Harderoporphyrin: a misnomer
✍ Scribed by A. Gorchein; M. Danton; C. K. Lim
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 102 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0269-3879
- DOI
- 10.1002/bmc.480
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The combination of recessive early‐onset parkinsonism and pyramidal tract signs caused by pallidopyramidal degeneration is known as pallidopyramidal disease or syndrome (PPD/S). We investigated whether patients diagnosed as Davison's PPD/S showed any definite proof of pyramidal and pall
Chew et al. 1 studied the long-term natural history of Unverricht-Lundborg disease (ULD, progressive myoclonic epilepsy of Unverricht-Lundborg type, EPM1, OMIM #254800) in 8 patients with mutations in the cystatin B gene (CSTB). 1 Working in the area of Southern Sweden where Herman Lundborg (1868-19