Literature DB >> 14465634

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

F LINNEWEH.   

Abstract

Entities:  

Keywords:  ENZYMES/metabolism; GENETICS

Mesh：

Substances：

Year:  1962        PMID： 14465634     DOI： 10.1007/BF01478627

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


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  40 in total

1.  Glucuronic acid conjugation by patients with familial nonhemolytic jaundice and their relatives.

Authors:  B CHILDS; J B SIDBURY; C J MIGEON
Journal:  Pediatrics       Date:  1959-05       Impact factor: 7.124

2.  [On the biochemical genetics of galactosemia].

Authors:  R GITZELMANN; B HADORN
Journal:  Helv Paediatr Acta       Date:  1961-04

3.  The heterozygous carrier in galactosaemia.

Authors:  D Y HSIA; I HUANG; S G DRISCOLL
Journal:  Nature       Date:  1958-11-15       Impact factor: 49.962

4.  The enzymic defect of hereditary methemoglobinemia: diaphorase.

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

5.  On distribution and inheritance of atypical forms of human serum cholinesterase, as indicated by dibucaine numbers.

Authors:  W KALOW; N STARON
Journal:  Can J Biochem Physiol       Date:  1957-12

6.  A genetic study of a defect in glutathione metabolism of the erythrocyte.

Authors:  B CHILDS; W ZINKHAM; E A BROWNE; E L KIMBRO; J V TORBERT
Journal:  Bull Johns Hopkins Hosp       Date:  1958-01

7.  The glutathione instability of drug-sensitive red cells; a new method for the in vitro detection of drug sensitivity.

Authors:  E BEUTLER
Journal:  J Lab Clin Med       Date:  1957-01

8.  Assay of L-phenylalanine as phenylethylamine after enzymatic decarboxylation; application to isotopic studies.

Authors:  S UDENFRIEND; J R COOPER
Journal:  J Biol Chem       Date:  1953-08       Impact factor: 5.157

9.  Congenital familial nonhemolytic jaundice with kernicterus.

Authors:  J F CRIGLER; V A NAJJAR
Journal:  Pediatrics       Date:  1952-08       Impact factor: 7.124

10.  Studies on cell lines developed from the tissues of patients with galactosemia.

Authors:  R S KROOTH; A N WEINBERG
Journal:  J Exp Med       Date:  1961-06-01       Impact factor: 14.307
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  4 in total

Review 1.  [ON THE ROLE OF BLOOD CELLS IN THE DIAGNOSIS OF HEREDITARY METABOLIC DISEASES].

Authors:  F LINNEWEH
Journal:  Klin Wochenschr       Date:  1963-10-01

2.  [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

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

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

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

Authors:  W Schröter
Journal:  Klin Wochenschr       Date:  1965-11-01
  4 in total

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