Literature DB >> 14092943

[ON THE ROLE OF BLOOD CELLS IN THE DIAGNOSIS OF HEREDITARY METABOLIC DISEASES].

F LINNEWEH.   

Abstract

Entities:  

Keywords:  ALANINE AMINOTRANSFERASE; ALDOLASE; ANEMIA, HEMOLYTIC; ASPARTATE AMINOTRANSFERASE; BLOOD CELLS; ENZYME TESTS; FAVISM; GENETICS, HUMAN; GLUCOSEPHOSPHATE DEHY- DROGENASE DEFICIENCY; GLUCOSEPHOSPHATE DEHYDROGENASE; MALATE DEHYDROGENASE; METABOLIC DISEASES; METHEMOGLOBINEMIA; OXIDOREDUCTASES; PHOSPHATASES; PHOSPHOTRANSFERASES; PURPURA, THROMBOPENIC; REVIEW; SUCCINATE DEHYDROGENASE

Mesh：

Substances：

Year:  1963        PMID： 14092943     DOI： 10.1007/bf01478534

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


× No keyword cloud information.
  20 in total

1.  Leukocyte debranching enzyme in glycogen storage disease.

Authors:  H E WILLIAMS; E M KENDIG; J B FIELD
Journal:  J Clin Invest       Date:  1963-05       Impact factor: 14.808

2.  Phosphorylase activity in leucocytes from patients with glycogen-storages disease.

Authors:  W C HULSMANN; T L OEI
Journal:  Lancet       Date:  1961-09-09       Impact factor: 79.321

3.  Metabolism of the white blood cells in maple-syrup-urine disease.

Authors:  J DANCIS; J HUTZLER; M LEVITZ
Journal:  Biochim Biophys Acta       Date:  1960-09-23

4.  A nanomole adaption of the automatic amino acid analysis according to Spackman, Stein, and Moore (1958).

Authors:  E KIRSTEN; R KIRSTEN
Journal:  Biochem Biophys Res Commun       Date:  1962-02-20       Impact factor: 3.575

5.  The enzymic defect of hereditary methemoglobinemia: diaphorase.

Authors:  E M SCOTT; I V GRIFFITH
Journal:  Biochim Biophys Acta       Date:  1959-08

6.  A study of subjects with erythrocyte glucose-6-phosphate dehydrogenase deficiency: investigation of platelet enzymes.

Authors:  B RAMOT; A SZEINBERG; A ADAM; C SHEBA; D GAFNI
Journal:  J Clin Invest       Date:  1959-09       Impact factor: 14.808

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

Authors:  H D WALLER; G W LOHR; M TABATABAI
Journal:  Klin Wochenschr       Date:  1957-10-15

8.  The reduction of methaemoglobin in red blood cells and studies on the cause of idiopathic methaemoglobinaemia.

Authors:  Q H Gibson
Journal:  Biochem J       Date:  1948       Impact factor: 3.857

9.  PYRIMIDINE METABOLISM IN MAN. IV. THE ENZYMATIC DEFECT OF OROTIC ACIDURIA.

Authors:  L H Smith; M Sullivan; C M Huguley
Journal:  J Clin Invest       Date:  1961-04       Impact factor: 14.808

10.  [Advances in the recognition of heterozygous characteristics in hereditary enzymopathies].

Authors:  F LINNEWEH
Journal:  Klin Wochenschr       Date:  1962-06-01
View more
  5 in total

1.  [ANOTHER HETEROZYGOTE TEST FOR THE MAPLE SYRUP URINE DISEASE].

Authors:  F LINNEWEH; M EHRLICH; E H GRAUL; H HUNDESHAGEN
Journal:  Klin Wochenschr       Date:  1963-10-01

2.  [ON CYSTINE METABOLISM IN CYSTINOSIS].

Authors:  F LINNEWEH; E SCHAUMLOEFFEL; E H GRAUL; H HUNDESHAGEN; E KIRSTEN; R KIRSTEN; W BARTHELMAI
Journal:  Klin Wochenschr       Date:  1964-10-15

Review 3.  [Problems of quantitative diagnosis of hereditary metabolic diseases].

Authors:  F Linneweh
Journal:  Klin Wochenschr       Date:  1965-10-15

4.  [Oxygen consumption of erythrocytes from psoriatic patients].

Authors:  H Holzmann; B Morsches; J Kunz
Journal:  Klin Wochenschr       Date:  1970-02-15

5.  [Studies of the activity of glucose phosphate isomerase in thrombocytes and leukocytes of patients with florid psoriasis vulgaria].

Authors:  H Holzmann; B Morsches; W Ohler
Journal:  Klin Wochenschr       Date:  1967-03-15
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.