Hereditary methemoglobinemia due to cytochrome b5 reductase deficiency in blood cells without associated neurologic and mental disorders

Studies with a murine monoclonal antibody that abolishes ristocetin- induced binding of von Willebrand factor to platelets: additional evidence in support of GPIb as a platelet receptor for von Willebrand factor

1983 • 469 citations

Isolation and Characterization of Plasma Membranes from Human Blood Platelets

1970 • 429 citations

A Function of Cytochrome b5 in Fatty Acid Desaturation by Rat Liver Microsomes

1971 • 389 citations

Purification of glycoproteins IIb and III from human platelet plasma membranes and characterization of a calcium-dependent glycoprotein IIb-III complex.

1982 • 337 citations

Catalysis of Methaemoglobin Reduction by Erythrocyte Cytochrome b5 and Cytochrome b5 Reductase

1971 • 282 citations

Characterization of the platelet membrane glycoprotein abnormalities in Bernard-Soulier syndrome and comparison with normal by surface-labeling techniques and high-resolution two-dimensional gel electrophoresis.

1982 • 245 citations

Additional glycoprotein defects in Bernard-Soulier's syndrome: confirmation of genetic basis by parental analysis

1983 • 186 citations

THE RELATION OF DIAPHORASE OF HUMAN ERYTHROCYTES TO INHERITANCE OF METHEMOGLOBINEMIA

1960 • 177 citations

Monoclonal Antibody to Human Platelet Glycoprotein I I. IMMUNOLOGICAL STUDIES

1981 • 166 citations

New method for determining ferrihemoglobin reductase (NADH-methemoglobin reductase) in erythrocytes.

1968 • 151 citations

The enzymic defect of hereditary methemoglobinemia: diaphorase

1959 • 144 citations

Purification and preliminary physicochemical characterization of human platelet membrane glycoprotein V.

1981 • 137 citations

Generalised deficiency of cytochrome b5 reductase in congenital methaemoglobinaemia with mental retardation

1975 • 132 citations

Requirement for cytochrome b₅ in microsomal stearyl coenzyme A desaturation

1972 • 127 citations

Purification and characterization of a calcium dependent sulfhydryl protease from human platelets

1981 • 118 citations

Electrophoresis of red cell NADH- and NADPH-diaphorases in normal subjects and patients with congenital methemoglobinemia

1967 • 116 citations

Further studies of the human platelet receptor for quinine- and quinine-dependent antibodies.

1981 • 86 citations

The effects of aggregated immunoglobulins on human blood platelets in relation to their complement-fixing abilities. I. Studies of immunoglobulins of different types.

1972 • 78 citations

Drug-Antibody-Platelet Interaction in Quinine- and Quinidine-induced Thrombocytopenia

1982 • 70 citations

Quinidine-induced thrombocytopenia and leukopenia: demonstration and characterization of distinct antiplatelet and antileukocyte antibodies

1983 • 69 citations

Isolation and structural characterization of the polypeptide subunits of membrane glycoprotein IIb-IIIa from human platelets

1982 • 68 citations

Purification and Properties of Soluble NADH-Cytochrome b5 Reductase of Rabbit Erythrocytes1

1982 • 41 citations

Monoclonal antibodies against antigens of the human platelet surface: preparation and properties

1984 • 36 citations

Structural analysis of human platelet membrane glycoprotein I complex.

1979 • 36 citations

Studies on quinine‐ and quinidine‐dependent antibodies against platelets and their reaction with platelets in the Bernard‐Soulier syndrome

1982 • 33 citations

HYBRIDOMAS SECRETING MONOCLONAL ANTIBODY TO TOXOPLASMA GONDII

1981 • 32 citations

The Metabolism of Methemoglobin in Human Erythrocytes

1975 • 31 citations

Mental Retardation in Methemoglobinemia Due to Diaphorase Deficiency

1965 • 31 citations

Factor VIII/von Willebrand Factor has potent lectin activity

1984 • 30 citations

Hereditary methemoglobinemia with and without mental retardation

1966 • 29 citations

Characterization of calcium-dependent binding of endogenous factor VIII/von Willebrand factor to surface activated platelets

1984 • 22 citations

Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b₅ reductase deficiency: First report of two cases

1981 • 13 citations

Cytochrome b5 reductase activity in erythrocytes and leukocytes as related to sex and age.

1984 • 13 citations

Congenital Methemoglobin- Reductase (Cytochrome b<sub>5</sub> Reductase) Deficiency Associated with Mental Retardation in a Spanish Girl

1978 • 10 citations

Erythrocyte enzymes in groups of Rattus norvegicus with genetic differences in 2,3-diphosphoglycerate levels

1979 • 10 citations

NADH-Cytochrome b<sub>5</sub> Reductase in Platelets and Leukocytes with Special Reference to Normal Levels and to Levels in Carriers of Hereditary Methemoglobinemia with or without Neurological Symptoms

1980 • 6 citations

Leukocyte Diaphorase Deficiency in Congenital Methemoglobinemia: a Valuable Prognostic Indicator

1977 • 4 citations

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