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. 1978 Nov;1(11):699-710.

[Article in French]

[Article in French]

J Libert. J Fr Ophtalmol. 1978 Nov.

. 1978 Nov;1(11):699-710.

No abstract available

Chemical diagnosis of inborn lysosomal storage disorders involving the eye.
Dawson G, Tsay GC. Dawson G, et al. Birth Defects Orig Artic Ser. 1976;12(3):1-13. Birth Defects Orig Artic Ser. 1976. PMID: 821555 Review. No abstract available.
Inborn errors of lysosomal catabolism--principles of heterozygote detection.
Jolly RD, Desnick RJ. Jolly RD, et al. Am J Med Genet. 1979;4(3):293-307. doi: 10.1002/ajmg.1320040313. Am J Med Genet. 1979. PMID: 117711 Review.
[Lysosomal storage diseases: clinical variety and genetic heterogeneity (author's transl)].
Gitzelmann R, Wiesmann UN, Spycher MA. Gitzelmann R, et al. Verh Dtsch Ges Pathol. 1976:101-5. Verh Dtsch Ges Pathol. 1976. PMID: 828812 German. No abstract available.
[Prenatally recognizable enzymopathies, metabolic disorders].
Bickel H. Bickel H. Monatsschr Kinderheilkd (1902). 1975 May;123(5):206-17. Monatsschr Kinderheilkd (1902). 1975. PMID: 815786 German. No abstract available.
Enzymatic and biochemical diagnosis of inborn lysosomal diseases with neurological symptoms.
Hultberg B, Ockerman PA, Sjöblad S. Hultberg B, et al. Eur Neurol. 1972;7(1):101-18. doi: 10.1159/000114417. Eur Neurol. 1972. PMID: 4259742 No abstract available.