Adult mucolipidosis with β-galactosidase and neuraminidase deficiencies

Author:

Kuriyama Masaru,Okada Shintaro,Tanaka Yukio,Umezaki Hirotoshi

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference31 articles.

1. Determination of pentose in the presence of large quantities of glucose;Brown;Arch. Biochem.,1946

2. Mucolipidosis I — Increased sialic acid content and deficiency of an α-N-acetylneuraminidase in cultured fibroblasts;Cantz;Biochem. biophys. Res. Commun.,1977

3. A new specific color reaction of hexuronic acids;Dische;J. biol. Chem.,1947

4. Sialidosis (mucolipidosis I);Durand;Helv. paediat. Acta,1977

5. Two siblings with mucolipidosis;Fukunaga;Clin. Neurol. (Tokyo),1976

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1. Glycolipid and Glycoprotein Degradation;Advances in Enzymology - and Related Areas of Molecular Biology;2006-11-22

2. Juvenile galactosialidosis in a white male: A new variant;American Journal of Medical Genetics;1988-12

3. Type III (chronic) GM1-gangliosidosis;Journal of the Neurological Sciences;1985-12

4. Electrophysiological studies of myoclonus in sialidosis type 2;Electroencephalography and Clinical Neurophysiology;1985-01

5. Cardiac involvement in diseases characterized by β-galactosidase deficiency;The Journal of Pediatrics;1985-01

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