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 |
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ASJC Scopus subject areas
- Medicine(all)
Cite this
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 journal › Article
}
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 -