(Q39841083)

15 September 2017

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title

Inherited glucosephosphate isomerase deficiency. A review of known variants and some aspects of the pathomechanism of the deficiency (English)

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15 September 2017

H Arnold

1

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15 September 2017

publication date

1 December 1979

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15 September 2017

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15 September 2017

volume

39

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15 September 2017

issue

6

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15 September 2017

page(s)

405-417

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Unique phenotypic expression of glucosephosphate isomerase deficiency

15 September 2017

cites work

1 reference

12 December 2020

A new variant of glucosephosphate isomerase deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

Inherited variations in human phosphohexose isomerase

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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

"Acquired" red cell enzyme defects in hematological diseases

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12 December 2020

Glucosephosphate isomerase deficiency type Liège: a new variant with congenital nonspherocytic hemolytic anemia

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12 December 2020

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

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12 December 2020

Acquired erythroenzymopathies in blood disorders: study of 200 cases

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12 December 2020

Glucose phosphate isomerase deficiency with hereditary nonspherocytic hemolytic anemia

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12 December 2020

Glucosephosphate isomerase deficiency in a Dutch family

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12 December 2020

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

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12 December 2020

Haematological studies in a new variant of glucosephosphate isomerase deficiency (GPI Utrecht)

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12 December 2020

Pseudoisoenzymes of rabbit muscle phosphoglucose isomerase

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12 December 2020

Occurrence of Defective Hexosephosphate Isomerization in Human Erythrocytes and Leukocytes

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Glucosephosphate-Isomerase (GPI) Deficiency: GPI Elyria

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12 December 2020

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

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12 December 2020

Formal genetics of phosphoglucose isomerase (EC:5.3.1.9). Studies of a family with PGI-deficiency

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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

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

1 reference

12 December 2020

Causal mechanisms of multiple acquired red cell enzyme defects in a patient with acquired dyserythropoiesis

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Haemolytic Anaemia Associated with Glucosephosphate Isomerase (GPI) Deficiency in a Black South African Child

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12 December 2020

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

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12 December 2020

Hereditary Glucosephosphate Isomerase Deficiency: A Review

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12 December 2020

The kinetics of phosphoglucoisomerase

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12 December 2020

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

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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

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12 December 2020

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

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12 December 2020

Molecular and functional anomalies in two new mutant glucose-phosphate-isomerase variants with enzyme deficiency and chronic hemolysis

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12 December 2020

Glucosephosphate isomerase deficiency, a new variant in a Dutch family. Case report

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12 December 2020

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

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12 December 2020

Glucose-phosphate isomerase deficiency due to a new variant (GP I barcelona) and to a silent gene: Biochemical, immunological and genetic studies

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12 December 2020

A New variant of glucosephosphate isomerase deficiency: GPI-kortrijk

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12 December 2020

Genetic and Molecular Mechanisms of the Congenital Defects in Glucose Phosphate Isomerase Activity: Studies of Four Families

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12 December 2020

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

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12 December 2020

Congenital nonspherocytic hemolytic anemia associated with glucosephosphate isomerase deficiency: variant Paderborn

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12 December 2020

A point mutation increasing the stability of human phosphoglucose isomerase

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12 December 2020

Identifiers

DOI

10.1007/BF01008661

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15 September 2017

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