12 results on '"Harzer, K."'
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2. THE PATTERNS OF ARYLSULPHATASES A AND B IN HUMAN NORMAL AND METACHROMATIC LEUCODYSTROPHY TISSUES AND THEIR RELATIONSHIP TO THE CEREBROSIDE SULPHATASE ACTIVITY.
3. ENZYME ALTERATIONS AND LIPID STORAGE IN THREE VARIANTS OF TAY-SACHS DISEASE.
4. AGE-DEPENDENT VARIATIONS OF THE HUMAN N-ACETYL-β-D-HEXOSAMINIDASES.
5. Incorporation of labelled glucose into the individual major gangliosides of the brain of young rats.
6. Sulfatides in Prenatal Metachromatic Leukodystrophy.
7. Partial Purification of Acid Sphingomyelinase from Normal and Pathological (M. Niemann-Pick Type C) Human Brain.
8. Resolution of tissue sphingomyelinase isoelectric profile in multiple components is extraction-dependent: evidence for a component defect in Niemann-Pick disease type C is spurious.
9. A simple sphingomyelinase determination for Niemann-Pick disease: differential diagnosis of types A, B and C.
10. AGE-DEPENDENT VARIATIONS OF THE HUMAN N-ACETYL-?-D-HEXOSAMINIDASES
11. Brain galactolipid content in a patient with pseudoarylsulfatase A deficiency and coincidental diffuse disseminated sclerosis, and in patients with metachromatic, adreno-, and other leukodystrophies.
12. Letters: A simple sphingomyelinase determination for Niemann-Pick disease: differential diagnosis of types A, B and C.
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