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Academic Journal

Estimating the impact of different types hearing loss on cognitive decline and the joint effect of hearing loss and depression on cognitive decline among older adults in China.

  • Authors : Qin A; Centre for Health Management and Policy Research, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China; National Health Commission (NHC) Key Laboratory of Health Economics and Policy Research (Shandong University), Jinan, Shandong 250012, China

Subjects: Cognitive Dysfunction*/Cognitive Dysfunction*/Cognitive Dysfunction*/diagnosis ; Hearing Loss*/Hearing Loss*/Hearing Loss*/epidemiology ; Hearing Loss*/Hearing Loss*/Hearing Loss*/complications

  • Source: Journal of affective disorders [J Affect Disord] 2024 Apr 15; Vol. 351, pp. 58-65. Date of Electronic Publication: 2024 Jan 28.Publisher: Elsevier/North-Holland Biomedical Press Country of Publication: Netherlands NLM ID: 7906073 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Effects of cooking with solid fuel on hearing loss in Chinese adults-Based on two cohort studies.

  • Authors : Mao XY; Zhejiang Chinese Medicine University, Hangzhou, China.; Zheng M

Subjects: Cooking* ; Hearing Loss*/Hearing Loss*/Hearing Loss*/epidemiology ; Hearing Loss*/Hearing Loss*/Hearing Loss*/etiology

  • Source: Scientific reports [Sci Rep] 2024 May 10; Vol. 14 (1), pp. 10763. Date of Electronic Publication: 2024 May 10.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Case report of a novel mutation in the TNC gene in Chinese patients with nonsyndromic hearing loss.

  • Authors : Li S; Department of Laboratory Medicine, Handan Central Hospital, Hebei Medical University, Handan, Hebei, China.; Li S

Subjects: Deafness*/Deafness*/Deafness*/genetics ; Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics ; Hearing Loss, Sensorineural*/Hearing Loss, Sensorineural*/Hearing Loss, Sensorineural*/genetics Nonsyndromic Deafness

  • Source: Medicine [Medicine (Baltimore)] 2024 Apr 19; Vol. 103 (16), pp. e37702.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Distribution of mitochondrial MT-RNR1, MT-TL1, MT-TS1, MT-TK and MT-TE genes variants associated with hearing loss in Southwestern China.

  • Authors : Zhou S; Department of Medical Genetics, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China; The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China.

Subjects: Genes, Mitochondrial* ; Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics; Humans

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2024 Jun; Vol. 181, pp. 111979. Date of Electronic Publication: 2024 May 09.Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Unveiling a novel GJB2 dominant K22T mutation in a Chinese family with hearing loss.

  • Authors : Ji H; Department of the Affiliated Eye and ENT Hospital, State Key Laboratory of Medical Neurobiology, ENT Institute and Otorhinolaryngology, Fudan University, Shanghai 200031, China.; NHC Key Laboratory of Hearing Medicine, Fudan University, Shanghai 200031, China.

Subjects: Connexin 26*/Connexin 26*/Connexin 26*/genetics ; Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics; Adult

  • Source: Acta biochimica et biophysica Sinica [Acta Biochim Biophys Sin (Shanghai)] 2024 Jun 25; Vol. 56 (6), pp. 945-951.Publisher: China Science Publishing & Media Ltd Country of Publication: China NLM ID: 101206716

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Academic Journal

MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population.

  • Authors : Zhang L; College of Otolaryngology Head and Neck Surgery, National Clinical Research Center for Otolaryngologic Diseases, Sixth Medical Center of the PLA General Hospital, Chinese PLA Medical School, 6# Fucheng Road, Beijing, 100048, China.; State Key Lab of Hearing Science, Ministry of Education, Beijing, China.

Subjects: Deafness*/Deafness*/Deafness*/ethnology ; Deafness*/Deafness*/Deafness*/genetics ; Hearing Loss, Sensorineural*/Hearing Loss, Sensorineural*/Hearing Loss, Sensorineural*/ethnology Deafness, Autosomal Recessive

  • Source: BMC medical genomics [BMC Med Genomics] 2024 Jan 23; Vol. 17 (1), pp. 32. Date of Electronic Publication: 2024 Jan 23.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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Academic Journal

[Genetic and phenotypic analysis of MYO15A rare variants associated with autosomal recessive hearing loss].

  • Authors : Lin Y; Department of Otolaryngology-Head and Neck Surgery,Shanghai Ninth People's Hospital,Shanghai Jiao Tong University School of Medicine,Shanghai,200125,China.; Ear Institute,Shanghai Jiao Tong University School of Medicine.

Subjects: Deafness*/Deafness*/Deafness*/genetics ; Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics ; Hearing Loss, Sensorineural*/Hearing Loss, Sensorineural*/Hearing Loss, Sensorineural*/genetics

  • Source: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery [Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi] 2024 Jan; Vol. 38 (1), Publisher: Lin chuang er bi yan hou tou jing wai ke za zhi bain ji bu Country of Publication: China NLM ID: 101303164 Publication

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Academic Journal

Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.

  • Authors : Xiong Y; The Frist Department of Clinical Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, 350122, Fujian Province, China.; Chen M

Subjects: Deafness*/Deafness*/Deafness*/diagnosis ; Deafness*/Deafness*/Deafness*/genetics ; Hearing Loss*/Hearing Loss*/Hearing Loss*/diagnosis Nonsyndromic Deafness

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2024 Jan; Vol. 176, pp. 111777. Date of Electronic Publication: 2023 Nov 21.Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Novel, pathogenic insertion variant of GSDME associates with autosomal dominant hearing loss in a large Chinese pedigree.

  • Authors : Cheng J; Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China.; Li T

Subjects: Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics ; Deafness*/Deafness*/Deafness*/genetics ; Hearing Loss, Sensorineural*/Hearing Loss, Sensorineural*/Hearing Loss, Sensorineural*/geneticsNonsyndromic Deafness

  • Source: Journal of cellular and molecular medicine [J Cell Mol Med] 2024 Jan; Vol. 28 (1), pp. e18004. Date of Electronic Publication: 2023 Oct 20.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101083777 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Association between depression status and hearing loss among older adults: The role of outdoor activity engagement.

  • Authors : Lu Z; College of management, Shandong University of Traditional Chinese Medicine, Jinan 250001, China.; Yu D

Subjects: Depression*/Depression*/Depression*/epidemiology ; Depression*/Depression*/Depression*/diagnosis ; Hearing Loss*/Hearing Loss*/Hearing Loss*/epidemiology

  • Source: Journal of affective disorders [J Affect Disord] 2024 Jan 15; Vol. 345, pp. 404-409. Date of Electronic Publication: 2023 Oct 23.Publisher: Elsevier/North-Holland Biomedical Press Country of Publication: Netherlands NLM ID: 7906073 Publication Model: Print-Electronic Cited Medium:

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