Search Results - "Hafren, Lena"

Effects of social distancing on the incidence of Bell's palsy and sudden sensorineural hearing loss by Hafrén, Lena, Saarinen, Riitta, Lundberg, Marie

“…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…”
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Inheritance of NSAID‐Exacerbated Respiratory Disease by Suikkila, Anna, Lyly, Annina, Hafrén, Lena, Saarinen, Riitta, Klockars, Tuomas

“…Nonsteroidal anti‐inflammatory drug (NSAID)–exacerbated respiratory disease (N‐ERD) has been considered an acquired condition. Positive first‐degree family…”
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Inflammatory Cytokines in Middle Ear Effusion of Patients With Asthma, Chronic Rhinosinusitis With Nasal Polyps With or Without NSAID Intolerance by Suikkila, Anna, Lyly, Annina, Savinko, Terhi, Vento, Seija I, Saarinen, Riitta, Hafrén, Lena

“…To measure the inflammatory cytokines of middle ear effusion (MEE) in otitis media (OM) associated with asthma and chronic rhinosinusitis with nasal polyps…”
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Removal of parotid sialoliths; techniques, complications, and success rate—A cohort study by Hafrén, Lena, Mäkinen, Laura K., Haapaniemi, Aaro, Jokela, Johanna, Saarinen, Riitta

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Malignant lymphoma presenting as bilateral sensorineural hearing loss—A case report by Raunio, Frida, Kelppe, Jetta, Hafrén, Lena

“…Bilateral Sensorineural Hearing Loss is a rare disease that is often associated with other complex medical conditions. Primary central nervous system lymphoma…”
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Asthma is Underdiagnosed and Often Uncontrolled in Preoperative Patients With Chronic Rhinosinusitis With Nasal Polyps by Genberg, Emma, Kauppi, Paula, Sahlman, Johanna, Laulajainen-Hongisto, Anu, Lilja, Markus, Hammarén-Malmi, Sari, Hafrén, Lena, Mäkitie, Antti, Vento, Seija, Toppila-Salmi, Sanna, Virkkula, Paula

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Aspergillus Sinusitis: Risk Factors and Phenotyping by Hafrén, Lena, Saarinen, Riitta, Kurimo, Rane, Viljanen, Milla, Lundberg, Marie

“…: can cause fungal rhinosinusitis (FRS). We aimed to identify risk factors for sinonasal disease. Patients with a positive sinonasal mycological culture for…”
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Digital otoscopy in remote consultations by Appelberg, Erik, Viitasalo, Sanna, Hafrén, Lena, Laakso, Juha, Suutarla, Samuli, Hopsu, Erkki, Sinkkonen, Saku T.

“…Introduction Otoscopes and otomicroscopes are the most commonly used instruments for visualizing the ear. Digital otoscopy (DO) could be used to improve…”
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Patient-Reported Control of Asthma, Nasal Polyposis, and Middle-Ear Symptoms in NSAID-Exacerbated Respiratory Disease by Suikkila, Anna, Hafrén, Lena, Lyly, Annina, Klockars, Tuomas, Saarinen, Riitta

“…Non-steroidal anti-inflammatory drug (NSAID)-exacerbated respiratory disease (NERD) is an adult-onset inflammatory condition of the upper and lower airways. It…”
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A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11 by Bhutta, Mahmood F., Lambie, Jane, Hobson, Lindsey, Goel, Anuj, Hafrén, Lena, Einarsdottir, Elisabet, Mattila, Petri S., Farrall, Martin, Brown, Steve, Burton, Martin J.

“…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…”
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Otitis media susceptibility and shifts in the head and neck microbiome due to SPINK5 variants by Frank, Daniel N, Giese, Arnaud P J, Hafren, Lena, Bootpetch, Tori C, Yarza, Talitha Karisse L, Steritz, Matthew J, Pedro, Melquiadesa, Labra, Patrick John, Daly, Kathleen A, Tantoco, Ma Leah C, Szeremeta, Wasyl, Reyes-Quintos, Maria Rina T, Ahankoob, Niaz, Llanes, Erasmo Gonzalo D V, Pine, Harold S, Yousaf, Sairah, Ir, Diana, Einarsdottir, Elisabet, de la Cruz, Rhodieleen Anne R, Lee, Nanette R, Nonato, Rachelle Marie A, Robertson, Charles E, Ong, Kimberly Mae C, Magno, Jose Pedrito M, Chiong, Alessandra Nadine E, Espiritu-Chiong, Ma Carmina, San Agustin, Maria Luz, Cruz, Teresa Luisa G, Abes, Generoso T, Bamshad, Michael J, Cutiongco-de la Paz, Eva Maria, Kere, Juha, Nickerson, Deborah A, Mohlke, Karen L, Riazuddin, Saima, Chan, Abner, Mattila, Petri S, Leal, Suzanne M, Ryan, Allen F, Ahmed, Zubair M, Chonmaitree, Tasnee, Sale, Michele M, Chiong, Charlotte M, Santos-Cortez, Regie Lyn P

“…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…”
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Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus by Hafrén, Lena, Einarsdottir, Elisabet, Kentala, Erna, Hammarén-Malmi, Sari, Bhutta, Mahmood F, MacArthur, Carol J, Wilmot, Beth, Casselbrant, Margaretha, Conley, Yvette P, Weeks, Daniel E, Mandel, Ellen M, Vaarala, Outi, Kallio, Anna, Melin, Merit, Nieminen, Janne K, Leinonen, Eira, Kere, Juha, Mattila, Petri S

“…Predisposition to childhood otitis media (OM) has a strong genetic component, with polymorphisms in innate immunity genes suspected to contribute to risk…”
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The role of CDHR3 in susceptibility to otitis media by Hirsch, Scott D., Elling, Christina L., Bootpetch, Tori C., Scholes, Melissa A., Hafrén, Lena, Streubel, Sven-Olrik, Pine, Harold S., Wine, Todd M., Szeremeta, Wasyl, Prager, Jeremy D., Einarsdottir, Elisabet, Yousaf, Ayesha, Baschal, Erin E., Rehman, Sakina, Bamshad, Michael J., Nickerson, Deborah A., Riazuddin, Saima, Leal, Suzanne M., Ahmed, Zubair M., Yoon, Patricia J., Kere, Juha, Chan, Kenny H., Mattila, Petri S., Friedman, Norman R., Chonmaitree, Tasnee, Frank, Daniel N., Ryan, Allen F., Santos-Cortez, Regie Lyn P.

“…Otitis media (OM) is common in young children and can cause hearing loss and speech, language, and developmental delays. OM has high heritability; however,…”
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Panel 3: Genomics, precision medicine and targeted therapies by Santos-Cortez, Regie Lyn P., Bhutta, Mahmood F., Earl, Joshua P., Hafrén, Lena, Jennings, Michael, Mell, Joshua C., Pichichero, Michael E., Ryan, Allen F., Tateossian, Hilda, Ehrlich, Garth D.

“…To review the most recent advances in human and bacterial genomics as applied to pathogenesis and clinical management of otitis media. PubMed articles…”
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A2ML1 and otitis media: novel variants, differential expression, and relevant pathways by Larson, Eric D., Magno, Jose Pedrito M., Steritz, Matthew J., Llanes, Erasmo Gonzalo d.V., Cardwell, Jonathan, Pedro, Melquiadesa, Roberts, Tori Bootpetch, Einarsdottir, Elisabet, Rosanes, Rose Anne Q., Greenlee, Christopher, Santos, Rachel Ann P., Yousaf, Ayesha, Streubel, Sven‐Olrik, Santos, Aileen Trinidad R., Ruiz, Amanda G., Lagrana‐Villagracia, Sheryl Mae, Ray, Dylan, Yarza, Talitha Karisse L., Scholes, Melissa A., Anderson, Catherine B., Acharya, Anushree,  , University of Washington Center for Mendelian Genomics, Gubbels, Samuel P., Bamshad, Michael J., Cass, Stephen P., Lee, Nanette R., Shaikh, Rehan S., Nickerson, Deborah A., Mohlke, Karen L., Prager, Jeremy D., Cruz, Teresa Luisa G., Yoon, Patricia J., Abes, Generoso T., Schwartz, David A., Chan, Abner L., Wine, Todd M., Cutiongco‐de la Paz, Eva Maria, Friedman, Norman, Kechris, Katerina, Kere, Juha, Leal, Suzanne M., Yang, Ivana V., Patel, Janak A., Tantoco, Ma. Leah C., Riazuddin, Saima, Chan, Kenny H., Mattila, Petri S., Reyes‐Quintos, Maria Rina T., Ahmed, Zubair M., Jenkins, Herman A., Chonmaitree, Tasnee, Hafrén, Lena, Chiong, Charlotte M., Santos‐Cortez, Regie Lyn P.

“…A genetic basis for otitis media is established, however, the role of rare variants in disease etiology is largely unknown. Previously a duplication variant…”
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Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion by Einarsdottir, Elisabet, Hafrén, Lena, Leinonen, Eira, Bhutta, Mahmood F., Kentala, Erna, Kere, Juha, Mattila, Petri S.

“…To identify genetic risk factors of childhood otitis media (OM), a genome-wide association study was performed on Finnish subjects, 829 affected children, and…”
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Panel 3: Genetics and Precision Medicine of Otitis Media by Lin, Jizhen, Hafrén, Hena, Kerschner, Joseph, Li, Jian-Dong, Brown, Steve, Zheng, Qing Y., Preciado, Diego, Nakamura, Yoshihisa, Huang, Qiuhong, Zhang, Yan

“…Objective The objective is to perform a comprehensive review of the literature up to 2015 on the genetics and precision medicine relevant to otitis media. Data…”
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Multi-omic studies on missense PLG variants in families with otitis media by Bootpetch, Tori C., Hafrén, Lena, Elling, Christina L., Baschal, Erin E., Manichaikul, Ani W., Pine, Harold S., Szeremeta, Wasyl, Scholes, Melissa A., Cass, Stephen P., Larson, Eric D., Chan, Kenny H., Ishaq, Rafaqat, Prager, Jeremy D., Shaikh, Rehan S., Gubbels, Samuel P., Yousaf, Ayesha, Wine, Todd M., Bamshad, Michael J., Yoon, Patricia J., Jenkins, Herman A., Nickerson, Deborah A., Streubel, Sven-Olrik, Friedman, Norman R., Frank, Daniel N., Einarsdottir, Elisabet, Kere, Juha, Riazuddin, Saima, Daly, Kathleen A., Leal, Suzanne M., Ryan, Allen F., Mattila, Petri S., Ahmed, Zubair M., Sale, Michele M., Chonmaitree, Tasnee, Santos-Cortez, Regie Lyn P.

“…Otitis media (OM), a very common disease in young children, can result in hearing loss. In order to potentially replicate previously reported associations…”
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ABO Genotype and Blood Type Are Associated with Otitis Media by Wiesen, Brett M, Hafrén, Lena, Einarsdottir, Elisabet, Kere, Juha, Mattila, Petri S, Santos-Cortez, Regie Lyn P

“…To determine if there is an association between variants or blood types and otitis media. DNA samples from 214 probands from Finnish families with recurrent…”
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Genetic background and the risk of otitis media by Hafrén, Lena, Kentala, Erna, Järvinen, Tiina M, Leinonen, Eira, Onkamo, Päivi, Kere, Juha, Mattila, Petri S

“…Abstract Objective Otitis media is a multifactorial disease where genetic background may have an important role. For genome-wide association studies, it is…”
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