Zobrazeno 1 - 3
of 3
pro vyhledávání: '"E C Sener"'
Publikováno v:
British Journal of Ophthalmology. 85:1174-1178
AIM—To determine whether a newly identified thrombophilia factor, activated factor VII (FVIIa), is associated with retinal vein occlusion (RVO). METHODS—54 consecutive cases with RVO seen between March and September 1999 were included in the stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42a6866ddc1e1b3e0fe61fc8a797e60
https://doi.org/10.1136/bjo.85.10.1174
https://doi.org/10.1136/bjo.85.10.1174
Autor:
S, Oruç, E C, Sener
Publikováno v:
International ophthalmology. 23(2)
To evaluate the effects of topical timolol and apraclonidine on retrobulbar blood flow velocity waveforms in a group of healthy volunteers.Apraclonidine 1% and timolol maleate 0.5% single dose administrations were crossed over double masked in 12 hea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c7feafc4cc009d6f4532d04ff03e7d7e
https://pubmed.ncbi.nlm.nih.gov/11196122
https://pubmed.ncbi.nlm.nih.gov/11196122
Autor:
Ingo Meuthen, Janet Kerwin, Teresa de Berardinis, Alfons Meindl, Costantino Schiavi, Robyn V. Jamieson, Christina Pieh, Hagit N. Baris, Bettina Wabbels, Feray Koc, Wei He, Scott L. Pomeroy, Maree Flaherty, Joseph L. Demer, David A. Mackey, Emin Cumhur Sener, Jonathan B Ruddle, Lionel Van Maldergem, Louise J. Sabol, Susan Lindsay, Nicolas Uzcategui, Irene Gottlob, David F. Callen, Max A. Tischfield, Richard L. Robertson, Clara E. de Uzcategui, Thomas D. Bird, Janet S. Soul, Alex V. Levin, Marco Pastore-Trossello, Thomas Meitinger, Hans Ulrik Møller, Elizabeth C. Engle, Mary Louise Z. Collins, David G. Hunter, Maria Descartes, Edward J. Doherty, Mohan L. Gupta, Adriano Magli, Agnes M. F. Wong, Caroline Andrews, Chen Wu, Elias I. Traboulsi, Wai-Man Chan, Michael T. Geraghty, David Pellman, Anna Newlin, G. Rudolph, Heide Hellebrand
none 49 We report that eight heterozygous missense mutations in TUBB3, encoding the neuron-specific beta-tubulin isotype III, result in a spectrum of human nervous system disorders that we now call the TUBB3 syndromes. Each mutation causes the ocular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b601b8af477f5b7fbdfc8f57b962a518
http://hdl.handle.net/11585/89525
http://hdl.handle.net/11585/89525
