Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Teresa Luisa G. Cruz"'
Publikováno v:
World Journal of Otorhinolaryngology-Head and Neck Surgery, Vol 8, Iss 4, Pp 287-296 (2022)
Abstract Background Otologic and vestibular symptoms have been seen in patients confirmed to have COVID‐19 disease. Further discussion of these symptoms may provide insight into short‐ and long‐term management for these patients. Objective The
Externí odkaz:
https://doaj.org/article/7e47d9ce60ed4a1fbc1dd92e3f362900
Publikováno v:
Philippine Journal of Otolaryngology Head and Neck Surgery, Vol 32, Iss 2 (2018)
Objective: To determine the prevalence rate of follow-up among infants who had a “refer” result on initial newborn hearing screening and to identify reasons for default by parents or guardians. Method: Study Design: Cross-sectional study
Externí odkaz:
https://doaj.org/article/c931609aaeae4a3d877139e0d747c267
Publikováno v:
International Journal of Health Promotion and Education. :1-11
Autor:
Regie Lyn P. Santos-Cortez, Kimberly Mae C. Ong, Angeli Carlos-Hiceta, Ma. Leah C. Tantoco, Talitha Karisse L. Yarza, Ma. Luz San Agustin, Melquiadesa Pedro, Teresa Luisa G. Cruz, Eva Maria Cutiongco-de la Paz, Generoso T. Abes, Erasmo Gonzalo d.V. Llanes, Abner L. Chan, Charlotte M. Chiong, Maria Rina T. Reyes-Quintos
Publikováno v:
Genetic Testing and Molecular Biomarkers. 27:12-17
Autor:
Charles E. Robertson, Alessandra Nadine E. Chiong, Michèle M. Sale, Nanette R. Lee, Kimberly Mae C. Ong, Sairah Yousaf, Jose Pedrito M. Magno, Diana Ir, Patrick John Labra, Petri S. Mattila, Maria Luz San Agustin, Generoso T. Abes, Erasmo Gonzalo D V Llanes, Ma. Carmina Espiritu-Chiong, Maria Rina T. Reyes-Quintos, Tori C. Bootpetch, Wasyl Szeremeta, Allen F. Ryan, Teresa Luisa G. Cruz, Arnaud P. J. Giese, Suzanne M. Leal, Rachelle Marie A. Nonato, Zubair M. Ahmed, Abner L. Chan, Karen L. Mohlke, Rhodieleen Anne R. de la Cruz, Regie Lyn P. Santos-Cortez, Matthew J. Steritz, Tasnee Chonmaitree, Daniel N. Frank, Eva Maria Cutiongco-de la Paz, Melquiadesa Pedro, Elisabet Einarsdottir, Talitha Karisse L. Yarza, Juha Kere, Deborah A. Nickerson, Lena Hafrén, Niaz Ahankoob, Michael J. Bamshad, Kathleen Daly, Ma. Leah C. Tantoco, Charlotte M. Chiong, Harold S. Pine, Saima Riazuddin
Publikováno v:
Journal of Medical Genetics. 58:442-452
BackgroundOtitis media (OM) susceptibility has significant heritability; however, the role of rare variants in OM is mostly unknown. Our goal is to identify novel rare variants that confer OM susceptibility.MethodsWe performed exome and Sanger sequen
Publikováno v:
World journal of otorhinolaryngology - head and neck surgery.
Otologic and vestibular symptoms have been seen in patients confirmed to have COVID-19 disease. Further discussion of these symptoms may provide insight into short- and long-term management for these patients.The aim of this review was to describe th
Autor:
Nanette R. Lee, Maria Rina T. Reyes-Quintos, Teresa Luisa G. Cruz, Karen L. Mohlke, Tori C. Bootpetch, Talitha Karisse L. Yarza, Regie Lyn P. Santos-Cortez, Charlotte M. Chiong, Abner L. Chan, Celina Ann M. Tobias-Grasso, Eva Maria Cutiongco-de la Paz, Mary Ellen Chiong Perez, Ma. Leah C. Tantoco
Publikováno v:
Genes, Vol 12, Iss 566, p 566 (2021)
Genes
Volume 12
Issue 4
Genes
Volume 12
Issue 4
Background: Hearing loss remains an important global health problem that is potentially addressed through early identification of a genetic etiology, which helps to predict outcomes of hearing rehabilitation such as cochlear implantation and also to
Autor:
Talitha Karisse L. Yarza, Teresa Luisa G. Cruz, Carlos Diego A. Rozul, Jaymilyn V. Catangay-Ombao
Publikováno v:
Acta Medica Philippina.
Objective. The current paper aimed to discuss developing the online newborn hearing screening certification course and revisions made from pre-pandemic face-to-face strategies to the online implementation in response to COVID-19 limitations. Furtherm
Autor:
Daniel N, Frank, Arnaud P J, Giese, Lena, Hafren, Tori C, Bootpetch, Talitha Karisse L, Yarza, Matthew J, Steritz, Melquiadesa, Pedro, Patrick John, Labra, Kathleen A, Daly, Ma Leah C, Tantoco, Wasyl, Szeremeta, Maria Rina T, Reyes-Quintos, Niaz, Ahankoob, Erasmo Gonzalo D V, Llanes, Harold S, Pine, Sairah, Yousaf, Diana, Ir, Elisabet, Einarsdottir, Rhodieleen Anne R, de la Cruz, Nanette R, Lee, Rachelle Marie A, Nonato, Charles E, Robertson, Kimberly Mae C, Ong, Jose Pedrito M, Magno, Alessandra Nadine E, Chiong, Ma Carmina, Espiritu-Chiong, Maria Luz, San Agustin, Teresa Luisa G, Cruz, Generoso T, Abes, Michael J, Bamshad, Eva Maria, Cutiongco-de la Paz, Juha, Kere, Deborah A, Nickerson, Karen L, Mohlke, Saima, Riazuddin, Abner, Chan, Petri S, Mattila, Suzanne M, Leal, Allen F, Ryan, Zubair M, Ahmed, Tasnee, Chonmaitree, Michele M, Sale, Charlotte M, Chiong, Regie Lyn P, Santos-Cortez
Publikováno v:
J Med Genet
BACKGROUND: Otitis media (OM) susceptibility has significant heritability, however the role of rare variants in OM is mostly unknown. Our goal is to identify novel rare variants that confer OM susceptibility. METHODS: We performed exome and Sanger se
Autor:
Rachel Ann P Santos, Melquiadesa Pedro, Talitha Karisse L. Yarza, Charlotte M. Chiong, Janak A. Patel, Christopher Greenlee, Zubair M. Ahmed, Rose Anne Q Rosanes, Rehan S. Shaikh, Melissa A. Scholes, Matthew J. Steritz, Norman R. Friedman, Todd Wine, Abner L. Chan, Ma. Leah C. Tantoco, Patricia J. Yoon, Tori Bootpetch Roberts, Erasmo Gonzalo D V Llanes, Jeremy D. Prager, Anushree Acharya, Eric D. Larson, Karen L. Mohlke, Saima Riazuddin, Maria Rina T. Reyes-Quintos, Jose Pedrito M. Magno, Generoso T. Abes, Tasnee Chonmaitree, Petri S. Mattila, Teresa Luisa G. Cruz, Lena Hafrén, Elisabet Einarsdottir, Ayesha Yousaf, Catherine B. Anderson, Juha Kere, Jonathan Cardwell, Amanda G. Ruiz, Michael J. Bamshad, Herman A. Jenkins, Ivana V. Yang, Deborah A. Nickerson, Samuel P. Gubbels, Sven-Olrik Streubel, Suzanne M. Leal, Katerina Kechris, David A. Schwartz, Sheryl Mae Lagrana-Villagracia, Regie Lyn P. Santos-Cortez, Aileen Trinidad R Santos, Nanette R. Lee, Kenny H. Chan, Dylan Ray, Eva Maria Cutiongco-de la Paz, Stephen P. Cass
Publikováno v:
Hum Mutat
A genetic basis for otitis media is established, however, the role of rare variants in disease etiology is largely unknown. Previously a duplication variant within A2ML1 was identified as a significant risk factor for otitis media in an indigenous Fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffa230c38770ef2c2a612a2e6653a5b4
http://hdl.handle.net/10138/312957
http://hdl.handle.net/10138/312957