H. Arnold

PROFILE

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Aliases
H Arnold, Heidwolf Arnold
Publication record
46 papers · 287 citations · H-index 8

PAPERS

A rare combination of two inherited disorders in one patient: pyruvate kinase deficiency and hemochromatosis
20091 citationsauthor #1
Detection of phosphohexose isomerase deficiency in human fibroblast cultures
20047 citationsauthor #4
Combined erythrocyte glucosephosphate isomerase (GPI) and glucose-6-phosphate dehydrogenase (G6PD) deficiency in an italian family
20042 citationsauthor #1
Evidence for linkage between the locus for the AB0-system and the locus for phosphoglucoseisomerase (PGI)
20041 citationsauthor #3
The polymorphism of nucleosid effect in pyruvate kinase deficiency
20041 citationsauthor #4
Phase II Study of 1-(2-Chloroethyl)-3-(2-Hydroxyethyl)-1-Nitrosourea (HECNU) in Patients with Advanced Stomach and Large Bowel Cancers
19890 citationsauthor #3
High-dose desferoxamine and Diamond-Blackfan anemia.
19861 citationsauthor #2
Hemolytic anemia with pyruvate kinase deficiency presenting as paravertebral myelolipoma
19845 citationsauthor #3
[Hereditary erythrocyte pyruvate kinase abnormality: another kindred from Aargau Canton].
19840 citationsauthor #2
Cytotoxic activity in the serum of a patient with metastasizing nephroblastoma given intravenous infusions of alkyl-lysophospholipids in a phase I study
19820 citationsauthor #2
Augsburg-type glucosephosphate isomerase deficiency
19802 citationsauthor #1
[Erythrocyte enzymes and drugs].
19780 citationsauthor #2
[Controlled desferrioxamine treatment of congenital anaemia and transfusion siderosis (author's transl)].
19782 citationsauthor #1
[Standardized treatment of adult acute leukemia].
19780 citationsauthor #5
Creatine kinase in human erythrocytes: A newly detected genetic anomaly
19783 citationsauthor #1
Mechanisms for acquired red cell enzyme defects [letter]
19774 citationsauthor #1
Mechanisms for acquired red cell enzyme defects.
19773 citationsauthor #1
[Expenditure and success in the treatment of drug addicts].
19770 citationsauthor #1
[Psychiatric services].
19770 citationsauthor #1
Acquired pyruvate kinase deficiency with hemolysis in preleukemia.
19779 citationsauthor #2
[Social medical aspects of hypertension problems (author's transl)].
19770 citationsauthor #1
Effect of riboflavin treatment on human red cell pyruvate kinase deficiency.
19765 citationsauthor #2
Immunological studies on glucosephosphate isomerase deficiency: Instability and impaired synthesis of the defective enzyme
19755 citationsauthor #1
[Indication for splenectomy in hematologic diseases. Current views].
19752 citationsauthor #3
[Indication for splenectomy in hematologic diseases].
19751 citationsauthor #2
Glucose Phosphate Isomerase Deficiency with Congenital Nonspherocytic Hemolytie Anemia: A New Variant (Type Nordhorn). II. Purification and Biochemical Properties of the Defective Enzyme
197423 citationsauthor #1
[Bee hexokinase and the toxicity of mannose to bees (author's transl)].
19741 citationsauthor #1
[Concerning tissue-specific isoenzymes of glucosephosphate isomerase in man (author's transl)].
19740 citationsauthor #1
[Hereditary red cell enzyme defects: expressivity and molecular heterogeneity of abnormal enzyme proteins (author's transl)].
19740 citationsauthor #2
On the molecular basis of pyruvate kinase deficiency.
197416 citationsauthor #2
Isolelectric focusing of human red blood cell glutathione reductase saturated and unsaturated with flavin-adenin-dinucleotid
19740 citationsauthor #3
"Acquired" red cell enzyme defects in hematological diseases.
197428 citationsauthor #1
Genetic abnormalities in glutathione metabolism as a cause of drug-induced haemolytic anaemia.
19740 citationsauthor #1
Kurze wissenschaftliche Mitteilungen Isoeleetrie Focusing of Human Red Blood Cell 6)lutathione Reduetase Saturated and Unsaturated with Flavin-Adenin-Dinueleotid *
19740 citationsauthor #4
Proceedings: The effect of mannose on adenine nucleotide content in the isolated perfused rat liver.
19740 citationsauthor #3
[Pharmacogenetic causes in manifestation of hematologic diseases].
19730 citationsauthor #3
[Glucose phosphate isomerase type Recklinghausen: a new enzyme variant with haemolytic anaemia (author's transl)].
19730 citationsauthor #1
Hereditary deficiency of glucosephosphate isomerase as a cause of nonspherocytic hemolytic anemia
19739 citationsauthor #2
The molecular heterogeneity of red cell enzymopathies.
19731 citationsauthor #3
Additional diagnostic procedures for the detection of abnormal red cell pyruvate kinase.
197366 citationsauthor #2
[Glucose-6-P-dehydrogenase type bodensee (a new enzyme variant)].
19710 citationsauthor #3
Purification and properties of pyruvate kinase in normal and in pyruvate kinase deficient human red blood cells.
197173 citationsauthor #4
[Clinical studies on hereditary nonspherocytic anemia with erythrocyte pyruvate kinase deficiency].
19711 citationsauthor #3
[Formal genetics of phosphoglucose isomerase (EC:5.3.1.9). Studies of a family with PGI-deficiency].
197015 citationsauthor #2
[Clinical and biochemical studies of glucosephosphate isomerase of normal human erythrocytes and in glucosephosphate isomerase deficiency].
19700 citationsauthor #1
[CONTRIBUTION TO THE BIOCHEMISTRY OF AN EXPERIMENTAL LIVER CIRRHOSIS AND ON THE POSSIBILITY OF CONTROLLING IT PHARMACOLOGICALLY].
19630 citationsauthor #1

TIMELINE

1963 0 citations

1970 15 citations

1971 74 citations

1973 76 citations

1974 68 citations

1975 8 citations

1976 5 citations

1977 16 citations

1978 5 citations

1980 2 citations

1982 0 citations

1984 5 citations

1986 1 citations

1989 0 citations

2004 11 citations

2009 1 citations

H. Arnold

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