[Tay-Sachs disease with hexosaminidase deficiency. Clinical, morphological and biochemical findings in a case with visceral storage of renal globosides]

[Article in German]

[Article in German]

H Pilz et al. Dtsch Med Wochenschr. 1968.

. 1968 Sep 27;93(39):1833-9 passim.

doi: 10.1055/s-0028-1110836.

No abstract available

Cited by

[Endogenous storage diseases of the lung. Attempt at classification clinical diagnosis and problems].
Bassermann FJ. Bassermann FJ. Pneumonologie. 1971;145:265-78. doi: 10.1007/BF02095042. Pneumonologie. 1971. PMID: 4942797 Review. German. No abstract available.
[Infantile amaurotic idiocy and related forms as ganglioside storage diseases].
Sandhoff K, Jatzkewitz H, Peters G. Sandhoff K, et al. Naturwissenschaften. 1969 Jul;56(7):356-62. doi: 10.1007/BF00596925. Naturwissenschaften. 1969. PMID: 5360899 German. No abstract available.
The metabolism of Tay-Sachs ganglioside: catabolic studies with lysosomal enzymes from normal and Tay-Sachs brain tissue.
Tallman JF, Johnson WG, Brady RO. Tallman JF, et al. J Clin Invest. 1972 Sep;51(9):2339-45. doi: 10.1172/JCI107045. J Clin Invest. 1972. PMID: 4639018 Free PMC article.
[Enzymatic studies on the blood of carriers of a Tay-Sachs disease variant (variant O)].
Harzer K, Sandhoff K, Schall H, Kollmann F. Harzer K, et al. Klin Wochenschr. 1971 Nov 1;49(21):1189-91. doi: 10.1007/BF01732464. Klin Wochenschr. 1971. PMID: 5124584 German. No abstract available.
The AB-variant of GM2-gangliosidosis. Clinical, biochemical, and pathological studies of two patients.
Goldman JE, Yamanaka T, Rapin I, Adachi M, Suzuki K, Suzuki K. Goldman JE, et al. Acta Neuropathol. 1980;52(3):189-202. doi: 10.1007/BF00705807. Acta Neuropathol. 1980. PMID: 6255724