Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1990 | 1 |
1996 | 1 |
2017 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Tumefactive lesions in retinal vasculopathy with cerebral leucoencephalopathy and systemic manifestations (RVCL-S): a role for neuroinflammation?
J Neurol Neurosurg Psychiatry. 2017 Aug 9:jnnp-2017-316142. doi: 10.1136/jnnp-2017-316142. Online ahead of print.
J Neurol Neurosurg Psychiatry. 2017.
PMID: 28794152
No abstract available.
Characterisation of four novel fibrillin-1 (FBN1) mutations in Marfan syndrome.
Adès LC, Haan EA, Colley AF, Richard RI.
Adès LC, et al. Among authors: colley af.
J Med Genet. 1996 Aug;33(8):665-71. doi: 10.1136/jmg.33.8.665.
J Med Genet. 1996.
PMID: 8863159
Free PMC article.
Item in Clipboard
Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p11.2 p11.2) (Smith-Magenis syndrome).
Colley AF, Leversha MA, Voullaire LE, Rogers JG.
Colley AF, et al.
J Paediatr Child Health. 1990 Feb;26(1):17-21. doi: 10.1111/j.1440-1754.1990.tb02372.x.
J Paediatr Child Health. 1990.
PMID: 2331413
Item in Clipboard
Cite
Cite