Gargoylism (mucopolysaccharidosis type II). accumulation of glycosaminoglycans, gangliosides and glycoproteins and activity of some related glycolytic enzymes in liver, spleen and brain
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference30 articles.
1. THE GENETIC MUCOPOLYSACCHARIDOSES
2. BRAIN GANGLTOSIDE PATTERN IN THREE FORMS OF AMAUROTIC IDIOCY AND IN GARGOYLISM
3. ULTRASTKUCTURAL AND BIOCHEMICAL OBSERVATIONS ON A CASE OF SYSTEMIC LATE INFANTILE LIPIDOSIS AND ITS RELATIONSHIP TO TAY-SACHS DISEASE AND GARGOYLISM
4. STRUCTURE COMPARISON OF THE MAJOR MONOSIALOGANGLIOSIDES FROM BRAINS OF NORMAL HUMAN, GARGOYLISM, AND LATE INFANTILE SYSTEMIC LIPIDOSIS. PART I
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2. HUNTER'S SYNDROME. An Ultrastructural Study of an Autopsy Case;Pathology International;1988-09
3. Further studies on hepatic acidic glycosaminoglycans in the Hurler syndrome;Experientia;1978-05
4. NEUROCHEMISTRY OF THE MUCOPOLYSACCHARIDOSES: BRAIN LIPIDS AND LYSOSOMAL ENZYMES IN PATIENTS WITH FOUR TYPES OF MUCOPOLYSACCHARIDOSIS AND IN NORMAL CONTROLS;Journal of Neurochemistry;1978-05
5. NEUROCHEMISTRY OF THE MUCOPOLYSACCHARIDOSES: BRAIN GLYCOSAMINOGLYCANS IN NORMALS AND FOUR TYPES OF MUCOPOLYSACCHARIDOSES;Journal of Neurochemistry;1976-05
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