Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Lena Hafrén"'
Publikováno v:
Laryngoscope Investigative Otolaryngology, Vol 9, Iss 5, Pp n/a-n/a (2024)
Abstract Objectives To study the predisposing factors, treatment, and complications of Aspergillus otitis externa. Methods A retrospective analysis of patients diagnosed with Aspergillus otitis externa at the Department of Otorhinolaryngology, Helsin
Externí odkaz:
https://doaj.org/article/6037cfc839af4fc9a09d8212a5713dae
Autor:
Erik Appelberg, Sanna Viitasalo, Lena Hafrén, Juha Laakso, Samuli Suutarla, Erkki Hopsu, Saku T. Sinkkonen
Publikováno v:
Laryngoscope Investigative Otolaryngology, Vol 9, Iss 4, Pp n/a-n/a (2024)
Abstract Introduction Otoscopes and otomicroscopes are the most commonly used instruments for visualizing the ear. Digital otoscopy (DO) could be used to improve diagnostics in primary health care by utilizing image enlargement. The aim of the study
Externí odkaz:
https://doaj.org/article/0e3f769940f044aebb88cacc601ca906
Publikováno v:
Clinical Case Reports, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract Bilateral Sensorineural Hearing Loss is a rare disease that is often associated with other complex medical conditions. Primary central nervous system lymphoma is an uncommon and aggressive variant of non‐Hodgkin lymphoma that can mimic man
Externí odkaz:
https://doaj.org/article/bcb5ea871d204b7a88b8a238b842e74b
Publikováno v:
Frontiers in Allergy, Vol 2 (2021)
Non-steroidal anti-inflammatory drug (NSAID)—exacerbated respiratory disease (NERD) is an adult-onset inflammatory condition of the upper and lower airways. It is characterized by the co-existence of asthma, nasal polyposis, and hypersensitivity to
Externí odkaz:
https://doaj.org/article/d6741337dcbf4014b09678b2bab8a83c
Autor:
Mahmood F. Bhutta, Jane Lambie, Lindsey Hobson, Anuj Goel, Lena Hafrén, Elisabet Einarsdottir, Petri S. Mattila, Martin Farrall, Steve Brown, Martin J. Burton
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Abstract Chronic otitis media with effusion (COME) is the most common cause of hearing loss in children, and known to have high heritability. Mutant mouse models have identified Fbxo11, Evi1, Tgif1, and Nisch as potential risk loci. We recruited chil
Externí odkaz:
https://doaj.org/article/4e3ad4f89c544c7ca34f1dfdf0d95724
Autor:
Lena Hafrén, Elisabet Einarsdottir, Erna Kentala, Sari Hammarén-Malmi, Mahmood F Bhutta, Carol J MacArthur, Beth Wilmot, Margaretha Casselbrant, Yvette P Conley, Daniel E Weeks, Ellen M Mandel, Outi Vaarala, Anna Kallio, Merit Melin, Janne K Nieminen, Eira Leinonen, Juha Kere, Petri S Mattila
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0132551 (2015)
Predisposition to childhood otitis media (OM) has a strong genetic component, with polymorphisms in innate immunity genes suspected to contribute to risk. Studies on several genes have been conducted, but most associations have failed to replicate in
Externí odkaz:
https://doaj.org/article/25a3ab538da14180bfb286e67f411501
Publikováno v:
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.
Nonsteroidal anti-inflammatory drug (NSAID)-exacerbated respiratory disease (N-ERD) has been considered an acquired condition. Positive first-degree family history has been reported in 1% of cases. The geographic and genetic isolation of the Finnish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb13f713d782772ecc337cd0fb17d275
https://pubmed.ncbi.nlm.nih.gov/35639475
https://pubmed.ncbi.nlm.nih.gov/35639475
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c1f3273286a54b911b866b3c1c6e874
https://doi.org/10.1136/jmedgenet-2020-106844
https://doi.org/10.1136/jmedgenet-2020-106844
Background The aetiology of idiopathic facial nerve palsy (Bell's palsy, BP) and sudden sensorineural hearing loss (SSNHL) are not known. It has been proposed that common respiratory tract viruses play a part in the pathophysiology of these diseases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8fd4e7285d368fedd64a663b7c214d1
http://hdl.handle.net/10138/354019
http://hdl.handle.net/10138/354019
Autor:
Tori C. Bootpetch, Todd Wine, Melissa A. Scholes, Patricia J. Yoon, Michael J. Bamshad, Sven-Olrik Streubel, Daniel N. Frank, Stephen P. Cass, Harold S. Pine, Tasnee Chonmaitree, Michèle M. Sale, Herman A. Jenkins, Ayesha Yousaf, Elisabet Einarsdottir, Erin E. Baschal, Ani Manichaikul, Juha Kere, Kenny H. Chan, Petri S. Mattila, Christina L Elling, Jeremy D. Prager, Regie Lyn P. Santos-Cortez, Lena Hafrén, Norman R. Friedman, Wasyl Szeremeta, Eric D. Larson, Saima Riazuddin, Allen F. Ryan, Rehan S. Shaikh, Rafaqat Ishaq, Suzanne M. Leal, Deborah A. Nickerson, Kathleen Daly, Samuel P. Gubbels, Zubair M. Ahmed
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Otitis media (OM), a very common disease in young children, can result in hearing loss. In order to potentially replicate previously reported associations between OM and PLG, exome and Sanger sequencing, RNA-sequencing of saliva and middle ear sample
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29baf8c7c7adbb1c2ce8a28870aa6d39
http://hdl.handle.net/10138/320494
http://hdl.handle.net/10138/320494