Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl) (Q40016315)

16 September 2017

1 reference

reason for deprecated rank

title

Enzymdefekte in Glykolyse und Nukleotidstoffwechsel roter Blutzellen bei nichtsph�rocyt�ren h�molytischen An�mien (German)

marking inconsistent with the registered/official identifier/name

1 reference

reason for deprecated rank

25 December 2022

Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl) (English)

marking inconsistent with the registered/official identifier/name

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A184346

25 December 2022

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25 December 2022

author name string

H. D. Waller

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A184346

25 December 2022

H. C. Benöhr

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A184346

25 December 2022

language of work or name

German

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publication date

1 September 1976

1 reference

full work available at URL

16 September 2017

http://link.springer.com/content/pdf/10.1007/BF01469302.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF01469302/fulltext.html

25 December 2022

1 reference

http://link.springer.com/content/pdf/10.1007/BF01469302

25 December 2022

1 reference

25 December 2022

published in

Klinische Wochenschrift

1 reference

16 September 2017

volume

54

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16 September 2017

issue

17

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16 September 2017

page(s)

803-821

1 reference

Hereditary Glucosephosphate Isomerase Deficiency: A Review

16 September 2017

cites work

1 reference

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An inherited molecular lesion of erythrocyte pyruvate kinase. Identification of a kinetically aberrant isozyme associated with premature hemolysis

21 January 2018

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Human erythrocyte phosphofructokinase: its purification and some properties.

21 January 2018

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Chronic hemolytic anemia associated with erythrocyte enolase deficiency exacerbated by ingestion of nitrofurantoin

21 January 2018

1 reference

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Muscle Phosphofructokinase Deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01469302

Glutathione (author's transl)

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12 December 2020

Unique phenotypic expression of glucosephosphate isomerase deficiency

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Hereditary non-spherocytic hemolytic anemia of the pyruvate-kinase deficient type

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A new type of phosphofructokinase deficiency hereditary nonspherocytic hemolytic anemia.

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HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY

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12 December 2020

HEREDITARY NON-SPHEROCYTIC HAEMOLYTIC ANAEMIA. A STUDY OF RED-CELL CARBOHYDRATE METABOLISM IN TWELVE CASES OF PYRUVATE-KINASE DEFICIENCY

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12 December 2020

[Problems of erythrocyte metabolism in anemias with pyruvate kinase deficiency]

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12 December 2020

Electrophoretic and kinetic studies of mutant erythrocyte pyruvate kinases

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12 December 2020

Glucose phosphate isomerase type Recklinghausen: a new enzyme variant with haemolytic anaemia (author's transl)

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12 December 2020

The mechanism of precursor modulation of human pyruvate kinase I by fructose diphosphate

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12 December 2020

Some properties of abnormal red blood cell pyruvate kinase

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12 December 2020

Glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Report of the first case found in Japanese

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12 December 2020

Evidence against the occurrence of tissue-specific variants and isoenzymes of phosphoglucose isomerase

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12 December 2020

Hemolytic anemia and hexokinase deficiency associated with malformations

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12 December 2020

Liver pyruvate kinase (PK) isozymes in a PK-deficient patient

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12 December 2020

Hereditary high ATP content of human erythrocytes

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12 December 2020

Detection of glucose-phosphate isomerase deficiency by a screening procedure

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12 December 2020

Life-Span and Organ Sequestration of the Red Cells in Pyruvate Kinase Deficiency

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12 December 2020

Hereditary elliptocytosis and pyruvate kinase deficiency of the erythrocytes

1 reference

12 December 2020

Congenital hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes, polynuclear cells and lymphocytes

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12 December 2020

[Hexokinase deficiency in hemolytic anemia]

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12 December 2020

[Familial diphosphoglycerate mutase deficiency: hematological and biochemical study]

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12 December 2020

Erythrocyte and leukocyte phosphoglycerate kinase deficiency with neurologic disease

1 reference

12 December 2020

A new type of pyruvate-kinase deficiency of human erythrocytes.

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12 December 2020

Inherited variations in human phosphohexose isomerase

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12 December 2020

Distribution of fructose diphosphate aldolase variants in biological systems

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12 December 2020

Interconvertible Kinetic and Physical Forms of Human Erythrocyte Pyruvate Kinase

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12 December 2020

Studies on erythrocyte metabolism in a case with hereditary deficiency of H-subunit of lactate dehydrogenase

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12 December 2020

[On the effect of glycolytic intermediary products on the 2,3-PGase activity of red blood cells]

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12 December 2020

Familial diphosphoglyceratemutase deficiency. Influence on the oxygen affinity curves of hemoglobin

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12 December 2020

Studies on pyruvate kinase (PK) deficiency. II. Electrophoretic, kinetic and immunological studies on pyruvate kinase of erythrocytes and other tissues.

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12 December 2020

Fine structure of the spleen and liver in glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Selective reticulocyte destruction as a mechanism of hemolysis

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12 December 2020

Red Cell Aldolase Deficiency in Hereditary Spherocytosis

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12 December 2020

Familial hemolytic anemia resulting from an abnormal red blood cell pyruvate kinase

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12 December 2020

Hereditary deficiency of subunit H of lactate dehydrogenase

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12 December 2020

Clinical heterogeneity of erythrocyte pyruvate kinase deficiency. Evidence of an impaired utilization of ATP in a clinically severe form

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12 December 2020

[Congenital pyruvate kinase deficiency in erythrocytes: kinetic study of the enzyme and metabolic consequences]

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12 December 2020

Red cell aldolase deficiency and hemolytic anemia: a new syndrome

1 reference

12 December 2020

Membrane-localized pyruvate kinase of red blood cells in hemolytic anemia associated with pyruvate kinase deficiency

1 reference

12 December 2020

Detection of phosphohexose isomerase deficiency in human fibroblast cultures

1 reference

12 December 2020

Hereditary Deficiency of Adenylate Kinase in Red Blood Cells

1 reference

12 December 2020

Multiple forms of fructose diphosphate aldolase in mammalian tissues

1 reference

12 December 2020

A Low KmPhosphoenolpyruvate Mutant in the Amish with Red Cell Pyruvate Kinase Deficiency

1 reference

12 December 2020

Glucose phosphate isomerase deficiency with hereditary hemolytic anemia in a Spanish family: Clinical and familial studies

1 reference

12 December 2020

Red-cell metabolism in non-spherocytic congenital haemolytic anaemia

1 reference

12 December 2020

Electrophoretic separation of isoenzymes of glutathione reductase and pyruvate kinase in human erythrocytes

1 reference

12 December 2020

Anomalies of glycolysis during hemolytic anemia due to deficiency of pyruvate kinase in the erythrocytes

1 reference

12 December 2020

A NEW INHERITED ABNORMALITY OF HUMAN ERYTHROCYTES: ELEVATED ERYTHROCYTIC ADENOSINE TRIPHOSPHATE

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12 December 2020

Acquired red cell pyruvate kinase deficiency in leukemias and related disorders

1 reference

12 December 2020

Glucose phosphate isomerase deficiency with hereditary nonspherocytic hemolytic anemia

1 reference

12 December 2020

Evidence of the decreased muscle enzyme activity in erythrocyte phosphoglycerate kinase deficiency

1 reference

12 December 2020

A new variant of red blood cell pyruvate kinase deficiency

1 reference

12 December 2020

[Hematologic enzymology]

1 reference

12 December 2020

Hereditary deficiency of glucosephosphate isomerase as a cause of nonspherocytic hemolytic anemia.

1 reference

12 December 2020

Genetic enzyme deficiencies of the hexokinase and the transport-adenosine triphosphate phosphohydrolase of the erythrocytes

1 reference

12 December 2020

[Congenital non spherocytic hemolytic anemia caused by pyruvate kinase abnormalities]

1 reference

12 December 2020

Congenital nonspherocytic hemolytic anemia associated with an unusual erythrocyte hexokinase abnormality

1 reference

12 December 2020

Red cell aldolase and other enzyme activities in hereditary spherocytosis

1 reference

12 December 2020

Four New Pyruvate Kinase (PK) Variants and a Classical PK Deficiency

1 reference

12 December 2020

Nonspherocytic haemolytic anaemia and severe jaundice in a newborn with partial pyruvate kinase deficiency

1 reference

12 December 2020

EXTREME HEMOLYSIS AND RED-CELL DISTORTION IN ERYTHROCYTE PYRUVATE KINASE DEFICIENCY. I. MORPHOLOGY, ERYTHROKINETICS AND FAMILY ENZYME STUDIES

1 reference

12 December 2020

Phosphoglycerate kinase (PKG) deficiency hereditary nonspherocytic hemolytic anemia: report of a case found in a Japanese family.

1 reference

12 December 2020

Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome

1 reference

12 December 2020

Hereditary hemolytic anemia with hexokinase deficiency. Role of hexokinase in erythrocyte aging

1 reference

12 December 2020

[Hemolysis and absence of glucose-6-phosphate dehydrogenase in erythrocytes; an enzyme abnormality of erythrocytes]

1 reference

12 December 2020

Studies on erythrocyte glycolysis. I. Determination of the glycolytic intermediates in human erythrocytes

1 reference

12 December 2020

Adenosine-triphosphatase deficiency in a family with non-spherocytic haemolytic anaemia

1 reference

12 December 2020

Red cell glycolysis in a case of 3-phosphoglycerate kinase deficiency.

1 reference

12 December 2020

Further evidence of molecular alteration and aberration of erythrocyte pyruvate kinase

1 reference

12 December 2020

Occurrence of Defective Hexosephosphate Isomerization in Human Erythrocytes and Leukocytes

1 reference

12 December 2020

Glucosephosphate isomerase deficiency: evidence for in vivo instability of an enzyme variant with hemolysis

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12 December 2020

Red cell pyruvate kinase deficiency. The effect of splenectomy

1 reference

12 December 2020

[Concerning tissue-specific isoenzymes of glucosephosphate isomerase in man (author's transl)]

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12 December 2020

Evidence for molecular alteration of pyruvate kinase as a consequence of erythrocyte aging

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12 December 2020

[Erythrocyte and leucocyte 3-phosphoglycerate kinase deficiency. Studies of properties of the enzyme, phagocytic activity of the polymorphonuclear leucoytes and a review of the literature]

1 reference

12 December 2020

Purification and characterization of human phosphoglucose isomerase

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12 December 2020

Glucosephosphate-Isomerase (GPI) Deficiency: GPI Elyria

1 reference

12 December 2020

Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia

1 reference

12 December 2020

Enzymatic deficiency in primaquine-sensitive erythrocytes

1 reference

12 December 2020

[Coexistence of 2 types of kinetically different pyruvate kinase in normal human erythrocytes]

1 reference

12 December 2020

Immunological studies on glucosephosphate isomerase deficiency: Instability and impaired synthesis of the defective enzyme

1 reference

12 December 2020

A new erythroenzymopathy: congenital non-spherocytic hemolytic anemia and hereditary erythrocytic adenylate kinase deficiency

1 reference

12 December 2020

Erythrocyte pyruvate kinase in healthy subjects and in nonspherocytic hemolytic pyruvate-kinase deficiency anemia

1 reference

12 December 2020

[Observation of a case of partial deficiency of intraerythrocyte ATPase]

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12 December 2020

Electrophoretic and kinetic studies of glucosephosphate isomerase (GPI) in two different Japanese families with GPI deficiency

1 reference

12 December 2020

Metabolism in haemolytic states

1 reference

12 December 2020

Glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Report of the second case found in Japanese

1 reference

12 December 2020

Purification and properties of pyruvate kinase in normal and in pyruvate kinase deficient human red blood cells

1 reference

12 December 2020

[Hereditary red cell enzyme defects: expressivity and molecular heterogeneity of abnormal enzyme proteins (author's transl)]

1 reference

12 December 2020

Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia

1 reference

12 December 2020

A specific erythrocyte glycolytic enzyme defect (pyruvate kinase) in three subjects with congenital non-spherocytic hemolytic anemia

1 reference

12 December 2020

2,3-PGase deficiency as a possible cause of increased ATP-content

1 reference

12 December 2020

Pyruvate kinase deficiency

1 reference

12 December 2020

Selective reticulocyte destruction in erythrocyte pyruvate kinase deficiency

1 reference

12 December 2020

Molecular mechanism of erythrocyte pyruvate kinase deficiency

1 reference

12 December 2020

Combined Glucosephosphate Isomerase and Glucose-6-Phosphate Dehydrogenase Deficiency of the Erythrocytes: A New Haemolytic Syndrome

1 reference

12 December 2020

Characterization of two new variants of glucose-phosphate-isomerase deficiency with hereditary nonspherocytic hemolytic anemia

1 reference

12 December 2020

Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). I. Clinical and genetic studies

1 reference

12 December 2020

Characterization of erythrocyte membrane-associated enzymes (glyceraldehyde-3-phosphate dehydrogenase and phosphoglyceric kinase)

1 reference

12 December 2020

Studies on pyruvate kinase (PK) deficiency. I. Clinical, hematological and erythrocyte enzyme studies.

1 reference

12 December 2020

Mechanism of fructose diphosphate activation of a mutant pyruvate kinase from human red cells

1 reference

12 December 2020

Three cases in two families with congenital nonspherocytic hemolytic anemia due to defective glucosephosphate isomerase: GPI Matsumoto

1 reference

12 December 2020

Pyruvate kinase (PK) deficiency hereditary nonspherocytic hemolytic anemia

1 reference

12 December 2020

[Relative deficiency of glutathione reductase and or pyruvate kinase in erythrocytes in aplastic anemia and acute leukemia]

1 reference

12 December 2020

Erythrocyte phosphofructokinase deficiency associated with an unstable variant of muscle phosphofructokinase

1 reference

12 December 2020

Enzyme defects in bone-marrow insufficiency

1 reference

12 December 2020

Normalisation of red blood cell pyruvate kinase in pyruvate kinase deficiency by riboflavin treatment

1 reference

12 December 2020

Phosphoglycerate kinase: an X-linked polymorphism in man

1 reference

12 December 2020

[CONGENITAL 2,3-DIPHOSPHOGLYCEROMUTASE DEFICIENCY.]

1 reference

12 December 2020

Multimolecular forms of pyruvate kinase from rat and other mammalian tissues. I. Electrophoretic studies

1 reference

12 December 2020

Hereditary nonspherocytic hemolysis with erythrocyte phosphofructokinase deficiency

1 reference

12 December 2020

An unusual hematological syndrome with pyruvate-kinase deficiency and thalassemia minor in the kindreds

1 reference

12 December 2020

The polymorphism of nucleosid effect in pyruvate kinase deficiency

1 reference

12 December 2020

Physical and kinetic properties of human phosphofructokinase from skeletal muscle and erythrocytes

1 reference

12 December 2020

Additional kinetic distinctions between normal pyruvate kinase and a mutant isozyme from human erythrocytes. Correction of the kinetic anomaly by fructose-1,6-diphosphate

1 reference

12 December 2020

Regulation of glycolysis in human red cells.

1 reference

12 December 2020

Sequestration and destruction of reticulocyte in the spleen in pyruvate kinase deficiency hereditary nonspherocytic hemolytic anemia

1 reference

12 December 2020

Functionally abnormal pyruvate kinase in congenital hemolytic anemia

1 reference

12 December 2020

Neonatal Hemolysis Due to a Transient Severity of Inherited Pyruvate Kinase Deficiency

1 reference

12 December 2020

[Excessive erythrocyte ATP level feature of a hereditary nonspherocytic hemolytic anemia in disturbed ATP utilization and a red cell metabolic anomaly without disease value]

1 reference

12 December 2020

Erythrocyte pyruvate kinase deficiency in non-spherocytic hemolytic anemia: a system of multiple genetic markers?

1 reference

12 December 2020

On the molecular basis of pyruvate kinase deficiency. I. Primary defect or conseqence of increased glutathione disulfide concentration

1 reference

12 December 2020

Defective Erythrocyte Pyruvate Kinase with Impaired Kinetics and Reduced Optimal Activity

1 reference

12 December 2020

Control of glycolysis in the human red blood cell

1 reference

12 December 2020

Tissue distribution of human pyruvate kinase isozymes

1 reference

12 December 2020

Clinical and biochemical studies of glucosephosphate isomerase of normal human erythrocytes and in glucosephosphate isomerase deficiency

1 reference

12 December 2020

Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). II. Purification and biochemical properties of the defective enzyme

1 reference

12 December 2020

A new variant of glucosephosphate isomerase deficiency (GPI-Utrecht)

1 reference

12 December 2020

Hemolytic anemia with impaired hexokinase activity

1 reference

12 December 2020

Hexokinase deficiency in blood cells in a group of kin with familial panmyelopathy (Fanconi type)

1 reference

12 December 2020

On the molecular basis of pyruvate kinase deficiency.

1 reference

12 December 2020

Erythrocyte 2, 3-diphosphoglycerate mutase: an optical test in hemolysates

1 reference

12 December 2020

STUDIES IN CONGENITAL NON-SPHEROCYTIC HAEMOLYTIC ANAEMIAS WITH SPECIFIC ENZYME DEFECTS

1 reference

12 December 2020

A CASE OF CONGENITAL ATYPICAL HAEMOLYTIC ANAEMIA WITH PYRUVATE KINASE DEFICIENCY

1 reference

12 December 2020

Additional diagnostic procedures for the detection of abnormal red cell pyruvate kinase

1 reference

12 December 2020

Pyruvate kinase in human erythrocytes

1 reference

12 December 2020

Human erythrocyte pyruvate kinase. Its purification and some properties

1 reference

12 December 2020

Hereditary hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency--a new enzyme defect of human erythrocytes

1 reference

12 December 2020

Chronic idiopathic infantile pancytopenia. A new syndrome with relative pyravate kinase and glutachione reductase deficiency of erythocytes and hyperplasia of the erythropoietic tissue

1 reference

12 December 2020

Atypical pyruvate kinase in a patient with haemolytic anaemia

1 reference

12 December 2020

The effect of urea and temperature on red blood cell pyruvate kinase

1 reference

12 December 2020

Enzymatic basis for the coexistence of myopathy and hemolytic disease in inherited muscle phosphofructokinase deficiency

1 reference

12 December 2020

[Hereditary non-spherocytic hemolytic anemia caused by glucosephosphate isomerase deficiency: 1. case observed in Switzerland]

1 reference

12 December 2020

Hereditary hemolytic anemia with human erythrocyte pyrimidine 5'-nucleotidase deficiency

1 reference

12 December 2020

Congenital non-spherocytic hemolytic anemia by 2,3-diphosphoglycerate mutase deficiency of the erythrocytes in early infancy

1 reference

12 December 2020

ADENOSINE-TRIPHOSPHATASE DEFICIENCY IN PATIENTS WITH NON-SPHEROCYTIC HAEMOLYTIC ANAEMIA

1 reference

12 December 2020

Enzymatic Deficiency in Primaquine-Sensitive Erythrocytes

series ordinal

50

1 reference

25 December 2022

Identifiers

DOI

10.1007/BF01469302

1 reference

16 September 2017

1 reference