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22 in total

Review 1. Biochemistry and genetics of gangliosidoses.

Authors: K Sandhoff; H Christomanou
Journal: Hum Genet Date: 1979 Impact factor: 4.132

2. MR imaging and proton spectroscopy of neuronal injury in late-onset GM2 gangliosidosis.

Authors: Matilde Inglese; Annette O Nusbaum; Gregory M Pastores; John Gianutsos; Edwin H Kolodny; Oded Gonen
Journal: AJNR Am J Neuroradiol Date: 2005-09 Impact factor: 3.825

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

5. [Clinical and ultrastructural observations in a case of juvenile amaurotic idiocy with protracted course (author's transl)].

Authors: G Ebhardt; J Cervós-Navarro; P Bürgel
Journal: Arch Psychiatr Nervenkr (1970) Date: 1973-11-27

6. Gangliosidosis with total hexosaminidase deficiency: clinical, biochemical and ultrastructural studies and comparison with conventional cases of Tay-Sachs disease.

Authors: G Fontaine; A Résibois; M Tondeur; G Jonniaux; J P Farriaux; W Voet; E Maillard; H Loeb
Journal: Acta Neuropathol Date: 1973-01-30 Impact factor: 17.088

Juvenile GM2-gangliosidosis. Clinical variant of Tay-Sachs disease or a new disease.

Review 1. Biochemistry and genetics of gangliosidoses.

2. MR imaging and proton spectroscopy of neuronal injury in late-onset GM2 gangliosidosis.

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.

5. [Clinical and ultrastructural observations in a case of juvenile amaurotic idiocy with protracted course (author's transl)].

6. Gangliosidosis with total hexosaminidase deficiency: clinical, biochemical and ultrastructural studies and comparison with conventional cases of Tay-Sachs disease.

7. Late onset GM2-gangliosidosis. Clinical, pathological, and biochemical studies on 8 patients.

8. Corneal clouding in GM1-generalized gangliosidosis.

9. The AB-variant of GM2-gangliosidosis. Clinical, biochemical, and pathological studies of two patients.

10. Fine structure of cutaneous nerves in ganglioside storage disease.