Lipid storage diseases: review of the cases admitted to the Istituto Neurologico

A. D'Angelo; A. Moise; M. Rimoldi; B. Bertagnolio; A. Ottolenghi; G. Tettamanti; S. Di Donato

Lipid storage diseases: review of the cases admitted to the Istituto Neurologico

A. D'Angelo, A. Moise, M. Rimoldi, B. Bertagnolio, A. Ottolenghi, G. Tettamanti, S. Di Donato

Research output: Contribution to journal › Article › peer-review

Abstract

Lipidoses are inborn errors of metabolism resulting in a progressive accumulation of lipid material in the nervous system and visceral organs due to a genetic absence or disfunction of an acid hydrolase acting on tissue complex lipids as well as on other substances. The previously described biochemical procedures set up for the detection of lipidoses were applied. In 11 patients, 7 patients by metachromatic leukodystrophy (MLD); 2 by GM ₁ -gangliosidosis; 2 by GM ₂ -gangliosidosis.

Original language	English
Pages (from-to)	71-78
Number of pages	8
Journal	Biochemistry and Experimental Biology
Volume	13
Issue number	1
Publication status	Published - 1977

ASJC Scopus subject areas

Medicine(all)

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abstract = "Lipidoses are inborn errors of metabolism resulting in a progressive accumulation of lipid material in the nervous system and visceral organs due to a genetic absence or disfunction of an acid hydrolase acting on tissue complex lipids as well as on other substances. The previously described biochemical procedures set up for the detection of lipidoses were applied. In 11 patients, 7 patients by metachromatic leukodystrophy (MLD); 2 by GM 1 -gangliosidosis; 2 by GM 2 -gangliosidosis.",

author = "A. D'Angelo and A. Moise and M. Rimoldi and B. Bertagnolio and A. Ottolenghi and G. Tettamanti and {Di Donato}, S.",

year = "1977",

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AU - D'Angelo, A.

AU - Moise, A.

AU - Rimoldi, M.

AU - Bertagnolio, B.

AU - Ottolenghi, A.

AU - Tettamanti, G.

AU - Di Donato, S.

PY - 1977

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AB - Lipidoses are inborn errors of metabolism resulting in a progressive accumulation of lipid material in the nervous system and visceral organs due to a genetic absence or disfunction of an acid hydrolase acting on tissue complex lipids as well as on other substances. The previously described biochemical procedures set up for the detection of lipidoses were applied. In 11 patients, 7 patients by metachromatic leukodystrophy (MLD); 2 by GM 1 -gangliosidosis; 2 by GM 2 -gangliosidosis.

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