Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 1
2005 2
2006 5
2007 6
2008 3
2009 2
2010 3
2011 5
2012 5
2013 4
2014 1
2015 7
2016 2
2017 4
2018 2
2019 2
2020 2
2021 1
Text availability
Article attribute
Article type
Publication date

Search Results

48 results
Results by year
Filters applied: . Clear all
Page 1
Role of GUCA1C in Primary Congenital Glaucoma and in the Retina: Functional Evaluation in Zebrafish.
Morales-Cámara S, Alexandre-Moreno S, Bonet-Fernández JM, Atienzar-Aroca R, Aroca-Aguilar JD, Ferre-Fernández JJ, Méndez CD, Morales L, Fernández-Sánchez L, Cuenca N, Coca-Prados M, Martínez-de-la-Casa JM, Garcia-Feijoo J, Escribano J. Morales-Cámara S, et al. Among authors: escribano j. Genes (Basel). 2020 May 14;11(5):550. doi: 10.3390/genes11050550. Genes (Basel). 2020. PMID: 32422965 Free PMC article.
CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix.
Bonet-Fernández JM, Aroca-Aguilar JD, Corton M, Ramírez AI, Alexandre-Moreno S, García-Antón MT, Salazar JJ, Ferre-Fernández JJ, Atienzar-Aroca R, Villaverde C, Iancu I, Tamayo A, Méndez-Hernández CD, Morales-Fernández L, Rojas B, Ayuso C, Coca-Prados M, Martinez-de-la-Casa JM, García-Feijoo J, Escribano J. Bonet-Fernández JM, et al. Among authors: escribano j. Hum Genet. 2020 Oct;139(10):1209-1231. doi: 10.1007/s00439-020-02164-0. Epub 2020 Apr 9. Hum Genet. 2020. PMID: 32274568
Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma.
Medina-Trillo C, Aroca-Aguilar JD, Ferre-Fernández JJ, Alexandre-Moreno S, Morales L, Méndez-Hernández CD, García-Feijoo J, Escribano J. Medina-Trillo C, et al. Among authors: escribano j. PLoS One. 2019 Jan 18;14(1):e0211029. doi: 10.1371/journal.pone.0211029. eCollection 2019. PLoS One. 2019. PMID: 30657791 Free PMC article.
Transforming growth factor beta-induced p.(L558P) variant is associated with autosomal dominant lattice corneal dystrophy type IV in a large cohort of Spanish patients.
Campos-Mollo E, Varela-Conde Y, Arriola-Villalobos P, Cabrera-Beyrouti R, Benítez-Del-Castillo JM, Maldonado MJ, Escribano J. Campos-Mollo E, et al. Among authors: escribano j. Clin Exp Ophthalmol. 2019 Sep;47(7):871-880. doi: 10.1111/ceo.13532. Epub 2019 May 22. Clin Exp Ophthalmol. 2019. PMID: 31056827
Recent patents and developments in glaucoma biomarkers.
Colligris B, Crooke A, Gasull X, Escribano J, Herrero-Vanrell R, Benitez-del-Castillo JM, García-Feijoo J, Pintor J. Colligris B, et al. Among authors: escribano j. Recent Pat Endocr Metab Immune Drug Discov. 2012 Sep;6(3):224-34. doi: 10.2174/187221412802481739. Recent Pat Endocr Metab Immune Drug Discov. 2012. PMID: 22827637 Review.
48 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page