Pinguecula research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Pinguecula treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
Designed by medical professionals, for medical professionals, with doctorAsyou you can visualize research in a unique evidence dashboard. You can also export, save and sort results.
Sign up for free for full access.
All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 19 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
Sort by
Date
Institutional score
Impact
Patients
List order
Sort
Categories
Studies
26272 Unclassified
9111 Research
8464 Reviews
8322 Case Reports
3836 Other Trials
2928 Advanced Trials
1699 Early Trials
148 Meta-Analysis
Guidelines
67 Guidelines
31 Consensuses
26 Cochrane
Congresses
5139 Abstracts
Research
Further pharmacological and genetic evidence for the efficacy of PlGF inhibition in cancer and eye disease.
Van de Veire Sara, Stalmans Ingeborg, Heindryckx Femke, Oura Hajimu, Tijeras-Raballand Annemilaï ...
Cell Vol 141(1)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 02 Apr 2010
Research
Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Eye Disease.
Chou Christopher M, Nelson Christine, Tarlé Susan A, Pribila Jonathan T, Bardakjian Tanya ...
Cell Vol 161(3)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 23 Apr 2015
Research
Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients.
Olschwang S, Tiret A, Laurent-Puig P, Muleris M, Parc R ...
Cell Vol 75(5)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 03 Dec 1993
Research
Add to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 23 Apr 2015
Research
A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy.
Chen Z Y, Battinelli E M, Fielder A, Bundey S, Sims K ...
Nature genetics Vol 5(2)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 Oct 1993
Research
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
Arts Heleen H, Doherty Dan, van Beersum Sylvia E C, Parisi Melissa A, Letteboer Stef J F ...
Nature genetics Vol 39(7)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 Jul 2007
Research
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.
Delous Marion, Baala Lekbir, Salomon Rémi, Laclef Christine, Vierkotten Jeanette ...
Nature genetics Vol 39(7)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 Jul 2007
Research
Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.
Yamamoto H, Simon A, Eriksson U, Harris E, Berson E L ...
Nature genetics Vol 22(2)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 Jun 1999
Research
Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes.
Kantarci Sibel, Al-Gazali Lihadh, Hill R Sean, Donnai Dian, Black Graeme C M ...
Nature genetics Vol 39(8)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 Aug 2007
Research
Biochemical defects in ABCR protein variants associated with human retinopathies.
Sun H, Smallwood P M, Nathans J
Nature genetics Vol 26(2)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 Oct 2000
View
per page
Page
1
2
3
4
5
6
7
8
9
10
Last
