Results 91 to 100 of about 6,571 (239)

Lymphatic Vessels in the Inner Ear of Patients With Meniere Disease: A Novel Pathological Finding

OTO Open, Volume 8, Issue 3, July–September 2024.
Abstract Background Meniere disease, characterized by intermittent episodes of vertigo, fluctuating sensorineural hearing loss, tinnitus, and aural pressure, is a common cause of vertigo in humans. The pathogenesis of Meniere disease remains unknown.
Daogong Zhang, Xiaofei Li, Yafeng Lv, Yongdong Song, Ligang Kong, Boqin Li, Jinfeng Zheng, Nicolas Pérez‐Fernández, Zhaomin Fan, Haibo Wang   +9 more
wiley   +1 more source

Intratympanic corticosteroids in Ménière's disease: A mini-review [PDF]

, 2017
This article reviews the effectiveness of intratympanic corticosteroids for vertigo control in Ménière's disease at 2-years follow-up according to the guidelines expressed by the American Academy of Otolaryngology-Head & Neck Surgery.
AAO-HNS, Albu, Albu, Atrache Al Attrache, Barrs, Bird, Boleas-Aguirre, Brookes, Casani, Dodson, Doyle, Espinosa-Sanchez, Frejo, Frejo, Fukushima, Gabra, Garduño-Anaya, Gazquez, Greco, Hamid, Herraiz, Hirvonen, Itoh, James, Kayan, Lavigne, Lee, Leng, Liu, Martin Sanz, Martin-Sanz, McCabe, McRackan, Miller, Minor, Moffat, Paragache, Parnes, Patel, Phillips, Pondugula, Pullens, Pullens, Rauch, Rauch, Ren, Riente, Sajjadi, Sakata, Salt, Sennaroğlu, She, Shea, Shin, Shirwany, Silverstein, Silverstein, Suzuki, Söderman, Thirlwall, Trune, Trune, van Sonsbeek, Wick, Wladislavosky-Waserman, Xenellis   +65 more
core   +2 more sources

Prevalence and prognosis of hypoxia‐inducible factor‐2α (HIF‐2α) pathway gene mutations across advanced solid tumors

Cancer Medicine, Volume 13, Issue 11, June 2024.
Abstract Introduction Hypoxia‐inducible factor‐2α (HIF‐2α) modulates the hypoxic response pathway in tumors; however, mutations in pathways (including SDHA, SDHB, SDHC, SDHD, FH, and VHL genes) that are suspected to activate HIF‐2α are poorly understood, with limited understanding of the prevalence and clinical prognosis.
Wenjun Zhong, Jiemin Ma, Cai Chen, E. J. Dettman, Razvan Cristescu, Girish S. Naik, Fan Jin, Changxia Shao   +7 more
wiley   +1 more source

Unraveling the Genetic Basis of Combined Deafness and Male Infertility Phenotypes through High‐Throughput Sequencing in a Unique Cohort from South India

Advanced Genetics, Volume 5, Issue 2, June 2024.
A comprehensive analysis of the genetic makeup of a unique cohort of males with hearing impairment and infertility uncovers a wide range of gene variations spanning seven chromosomes, highlighting significant genetic heterogeneity within this disorder.
Jeffrey Justin Margret, Chandru Jayasankaran, Pavithra Amritkumar, Hela Azaiez, C. R. Srikumari Srisailapathy   +4 more
wiley   +1 more source

When alarm bells ring: emergency tinnitus [PDF]

, 2016
OBJECTIVE: The aim of this study is to develop a diagnostic-therapeutic algorithm for those suffering from tinnitus who seek emergency aid. MATERIALS AND METHODS: A literature review has been performed on articles from the last 30 years. RESULTS: It is
Altissimi, Giancarlo, Cianfrone, Giancarlo, Ciofalo, Andrea, Greco, Antonio, Marinelli, C, Mazzei, F, Orlando, Maria Patrizia, Salviati, M, Testugini, C, Turchetta, Rosaria, Vincentiis, M. DE   +10 more
core  

Síndrome de Pendred causada por mutação em homozigoze no gene SLC26A4 em uma família brasileira consangüínea [PDF]

, 2008
Pendred Syndrome (PS) is an autossomal recessive disorder characterized by sensorineural deafness, goiter and iodide organification defect. The hearing loss is associated with inner ear abnormalities, ranging from an isolated enlarged vestibular aqueduct
Bahmad Júnior, Fayez, Barra, Gustavo Barcelos, Batista, Ana R. T., Cherulli, Bruno Luis Barbosa, Costa, Patrícia Godoy Garcia, Figueiredo, Larissa Pereira Gomes, Freitas, Ana Carolina Rezende de, Garcia, Érica Correia, Motta, Luiz Augusto Casulari Roxo da, Nascimento, Paula P., Neves, Francisco de Assis Rocha, Porto, Adriana Lofrano Alves, Vaz, Rodrigo Ferreira   +12 more
core   +1 more source

Endolymphatic sac tumor

Chinese Journal of Contemporary Neurology and Neurosurgery, 2019
DOI: 10.3969/j.issn.1672-6731.2019.02 ...
Xiao-ling YAN
doaj  

Cause, severity, and efficacy of treatment for hearing loss in children with Trisomy 18: A single institution‐based retrospective study

American Journal of Medical Genetics Part A, Volume 194, Issue 4, April 2024.
Abstract Trisomy 18 is a common chromosomal aberration syndrome, characterized by variable clinical manifestations, including cardiovascular, pulmonary, genitourinary, and musculoskeletal findings, leading to a shorter survival and severe developmental delay in survivors.
Ririko Sato, Hidekane Yoshimura, Tomoki Kosho, Yutaka Takumi   +3 more
wiley   +1 more source

Embryonic development in the bonnethead (Sphyrna tiburo), a viviparous hammerhead shark

Developmental Dynamics, Volume 253, Issue 3, Page 351-362, March 2024.
Abstract Background The hammerhead sharks (family Sphyrnidae) are an immediately recognizable group of sharks due to their unique head shape. Though there has long been an interest in hammerhead development, there are currently no explicit staging tables published for any members of the group.
Steven R. Byrum, Bryan S. Frazier, R. Dean Grubbs, Gavin J. P. Naylor, Gareth J. Fraser   +4 more
wiley   +1 more source

Intracellular and Extracellular Elemental Composition of the Endolymphatic Sac Studied by X-Ray Microanalysis [PDF]

, 1993
X-ray microanalysis was performed along with light microscopy (LM) on rapidly frozen and cryo-sectioned endolymphatic sac tissues of adult guinea pigs, to determine the elemental composition of the different cell types in this tissue as well as the ...
Wroblewski, Romuald
core   +1 more source