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 journalArticle

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 languageEnglish
Pages (from-to)71-78
Number of pages8
JournalBiochemistry and Experimental Biology
Volume13
Issue number1
Publication statusPublished - 1977

Fingerprint

Gangliosidoses
Lipidoses
Metachromatic Leukodystrophy
Lipids
Inborn Errors Metabolism
Autonomic Nervous System
Hydrolases
Acids

ASJC Scopus subject areas

  • Medicine(all)

Cite this

D'Angelo, A., Moise, A., Rimoldi, M., Bertagnolio, B., Ottolenghi, A., Tettamanti, G., & Di Donato, S. (1977). Lipid storage diseases: review of the cases admitted to the Istituto Neurologico. Biochemistry and Experimental Biology, 13(1), 71-78.

Lipid storage diseases : review of the cases admitted to the Istituto Neurologico. / D'Angelo, A.; Moise, A.; Rimoldi, M.; Bertagnolio, B.; Ottolenghi, A.; Tettamanti, G.; Di Donato, S.

In: Biochemistry and Experimental Biology, Vol. 13, No. 1, 1977, p. 71-78.

Research output: Contribution to journalArticle

D'Angelo, A, Moise, A, Rimoldi, M, Bertagnolio, B, Ottolenghi, A, Tettamanti, G & Di Donato, S 1977, 'Lipid storage diseases: review of the cases admitted to the Istituto Neurologico', Biochemistry and Experimental Biology, vol. 13, no. 1, pp. 71-78.
D'Angelo A, Moise A, Rimoldi M, Bertagnolio B, Ottolenghi A, Tettamanti G et al. Lipid storage diseases: review of the cases admitted to the Istituto Neurologico. Biochemistry and Experimental Biology. 1977;13(1):71-78.
D'Angelo, A. ; Moise, A. ; Rimoldi, M. ; Bertagnolio, B. ; Ottolenghi, A. ; Tettamanti, G. ; Di Donato, S. / Lipid storage diseases : review of the cases admitted to the Istituto Neurologico. In: Biochemistry and Experimental Biology. 1977 ; Vol. 13, No. 1. pp. 71-78.
@article{8b53c0ddf25b42548e78f523ba408547,
title = "Lipid storage diseases: review of the cases admitted to the Istituto Neurologico",
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",
language = "English",
volume = "13",
pages = "71--78",
journal = "Biochemistry and Experimental Biology",
issn = "0366-0060",
number = "1",

}

TY - JOUR

T1 - Lipid storage diseases

T2 - review of the cases admitted to the Istituto Neurologico

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

Y1 - 1977

N2 - 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.

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.

UR - http://www.scopus.com/inward/record.url?scp=0017588545&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0017588545&partnerID=8YFLogxK

M3 - Article

VL - 13

SP - 71

EP - 78

JO - Biochemistry and Experimental Biology

JF - Biochemistry and Experimental Biology

SN - 0366-0060

IS - 1

ER -