Literature DB >> 6111988

[Problems in the diagnosis of metachromatic leukodystrophy by arylsulfatase-A assay in white blood cells. Genetic study of normal enzyme values in 64 mother and child pairs (author's transl)].

K Harzer, K I Gussmann.   

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Year:  1981        PMID： 6111988     DOI： 10.1007/bf01833158

Source DB:  PubMed          Journal:  Arch Psychiatr Nervenkr (1970)


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  4 in total

1.  The assay of arylsulphatases A and B in human urine.

Authors:  H BAUM; K S DODGSON; B SPENCER
Journal:  Clin Chim Acta       Date:  1959-05       Impact factor: 3.786

2.  [Procedure for the diagnosis of sphingolipidoses or allied diseases in adult patients with neurological or psychiatric symptoms (author's transl)].

Authors:  H Pilz; R Heipertz; D Seidel
Journal:  Nervenarzt       Date:  1979-12       Impact factor: 1.214

3.  Metachromatic leukodystrophy: ambiguity of heterozygote identification.

Authors:  H Kihara; M T Porter; A L Fluharty; M L Scott; S D De la Flor; J L Trammell; R N Nakamura
Journal:  Am J Ment Defic       Date:  1973-01

4.  [Metachromatic leucodystrophy. A genetic study of a familial adult form of metachromatic leucodystrophy (author's transl)].

Authors:  E Czmok; F Regli; K Harzer; H U Benz
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1974
  4 in total
  1 in total

1.  Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymograms.

Authors:  B Kustermann-Kuhn; K Harzer
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
  1 in total

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