Three families with unstable hemoglobinopathies (Köln, Olmsted and Santa Ana) causing hemolytic anemia with inclusion bodies and pigmenturia

Improved method for the determination of blood glutathione.

1963 • 6,733 citations

MICRODETERMINATION OF OXYHEMOGLOBIN, METHEMOGLOBIN, AND SULFHEMOGLOBIN IN A SINGLE SAMPLE OF BLOOD

1938 • 1,194 citations

PROTEIN COAGULATION AND ITS REVERSAL

1930 • 493 citations

The glutathione instability of drug-sensitive red cells; a new method for the in vitro detection of drug sensitivity.

1957 • 456 citations

Autohemolysis and Other Changes Resulting from the Incubation in Vitro of Red Cells from Patients with Congenital Hemolytic Anemia

1954 • 289 citations

Pyruvate Kinase (PK) Deficiency Hereditary Nonspherocytic Hemolytic Anemia

1962 • 267 citations

DIAGNOSTIC LABORATORY HEMATOLOGY

1955 • 248 citations

PURIFICATION AND PROPERTIES OF d-GLUCOSE-6-PHOSPHATE DEHYDROGENASE

1955 • 214 citations

Hydrogen Peroxide Toxicity and Detoxification in the Erythrocytes of Newborn Infants

1967 • 206 citations

The hemolytic effect of primaquine. VI. An in vitro test for sensitivity of erythrocytes to primaquine.

1955 • 198 citations

Hereditary Heinz‐Body Anaemia

1964 • 187 citations

Hereditary Hemolytic Anemia with Hexokinase Deficiency

1967 • 183 citations

Inclusions of Hemoglobin in Erythroblasts and Erythrocytes of Thalassemia

1963 • 168 citations

Haemoglobin Köln (β–98 Valine → Methionine): An Unstable Protein Causing Inclusion-Body Anaemia

1966 • 167 citations

Haemoglobin Hammersmith (β 42 (CD1) Phe→Ser)

1967 • 149 citations

HEMOGLOBIN CATABOLISM

1958 • 148 citations

Congenital Heinz‐Body Anaemia

1964 • 132 citations

A Simple Visual Screening Test for Glucose-6-Phosphate Dehydrogenase Deficiency Employing Ascorbate and Cyanide

1966 • 97 citations

Haemoglobin Genova: β28 (B10) Leucine→Proline

1967 • 91 citations

Haemoglobin Sydney: β67 (EII) Valine→ Alanine : an Emerging Pattern of Unstable Haemoglobins

1967 • 85 citations

Erythrocyte Glutathione Reductase

1963 • 84 citations

Haemoglobin Torino – α43 (CDI) Phenylalanine→Valine

1968 • 74 citations

Hereditary Heinz-body Anaemia, Thrombocyttopenia, and Haemoglobinopathy (Hb Koln) in a Glasgow Family

1964 • 72 citations

HemoglobinBibba or α2136Proβ2, an unstable α chain abnormal hemoglobin

1968 • 72 citations

Hemoglobin H; clinical, laboratory, and genetic studies of a family with a previously undescribed hemoglobin.

1956 • 71 citations

Hemoglobin Zürich

1965 • 69 citations

SPECTROPHOTOMETRIC MICROMETHOD FOR THE QUANTITATIVE DETERMINATION OF THE FREE ERYTHROCYTE PROTOPORPHYRIN

1948 • 68 citations

Studies on the Formation of Heinz Bodies. II. The Nature and Significance of Heinz Bodies

1961 • 59 citations

Congenital Hemolytic Disease Associated with Red Cell Inclusion Bodies, Abnormal Pigment Metabolism and an Electrophoretic Hemoglobin Abnormality

1960 • 50 citations

Über Mesobilifuscin, ein neues physiologisches Abbauprodukt des Häms bzw. Hämatins

1939 • 46 citations

Congenital Hemolytic Anemia with Abnormal Pigment Metabolism and Red Cell Inclusion Bodies: a New Clinical Syndrome

1958 • 44 citations

Diagnostic Laboratory Hematology.

1964 • 44 citations

Familial Hemolytic Anemia with Erythrocyte Inclusion Bodies and a Defect in Pigment Metabolism

1959 • 44 citations

STUDIES OF THE DIPYRRYLMETHENE (“FUSCIN”) PIGMENTS. I. THE ANABOLIC SIGNIFICANCE OF THE FECAL MESOBILIFUSCIN*

1959 • 40 citations

Köln Haemoglobinopathy: FURTHER DATA AND A COMPARISON WITH OTHER HEREDITARY HEINZ BODY ANAEMIAS

1967 • 37 citations

HEMOLYTIC DISEASE ASSOCIATED WITH THE PRODUCTION OF ABNORMAL HEMOGLOBIN AND INTRAERYTHROCYTIC HEINZ BODIES.

1963 • 31 citations

Hemoglobin tacoma ? A ?-chain variant

1966 • 30 citations

Dipyrrolic urinary pigments in congenital Heinz-body anaemia due to Hb kA ln and in thalassaemia.

1966 • 27 citations

Hämoglobin-Köln-Krankheit: Familiäre hypochrome hämolytische Anämie mit Hämoglobinanomalie

1965 • 26 citations

Familial Haemolytic Anaemia with Erythrocyte Inclusion Bodies, Bilifuscinuria and Abnormal Haemoglobin (Haemoglobin Galliera Genova)

1965 • 26 citations

Man's Haemoglobins. Including the Haemoglobinopathies and their Investigation.

1975 • 24 citations

STUDIES OF THE DIPYRRYLMETHENE (“FUSCIN”) PIGMENTS. II. THE CONTRASTING RATIOS AND SIGNIFICANCE OF THE FECAL UROBILINOGEN AND MESOBILIFUSCIN IN CERTAIN ANEMIAS*

1959 • 19 citations

A West Australian Family with a Haemolytic Disorder Associated with Haemoglobin Köln

1967 • 19 citations

Man's Haemoglobins, Including the Haemoglobinopathies and Their Investigation.

1966 • 13 citations

Compensated hereditary haemolytic disease resulting from an unstable haemoglobin fraction.

1967 • 13 citations

COMPENSATED HEREDITARY HAEMOLYTIC DISEASE RESULTING FROM AN UNSTABLE HAEMOGLOBIN FRACTION

1967 • 10 citations

[27] 6-Phosphogluconate dehydrogenase—Clinical aspects

1966 • 9 citations

A technique for the processing of blood samples for subsequent assay of ATP, and an investigation of the method of standardization of the firefly-luciferase ATP assay

1966 • 6 citations

Angeborene hämolytische Anämie mit Mesobilifuscinurie und Innenkörperbildung nach Splenectomie

1964 • 6 citations

The experimental production of Heinz bodies in various hemoglobinopathies and the thalassemic syndromes.

1958 • 5 citations

Inclusion Body Anemia With Pigmenturia

1964 • 4 citations