Literature DB >> 4982580

Hereditary deficiency of adenylate kinase in red blood cell.

A Szeinberg, D Kahana, S Gavendo, J Zaidman, J Ben-Ezzer.   

Abstract

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Year:  1969        PMID： 4982580     DOI： 10.1159/000208770

Source DB:  PubMed          Journal:  Acta Haematol        ISSN： 0001-5792            Impact factor:   2.195


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  7 in total

1.  Uridine monophosphate kinase: A new genetic polymorphism with possible clinical implications.

Authors:  E R Giblett; J E Anderson; S H Chen; Y S Teng; F Cohen
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

2.  [Forensic importance of spectrophotometric tests of the isoenzyme systems red cell acid phosphatase and glutamatic-pyruvic transaminase in settlement of paternity disputes (author's transl)].

Authors:  K G Heide; N Petersen; B Brinkmann
Journal:  Z Rechtsmed       Date:  1974-06-18

3.  [A new allele of AK-Polymorphism: AK0 (author's transl)].

Authors:  J Weissmann; O Pribilla
Journal:  Z Rechtsmed       Date:  1981

Review 4.  [Red cell enzyme polymorphisms in forensic serology].

Authors:  B Brinkmann
Journal:  Z Rechtsmed       Date:  1971

5.  PGI*3(Israel), a new, unstable allele in the phosphoglucose isomerase system.

Authors:  B Bonné-Tamir; S S Papiha; S Ashbel; F Brok-Simoni; G Kende; B Ramot
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

Review 6.  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

Review 7.  [Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl)].

Authors:  H D Waller; H C Benöhr
Journal:  Klin Wochenschr       Date:  1976-09-01
  7 in total

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