Fluorescence-based diagnosis of lipid storage diseases by analysis of the culture medium of skin fibroblasts

Author:

Vered Agmon,Eugenio Monti,Arie Dagan,Augusto Preti,Sergio Marchesini,Shimon Gatt

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference34 articles.

1. Glucosylceramide lipidoses: Gaucher disease;Barranger,1989

2. Galactosylceramide lipidosis: globoid cell leuko-dystrophy (Krabbe disease);Suzuki,1989

3. Fabry disease: α-galactosidase deficiency: Schindler's disease: α-N-acetyhexosaminidase deficiency;Desnick,1989

4. Metachromatic leukodystrophy and multiple sulfatase deficiency: sulfatide lipidosis;Kolodny,1989

5. β-Galactosidase deficiency (GM1-gangliosidosis; galactosyl-sialidosis and Morqio syndrome, type B); ganglioside sialidase deficiency (mucolipodosis IV);Obrien,1989

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