PMC Articles for MedGen (Select 99093) - PMC - NCBI

Result Filters

Links from MedGen

Items: 1 to 20 of 35

<< First< Prev

Page of 2

Select item 63546711.

A tale of 1 year: a case of bilateral conductive hearing loss due to bilateral ossicular chain disruption post head trauma

Mariam Aljehani, Mansour Alshamani

J Surg Case Rep. 2019 Jan; 2019(1): rjy353. Published online 2019 Jan 31. doi: 10.1093/jscr/rjy353

PMCID:: PMC6354671

Abstract Article PDF–182K

Select item 70693242.

Bilateral superior semicircular canal dehiscence: bilateral conductive hearing loss with subtle vestibular symptoms

Diogo Pereira, Abílio Leonardo, Delfim Duarte, Nuno Oliveira

BMJ Case Rep. 2020; 13(3): e233042. Published online 2020 Mar 12. doi: 10.1136/bcr-2019-233042

PMCID:: PMC7069324

Abstract Article PDF–982K

Select item 71164333.

The Merits of Bilateral Application of Bone-Conduction Devices in Children With Bilateral Conductive Hearing Loss

Chrisje A. den Besten, Katharina Vogt, Arjan J. Bosman, Ad F. M. Snik, Myrthe K. S. Hol, Martijn J. H. Agterberg

Ear Hear. Author manuscript; available in PMC 2020 Dec 3.

Published in final edited form as: Ear Hear. 2020 Sep 1; 41(5): 1327–1332. doi: 10.1097/AUD.0000000000000853

PMCID:: PMC7116433

Abstract Article PDF–581K

Select item 77586724.

Successive ipsilateral surgery of Vibrant Soundbridge and Bonebridge devices for congenital bilateral conductive hearing loss: a case report

Yujie Liu, Ran Ren, Shouqin Zhao

J Int Med Res. 2020 Dec; 48(12): 0300060520972280. Published online 2020 Dec 22. doi: 10.1177/0300060520972280

PMCID:: PMC7758672

Abstract Article PDF–497K

Select item 10506705.

Possible autosomal recessive inheritance of progressive hearing loss with stapes fixation.

C Thies, M Handrock, K Sperling, A Rcis

J Med Genet. 1996 Jul; 33(7): 597–599. doi: 10.1136/jmg.33.7.597

PMCID:: PMC1050670

Summary Page Browse PDF–594K

Select item 110074856.

Audiologic and Otologic Clinical Manifestations of Loeys-Dietz Syndrome: A Heritable Connective Tissue Disorder

Jun W. Jeon, Julie Christensen, Jennifer Chisholm, Christopher Zalewski, Marjohn Rasooly, Caeden Dempsey, Alaina Magnani, Pamela Frischmeyer-Guerrerio, Carmen C. Brewer, Hung Jeffrey Kim

Otolaryngol Head Neck Surg. Author manuscript; available in PMC 2024 Apr 11.

Published in final edited form as: Otolaryngol Head Neck Surg. 2022 Feb; 166(2): 357–362. Published online 2021 May 11. doi: 10.1177/01945998211008899

PMCID:: PMC11007485

Abstract Article PDF–345K

Select item 101285577.

KBG综合征的听力学表型1例报告并文献回顾

苏文文, 夏雨奇, 夏彩风, 刘玉和

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2022 Oct 3; 36(10): 797–801. Chinese. doi: 10.13201/j.issn.2096-7993.2022.10.014

PMCID:: PMC10128557

Abstract Article PDF–6.4M

Select item 30429088.

Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome

Saima Riazuddin, Zubair M Ahmed, Rashmi S Hegde, Shaheen N Khan, Idrees Nasir, Uzma Shaukat, Sheikh Riazuddin, John A Butman, Andrew J Griffith, Thomas B Friedman, Byung Yoon Choi

BMC Med Genet. 2011; 12: 21. Published online 2011 Feb 9. doi: 10.1186/1471-2350-12-21

PMCID:: PMC3042908

Abstract Article PDF–1.6M

Select item 66315389.

TCOF1 pathogenic variants identified by Whole-exome sequencing in Chinese Treacher Collins syndrome families and hearing rehabilitation effect

Xinmiao Fan, Yibei Wang, Yue Fan, Huiqian Du, Nana Luo, Shuyang Zhang, Xiaowei Chen

Orphanet J Rare Dis. 2019; 14: 178. Published online 2019 Jul 15. doi: 10.1186/s13023-019-1136-z

PMCID:: PMC6631538

Abstract Article PDF–1.1M

Select item 541149110.

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

Jing Guan, Dayong Wang, Wenjian Cao, Yali Zhao, Renqian Du, Hu Yuan, Qiong Liu, Lan Lan, Liang Zong, Ju Yang, Zifang Yin, Bing Han, Feng Zhang, Qiuju Wang

J Hum Genet. 2016 Nov; 61(11): 917–922. Published online 2016 Jul 7. doi: 10.1038/jhg.2016.86

PMCID:: PMC5411491

Abstract Article PDF–2.3M

Select item 450290511.

Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family

Zhongxia Qi, Linda Jo Bone Jeng, Anne Slavotinek, Jingwei Yu

BMC Med Genomics. 2015; 8: 38. Published online 2015 Jul 15. doi: 10.1186/s12920-015-0113-1

PMCID:: PMC4502905

Abstract Article PDF–3.6M

Select item 840422212.

Interstitial duplication of 20q11.22q13.11: A case report and review of literature

Logan Goetzinger, Rachel D. Starks, Kyle Dillahunt, Heather Major, Jaime M. Nagy, Alpa Sidhu

Mol Genet Genomic Med. 2021 Aug; 9(8): e1755. Published online 2021 Jul 16. doi: 10.1002/mgg3.1755

PMCID:: PMC8404222

Abstract Article PDF–632K

Select item 560688313.

Novel compound heterozygous mutations in TELO2 in a patient with severe expression of You‐Hoover‐Fong syndrome

Shahida Moosa, Janine Altmüller, Troels Lyngbye, Rikke Christensen, Yun Li, Peter Nürnberg, Gökhan Yigit, Ida Vogel, Bernd Wollnik

Mol Genet Genomic Med. 2017 Sep; 5(5): 580–584. Published online 2017 Jul 28. doi: 10.1002/mgg3.287

PMCID:: PMC5606883

Abstract Article PDF–1.3M

Select item 682856414.

Prevalence of Mild Hearing Loss in Schoolchildren and its Association with their School Performance

Reem Elbeltagy

Int Arch Otorhinolaryngol. 2020 Jan; 24(1): e93–e98. Published online 2019 Nov 4. doi: 10.1055/s-0039-1695024

PMCID:: PMC6828564

Abstract Article PDF–177K

Select item 553511115.

Saddle-nose and bilateral cauliflower ear deformities with pyoderma gangrenosum-like ulcers, cavitary pulmonary lesions, digital gangrene and pulselessness in a young female

Sweta Subhadarshani, Vishal Gupta, Anurag Chahal, Kaushal K Verma

BMJ Case Rep. 2017; 2017: bcr2017220434. Published online 2017 Jun 15. doi: 10.1136/bcr-2017-220434

PMCID:: PMC5535111

Abstract Article PDF–2.1M

Select item 444356916.

First experience in Italy with a new transcutaneous bone conduction implant

P. MARSELLA, A. SCORPECCI, G. DALMASSO, C. PACIFICO

Acta Otorhinolaryngol Ital. 2015 Feb; 35(1): 29–33.

PMCID:: PMC4443569

Abstract Article PDF–302K

Select item 432059817.

Surgical treatment of scoliosis in Treacher Collins syndrome: a case report

Christos Karampalis, Nikolaos Bounakis, Athanasios I Tsirikos

J Med Case Rep. 2014; 8: 446. Published online 2014 Dec 19. doi: 10.1186/1752-1947-8-446

PMCID:: PMC4320598

Abstract Article PDF–1.7M

Select item 391387118.

A Sensitive Period for the Impact of Hearing Loss on Auditory Perception

Bradley N. Buran, Emma C. Sarro, Francis A. M. Manno, Ramanjot Kang, Melissa L. Caras, Dan H. Sanes

J Neurosci. 2014 Feb 5; 34(6): 2276–2284. doi: 10.1523/JNEUROSCI.0647-13.2014

PMCID:: PMC3913871

Abstract Article PDF–346K

Select item 340604919.

Diminished Behavioral and Neural Sensitivity to Sound Modulation Is Associated with Moderate Developmental Hearing Loss

Merri J. Rosen, Emma C. Sarro, Jack B. Kelly, Dan H. Sanes

PLoS One. 2012; 7(7): e41514. Published online 2012 Jul 26. doi: 10.1371/journal.pone.0041514

PMCID:: PMC3406049

Abstract Article PDF–1.6M

Select item 322273520.

Nasopharyngeal cancer mimicking otitic barotrauma in a resource-challenged center: a case report

Adekunle Daniel, Ayotunde James Fasunla

J Med Case Reports. 2011; 5: 532. Published online 2011 Oct 31. doi: 10.1186/1752-1947-5-532

PMCID:: PMC3222735

Abstract Article PDF–533K

<< First< Prev

Page of 2

Supplemental Content

Filter your results:

All (35)
NIH grants (5)
Embargoed (0)

Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

PMC Articles for MedGen (Select 99093) (35)
PMC
txid713[Organism:exp] (133278)
Identical Protein Groups
GSM753444[Accession] (3)
GEO DataSets
GSE107839[Accession] (27)
GEO DataSets
conotoxin pl14.1 precursor [Conus planorbis]
conotoxin pl14.1 precursor [Conus planorbis]
gi|91177670|gb|ABE27007.1|

Protein

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Literature > PubMed Central (PMC)