Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: ABR[original query] |
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Auditory function associated with Col11a1 haploinsufficiency in chondrodysplasia (cho) mice. Hearing research 2003 1 175 (1-2): 178-82. Szymko-Bennett Yvonne M, Kurima Kiyoto, Olsen Bjorn, Seegmiller Robert, Griffith Andrew |
[Mutations of GJB2 gene in infants with non-syndromic hearing impairment]. Zhonghua yi xue za zhi 2005 Mar 85 (10): 689-92. Shi Gui-Zhi, Gong Lu-Xia, Nie Wen-Ying, Lin Qian, Xiang Li-Li, Xu Xiao-Hu, Qi Yi-She |
Incidence of the 35delG/GJB2 mutation in low-risk newborns. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2008 Jul 21 (7): 463-8. Zaputovic Sanja, Stanojevic Milan, Medica Igor, Peterlin Borut, Petrovic Ol |
Prevalence of A1555G mitochondrial mutation in Chinese newborns and the correlation with neonatal hearing screening. International journal of pediatric otorhinolaryngology 2011 Apr 75 (4): 532-4. Chen Guanming, Wang Xiyin, Fu Siqi |
OTOF mutation screening in Japanese severe to profound recessive hearing loss patients. BMC medical genetics 2013 Sep 14 (1): 1. Iwasa YI, Nishio SY, Yoshimura H, Kanda Y, Kumakawa K, Abe S, Naito Y, Nagai K, Usami SI |
[Clinical and electrophysiological and molecular genetic characteristics of the course of relapsing-remitting multiple sclerosis]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinsko? promyshlennosti Rossi?sko? Federatsii, Vserossi?skoe obshchestvo nevrologov [i] Vserossi?skoe obshchestvo psikhiatrov 2013 113 (10): 55-9. Delov R A, Rozhdestvenski? A S, Marks E A, Smialovski? V E, Khanokh E V, Kakulia A V, Sokolova E A, Agapova O |
[Audiologic features of mitochondrial DNA A3243G mutation and its correlation with mutation rate]. Zhonghua yi xue za zhi 2012 Oct 92 (40): 40. Xue JF, Chen L, Ma YN, Zhao DH, Duan JB, Wang ZX, Qi Y, Liu YH |
[The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances]. Vestnik otorinolaringologii 2014 (2): 37-43. Lalaiants M R, Markova T G, Bakhshinian V V, Bliznets E A, Poliakov A V, Tavartikiladze G |
Prevalence and audiological profiles of GJB2 mutations in a large collective of hearing impaired patients. Hearing research 2016 Jan . Burke W F, Warnecke A, Schöner-Heinisch A, Lesinski-Schiedat A, Maier H, Lenarz |
Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinics. Journal of translational medicine 2018 11 16 (1): 330. Kim Bong Jik, Jang Jeong Hun, Han Jin Hee, Park Hye-Rim, Oh Doo Yi, Lee Seungmin, Kim Min Young, Kim Ah Reum, Lee Chung, Kim Nayoung K D, Park Woong-Yang, Choung Yun-Hoon, Choi Byung Yo |
Genetic screening as an adjunct to universal newborn hearing screening: literature review and implications for non-congenital pre-lingual hearing loss. International journal of audiology 2019 7 58 (12): 834-850. D'Aguillo Christine, Bressler Sara, Yan Denise, Mittal Rahul, Fifer Robert, Blanton Susan H, Liu Xuezho |
[OTOF-related auditory neuropathy spectrum disorder]. Vestnik otorinolaringologii 2020 6 85 (2): 21-25. Lalayants M R, Mironovich O L, Bliznets E A, Markova T G, Polyakov A V, Tavartkiladze G |
Mitochondrial calcium uniporter is essential for hearing and hair cell preservation in congenic FVB/NJ mice. Scientific reports 2021 5 11 (1): 9660. Manikandan Mayakannan, Walker Steven, Deshmukh Aditi R, Perea Elizabeth, Wang Danqi, Alagramam Kumar N, Stepanyan Rub |
Genetic Screening for 35delG Mutation in Egyptian Patients with Profound Sensorineural Hearing Loss Scheduled for Cochlear Implantation: A Population-Based Study. ORL; journal for oto-rhino-laryngology and its related specialties 2021 3 83 (3): 181-186. Mostafa Badr Eldin, El Sawi Mohammed Abdel, Sabry Sabry Magdi, Hassan Dalia Mohammed, Rezk Shafik Micha |
AudioChip: A Deep Phenotyping Approach for Deconstructing and Quantifying Audiological Phenotypes of Self-Reported Speech Perception Difficulties. Ear and hearing 2021 12 43 (3): 1023-1036. Bhatt Ishan Sunilkumar, Dias Raquel, Wineinger Nathan, Pratt Sheila, Wang Jin, Washnik Nilesh, Guthrie O'neil, Wilder Jason, Torkamani A |
Auditory processing disorder in children: the value of a multidisciplinary assessment. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2021 Jan . Rouillon Isabelle, de Lamaze Aude, Ribot Marlène, Collet Gregory, de Bollardière Théodora, Elmir Razane, Parodi Marine, Achard Sophie, Denoyelle Françoise, Loundon Natal |
A retrospective cohort study exploring the association between different mitochondrial diseases and hearing loss. Molecular genetics and metabolism 2022 2 135 (4): 333-341. van Kempen Carlijn M A, Beynon Andy J, Smits Jeroen J, Janssen Mirian C |
Genetic etiological analysis of auditory neuropathy spectrum disorder by next-generation sequencing. Frontiers in neurology 2022 12 13 1026695. Sun Lianhua, Lin Zhengyu, Zhang Jifang, Shen Jiali, Wang Xiaowen, Yang J |
A Prospective Study of Audiological Manifestations in Patients of Allergic Rhinitis. Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India 2022 12 74 (Suppl 2): 1256-1261. Mahajan Akriti, Manhas Monica, Kalsotra Parmod, Kalsotra Gopika, Gul Nave |
Tone-Burst Auditory Brainstem Response and Cortical Potentials in Diagnosis of Syndromic Auditory Neuropathy Spectrum Disorder. Journal of audiology & otology 2022 11 . Kaf Wafaa A, Reiter Samantha, Brodeur Amanda, White-Minnis Letitia, Deal Willi |
Impact of timing of prophylaxis commencement, F8 genotype and age on factor consumption and health-related quality of life in patients with severe haemophilia A. Haemophilia : the official journal of the World Federation of Hemophilia 2023 5 . Alexandros Arvanitakis, Pål Andre Holme, Erik Berntorp, Jan Asterma |
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- Page last updated:Apr 22, 2024
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