The many faces of COVID-19: managing uncertainty

por Sederer, Lloyd I
Publicado 2021

Integrating Care for Medical and Mental Illnesses

por McVeigh, Katharine H, Sederer, Lloyd I, Silver, Lynn, Levy, Joslyn
Publicado 2006

Making Room for Mental Health in the Medical Home

por Hogan, Michael F., Sederer, Lloyd I., Smith, Thomas E., Nossel, Ilana R.
Publicado 2010

COVID-19, Unemployment, and Behavioral Health Conditions: The Need for Supported Employment

por Drake, Robert E., Sederer, Lloyd I., Becker, Deborah R., Bond, Gary R.
Publicado 2021

Factors Influencing Buprenorphine Prescribing among Physicians in New York State

por Marino, Leslie A., Campbell, Aimee N., Nunes, Edward V., Sederer, Lloyd I., Dixon, Lisa B.
Publicado 2019

Characteristics of global naturopathic education, regulation, and practice frameworks: results from an international survey

por Dunn, J. M., Steel, A. E., Adams, J., Lloyd, I., De Groot, N., Hausser, T., Wardle, J.
Publicado 2021

Cataract management in children: a review of the literature and current practice across five large UK centres

por Self, J. E., Taylor, R., Solebo, A. L., Biswas, S., Parulekar, M., Dev Borman, A., Ashworth, J., McClenaghan, R., Abbott, J., O’Flynn, E., Hildebrand, D., Lloyd, I. C.
Publicado 2020

Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia

por Taylor, Rachel L., Soriano, Carla Sanjuro, Williams, Simon, Dzulova, Denisa, Ashworth, Jane, Hall, Georgina, Gale, Theodora, Lloyd, I. Christopher, Inglehearn, Chris F., Toomes, Carmel, Douzgou, Sofia, Black, Graeme C.
Publicado 2022

Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature

por Taylor, Rachel L., Handley, Mark T., Waller, Sarah, Campbell, Christopher, Urquhart, Jill, Meynert, Alison M., Ellingford, Jamie M., Donnelly, Deirdre, Wilcox, Gisela, Lloyd, I. Chris, Mundy, Helen, FitzPatrick, David R., Deshpande, Charu, Clayton-Smith, Jill, Black, Graeme C.
Publicado 2017

Molecular findings from 537 individuals with inherited retinal disease

por Ellingford, Jamie M, Barton, Stephanie, Bhaskar, Sanjeev, O'Sullivan, James, Williams, Simon G, Lamb, Janine A, Panda, Binay, Sergouniotis, Panagiotis I, Gillespie, Rachel L, Daiger, Stephen P, Hall, Georgina, Gale, Theodora, Lloyd, I Christopher, Bishop, Paul N, Ramsden, Simon C, Black, Graeme C M
Publicado 2016

Clinical and genetic variability in children with partial albinism

por Campbell, Patrick, Ellingford, Jamie M., Parry, Neil R. A., Fletcher, Tracy, Ramsden, Simon C., Gale, Theodora, Hall, Georgina, Smith, Katherine, Kasperaviciute, Dalia, Thomas, Ellen, Lloyd, I. Chris, Douzgou, Sofia, Clayton-Smith, Jill, Biswas, Susmito, Ashworth, Jane L., Black, Graeme C. M., Sergouniotis, Panagiotis I.
Publicado 2019

Clinical utility of genetic testing in 201 preschool children with inherited eye disorders

por Lenassi, Eva, Clayton-Smith, Jill, Douzgou, Sofia, Ramsden, Simon C., Ingram, Stuart, Hall, Georgina, Hardcastle, Claire L., Fletcher, Tracy A., Taylor, Rachel L., Ellingford, Jamie M., Newman, William D., Fenerty, Cecilia, Sharma, Vinod, Lloyd, I. Chris, Biswas, Susmito, Ashworth, Jane L., Black, Graeme C., Sergouniotis, Panagiotis I.
Publicado 2019

Translational pharmacology of an inhaled small molecule αvβ6 integrin inhibitor for idiopathic pulmonary fibrosis

por John, Alison E., Graves, Rebecca H., Pun, K. Tao, Vitulli, Giovanni, Forty, Ellen J., Mercer, Paul F., Morrell, Josie L., Barrett, John W., Rogers, Rebecca F., Hafeji, Maryam, Bibby, Lloyd I., Gower, Elaine, Morrison, Valerie S., Man, Yim, Roper, James A., Luckett, Jeni C., Borthwick, Lee A., Barksby, Ben S., Burgoyne, Rachel A., Barnes, Rory, Le, Joelle, Flint, David J., Pyne, Susan, Habgood, Anthony, Organ, Louise A., Joseph, Chitra, Edwards-Pritchard, Rochelle C., Maher, Toby M., Fisher, Andrew J., Gudmann, Natasja Stæhr, Leeming, Diana J., Chambers, Rachel C., Lukey, Pauline T., Marshall, Richard P., Macdonald, Simon J. F., Jenkins, R. Gisli, Slack, Robert J.
Publicado 2020