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25 in total

Review 1. Sialidosis: a review of human neuraminidase deficiency.

Authors: J A Lowden; J S O'Brien
Journal: Am J Hum Genet Date: 1979-01 Impact factor: 11.025

Review 2. Lysosomal membrane proteomics and biogenesis of lysosomes.

Authors: Richard D Bagshaw; Don J Mahuran; John W Callahan
Journal: Mol Neurobiol Date: 2005-08 Impact factor: 5.590

Review 3. Progress in investigations of sphingolipidoses.

Authors: M Adachi; L Schneck; B W Volk
Journal: Acta Neuropathol Date: 1978-08-07 Impact factor: 17.088

Review 4. The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported.

Authors: Gustavo H B Maegawa; Tracy Stockley; Michael Tropak; Brenda Banwell; Susan Blaser; Fernando Kok; Roberto Giugliani; Don Mahuran; Joe T R Clarke
Journal: Pediatrics Date: 2006-10-02 Impact factor: 7.124

Review 5. Mucopolysaccharidoses and mucolipidoses.

Authors: F Van Hoof
Journal: J Clin Pathol Suppl (R Coll Pathol) Date: 1974

6. GM1 gangliosidosis in skin fibroblast culture: enzymatic differences between types 1 and 2 and observations on a third variant.

Authors: L Pinsky; J Miller; B Shanfield; G Watters; L S Wolfe
Journal: Am J Hum Genet Date: 1974-09 Impact factor: 11.025

Late infantile systemic lipidosis. Major monosialogangliosidosis. Delineation of two types.

Review 1. Sialidosis: a review of human neuraminidase deficiency.

Review 2. Lysosomal membrane proteomics and biogenesis of lysosomes.

Review 3. Progress in investigations of sphingolipidoses.

Review 4. The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported.

Review 5. Mucopolysaccharidoses and mucolipidoses.

6. GM1 gangliosidosis in skin fibroblast culture: enzymatic differences between types 1 and 2 and observations on a third variant.

7. The genetic mucolipidoses. Diagnosis and differential diagnosis.

8. Nature of the mutation in adult beta-galactosidase deficient patients.

9. Gmi-gangliosidosis. A variant with high activity of hepatic neutral beta-galactosidase.

10. Experimental polymer storage disease in rabbits. An approach to the histogenesis of sphingolipidoses.