Literature DB >> 5862690

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

G W Löhr, H D Waller, F Anschütz, A Knopp.   

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Year:  1965        PMID： 5862690     DOI： 10.1007/bf01711251

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN： 0023-2173


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  16 in total

1.  [HYPOTHESIS OF CHROMOSOMAL TRANSLOCATION AS A GENETIC INTERPRETATION OF FANCONI'S FAMILIAL CONSTITUTIONAL PANMYELOPATHY].

Authors:  G FANCONI
Journal:  Helv Paediatr Acta       Date:  1964-06

2.  [STUDIES ON HEMOLYSIS IN FANCONI'S ANEMIA. INCREASE OF ATP-ASE AS A POSSIBLE CAUSE FOR DECEASED ATP VALUES].

Authors:  I SYLLM-RAPOPORT; D GMYREK; H J ALTENBRUNN; D SCHEUCH; G JACOBASCH
Journal:  Dtsch Med Wochenschr       Date:  1965-02-12       Impact factor: 0.628

3.  Chronic pancytopenia with multiple congenital abnormalities (Fanconi's anaemia).

Authors:  L R NILSSON
Journal:  Acta Paediatr       Date:  1960-07       Impact factor: 2.299

4.  [Enzymic determination of L(+)-lactic acid].

Authors:  H J HOHORST
Journal:  Biochem Z       Date:  1957

5.  Studies on the preservation of blood. V. The influence of the hydrogen ion concentration on certain changes in blood during storage.

Authors:  S KASHKET; D RUBINSTEIN; O F DENSTEDT
Journal:  Can J Biochem Physiol       Date:  1957-10

6.  [Study of forty cases of chronic idiopathic pancytopenia].

Authors:  J BERNARD; G MATHE; Y NAJEAN
Journal:  Sang       Date:  1958

7.  [Quantitative enzyme determination in erythrocytes].

Authors:  G W LOHR; H D WALLER; O KARGES
Journal:  Klin Wochenschr       Date:  1957-09-01

8.  [Not Available].

Authors:  M KIESE
Journal:  Naunyn Schmiedebergs Arch Exp Pathol Pharmakol       Date:  1947

9.  Spectrophotometric measurement of hexokinase and phosphohexokinase activity.

Authors:  E RACKER
Journal:  J Biol Chem       Date:  1947-03       Impact factor: 5.157

10.  [Panmyelopathies in childhood. Study of Fanconi's anemia].

Authors:  C GASSER
Journal:  Helv Paediatr Acta       Date:  1961-12
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  14 in total

Review 1.  Advances in hereditary red cell enzyme anomalies.

Authors:  A Kahn; J C Kaplan; J C Dreyfus
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

Review 2.  [Enzyme deficiencies of blood cells in bone marrow insufficiency (author's transl].

Authors:  H D Waller; H C Benöhr
Journal:  Klin Wochenschr       Date:  1978-05-15

3.  Human erythrocyte hexokinase deficiency. Characterization of a mutant enzyme with abnormal regulatory properties.

Authors:  G Rijksen; G E Staal
Journal:  J Clin Invest       Date:  1978-08       Impact factor: 14.808

4.  [Contribution to the pathogenesis of the Fanconi anemia].

Authors:  G W Löhr; H D Waller
Journal:  Blut       Date:  1967-09

5.  Chromosomal peculiarities and "in vitro" examinations in Fanconi's anaemia.

Authors:  D Schuler; A Kiss; F Fábián
Journal:  Humangenetik       Date:  1969

6.  [Hexokinase isoenzymes in normal erythrocytes of adults and newborns and in various hyperregenerative anemias].

Authors:  W Tillmann; W Schröter
Journal:  Klin Wochenschr       Date:  1969-07-15

7.  [Glutathione reduction in erythrocytes of healthy persons and enzyme defect carriers. Use of the azoester test by Kosower et al. in glucose-6-P-dehydrogenase and glutathione reductase deficiency].

Authors:  H D Waller; H C Benöhr; B Heuer; O Nerke
Journal:  Klin Wochenschr       Date:  1970-01-15

8.  Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients.

Authors:  J German
Journal:  Am J Hum Genet       Date:  1969-03       Impact factor: 11.025

9.  Clinical and cytogenetic observations during a six-year period in an adult with Fanconi's anaemia.

Authors:  T M Schroeder; P Drings; P Beilner; G Buchinger
Journal:  Blut       Date:  1977-02

Review 10.  Diagnosis of red blood cell enzymopathies in infants, children and adolescents.

Authors:  S P Samuel; T D Miale
Journal:  Indian J Pediatr       Date:  1987 May-Jun       Impact factor: 1.967
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