1 - 25 of 5
| Title | Date | Type | Setname | ||
|---|---|---|---|---|---|
| 1 |
 |
A Giant Tumefactive Virchow-Robin Space: A Rare Cause of a Homonymous Quadrantanopia | 2017-03 | Text | ehsl_novel_jno |
| 2 |
 |
A Tough NUT to Crack: A 47-Year-Old With Diplopia From a Rare Malignancy | 2019-09 | Text | ehsl_novel_jno |
| 3 |
 |
Eyelid Closure Downbeat Nystagmus: A Rare Cause of Insomnia | 2021-06 | Text | ehsl_novel_jno |
| 4 |
 |
Impacting the Care of Children with Rare Disease through the Medical Home Portal | 2015 | Text | ehsl_gradnu |
| 5 |
 |
Variable Presentation of Leber Hereditary Optic Neuropathy in Children of a Family Harboring a Rare m.13051GA mtDNA Mutation | 2020-12 | Text | ehsl_novel_jno |
1 - 25 of 5