AN OUTBREAK OF BESNOITIOSIS IN MINIATURE DONKEYS von Elsheikha, Hany M, Mackenzie, Charles D, Rosenthal, Benjamin M, Marteniuk, Judith V, Steficek, Barbara, Windsor, Sharon, Saeed, A. Mahdi, Mansfield, Linda S

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Direct detection of a common inversion mutation in the genetic diagnosis of severe hemophilia A [see comments] von Windsor, S, Taylor, SA, Lillicrap, D

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Direct Detection of a Common Inversion Mutation in the Genetic Diagnosis of Severe Hemophilia A von Windsor, Sharon, Taylor, Sherryl A.M., Lillicrap, David

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Absence of allelic loss on chromosome 5q by RFLP analysis in preleukemia von Shepherd, Lois, Cameron, Cherie, Galbraith, Peter, Windsor, Sharon, Lillicrap, David

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Absence of a bleeding tendency in severe acquired von Willebrand's disease: the role of platelet Von Willebrand factor in maintaining normal hemostasis von DROUIN, J, LILLICRAP, D. P, IZAGUIRRE, C. A, SUTHERLAND, M, WINDSOR, S, BENFORD, K, HOOGENDORN, H, GILES, A. R

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Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics von Cideciyan, Artur V, Aleman, Tomas S, Boye, Sanford L, Schwartz, Sharon B, Kaushal, Shalesh, Roman, Alejandro J, Pang, Ji-jing, Sumaroka, Alexander, Windsor, Elizabeth A.M, Wilson, James M, Flotte, Terence R, Fishman, Gerald A, Heon, Elise, Stone, Edwin M, Byrne, Barry J, Jacobson, Samuel G, Hauswirth, William W

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Human RPE65 Gene Therapy for Leber Congenital Amaurosis: Persistence of Early Visual Improvements and Safety at 1 Year von CIDECIYAN, Artur V, HAUSWIRTH, William W, ROMAN, Alejandro J, BYRNE, Barry J, JACOBSON, Samuel G, ALEMAN, Tomas S, KAUSHAL, Shalesh, SCHWARTZ, Sharon B, BOYE, Sanford L, WINDSOR, Elizabeth A. M, CONLON, Thomas J, SUMAROKA, Alexander, PANG, Ji-Jing

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ABCA4 disease progression and a proposed strategy for gene therapy von Cideciyan, Artur V., Swider, Malgorzata, Aleman, Tomas S., Tsybovsky, Yaroslav, Schwartz, Sharon B., Windsor, Elizabeth A.M., Roman, Alejandro J., Sumaroka, Alexander, Steinberg, Janet D., Jacobson, Samuel G., Stone, Edwin M., Palczewski, Krzysztof

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Vision 1 Year after Gene Therapy for Leber's Congenital Amaurosis von Windsor, Elizabeth A.M, Byrne, Barry J, Sumaroka, Alexander, Jacobson, Samuel G, Hauswirth, William W, Cideciyan, Artur V, Kaushal, Shalesh, Aleman, Tomas S, Schwartz, Sharon B, Boye, Sanford L, Conlon, Thomas J, Roman, Alejandro J

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Identifying Photoreceptors in Blind Eyes Caused by RPE65 Mutations: Prerequisite for Human Gene Therapy Success von Jacobson, Samuel G., Aleman, Tomas S., Cideciyan, Artur V., Sumaroka, Alexander, Schwartz, Sharon B., Elizabeth A. M. Windsor, Traboulsi, Elias I., Heon, Elise, Pittler, Steven J., Milam, Ann H., Maguire, Albert M., Palczewski, Krzysztof, Stone, Edwin M., Bennett, Jean, Nathans, Jeremy

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Human cone photoreceptor dependence on RPE65 isomerase von Jacobson, Samuel G, Aleman, Tomas S, Cideciyan, Artur V, Heon, Elise, Golczak, Marcin, Beltran, William A, Sumaroka, Alexander, Schwartz, Sharon B, Roman, Alejandro J, Windsor, Elizabeth A.M, Wilson, James M, Aguirre, Gustavo D, Stone, Edwin M, Palczewski, Krzysztof

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Normal Central Retinal Function and Structure Preserved in Retinitis Pigmentosa von Jacobson, Samuel G, Roman, Alejandro J, Aleman, Tomas S, Sumaroka, Alexander, Herrera, Waldo, Windsor, Elizabeth A. M, Atkinson, Lori A, Schwartz, Sharon B, Steinberg, Janet D, Cideciyan, Artur V

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Defining the Residual Vision in Leber Congenital Amaurosis Caused by RPE65 Mutations von Jacobson, Samuel G, Aleman, Tomas S, Cideciyan, Artur V, Roman, Alejandro J, Sumaroka, Alexander, Windsor, Elizabeth A. M, Schwartz, Sharon B, Heon, Elise, Stone, Edwin M

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Retinal Laminar Architecture in Human Retinitis Pigmentosa Caused by Rhodopsin Gene Mutations von Aleman, Tomas S, Cideciyan, Artur V, Sumaroka, Alexander, Windsor, Elizabeth A. M, Herrera, Waldo, White, D. Alan, Kaushal, Shalesh, Naidu, Anjani, Roman, Alejandro J, Schwartz, Sharon B, Stone, Edwin M, Jacobson, Samuel G

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Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amauros... von Cideciyan, Artur V, Aleman, Tomas S, Jacobson, Samuel G, Khanna, Hemant, Sumaroka, Alexander, Aguirre, Geoffrey K, Schwartz, Sharon B, Windsor, Elizabeth A.M, He, Shirley, Chang, Bo, Stone, Edwin M, Swaroop, Anand

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Remodeling of the Human Retina in Choroideremia: Rab Escort Protein 1 (REP-1) Mutations von Jacobson, Samuel G, Cideciyan, Artur V, Sumaroka, Alexander, Aleman, Tomas S, Schwartz, Sharon B, Windsor, Elizabeth A. M, Roman, Alejandro J, Stone, Edwin M, MacDonald, Ian M

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Pregnancy and neonatal outcomes of COVID‐19: coreporting of common outcomes from PAN‐COVID and AAP‐SONPM registries von Barnette, K., Perry, A., Lees, C. C., Nallapeta, Soum, Peers, Beth, Iliodromiti, Stamatina, Armstrong, Maggie, Mutema, Eric, Syson, Jen, Thornton, Danielle, Ajay, Bini, Woodward, Zoe, Mason, Nicky, Moller‐Christensen, Christine, Jaleel, Shazia, Revell, Kirsty, Amin, Allison, Sherris, Leanne, Mansfield, Roshni, Raven, Jamie‐Louise, Sukrutha, Veerareddy, Fayadh, Anam, Kausar, Sameena, Harrington, Andrea, Lear, Emily, Kousar, Rukhsana, Essien, Sandra, Gowans, Sharon, Huson, Coralie, Barker, Katie, Newport, Rachel, Garner, Zoe, Lee, Fidelma, Anderson, Michelle, Everden, Caroline, Jokhi, Roobin, O'Brien, Clare, Bishop, Linda, Heal, Carrie, Jones, Sharon, Cloherty, Karen, Kermack, Alexandra, Liebling, Rachel, Khare, Manjiri, Halawa, Sherry, Narayanan, Sankara, Brain, Jessie, Pandey, Bhavna, Dooks, Emma, Tarft, Hayley, Newman, Tabitha, Thomas, Amy, Woodhead, Amy, Stoddard, Emma, Rhead, Kat, Frankland, Lisa, Home, Marie, Holroyd, Kelly, Sutton‐Cole, Amy, Keeping, Vikki, Kelly‐Baxter, Mary, Upson, Gerry, Creeth, Annabel, Johnson, Sarah, Rand, James, Taylor, Sasha, Edwards, Alex, Grant, Rachael, Truslove, Tracy, Dunham, Tracey, Mathew, Asha, Goodier, Jenny, Jenkins, Elinor, Ambler, Sarah‐Jayne, Pepper, Stacey, Dixon, Caroline, Paulose, Minimol, Alvarez, Mary, Hardy, Rachel, Hodgen, Lesley, Glyn‐Jones, Liz, Pyart, Eleanor, Burnard, Sara, Gill, Many, Harwood, Helen, Parish, Gemma, Hake, Danielle, Maher, Sarah, Watkins, Eve, Lal, Komal, Yelnoorkar, Fiona, Coton, Zoe, Lever, Erin, Watts, Rujnita, Patterson, Molly, Hollands, Heidi, Riddles, Laura, Evans, Melanie, Wood, Diane, Elliott, Kerry

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Safety of recombinant adeno-associated virus type 2-RPE65 vector delivered by ocular subretinal injection von Jacobson, Samuel G, Acland, Gregory M, Aguirre, Gustavo D, Aleman, Tomas S, Schwartz, Sharon B, Cideciyan, Artur V, Zeiss, Caroline J, Komaromy, Andras M, Kaushal, Shalesh, Roman, Alejandro J, Windsor, Elizabeth A M, Sumaroka, Alexander, Pearce-Kelling, Susan E, Conlon, Thomas J, Chiodo, Vincent A, Boye, Sanford L, Flotte, Terence R, Maguire, Albert M, Bennett, Jean, Hauswirth, William W

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Photoreceptor Layer Topography in Children with Leber Congenital Amaurosis Caused by RPE65 Mutations von Jacobson, Samuel G, Cideciyan, Artur V, Aleman, Tomas S, Sumaroka, Alexander, Windsor, Elizabeth A. M, Schwartz, Sharon B, Heon, Elise, Stone, Edwin M

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Disease Boundaries in the Retina of Patients with Usher Syndrome Caused by MYO7A Gene Mutations von Jacobson, Samuel G, Aleman, Tomas S, Sumaroka, Alexander, Cideciyan, Artur V, Roman, Alejandro J, Windsor, Elizabeth A. M, Schwartz, Sharon B, Rehm, Heidi L, Kimberling, William J

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