Resultats de la cerca - Ken K. Nischal

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  1. 1
    Genetics of Congenital Corneal Opacification—Impact on Diagnosis and Treatment

    Genetics of Congenital Corneal Opacification—Impact on Diagnosis and Treatment per Ken K. Nischal

    Publicat 2015
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  2. 2
    Pediatric cataract: challenges and future directions

    Pediatric cataract: challenges and future directions per Anagha Medsinge, Ken K. Nischal

    Publicat 2015
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  3. 3
    Congenital aniridia: etiology, manifestations and management

    Congenital aniridia: etiology, manifestations and management per Monica Samant, Bharesh K. Chauhan, Kira L. Lathrop, Ken K. Nischal

    Publicat 2016
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  4. 4
    Incidence of early-onset glaucoma after infant cataract extraction with and without intraocular lens implantation

    Incidence of early-onset glaucoma after infant cataract extraction with and without intraocular lens implantation per Inez B. Wong, V D Sukthankar, Mario Cortina‐Borja, Ken K. Nischal

    Publicat 2009
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  5. 5
    Recurrent Retinal Detachment in Stickler Syndrome

    Recurrent Retinal Detachment in Stickler Syndrome per T. Chen, Marjan Fooladi, Michelle Alabek, Hannah L. Scanga, Kelly Tripi, Ken K. Nischal, Joseph N. Martel

    Publicat 2024
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  6. 6
    Susceptibility weighted imaging depicts retinal hemorrhages in abusive head trauma

    Susceptibility weighted imaging depicts retinal hemorrhages in abusive head trauma per Giulio Zuccoli, Ashok Panigrahy, Anshul Haldipur, Dennis Willaman, Janet E. Squires, Jennifer Wolford, Christin L. Sylvester, Ellen Mitchell, Lee Ann Lope, Ken K. Nischal, Rachel P. Berger

    Publicat 2013
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  7. 7
    Ophthalmology Practice During the Coronavirus Disease 2019 Pandemic: The University of Pittsburgh Experience in Promoting Clinic Safety and Embracing Video Visits

    Ophthalmology Practice During the Coronavirus Disease 2019 Pandemic: The University of Pittsburgh Experience in Promoting Clinic Safety and Embracing Video Visits per Andrew M. Williams, Gagan Kalra, Patrick W. Commiskey, Eve M. R. Bowers, Brian R. Rudolph, Mary D. Pitcher, Kunal K. Dansingani, Vishal Jhanji, Ken K. Nischal, José‐Alain Sahel, Evan L. Waxman, Roxana Fu

    Publicat 2020
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    Editorial
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  8. 8
    A proposal for an updated staging system for LCHADD retinopathy

    A proposal for an updated staging system for LCHADD retinopathy per Nida Wongchaisuwat, Melanie B. Gillingham, Paul Yang, Lesley Everett, Ashley Gregor, Cary O. Harding, José‐Alain Sahel, Ken K. Nischal, Hannah L. Scanga, Danielle A. Black, Jerry Vockley, Georgianne L. Arnold, Mark E. Pennesi

    Publicat 2024
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  9. 9
    Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features

    Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features per Michael Absoud, Ming Lim, W.K. Chong, Christian G De Goede, Katharine Foster, Roxana Gunny, Cheryl Hemingway, Philip Jardine, Rachel Kneen, Marcus Likeman, Ken K. Nischal, Michael Pike, Naomi Sibtain, William Whitehouse, Carole Cummins, Evangeline Wassmer

    Publicat 2012
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  10. 10
    IC3D Classification of Corneal Dystrophies—Edition 3

    IC3D Classification of Corneal Dystrophies—Edition 3 per Jayne S. Weiss, Christopher J. Rapuano, Berthold Seitz, Massimo Busin, Tero Kivelä, Nacim Bouheraoua, Cecilie Bredrup, Ken K. Nischal, Harshvardhan Chawla, Vincent Borderie, Kenneth R. Kenyon, Eung Kweon Kim, Hans Ulrik Møller, Francis L. Munier, Tim Berger, Walter Lisch

    Publicat 2024
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  11. 11
    Mutation of SALL2 causes recessive ocular coloboma in humans and mice

    Mutation of SALL2 causes recessive ocular coloboma in humans and mice per Daniel Kelberman, Lily Islam, Jörn Lakowski, Chiara Bacchelli, Estelle Chanudet, Francesco Lescai, AmitP Patel, Elia Stupka, A. Buck, Stephan Wolf, Philip L. Beales, Thomas S. Jacques, Maria Bitner‐Glindzicz, Alki Liasis, Ordan J. Lehmann, Jürgen Kohlhase, Ken K. Nischal, Jane C. Sowden

    Publicat 2014
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  12. 12
    Congenital aniridia beyond black eyes: From phenotype and novel genetic mechanisms to innovative therapeutic approaches

    Congenital aniridia beyond black eyes: From phenotype and novel genetic mechanisms to innovative therapeutic approaches per Alejandra Daruich, Melinda K. Duncan, Matthieu P. Robert, Neil Lagali, Elena V. Semina, Daniel Aberdam, Stefano Ferrari, Vito Romano, Cyril Burin des Roziers, Rabia Benkortebi, Nathalie de Vergnes, Michel Polak, Frédéric Chiambaretta, Ken K. Nischal, Francine Béhar‐Cohen, Sophie Valleix, Dominique Brémond‐Gignac

    Publicat 2022
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  13. 13
    IMI—Management and Investigation of High Myopia in Infants and Young Children

    IMI—Management and Investigation of High Myopia in Infants and Young Children per Ian Flitcroft, John Ainsworth, Audrey Chia, Susan A. Cotter, Elise Harb, Zi‐Bing Jin, Caroline C. W. Klaver, Anthony T. Moore, Ken K. Nischal, Kyoko Ohno‐Matsui, Evelyn A. Paysse, Michael X. Repka, Irina Yurievna Smirnova, Martin P. Snead, Virginie J. M. Verhoeven, Pavan K. Verkicharla

    Publicat 2023
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  14. 14
    Cerebroretinal microangiopathy with calcifications and cysts (CRMCC)

    Cerebroretinal microangiopathy with calcifications and cysts (CRMCC) per Tracy A. Briggs, Ghada M. H. Abdel‐Salam, Maryagnes R. Balicki, Peter Baxter, Enrico Bertini, Nick Bishop, B H Browne, David Chitayat, W.K. Chong, Maha M. Eid, William Halliday, Imelda Hughes, A. Klusmann‐Koy, Mary Kurian, Ken K. Nischal, Gillian Rice, John B.P. Stephenson, R. Surtees, J F Talbot, Nasrin Tehrani, John Tolmie, Carmel Toomes, Marjo S. van der Knaap, Yanick J. Crow

    Publicat 2007
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  15. 15
    Genetic Analysis of ‘PAX6-Negative’ Individuals with Aniridia or Gillespie Syndrome

    Genetic Analysis of ‘PAX6-Negative’ Individuals with Aniridia or Gillespie Syndrome per Morad Ansari, Jacqueline K. Rainger, Isabel M. Hanson, Kathleen A. Williamson, Freddie H. Sharkey, Louise Harewood, Angela Sandilands, Jill Clayton‐Smith, Hélène Dollfus, Pierre Bitoun, Françoise Meire, Judy Fantes, Brunella Franco, Birgit Lorenz, David S. Taylor, Fiona Stewart, Colin E. Willoughby, Meriel McEntagart, Peng T. Khaw, Carol L. Clericuzio, Lionel Van Maldergem, Denise Williams, Ruth Newbury‐Ecob, Elias I. Traboulsi, Eduardo Silva, Mukhlis M. Madlom, David Goudie, Brian W. Fleck, Dagmar Wieczorek, Juergen Kohlhase, Alice McTrusty, Carol Gardiner, Christopher Yale, Anthony T. Moore, Isabelle Russell‐Eggitt, Lily Islam, Melissa Lees, Philip L. Beales, Stephen J. Tuft, Juan B. Solano, Miranda Splitt, Jens Michael Hertz, Trine Prescott, Deborah Shears, Ken K. Nischal, Martine Doco‐Fenzy, Fabienne Prieur, I. Karen Temple, Katherine Lachlan, Giuseppe Damante, Danny Morrison, Veronica van Heyningen, David Fitzpatrick

    Publicat 2016
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  16. 16
    Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome

    Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome per Gillian Rice, Teresa Patrick, Rekha Parmar, Claire Taylor, Alec Aeby, Jean Aicardi, Rafael Artuch, Simon Attard Montalto, Carlos A. Bacino, Bruno Barroso, Peter Baxter, Willam S. Benko, Carsten Bergmann, Enrico Bertini, Roberta Biancheri, Edward Blair, Nenad Blau, David T. Bonthron, Tracy A. Briggs, Louise Brueton, Han G. Brunner, Christopher J. Burke, Ian Carr, Daniel R. Carvalho, Kate Chandler, H.‐J. Christen, Peter Corry, Frances M. Cowan, Helen Cox, Stefano D’Arrigo, John Dean, Corinne De Laet, Claudine De Praeter, Catherine Déry, Colin D. Ferrie, Kim Flintoff, Suzanna G.M. Frints, Àngels García‐Cazorla, Blanca Gener, Cyril Goizet, Françoise Goutières, Andrew Green, Agnès Guët, Ben C.J. Hamel, Bruce E. Hayward, Arvid Heiberg, Raoul C. M. Hennekam, Marie Husson, Andrew P. Jackson, Rasieka Jayatunga, Yong‐hui Jiang, Sarina G. Kant, Amy Kao, Mary D. King, Helen Kingston, Joerg Klepper, Marjo S. van der Knaap, Andrew J. Kornberg, Dieter Kotzot, W Kratzer, Didier Lacombe, Lieven Lagae, P. Landrieu, Giovanni Lanzi, Andrea Leitch, Ming Lim, John H. Livingston, Charles Marques Lourenço, E G Hermione Lyall, Sally Ann Lynch, Michael J. Lyons, Daphna Marom, John P. McClure, Robert McWilliam, Serge B. Melançon, Leena Mewasingh, Marie‐Laure Moutard, Ken K. Nischal, John R. Østergaard, Julie Prendiville, Magnhild Rasmussen, R. Curtis Rogers, Dominique Roland, Elisabeth Rosser, Kevin Rostásy, Agathe Roubertie, Amparo Sanchís, Raphael Schiffmann, Sabine Scholl‐Bürgi, Sunita Seal, Stavit A. Shalev, Concepción Sierra Córcoles, Gyan P. Sinha, Doriette Soler, Ronen Spiegel, John B.P. Stephenson, Uta Tacke, Tiong Yang Tan, Marianne Till, John Tolmie

    Publicat 2007
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