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Items: 1 to 20 of 965

1.

MiR-210 promotes sensory hair cell formation in the organ of corti.

Riccardi S, Bergling S, Sigoillot F, Beibel M, Werner A, Leighton-Davies J, Knehr J, Bouwmeester T, Parker CN, Roma G, Kinzel B.

BMC Genomics. 2016 Apr 27;17(1):309. doi: 10.1186/s12864-016-2620-7.

2.

Cochlear implant and inflammation reaction: Safety study of a new steroid-eluting electrode.

Astolfi L, Simoni E, Giarbini N, Giordano P, Pannella M, Hatzopoulos S, Martini A.

Hear Res. 2016 Apr 21. pii: S0378-5955(15)30193-3. doi: 10.1016/j.heares.2016.04.005. [Epub ahead of print]

PMID:
27109196
3.

Long-Term Follow-Up with Video of a Patient with Deafness-Dystonia Syndrome Treated with DBS-GPi.

Dulski J, Schinwelski M, Mandat T, Pienczk-Ręcławowicz K, Sławek J.

Stereotact Funct Neurosurg. 2016;94(2):123-5. doi: 10.1159/000445078. Epub 2016 Apr 22.

PMID:
27100856
4.

Genetics: A New Frontier in Otology.

Kameswaran M, Sudhamaheswari S, Natarajan K.

Indian J Otolaryngol Head Neck Surg. 2016 Mar;68(1):1-5. doi: 10.1007/s12070-016-0972-6. Epub 2016 Mar 11.

PMID:
27066400
5.

Genetic Correction of Induced Pluripotent Stem Cells From a Deaf Patient With MYO7A Mutation Results in Morphologic and Functional Recovery of the Derived Hair Cell-Like Cells.

Tang ZH, Chen JR, Zheng J, Shi HS, Ding J, Qian XD, Zhang C, Chen JL, Wang CC, Li L, Chen JZ, Yin SK, Huang TS, Chen P, Guan MX, Wang JF.

Stem Cells Transl Med. 2016 May;5(5):561-71. doi: 10.5966/sctm.2015-0252. Epub 2016 Mar 24.

PMID:
27013738
6.

Enzyme replacement therapy with galsulfase for mucopolysaccharidosis type VI.

Brunelli MJ, Atallah ÁN, da Silva EM.

Cochrane Database Syst Rev. 2016 Mar 4;3:CD009806. doi: 10.1002/14651858.CD009806.pub2. Review.

PMID:
26943923
7.

Human audiometric thresholds do not predict specific cellular damage in the inner ear.

Landegger LD, Psaltis D, Stankovic KM.

Hear Res. 2016 Feb 27;335:83-93. doi: 10.1016/j.heares.2016.02.018. [Epub ahead of print]

PMID:
26924453
8.

Advances in the Classification and Treatment of Osteogenesis Imperfecta.

Thomas IH, DiMeglio LA.

Curr Osteoporos Rep. 2016 Feb;14(1):1-9. doi: 10.1007/s11914-016-0299-y.

PMID:
26861807
9.

Ototoxicity and cancer therapy.

Landier W.

Cancer. 2016 Feb 9. doi: 10.1002/cncr.29779. [Epub ahead of print]

PMID:
26859792
10.
11.

The expression pattern and inhibitory influence of Tenascin-C on the growth of spiral ganglion neurons suggest a regulatory role as boundary formation molecule in the postnatal mouse inner ear.

Kwiatkowska M, Reinhard J, Roll L, Kraft N, Dazert S, Faissner A, Volkenstein S.

Neuroscience. 2016 Apr 5;319:46-58. doi: 10.1016/j.neuroscience.2016.01.039. Epub 2016 Jan 23.

PMID:
26812032
12.

Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing.

Yoshimura H, Miyagawa M, Kumakawa K, Nishio SY, Usami SI.

J Hum Genet. 2016 Jan 21. doi: 10.1038/jhg.2015.168. [Epub ahead of print]

PMID:
26791358
13.

Wolfram Syndrome: Diagnosis, Management, and Treatment.

Urano F.

Curr Diab Rep. 2016 Jan;16(1):6. doi: 10.1007/s11892-015-0702-6. Review.

14.

Musculoskeletal manifestations of Fabry disease: A retrospective study.

Lidove O, Zeller V, Chicheportiche V, Meyssonnier V, Sené T, Godot S, Ziza JM.

Joint Bone Spine. 2015 Dec 14. pii: S1297-319X(15)00273-0. doi: 10.1016/j.jbspin.2015.11.001. [Epub ahead of print]

PMID:
26697993
15.

Care of Adults With Intellectual and Developmental Disabilities: Down Syndrome.

Wilson B, Jones KB, Weedon D, Bilder D.

FP Essent. 2015 Dec;439:20-5. Review.

PMID:
26669211
16.

The Mouse Round-window Approach for Ototoxic Agent Delivery: A Rapid and Reliable Technique for Inducing Cochlear Cell Degeneration.

Stevens SM, Brown LN, Ezell PC, Lang H.

J Vis Exp. 2015 Nov 26;(105). doi: 10.3791/53131.

PMID:
26650771
17.

Methionine Sulfoxide Reductase B3-Targeted In Utero Gene Therapy Rescues Hearing Function in a Mouse Model of Congenital Sensorineural Hearing Loss.

Kim MA, Cho HJ, Bae SH, Lee B, Oh SK, Kwon TJ, Ryoo ZY, Kim HY, Cho JH, Kim UK, Lee KY.

Antioxid Redox Signal. 2016 Apr 10;24(11):590-602. doi: 10.1089/ars.2015.6442. Epub 2016 Jan 21.

PMID:
26649646
18.

SLC39A8 Deficiency: A Disorder of Manganese Transport and Glycosylation.

Park JH, Hogrebe M, Grüneberg M, DuChesne I, von der Heiden AL, Reunert J, Schlingmann KP, Boycott KM, Beaulieu CL, Mhanni AA, Innes AM, Hörtnagel K, Biskup S, Gleixner EM, Kurlemann G, Fiedler B, Omran H, Rutsch F, Wada Y, Tsiakas K, Santer R, Nebert DW, Rust S, Marquardt T.

Am J Hum Genet. 2015 Dec 3;97(6):894-903. doi: 10.1016/j.ajhg.2015.11.003.

PMID:
26637979
19.

Molecular Structure and Regulation of P2X Receptors With a Special Emphasis on the Role of P2X2 in the Auditory System.

Mittal R, Chan B, Grati M, Mittal J, Patel K, Debs LH, Patel AP, Yan D, Chapagain P, Liu XZ.

J Cell Physiol. 2016 Aug;231(8):1656-70. doi: 10.1002/jcp.25274. Epub 2015 Dec 30. Review.

PMID:
26627116
20.

A COL4A5 mutation with glomerular disease and signs of chronic thrombotic microangiopathy.

Wuttke M, Seidl M, Malinoc A, Prischl FC, Kuehn EW, Walz G, Köttgen A.

Clin Kidney J. 2015 Dec;8(6):690-4. doi: 10.1093/ckj/sfv091. Epub 2015 Sep 29.

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