Sickle Cell Syndromes: HbS, Hb Camden, and α-Thalassemia; and HbS in Combination With Hb Tacoma

Blood, 1980-04, Vol.55 (4), p.655-660

1980

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Synthesis of Hemoglobin Abraham Lincoln (ß 32 leu →pro)

Blood, 1974-05, Vol.43 (5), p.657-664

1974

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HB Mizuho [β68(E12)LEU→PRO]. Second occurrence identified in a caucasian child with hemolytic anemia and dense erythrocyte inclusions

Hemoglobin, 1990, Vol.14 (2), p.129-136

1990

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Modelling whole blood oxygen equilibrium: comparison of nine different models fitted to normal human data

Advances in experimental medicine and biology, 1985, Vol.191, p.505

1985

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Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia

Pediatric research, 1976-06, Vol.10 (6), p.613-620

1976

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Hemoglobin Korle Bu in a Mexican Family

Hemoglobin, 1983, Vol.7 (2), p.185-189

1983

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Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia

Blood, 1980-01, Vol.55 (1), p.131-137

1980

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Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia

Blood, 1980-01, Vol.55 (1), p.131-137

1980

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Evaluation of Fagara zanthoxyloides root extract in sickle cell anemia blood in vitro

Lloydia, 1975-09, Vol.38 (5), p.387

1975

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Globin chain synthesis in sickle cell trait under conditions of folate antagonism

Acta haematologica, 1974-01, Vol.51 (4), p.236-239

1974

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Hb Rampa [alpha 95(G2)pro-->Ser (alpha 2)] in a family of European ancestry: DNA analysis confirms the CCG-->TCG mutation at codon 95 of the alpha 2-globin gene; clinical and laboratory features

Hemoglobin, 2002-11, Vol.26 (4), p.397-403

2002

Volltextzugriff (PDF)

HB Mizuho [β68(E12)LEU-PRO]. Second Occurrence Identified in A Caucasian Child with Hemolytic Anenia and Dense Erythrocyte Inclusions

Hemoglobin, 1990, Vol.14 (2), p.129-136

1990

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Hemoglobin Warsaw (Phe super( beta 42(CD1)) arrow right Val), an unstable variant with decreased oxygen affinity. Characterization of its synthesis, functional properties, and structure

The Journal of biological chemistry, 1990-01, Vol.265 (1), p.126-132

1990

Volltextzugriff (PDF)

Hb Mizuho ( beta 68(E12)Leu arrow right Pro). Second occurrence identified in a Caucasian child with hemolytic anemia and dense erythrocyte inclusions

Hemoglobin, 1990-01, Vol.14 (2), p.129-136

1990

Volltextzugriff (PDF)

Hb South Milwaukee ( beta 105 (G7) Leu arrow right Phe): A newly-identified hemoglobin variant with high oxygen affinity

American journal of hematology, 1990-01, Vol.34 (3), p.199-203

1990

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Effects in vitro of the proposed antisickling agent DBA

Nature (London), 1978-04, Vol.272 (5656), p.833-834

1978

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Hemoglobin-specific antibody in a multiply transfused patient with sickle cell disease

Juvenile myelomonocytic leukemia (JMML) with the hematologic phenotype of severe β thalassemia

Hemoglobin Warsaw (Phe beta 42(CD1)----Val), an unstable variant with decreased oxygen affinity. Characterization of its synthesis, functional properties, and structure

Fetal hemoglobin expression in transplant recipients of placental blood hematopoietic progenitor cells

Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia

Hemoglobin Lincoln Park: a betadelta fusion (anti-Lepore) variant with an amino acid deletion in the delta chain-derived segment

Similarities of the Erythrocytes in Juvenile Chronic Myelogenous Leukemia to Fetal Erythrocytes

Hb South milwaukee [β105 (G7) leu → Phe]: A newly‐identified hemoglobin variant with high oxygen affinity

Hb Warsaw (β42 Phe → Val): An unstable hemoglobin with decreased oxygen affinity. I. Hematologic and clinical expression

Two New Sickle Cell Syndromes: HbS, Hb Camden, and α-Thalassemia; and HbS in Combination With Hb Tacoma

Synthesis of Hemoglobin Abraham Lincoln (ß 32 leu →pro)

HB Mizuho [β68(E12)LEU→PRO]. Second occurrence identified in a caucasian child with hemolytic anemia and dense erythrocyte inclusions

Modelling whole blood oxygen equilibrium: comparison of nine different models fitted to normal human data

Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia

Hemoglobin Korle Bu in a Mexican Family

Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia

Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia

Evaluation of Fagara zanthoxyloides root extract in sickle cell anemia blood in vitro

Globin chain synthesis in sickle cell trait under conditions of folate antagonism

Hb Rampa [alpha 95(G2)pro-->Ser (alpha 2)] in a family of European ancestry: DNA analysis confirms the CCG-->TCG mutation at codon 95 of the alpha 2-globin gene; clinical and laboratory features

HB Mizuho [β68(E12)LEU-PRO]. Second Occurrence Identified in A Caucasian Child with Hemolytic Anenia and Dense Erythrocyte Inclusions

Hemoglobin Warsaw (Phe super( beta 42(CD1)) arrow right Val), an unstable variant with decreased oxygen affinity. Characterization of its synthesis, functional properties, and structure

Hb Mizuho ( beta 68(E12)Leu arrow right Pro). Second occurrence identified in a Caucasian child with hemolytic anemia and dense erythrocyte inclusions

Hb South Milwaukee ( beta 105 (G7) Leu arrow right Phe): A newly-identified hemoglobin variant with high oxygen affinity

Effects in vitro of the proposed antisickling agent DBA

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