Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mica Y. Bergman"'
Autor:
Jean Carruthers, Alice V. Pereira, John J. Martin, Jessica R. Chang, Allen M. Putterman, Jill A. Foster, Michael T. Yen, Liat Attas-Fox, Robert G. Fante, Ana Filipa Duarte, Kimberly K. Gokoffski, Martin H Devoto, Krishnapriya Kalyam, Morris E. Hartstein, Steven C. Dresner, John D. Ng, Hirohiko Kakizaki, Wendy W. Lee, Christine Greer, Jonathan W. Kim, David B. Samimi, Magdalene Yin Lin Ting, Francesco P. Bernardini, Eric B. Hamill, Vivek Ravindra Patel, Nathan W. Blessing, Margaret L. Pfeiffer, François Codère, Peter J. Dolman, John B. Holds, Mica Y. Bergman, Mark J. Lucarelli, Juan A. Delgado, Alessandro Gennai, Diana K. Lee, Wesley Brundridge, Nicholas R. Mahoney, Sandy Zhang-Nunes, Hans B. Heymann, Michael A. Burnstine, Jeremy Tan, Helen A. Merritt, Farzad Pakdel, Raman Malhotra, Maria Suzanne Sabundayo, Juliana Gildener-Leapman, Jennifer Murdock, Katja Ullrich, Christopher M. DeBacker, David E. E. Holck
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::836ee097463db4200c17354887bf6729
https://doi.org/10.1055/b-006-149698
https://doi.org/10.1055/b-006-149698
Autor:
Michael A. Burnstine, Mica Y. Bergman
Publikováno v:
Surgery in Thyroid Eye Disease ISBN: 9789813292192
When thyroid-associated ophthalmopathy results in vision-threatening compressive optic neuropathy, orbital ache, or significant aesthetic deformity, orbital decompression may be indicated. Several operative techniques exist, and the choice of which t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49c5c53cc071444bfcbfd542c25b850a
https://doi.org/10.1007/978-981-32-9220-8_13
https://doi.org/10.1007/978-981-32-9220-8_13
Autor:
Adam Weber, Mica Y Bergman, Juan C. Jiménez-Pérez, J. Javier Servat, Shu Hong Chang, Michael E. Migliori, Catherine Y. Liu, Victoria Starks, Catherine J. Choi, Bradford W. Lee, N. Grace Lee, Osiris Olvera-Morales, Livia Teo, Chau Pham, Liza M. Cohen, Nicholas R. Mahoney, Michael K. Yoon, Peter W. MacIntosh, Joseph Giacometti, Arpine Barsegian, Christina H. Choe, Senmiao Zhan, Omar Dajani, Anne Barmettler, Sonul Mehta, Ashley A. Campbell, Vinay K. Aakalu, Lucas Bonafede, Jeremiah P. Tao, Ann Q. Tran, Suzanne K. Freitag, Sanjai Jalaj, Julius T. Oatts, Roxana Fu, Shu Lang Liao, Lora R. Dagi Glass, Ian F. Dunn, Blair K. Armstrong, Mithra O. Gonzalez, Pete Setabutr, Honglei Liu, Michael T. Yen, Natalie Homer, José Luis Tovilla-Canales, Roman Shinder, Brittany A. Simmons, Alexandra T. Elliott, Seanna Grob, Kian Eftekhari, Edward J. Wladis, Prashant Yadav, Bryan J. Winn, Do Eon Rok, Gary J. Lelli, Sandy Zhang-Nunes, Wenya Linda Bi, Benjamin S. Bleier, Jason S. Mantagos, Larissa H. Habib, Natalie Wolkow, Hunter Yuen, Neil Shah, Kristen E. Dunbar, Michael Tseng, Emily Charlson, Christopher B. Chambers, Alison B. Callahan, Sarina K. Mueller, Nora K. Siegal, Daniel R. Lefebvre, Kyle J. Godfrey, Tieu Vy Nguyen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e301d148267b38565f9f9bd42bc5de27
https://doi.org/10.1055/b-006-163725
https://doi.org/10.1055/b-006-163725
Autor:
Mica Y. Bergman, Michael A. Burnstine, Steven C. Dresner, Margaret L. Pfeiffer, Helen A. Merritt, David B. Samimi
Publikováno v:
Ophthalmology. 125(12)
Autor:
Mica Y. Bergman, Sudha Nallasamy
Publikováno v:
Journal of Pediatric Genetics. :243-258
Genetic diseases of the macula and choroid have various inheritance patterns and varying degrees of impact on vision. Herein, we review the literature including most recent advances in the understanding of the genetics of these diseases. Although man
Autor:
Edwin J. Weeber, Shenfeng Qiu, Melinda M. Peters, Adeola R. Pratt-Davis, Kimberly M. Korwek, Mica Y. Bergman
Publikováno v:
Neurobiology of Learning and Memory. 85:228-242
The heterozygote reeler mouse (HRM) shows many neuroanatomical and biochemical features that are also present in some human cognitive disorders, such as schizophrenia. In the present study, hippocampal dependent plasticity and cognitive function of t
Autor:
Genevieve Konopka, Mica Y. Bergman, Pat Levitt, Eric M. Wexler, Gregory E. Osborn, Zohar Mukamel, Hongmei Dong, Daniel H. Geschwind
Autism spectrum disorder (ASD) is a highly heritable, behaviorally defined, heterogeneous disorder of unknown pathogenesis. Several genetic risk genes have been identified, including the gene encoding the receptor tyrosine kinase MET, which regulates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d7e43f0f41e467dd5bb422116950116
https://europepmc.org/articles/PMC3667610/
https://europepmc.org/articles/PMC3667610/
Candidate risk genes for autism spectrum disorder (ASD) have been identified, but the challenge of determining their contribution to pathogenesis remains. We previously identified two ASD risk genes encoding the receptor tyrosine kinase MET and the u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f9ef36d3f5ee717e88aa0d9ac1138ac
https://europepmc.org/articles/PMC3644181/
https://europepmc.org/articles/PMC3644181/
Publikováno v:
The Journal of comparative neurology. 513(5)
The establishment of appropriate neural circuitry depends on the coordination of multiple developmental events across space and time. These events include proliferation, migration, differentiation, and survival-all of which can be mediated by hepatoc
Publikováno v:
International Journal of Developmental Neuroscience. 26:836-836