Macular ischaemia as a marker for nephropathy in diabetic retinopathy.

Autor: Shukla Dhananjay, Kolluru Chandra, Singh Jatinder, John Rajesh, Soman Manoj, Gandhi Banushree, Kim R, Perumalsamy Namperumalsamy

Publikováno v: Indian Journal of Ophthalmology, Vol 52, Iss 3, Pp 205-10 (2004)

PURPOSE: To determine whether diabetic macular ischaemia is associated with ischaemic heart disease (IHD), hyperlipidaemia, hypertension (HTN) and nephropathy. METHODS: Prospective case-control study from January to December 2001, involving 102 type

Externí odkaz: https://doaj.org/article/ccf4d95eabb34e6c9095382d96d228d9

Angiogenic potential of vitreous from Proliferative Diabetic Retinopathy and Eales' Disease patients.

Autor: Ponnalagu Murugeswari, Dhananjay Shukla, Ramasamy Kim, Perumalsamy Namperumalsamy, Alan W Stitt, Veerappan Muthukkaruppan

Publikováno v: PLoS ONE, Vol 9, Iss 10, p e107551 (2014)

Proliferative Diabetic Retinopathy (PDR) and Eales' Disease (ED) have different aetiologies although they share certain common clinical symptoms including pre-retinal neovascularization. Since there is a need to understand if the shared end-stage ang

Externí odkaz: https://doaj.org/article/6fa9989d63504977b66a0fd5e471f613

Contributors

Autor: Michael Abràmoff, Gary W. Abrams, Anita Agarwal, Everett Ai, Lloyd M. Aiello, Lloyd Paul Aiello, Daniel M. Albert, Mathew W. Aschbrenner, Marcos Ávila, G. William Aylward, Matthew Bedell, Rubens Belfort, Jean Bennett, Chris Bergstrom, Cagri G. Besirli, Pramod S. Bhende, Susanne Binder, Alan C. Bird, Barbara A. Blodi, Mark S. Blumenkranz, H. Culver Boldt, Norbert Bornfeld, Ferdinando Bottoni, Michael E. Boulton, Sara J. Bowne, Milam A. Brantley, Neil M. Bressler, Susan B. Bressler, Andreas Bringmann, Daniel A. Brinton, Gary C. Brown, Justin C. Brown, Simon Brunner, Ronald A. Bush, Dingcai Cao, Antonio Capone, David Carruthers, Jerry D. Cavallerano, Usha Chakravarthy, Chi-Chao Chan, Waiman Chan, Steven Charles, David G. Charteris, Dong Feng Chen, Jeannie Chen, Youxin Chen, Carol Yim Lui Cheung, Emily Y. Chew, Allen Chiang, Michael F. Chiang, Ian J. Constable, Gabriel Coscas, Alan F. Cruess, Emmett T. Cunningham, Christine A. Curcio, Stephen P. Daiger, Bertil E. Damato, Janet L. Davis, Matthew D. Davis, Shelley Day, Patrick De Potter, Marc D. de Smet, Alastair K. Denniston, Ranjit S. Dhaliwal, Xiaoyan Ding, Diana V. Do, Guorui Dou, William A. Dunn, Justis P. Ehlers, Michael Engelbert, Lisa J. Faia, Benedetto Falsini, Amani A. Fawzi, Sharon Fekrat, Steven E. Feldon, Rodrigo A. Brant Fernandes, Henry A. Ferreyra, Deborah A. Ferrington, Frederick L. Ferris, Paul T. Finger, Steven K. Fisher, Gerald A. Fishman, Monika Fleckenstein, Harry W. Flynn, Andrew C. Fok, Wallace S. Foulds, William R. Freeman, Aurélien Freton, Martin Friedlander, Laura J. Frishman, Arthur D. Fu, Carlos Alexandre de Amorim Garcia Filho, Enrique Garcia-Valenzuela, Alain Gaudric, Mary Gayed, Mohamed A. Genead, Heinrich Gerding, Andrea Giani, Morton F. Goldberg, Dan S. Gombos, Lingam Gopal, Caroline Gordon, Hiroshi Goto, Evangelos S. Gragoudas, Maria B. Grant, W. Richard Green, Ronald G. Gregg, Zdenek Gregor, Giovanni Gregori, Kevin Gregory-Evans, Seanna Grob, Carl Groenewald, Hans E. Grossniklaus, Sandeep Grover, Vamsi K. Gullapalli, Aditi Gupta, Rudolf F. Guthoff, Paul Hahn, Julia A. Haller, J. William Harbour, Christos Haritoglou, Mary E. Hartnett, Barbara S. Hawkins, Shikun He, Martina C. Herwig, Florian M.A. Heussen, David R. Hinton, Frank G. Holz, Samuel K. Houston, Yan-Nian Hui, Mark S. Humayun, Yasushi Ikuno, David Isaac, Tatsuro Ishibashi, Douglas A. Jabs, Glenn J. Jaffe, Lee M. Jampol, Leonard Joffe, Mark Johnson, Mark W. Johnson, Robert N. Johnson, Antonia M. Joussen, Karina Julian, J. Michael Jumper, Peter K. Kaiser, Anselm Kampik, Robert Katamay, Christine N. Kay, Pearse A. Keane, M. Cristina Kenney, Khizer R. Khaderi, Mohamad A. Khodair, Ivana K. Kim, Tae Wan Kim, Bernd Kirchhof, Barbara E.K. Klein, Ronald Klein, Lazaros Konstantinidis, Igor Kozak, Baruch D. Kuppermann, Leanne T. Labriola, Timothy Y. Lai, Dennis S. Lam, Linda A. Lam, Maurice B. Landers, Anne Marie Lane, Erin B. Lavik, James F. Leary, Sun Young Lee, Thomas C. Lee, Loh-Shan B. Leung, David A. Lewis, Geoffrey P. Lewis, Anita Leys, Xiaoxin Li, Sandra Liakopoulos, Chang-Ping Lin, Phoebe Lin, David T. Liu, Nikolas J.S. London, Brandon J. Lujan, Yan Luo, Gerard A. Lutty, Robert MacLaren, Steven Madreperla, Albert M. Maguire, Martin A. Mainster, Nancy C. Mansfield, Arnold M. Markoe, Michael F. Marmor, Daniel F. Martin, Stephen C. Massey, Maureen A. McCall, Tara A. McCannel, J. Allen McCutchan, H. Richard McDonald, Milap P. Mehta, Petra Meier, Shannath Merbs, Travis A. Meredith, Carsten H. Meyer, William F. Mieler, Joan W. Miller, Rukhsana G. Mirza, Sayak K. Mitter, Robert A. Mittra, Yozo Miyake, Carlo Montemagno, Ala Moshiri, Prithvi Mruthyunjaya, Cristina Muccioli, Robert F. Mullins, Toshinori Murata, A. Linn Murphree, Robert P. Murphy, Philip I. Murray, Timothy G. Murray, Manish Nagpal, Perumalsamy Namperumalsamy, Sumit K. Nanda, Quan Dong Nguyen, Robert B. Nussenblatt, Kean T. Oh, Masahito Ohji, Kyoko Ohno-Matsui, Daniel Palanker, Purnima S. Patel, Anna C. Pavlick, David M. Peereboom, Mark E. Pennesi, Jay S. Pepose, Julian D. Perry, Carmen A. Puliafito, Polly A. Quiram, Rajiv Raman, Rajeev S. Ramchandran, Haripriya Vittal Rao, Narsing A. Rao, P. Kumar Rao, Sivakumar R. Rathinam, Franco M. Recchia, Kristin J. Redmond, Thomas A. Reh, Andreas Reichenbach, Robert Ritch, Philip J. Rosenfeld, Gary S. Rubin, Humberto Ruiz-Garcia, Stephen J. Ryan, SriniVas R. Sadda, Alfredo A. Sadun, Taiji Sakamoto, Alapakkam P. Sampath, Andrew P. Schachat, Steffen Schmitz-Valckenberg, Stephen G. Schwartz, Adrienne W. Scott, Jerry Sebag, Johanna M. Seddon, H. Nida Sen, Yasir Jamal Sepah, Sanjay Sharma, Tarun Sharma, Shwu-Jiuan Sheu, Carol L. Shields, Jerry A. Shields, Kei Shinoda, Dhananjay Shukla, Paul A. Sieving, Paolo A.S. Silva, Claudio Silveira, Arun D. Singh, Sylvia B. Smith, Wendy M. Smith, Lucia Sobrin, Akrit Sodhi, Elliott H. Sohn, Gisèle Soubrane, Leigh Spielberg, Sunil K. Srivastava, Oliver Stachs, Giovanni Staurenghi, Paul Sternberg, Edwin M. Stone, Ilene K. Sugino, Lori S. Sullivan, Paul Sullivan, Jennifer K. Sun, Janet S. Sunness, Ramin Tadayoni, Shibo Tang, Hiroko Terasaki, Matthew A. Thomas, John T. Thompson, Gabriele Thumann, Cynthia A. Toth, Michael T. Trese, Julie H. Tsai, Mary E. Turell, Patricia L. Turner, Nitin Udar, J. Niklas Ulrich, Russell N. Van Gelder, Jan C. van Meurs, Daniel Vítor Vasconcelos-Santos, Demetrios G. Vavvas, G. Atma Vemulakonda, Hao Wang, Yusheng Wang, James D. Weiland, Richard G. Weleber, Moody D. Wharam, Louisa Wickham, Peter Wiedemann, Henry E. Wiley, C.P. Wilkinson, David J. Wilson, Thomas J. Wolfensberger, David Wong, Ian Y. Wong, Tien Yin Wong, David M. Wu, Yanors Yandiev, Chang-Hao Yang, Chung-May Yang, Lawrence A. Yannuzzi, Miho Yasuda, Po-Ting Yeh, Zohar Yehoshua, Glenn Yiu, Young Hee Yoon, Hyeong Gon Yu, Alex Yuan, Marco A. Zarbin, Jun Jun Zhang, Kang Zhang, Mingwei Zhao, Peng Zhou

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e31f820a5a5039341726a180f8b6552c
https://doi.org/10.1016/b978-1-4557-0737-9.00159-4

Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy

Autor: Jeyabalan, Nallathambi, Dhananjay, Shukla, Anand, Rajendran, Perumalsamy, Namperumalsamy, Ramakrishnan, Muthulakshmi, Periasamy, Sundaresan

Publikováno v: Molecular vision. 12

To identify novel mutations in FZD4 gene that cause familial exudative vitreoretinopathy (FEVR) in Indian patients.The study was conducted on 75 subjects from 53 Indian families. These families were clinically diagnosed to have FEVR by fundus examina

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3a85260ceaad8b2df8ec669e0e563823
https://pubmed.ncbi.nlm.nih.gov/17093393

Genetic analysis of oculocutaneous albinism type 1 (OCA1) in Indian families: two novel frameshift mutations in the TYR Gene

Autor: Periasamy, Sundaresan, Asim Kumar, Sil, Alisdair R, Philp, Mary A, Randolph, Govindappa, Natchiar, Perumalsamy, Namperumalsamy

Publikováno v: Molecular vision. 10

Oculocutaneous albinism type 1 (OCA1) patients demonstrate a partial or total lack of melanin in the skin, hair and eye. OCA1 is an autosomal recessive genetic disorder caused by mutations in the TYR gene located at chromosome band 11q14-q25. The pur

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f30c075e25a460c716911256bbb1e185
https://pubmed.ncbi.nlm.nih.gov/15635296