Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Angele Nalbandian"'
Autor:
Lata Singh, Nasim Salimiaghdam, Kevin Schneider, Angele Nalbandian, Marilyn Chwa, Shari R Atilano, Andrea Bao, M Cristina Kenney
Publikováno v:
BMJ Open Ophthalmology, Vol 5, Iss 1 (2020)
Background We aim to determine the possible adverse effects of ciprofloxacin (CPFX) and tetracycline (TETRA), as examples of bactericidal and bacteriostatic agents, respectively, on cultured human retinal pigment epithelial cells (ARPE-19).Methods Ce
Externí odkaz:
https://doaj.org/article/b225632cc6f7451290919d020cd4be45
Publikováno v:
American Journal of Ophthalmology. 240:58-66
To study orthograde axonal transport with amyloid precursor protein (APP-A4) immunohistochemistry (IHC) in the retina and lamina cribrosa (LC) portion of the optic nerve in abusive head trauma (AHT) suspects.Retrospective, case-control study.Seventy-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86db1c214a4dfe434c3d98b65e0ea8d0
https://doi.org/10.1016/j.ajo.2022.02.018
https://doi.org/10.1016/j.ajo.2022.02.018
Autor:
Veronica Ferrari, Riccardo Cristofani, Maria E. Cicardi, Barbara Tedesco, Valeria Crippa, Marta Chierichetti, Elena Casarotto, Marta Cozzi, Francesco Mina, Mariarita Galbiati, Margherita Piccolella, Serena Carra, Thomas Vaccari, Angele Nalbandian, Virginia Kimonis, Tyler R. Fortuna, Udai B. Pandey, Maria C. Gagliani, Katia Cortese, Paola Rusmini, Angelo Poletti
Mutations in the valosin-containing protein (VCP) gene cause various lethal proteinopathies that mainly include inclusion body myopathy with Paget's disease of bone and frontotemporal dementia (IBMPFD) and amyotrophic lateral sclerosis (ALS). Differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44c1ced20d9cbccee8e3fbbbd646df8d
https://hdl.handle.net/11380/1287009
https://hdl.handle.net/11380/1287009
Autor:
Amanda, Gerling, Szu-Yun, Leu, Szu-Yen, Leu, Andrew J, Morton, Julio, Echegoyen, Angele, Nalbandian, Robert W, Lingua
Publikováno v:
Gerling, Amanda; Leu, Szu-Yen; Morton, Andrew J; Echegoyen, Julio; Nalbandian, Angele; & Lingua, Robert W. (2015). Reliability and Application Variability of a Commercially Available Infrared Videonystagmography Unit. Journal of Pediatric Ophthalmology & Strabismus, 52(2), 114-118. doi: 10.3928/01913913-20150114-04. UC Irvine: Institute for Clinical and Translational Science. Retrieved from: http://www.escholarship.org/uc/item/5n93w0pv
Purpose: Nystagmus is a condition of involuntary eye movement. The causes for nystagmus may be congenital, idiopathic, or acquired. Considerable debate exists on the therapeutic potential of various surgical techniques. Currently, there are neither s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95bb150fc2c7930ef519bb72927b3686
https://europepmc.org/articles/PMC4725705/
https://europepmc.org/articles/PMC4725705/
Autor:
Josephine S. Modica-Napolitano, Marianne E Kidd, Raffi Nalbandian, Chilinh C Nguyen, Angele Nalbandian
Publikováno v:
Cancer Letters. 198:59-68
This study assessed the selective growth inhibitory effect on cultured carcinoma cells by 3'-azido-3'-deoxythymidine (AZT), as a single agent, and in combination with delocalized lipophilic cations (DLCs) that are known to inhibit mitochondrial funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b17f54111cf7f66570c851ec3445f6fc
https://doi.org/10.1016/s0304-3835(03)00274-x
https://doi.org/10.1016/s0304-3835(03)00274-x
Autor:
Katrina J. Llewellyn, Angèle Nalbandian, Arianna Gomez, Don Wei, Naomi Walker, Virginia E. Kimonis
Publikováno v:
Neurobiology of Disease, Vol 76, Iss , Pp 77-86 (2015)
Genetic defects in the UBE3A gene, which encodes for the imprinted E6-AP ubiquitin E3 ligase (UBE3A), is responsible for the occurrence of Angelman syndrome (AS), a neurodegenerative disorder which arises in 1 out of every 12,000–20,000 births. Cla
Externí odkaz:
https://doaj.org/article/50d6741fa0c644ff929dfc72944f7ec6
Autor:
Katrina J Llewellyn, Angèle Nalbandian, Lan N Weiss, Isabela Chang, Howard Yu, Bibo Khatib, Baichang Tan, Vanessa Scarfone, Virginia E Kimonis
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0176919 (2017)
Valosin Containing Protein (VCP) disease is an autosomal dominant multisystem proteinopathy caused by mutations in the VCP gene, and is primarily associated with progressive muscle weakness, including atrophy of the pelvic and shoulder girdle muscles
Externí odkaz:
https://doaj.org/article/af6202955bc24f2880bea5ee6ef749fc
Autor:
Katrina J. Llewellyn, Angèle Nalbandian, Arianna Gomez, Don Wei, Naomi Walker, Anh Bui, Hannah Kim, Ivan Soltesz, Virginia E. Kimonis
Publikováno v:
Neurobiology of Disease, Vol 78, Iss , Pp 56- (2015)
Externí odkaz:
https://doaj.org/article/e0990bdef6a547838f5282b796e257c8
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0122888 (2015)
Mutations in the valosin containing protein (VCP) gene cause hereditary Inclusion body myopathy (hIBM) associated with Paget disease of bone (PDB), frontotemporal dementia (FTD), more recently termed multisystem proteinopathy (MSP). Affected individu
Externí odkaz:
https://doaj.org/article/5170ef3211304dc2837073b815c97eff
Autor:
Katrina J Llewellyn, Naomi Walker, Christopher Nguyen, Baichang Tan, Lbachir BenMohamed, Virginia E Kimonis, Angèle Nalbandian
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0131995 (2015)
The discovery of effective therapies and of disease mechanisms underlying valosin containing protein (VCP)-associated myopathies and neurodegenerative disorders remains elusive. VCP disease, caused by mutations in the VCP gene, are a clinically and g
Externí odkaz:
https://doaj.org/article/c9cf19ef26c44a0eab287f830120fe0b