Results 1 -
5
of
5
for
sachs
- Tay-Sachs disease is a rare, inherited disorder that is characterized by neurological problems caused by the death of ... nervous system).The most common form of Tay-Sachs disease, known as infantile Tay-Sachs disease, becomes ...
- ... GM2 gangliosidosis, AB variant Hexosaminidase activator deficiency Tay-Sachs disease, AB variant Genetic Testing Registry: Tay-Sachs disease, variant AB GM2-gangliosidosis, B, B1, AB ...
- ... ganglioside. The other two conditions are called Tay-Sachs disease and GM2-gangliosidosis, AB variant, which are ... burden of disease manifestations in late-onset Tay-Sachs and Sandhoff diseases. Orphanet J Rare Dis. 2020 ...
- ... Marangell LB, Miklowitz DJ, Nierenberg AA, Patel J, Sachs GS, Sklar P, Smoller JW, Laird N, Keshavan ...
- ... PFM1 PARIETAL FORAMINA 2; PFM2 PubMed Edwards LS, Sachs JR, Elster AD. Skull fractures through parietal foramina: ...