Literature DB >> 14092944

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

F LINNEWEH, M EHRLICH, E H GRAUL, H HUNDESHAGEN.   

Abstract

Keywords:  BLOOD; CARBON ISOTOPES; GENETICS, HUMAN; LEUCINE; MAPLE SYRUP URINE DISEASE

Mesh:

Substances:

Year:  1963        PMID: 14092944     DOI: 10.1007/BF01478535

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


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  5 in total

1.  THE DIAGNOSIS OF MAPLE SYRUP URINE DISEASE (BRANCHED- CHAIN KETOACIDURIA) BY THE IN VITRO STUDY OF THE PERIPHERAL LEUKOCYTE.

Authors:  J DANCIS; J HUTZLER; M LEVITZ
Journal:  Pediatrics       Date:  1963-08       Impact factor: 7.124

Review 2.  [ON THE ROLE OF BLOOD CELLS IN THE DIAGNOSIS OF HEREDITARY METABOLIC DISEASES].

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

3.  [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

4.  Maple syrup urine disease: branched-chain keto-aciduria.

Authors:  J DANCIS; M LEVITZ; R G WESTALL
Journal:  Pediatrics       Date:  1960-01       Impact factor: 7.124

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

Authors:  F LINNEWEH
Journal:  Klin Wochenschr       Date:  1962-06-01
  5 in total
  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.  [PROCEDURE FOR A SIMPLIFIED HETEROZYGOTE TEST FOR THE MAPLE SYRUP URINE DISEASE].

Authors:  H W GOEDDE; E RICHTER; M HUEFNER; B SIXEL
Journal:  Klin Wochenschr       Date:  1964-08-15

3.  Antenatal diagnosis of maple syrup urine disease.

Authors:  J J Hoo; E Latta; E Schaumlöffel
Journal:  Z Kinderheilkd       Date:  1974

4.  The absence of inactivation at two autosomal loci.

Authors:  B Sigman; S M Gartler
Journal:  Humangenetik       Date:  1966

Review 5.  [Problems of quantitative diagnosis of hereditary metabolic diseases].

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

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