FUNDUS AUTOFLUORESCENCE IMAGING IN A PATIENT WITH RAPIDLY DEVELOPING SCOTOMA

Por Gelman, Rony, Chen, Royce, Blonska, Anna, Barile, Gaetano, Sparrow, Janet R.
Publicado em 2012

Fundus Autofluorescence Findings in a Mouse Model of Retinal Detachment

Por Secondi, Roberta, Kong, Jian, Blonska, Anna M., Staurenghi, Giovanni, Sparrow, Janet R.
Publicado em 2012

The Bisretinoids of Retinal Pigment Epithelium

Por Sparrow, Janet R., Gregory-Roberts, Emily, Yamamoto, Kazunori, Blonska, Anna, Ghosh, Shanti Kaligotla, Ueda, Keiko, Zhou, Jilin
Publicado em 2011

Reticular Macular Disease is Associated with Multilobular Geographic Atrophy in Age-Related Macular Degeneration

Por Xu, Luna, Blonska, Anna M., Pumariega, Nicole M., Bearelly, Srilaxmi, Sohrab, Mahsa A., Hageman, Gregory S., Smith, R. Theodore
Publicado em 2013

Quantitative Fundus Autofluorescence in Mice: Correlation With HPLC Quantitation of RPE Lipofuscin and Measurement of Retina Outer Nuclear Layer Thickness

Por Sparrow, Janet R., Blonska, Anna, Flynn, Erin, Duncker, Tobias, Greenberg, Jonathan P., Secondi, Roberta, Ueda, Keiko, Delori, François C.
Publicado em 2013

Drusen Analysis in a Human-Machine Synergistic Framework

Por Smith, R. Theodore, Sohrab, Mahsa A., Pumariega, Nicole M., Mathur, Kanika, Haans, Raymond, Blonska, Anna, Uy, Karl, Despriet, Dominiek, Klaver, Caroline
Publicado em 2011

Complement Factor H 402H Variant and Reticular Macular Disease

Por Smith, R. Theodore, Merriam, Joanna E., Sohrab, Mahsa A., Pumariega, Nicole M., Barile, Gaetano, Blonska, Anna M., Haans, Raymond, Madigan, David, Allikmets, Rando
Publicado em 2011

Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio- facial/DiGeorge/22q11.2 deletion syndrome patients

Por Guo, Tingwei, McGinn, Donna McDonald, Blonska, Anna, Shanske, Alan, Bassett, Anne, Chow, Eva, Bowser, Mark, Sheridan, Molly, Beemer, Frits, Devriendt, Koen, Swillen, Ann, Breckpot, Jeroen, Digilio, M. Cristina, Marino, Bruno, Dallapiccola, Bruno, Carpenter, Courtney, Zheng, Xin, Johnson, Jacob, Chung, Jonathan, Higgins, Anne Marie, Philip, Nicole, Simon, Tony J., Coleman, Karlene, Heine-Suner, Damian, Rosell, Jordi, Kates, Wendy, Devoto, Marcella, Goldmuntz, Elizabeth, Zackai, Elaine, Wang, Tao, Shprintzen, Robert, Emanuel, Beverly, Morrow, Bernice
Publicado em 2011

Overt Cleft Palate Phenotype and TBX1 Genotype Correlations in Velo-cardio-facial/DiGeorge/22q11.2 Deletion Syndrome Patients

Por Herman, Sean B., Guo, Tingwei, McGinn, Donna M. McDonald, Blonska, Anna, Shanske, Alan L., Bassett, Anne S., Chow, Eva WC, Bowser, Mark, Sheridan, Molly, Beemer, Frits, Devriendt, Koen, Swillen, Ann, Breckpot, Jeroen, Digilio, M. Cristina, Marino, Bruno, Dallapiccola, Bruno, Carpenter, Courtney, Zheng, Xin, Johnson, Jacob, Chung, Jonathan, Higgins, Anne Marie, Philip, Nicole, Simon, Tony, Coleman, Karlene, Heine-Suner, Damian, Rosell, Jordi, Kates, Wendy, Devoto, Marcella, Zackai, Elaine, Wang, Tao, Shprintzen, Robert, Emanuel, Beverly S., Morrow, Bernice E.
Publicado em 2012

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

Por Guo, Tingwei, Repetto, Gabriela M., McDonald McGinn, Donna M., Chung, Jonathan H., Nomaru, Hiroko, Campbell, Christopher L., Blonska, Anna, Bassett, Anne S., Chow, Eva W.C., Mlynarski, Elisabeth E., Swillen, Ann, Vermeesch, Joris, Devriendt, Koen, Gothelf, Doron, Carmel, Miri, Michaelovsky, Elena, Schneider, Maude, Eliez, Stephan, Antonarakis, Stylianos E., Coleman, Karlene, Tomita-Mitchell, Aoy, Mitchell, Michael E., Digilio, M. Cristina, Dallapiccola, Bruno, Marino, Bruno, Philip, Nicole, Busa, Tiffany, Kushan-Wells, Leila, Bearden, Carrie E., Piotrowicz, Małgorzata, Hawuła, Wanda, Roberts, Amy E., Tassone, Flora, Simon, Tony J., van Duin, Esther D.A., van Amelsvoort, Thérèse A., Kates, Wendy R., Zackai, Elaine, Johnston, H. Richard, Cutler, David J., Agopian, A.J., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Emanuel, Beverly S., Morrow, Bernice E.
Publicado no Circ Cardiovasc Genet (2017)