Vreugde S - Search Results

1

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population.

Sobe T, Vreugde S, Shahin H, Berlin M, Davis N, Kanaan M, Yaron Y, Orr-Urtreger A, Frydman M, Shohat M, Avraham KB. Sobe T, et al. Among authors: vreugde s. Hum Genet. 2000 Jan;106(1):50-7. doi: 10.1007/s004390051009. Hum Genet. 2000. PMID: 10982182

2

Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor.

Frydman M, Vreugde S, Nageris BI, Weiss S, Vahava O, Avraham KB. Frydman M, et al. Among authors: vreugde s. Arch Otolaryngol Head Neck Surg. 2000 May;126(5):633-7. doi: 10.1001/archotol.126.5.633. Arch Otolaryngol Head Neck Surg. 2000. PMID: 10807331

3

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

Vreugde S, Erven A, Kros CJ, Marcotti W, Fuchs H, Kurima K, Wilcox ER, Friedman TB, Griffith AJ, Balling R, Hrabé De Angelis M, Avraham KB, Steel KP. Vreugde S, et al. Nat Genet. 2002 Mar;30(3):257-8. doi: 10.1038/ng848. Epub 2002 Feb 19. Nat Genet. 2002. PMID: 11850623

4

High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim.

Sobe T, Erlich P, Berry A, Korostichevsky M, Vreugde S, Avraham KB, Bonné-Tamir B, Shohat M. Sobe T, et al. Among authors: vreugde s. Am J Med Genet. 1999 Oct 29;86(5):499-500. Am J Med Genet. 1999. PMID: 10508996 No abstract available.

5

From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30.

Walsh T, Walsh V, Vreugde S, Hertzano R, Shahin H, Haika S, Lee MK, Kanaan M, King MC, Avraham KB. Walsh T, et al. Among authors: vreugde s. Proc Natl Acad Sci U S A. 2002 May 28;99(11):7518-23. doi: 10.1073/pnas.102091699. Proc Natl Acad Sci U S A. 2002. PMID: 12032315 Free PMC article.

6

USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses.

Adato A, Vreugde S, Joensuu T, Avidan N, Hamalainen R, Belenkiy O, Olender T, Bonne-Tamir B, Ben-Asher E, Espinos C, Millán JM, Lehesjoki AE, Flannery JG, Avraham KB, Pietrokovski S, Sankila EM, Beckmann JS, Lancet D. Adato A, et al. Among authors: vreugde s. Eur J Hum Genet. 2002 Jun;10(6):339-50. doi: 10.1038/sj.ejhg.5200831. Eur J Hum Genet. 2002. PMID: 12080385

7

Calcific tendinitis of the longus colli muscle.

De Maeseneer M, Vreugde S, Laureys S, Sartoris DJ, De Ridder F, Osteaux M. De Maeseneer M, et al. Among authors: vreugde s. Head Neck. 1997 Sep;19(6):545-8. doi: 10.1002/(sici)1097-0347(199709)19:6<545::aid-hed13>3.0.co;2-4. Head Neck. 1997. PMID: 9278764

8

Identification of the Bacterial Reservoirs for the Middle Ear Using Phylogenic Analysis.

Chan CL, Wabnitz D, Bassiouni A, Wormald PJ, Vreugde S, Psaltis AJ. Chan CL, et al. Among authors: vreugde s. JAMA Otolaryngol Head Neck Surg. 2017 Feb 1;143(2):155-161. doi: 10.1001/jamaoto.2016.3105. JAMA Otolaryngol Head Neck Surg. 2017. PMID: 27812691

9

Safety and Tolerability of Bacteriophage Therapy for Chronic Rhinosinusitis Due to Staphylococcus aureus.

Ooi ML, Drilling AJ, Morales S, Fong S, Moraitis S, Macias-Valle L, Vreugde S, Psaltis AJ, Wormald PJ. Ooi ML, et al. Among authors: vreugde s. JAMA Otolaryngol Head Neck Surg. 2019 Aug 1;145(8):723-729. doi: 10.1001/jamaoto.2019.1191. JAMA Otolaryngol Head Neck Surg. 2019. PMID: 31219531 Free PMC article.

10

The microbiome of otitis media with effusion.

Chan CL, Wabnitz D, Bardy JJ, Bassiouni A, Wormald PJ, Vreugde S, Psaltis AJ. Chan CL, et al. Among authors: vreugde s. Laryngoscope. 2016 Dec;126(12):2844-2851. doi: 10.1002/lary.26128. Epub 2016 Jun 23. Laryngoscope. 2016. PMID: 27335217

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