Literature DB >> 5171491

The biochemical differentiation between heterozygote carriers of metachromatic leucodystrophy and normal persons.

F Gabreëls, K Lamers, J Kok, M Loonen, E Lommen.   

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Year:  1971        PMID： 5171491     DOI： 10.1055/s-0028-1091795

Source DB:  PubMed          Journal:  Neuropadiatrie        ISSN： 0028-3797


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  3 in total

1.  A preclinical case of late adult metachromatic leukodystrophy? Manifestation only with lipid abnormalities in urine, enzyme deficiency and decrease of nerve conduction velocity.

Authors:  H Pilz; H C Hopf
Journal:  J Neurol Neurosurg Psychiatry       Date:  1972-06       Impact factor: 10.154

2.  [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

3.  Metachromatic leucodystrophy: review of 38 cases.

Authors:  R MacFaul; N Cavanagh; B D Lake; R Stephens; A E Whitfield
Journal:  Arch Dis Child       Date:  1982-03       Impact factor: 3.791
  3 in total

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