Animal model of human disease: GM2 gangliosidosis.

Tay-Sachs Disease: Generalized Absence of a Beta-D- <i>N</i> -Acetylhexosaminidase Component

Shintaro Okada, John S. O’Brien · Science · 1969 · 708 citations

Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs

Konrad Sandhoff, U. Andreae, Horst Jatzkewitz · Life Sciences · 1968 · 329 citations

Tay-sachs Disease, Exceptional Case, Immunology +3

G _M2 ‐gangliosidosis with total hexosaminidase deficiency

Yoshiyuki Suzuki, Jerry Jacob, Kinuko Suzuki et al. · Neurology · 1971 · 93 citations

Pathogenesis, Histopathology, Experimental Pathology +6

Juvenile GM2 gangliosidosis: Partial deficiency of bexosaminidase A

Shintaro Okada, M. Lois Veath, John S. O’Brien · The Journal of Pediatrics · 1970 · 63 citations

Parasitic Protozoa, Genetics, Pathogenesis +5

Juvenile GM2 Gangliosidosis

John H. Menkes · Archives of Neurology · 1971 · 49 citations

Parasitic Disease, Neurological Disorder, Pathology +26