X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
biography (5) 5
cornea (5) 5
humans (4) 4
index medicus (4) 4
keratoconus (4) 4
keratoconus - genetics (4) 4
polymorphism, single nucleotide (4) 4
cornea - metabolism (3) 3
cornea - pathology (3) 3
eye diseases (3) 3
genes (3) 3
genomes (3) 3
history (3) 3
keratoconus - ethnology (3) 3
keratoconus - pathology (3) 3
mutations (3) 3
adamts proteins - genetics (2) 2
adamts proteins - metabolism (2) 2
adult (2) 2
aged (2) 2
asian continental ancestry group (2) 2
association analysis (2) 2
australia - epidemiology (2) 2
cornea - abnormalities (2) 2
corneal diseases - ethnology (2) 2
corneal diseases - genetics (2) 2
corneal diseases - metabolism (2) 2
corneal diseases - pathology (2) 2
corneal dystrophies, hereditary - ethnology (2) 2
corneal dystrophies, hereditary - genetics (2) 2
corneal dystrophies, hereditary - metabolism (2) 2
corneal dystrophies, hereditary - pathology (2) 2
decorin (2) 2
decorin - genetics (2) 2
decorin - metabolism (2) 2
dna sequencing (2) 2
ehlers-danlos syndrome - ethnology (2) 2
ehlers-danlos syndrome - genetics (2) 2
ehlers-danlos syndrome - metabolism (2) 2
ehlers-danlos syndrome - pathology (2) 2
endocrinology & metabolism (2) 2
european continental ancestry group (2) 2
eye diseases, hereditary - ethnology (2) 2
eye diseases, hereditary - genetics (2) 2
eye diseases, hereditary - metabolism (2) 2
eye diseases, hereditary - pathology (2) 2
female (2) 2
fibrillin-1 - genetics (2) 2
fibrillin-1 - metabolism (2) 2
france history (2) 2
gene expression (2) 2
gene sequencing (2) 2
genetic predisposition to disease (2) 2
genetics & heredity (2) 2
genome, human (2) 2
genome-wide association (2) 2
genome-wide association study (2) 2
genomics (2) 2
glaucoma, open-angle - ethnology (2) 2
glaucoma, open-angle - genetics (2) 2
glaucoma, open-angle - metabolism (2) 2
glaucoma, open-angle - pathology (2) 2
internal medicine (2) 2
keratoconus - metabolism (2) 2
loeys-dietz syndrome - ethnology (2) 2
loeys-dietz syndrome - genetics (2) 2
loeys-dietz syndrome - metabolism (2) 2
loeys-dietz syndrome - pathology (2) 2
lumican (2) 2
lumican - genetics (2) 2
lumican - metabolism (2) 2
male (2) 2
marfan syndrome - ethnology (2) 2
marfan syndrome - genetics (2) 2
marfan syndrome - metabolism (2) 2
marfan syndrome - pathology (2) 2
medicine & public health (2) 2
mendelian randomization analysis (2) 2
middle aged (2) 2
multidisciplinary sciences (2) 2
myopia (2) 2
myopia - ethnology (2) 2
myopia - genetics (2) 2
myopia - metabolism (2) 2
myopia - pathology (2) 2
proteins (2) 2
proteoglycans - genetics (2) 2
proteoglycans - metabolism (2) 2
quantitative trait loci (2) 2
quantitative trait, heritable (2) 2
science (2) 2
transforming growth factor beta2 - genetics (2) 2
transforming growth factor beta2 - metabolism (2) 2
young adult (2) 2
1797-1877 (1) 1
610 medicine & health (1) 1
accident vasculaire cérébral (1) 1
acides aminés (1) 1
adamts proteins (1) 1
adolescent (1) 1
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
by Iglesias, Adriana I and Mishra, Aniket and Vitart, Veronique and Bykhovskaya, Yelena and Höhn, René and Springelkamp, Henriët and Cuellar-Partida, Gabriel and Gharahkhani, Puya and Bailey, Jessica N. Cooke and Willoughby, Colin E and Li, Xiaohui and Yazar, Seyhan and Nag, Abhishek and Khawaja, Anthony P and Polašek, Ozren and Siscovick, David and Mitchell, Paul and Tham, Yih Chung and Haines, Jonathan L and Kearns, Lisa S and Hayward, Caroline and Shi, Yuan and Van Leeuwen, Elisabeth M and Taylor, Kent D and Wang, Jie Jin and Rochtchina, Elena and Attia, John and Scott, Rodney and Holliday, Elizabeth G and Baird, Paul N and Xie, Jing and Inouye, Michael and Viswanathan, Ananth and Sim, Xueling and Bonnemaijer, Pieter and Rotter, Jerome I and Martin, Nicholas G and Zeller, Tanja and Mills, Richard A and Staffieri, Sandra E and Jonas, Jost B and Schmidtmann, Irene and Boutin, Thibaud and Kang, Jae H and Lucas, Sionne E. M and Wong, Tien Yin and Beutel, Manfred E and Wilson, James F and Allingham, R. Rand and Brilliant, Murray H and Budenz, Donald L and Christen, William G and Fingert, John and Friedman, David S and Gaasterland, Douglas and Gaasterland, Terry and Hauser, Michael A and Kraft, Peter and Lee, Richard K and Lichter, Paul R and Liu, Yutao and Loomis, Stephanie J and Moroi, Sayoko E and Pericak-Vance, Margaret A and Realini, Anthony and Richards, Julia E and Schuman, Joel S and Scott, William K and Singh, Kuldev and Sit, Arthur J and Vollrath, Douglas and Weinreb, Robert N and Wollstein, Gadi and Zack, Donald J and Zhang, Kang and Donnelly, Peter and Barroso, Ines and Blackwell, Jenefer M and Bramon, Elvira and Brown, Matthew A and Casas, Juan P and Corvin, Aiden and Deloukas, Panos and Duncanson, Audrey and Jankowski, Janusz and Markus, Hugh S and Mathew, Christopher G and Palmer, Colin N. A and Plomin, Robert and Rautanen, Anna and Sawcer, Stephen J and Trembath, Richard C and Wood, Nicholas W and Spencer, Chris C. A and Band, Gavin and Bellenguez, Céline and Freeman, Colin and Hellenthal, Garrett and Giannoulatou, Eleni and Pirinen, Matti and ... and Blue Mountains Eye Study-GWAS Grp and NEIGHBORHOOD Consortium and Wellcome Trust Case Control Consor and Blue Mountains Eye Study—GWAS group and Wellcome Trust Case Control Consortium 2 (WTCCC2)
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1 - 11
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide... 
DECORIN | CHROMATIN STATES | POLYMORPHISMS | RISK-FACTOR | MULTIDISCIPLINARY SCIENCES | MOUSE | GENE-EXPRESSION | MUTATIONS | HERITABILITY | LUMICAN | KERATOCONUS | Glaucoma | Cornea | Genes | Myopia | Association analysis | Genomes | Gene expression | Tissues | Connective tissues | Keratoconus | Collagen | Eye diseases | Extracellular matrix | Index Medicus
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 12/2017, Volume 58, Issue 14, pp. 6248 - 6256
PURPOSE. The Zinc Finger Protein 469 (ZNF469) gene has been proposed as a candidate gene for keratoconus due to the association of an upstream polymorphism... 
Cornea | Keratoconus | Genomics | Candidate genes | DNA sequencing | POPULATION | keratoconus | cornea | FORMAT | DISCOVERY | GENETIC-VARIATION | BRITTLE CORNEA SYNDROME | candidate genes | FRAMEWORK | OPHTHALMOLOGY | genomics | MUTATIONS | DNA-SEQUENCING DATA | ASSOCIATION | THICKNESS | Index Medicus
Journal Article
Nature communications, ISSN 2041-1723, 01/2019, Volume 10, Issue 1, pp. 155 - 155
Emmanuelle Souzeau, who contributed to analysis of data, was inadvertently omitted from the author list in the originally published version of this Article.... 
Association analysis | Eye diseases | Data processing | Cornea | Genomes
Journal Article
Journal Article
Nature communications, ISSN 2041-1723, 05/2018, Volume 9, Issue 1, p. 1864
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide... 
Lumican - metabolism | Glaucoma, Open-Angle - genetics | Humans | Corneal Diseases - metabolism | Corneal Dystrophies, Hereditary - ethnology | Corneal Diseases - genetics | Ehlers-Danlos Syndrome - genetics | Corneal Dystrophies, Hereditary - pathology | Loeys-Dietz Syndrome - metabolism | Mendelian Randomization Analysis | Fibrillin-1 - metabolism | Cornea - pathology | Keratoconus - pathology | Corneal Diseases - pathology | Decorin - genetics | Gene Expression | Eye Diseases, Hereditary - pathology | Lumican - genetics | ADAMTS Proteins - metabolism | Proteoglycans - metabolism | Ehlers-Danlos Syndrome - ethnology | European Continental Ancestry Group | Myopia - pathology | Cornea - metabolism | Myopia - ethnology | Loeys-Dietz Syndrome - pathology | Corneal Diseases - ethnology | Marfan Syndrome - metabolism | Marfan Syndrome - pathology | Cornea - abnormalities | Quantitative Trait Loci | Proteoglycans - genetics | ADAMTS Proteins - genetics | Transforming Growth Factor beta2 - metabolism | Corneal Dystrophies, Hereditary - genetics | Glaucoma, Open-Angle - pathology | Keratoconus - metabolism | Loeys-Dietz Syndrome - ethnology | Glaucoma, Open-Angle - ethnology | Myopia - metabolism | Ehlers-Danlos Syndrome - pathology | Marfan Syndrome - ethnology | Keratoconus - genetics | Glaucoma, Open-Angle - metabolism | Fibrillin-1 - genetics | Eye Diseases, Hereditary - ethnology | Genome-Wide Association Study | Quantitative Trait, Heritable | Corneal Dystrophies, Hereditary - metabolism | Marfan Syndrome - genetics | Eye Diseases, Hereditary - genetics | Myopia - genetics | Asian Continental Ancestry Group | Keratoconus - ethnology | Ehlers-Danlos Syndrome - metabolism | Loeys-Dietz Syndrome - genetics | Polymorphism, Single Nucleotide | Transforming Growth Factor beta2 - genetics | Genome, Human | Decorin - metabolism | Eye Diseases, Hereditary - metabolism | Cornea | Decorin | Corneal Dystrophies, Hereditary | Myopia | Corneal Diseases | Marfan Syndrome | Keratoconus | ADAMTS Proteins | Lumican | Transforming Growth Factor beta2 | Ehlers-Danlos Syndrome | Glaucoma, Open-Angle | Fibrillin-1 | Eye Diseases, Hereditary | Proteoglycans | Wellcome Trust Case Control Consortium 2 (WTCCC2) | Blue Mountains Eye Study—GWAS group | Loeys-Dietz Syndrome | NEIGHBORHOOD Consortium
Journal Article
Molecular Genetics & Genomic Medicine, ISSN 2324-9269, 07/2018, Volume 6, Issue 4, pp. 555 - 564
We screened 51 known congenital or pediatric cataract genes in 33 probands from Bhutan, Cambodia, and Sri Lanka. We identified likely causative mutations in... 
mutation screening | congenital cataract | inherited eye disease | next‐generation sequencing | next-generation sequencing | SEVERE VISUAL IMPAIRMENT | PROTEIN | VARIANTS | GENETICS & HEREDITY | SCHOOLS | BLINDNESS | CHILDHOOD | FAMILY | Cataracts | Pediatrics | Identification methods | Genes | Patients | Gene sequencing | Proteins | Coding | Blindness | Children | Mutation | Schools | Visually handicapped people
Journal Article
2004, ISBN 9782874153778, 163
Book
1948, Grandes études historiques, 402
Book
1997, Collection histoire, ISBN 2907064304, 375
Book
by C Lucas and E Simon
Douleur et Analgesie, ISSN 1011-288X, 06/2017, Volume 30, Issue 2, p. 64
Le nerf trijumeau assure la sensibilité de l'hémiface homolatérale au travers de ses trois branches principales : nerf ophtalmique (V1), nerf maxillaire... 
Journal Article
1929, Les leçons de passé; pub. par Marcel Boulenger et P. Bessand-Massenet, 266
Book
Diabetes and Metabolism, ISSN 1262-3636, 2011, Volume 37, Issue 1, pp. A12 - A12
Objectif Différentes études récentes montrent que les recommandations thérapeutiques dans le diabète de type 2 (DT2) restent insuffisamment appliquées.... 
Internal Medicine | Endocrinology & Metabolism
Journal Article
Revue de Stomatologie et de Chirurgie Maxillo-faciale, ISSN 0035-1768, 2006, Volume 107, Issue 3, pp. 137 - 142
L’édentation partielle ou totale des patients après le traitement d’un cancer des voies aéro-digestives supérieures pose des difficultés de réhabilitation... 
Réhabilitation prothétique | Dental implants | Radiotherapy | Implants dentaires | Radiothérapie | Dental prosthesis
Journal Article
Journal Francais d'Ophtalmologie, ISSN 0181-5512, 2007, Volume 30, pp. 2S189 - 2S189
Journal Article
Annales francaises d'anesthesie et de reanimation, ISSN 0750-7658, 1985, Volume 4, Issue 1, pp. 9 - 13
L'hypotension provoquée par le nitroprussiate de sodium (NPS) active de nombreux systèmes vasoconstricteurs : catécholamines, rénine-angiotensine (ARP) et... 
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.