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Items: 1 to 50 of 81

1.

Radiologic recognition of cochlear implant magnet displacement.

Epperson MV, Born HL, Greinwald J Jr.

Int J Pediatr Otorhinolaryngol. 2019 Feb 8;120:64-67. doi: 10.1016/j.ijporl.2019.02.019. [Epub ahead of print]

PMID:
30771555
2.

Ocular Vestibular Evoked Myogenic Potentials: Normative Findings in Children.

Kuhn JJ, Lavender VH, Hunter LL, McGuire SE, Meinzen-Derr J, Keith RW, Greinwald JH.

J Am Acad Audiol. 2018 May;29(5):443-450. doi: 10.3766/jaaa.17086.

PMID:
29708493
3.

Vestibular pathology in children with enlarged vestibular aqueduct.

Yang CJ, Lavender V, Meinzen-Derr JK, Cohen AP, Youssif M, Castiglione M, Manickam V, Bachmann KR, Greinwald JH.

Laryngoscope. 2016 Oct;126(10):2344-50. doi: 10.1002/lary.25890. Epub 2016 Feb 10.

PMID:
26864825
4.

Diagnostic Evaluation of Children with Sensorineural Hearing Loss.

Prosser JD, Cohen AP, Greinwald JH.

Otolaryngol Clin North Am. 2015 Dec;48(6):975-82. doi: 10.1016/j.otc.2015.07.004. Epub 2015 Oct 1. Review.

PMID:
26429334
5.

High-frequency sensorineural hearing loss in children.

Johnson K, Tabangin M, Meinzen-Derr J, Cohen AP, Greinwald JH.

Laryngoscope. 2016 May;126(5):1236-40. doi: 10.1002/lary.25544. Epub 2015 Aug 12.

PMID:
26266337
6.

Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss.

Nayak G, Varga L, Trincot C, Shahzad M, Friedman PL, Klimes I, Greinwald JH Jr, Riazuddin SA, Masindova I, Profant M, Khan SN, Friedman TB, Ahmed ZM, Gasperikova D, Riazuddin S, Riazuddin S.

Hum Genet. 2015 Apr;134(4):423-37. doi: 10.1007/s00439-015-1532-y. Epub 2015 Feb 10.

7.

Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss.

Pique LM, Brennan ML, Davidson CJ, Schaefer F, Greinwald J Jr, Schrijver I.

PeerJ. 2014 May 8;2:e384. doi: 10.7717/peerj.384. eCollection 2014.

8.

Codeine-related adverse drug reactions in children following tonsillectomy: a prospective study.

Prows CA, Zhang X, Huth MM, Zhang K, SaldaƱa SN, Daraiseh NM, Esslinger HR, Freeman E, Greinwald JH, Martin LJ, Sadhasivam S.

Laryngoscope. 2014 May;124(5):1242-50. doi: 10.1002/lary.24455. Epub 2013 Nov 13.

PMID:
24122716
9.

Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss.

Shahzad M, Sivakumaran TA, Qaiser TA, Schultz JM, Hussain Z, Flanagan M, Bhinder MA, Kissell D, Greinwald JH Jr, Khan SN, Friedman TB, Zhang K, Riazuddin S, Riazuddin S, Ahmed ZM.

Otolaryngol Head Neck Surg. 2013 Sep;149(3):478-87. doi: 10.1177/0194599813493075. Epub 2013 Jun 14.

10.

Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing loss.

Sivakumaran TA, Husami A, Kissell D, Zhang W, Keddache M, Black AP, Tinkle BT, Greinwald JH Jr, Zhang K.

Otolaryngol Head Neck Surg. 2013 Jun;148(6):1007-16. doi: 10.1177/0194599813482294. Epub 2013 Mar 22.

PMID:
23525850
11.

Significance of unilateral enlarged vestibular aqueduct.

Greinwald J, DeAlarcon A, Cohen A, Uwiera T, Zhang K, Benton C, Halstead M, Meinzen-Derr J.

Laryngoscope. 2013 Jun;123(6):1537-46. doi: 10.1002/lary.23889. Epub 2013 Feb 9.

PMID:
23401162
12.

Minimal access and standard cochlear implantation: a comparative study.

Prager JD, Neidich MJ, Perkins JN, Meinzen-Derr J, Greinwald JH Jr.

Int J Pediatr Otorhinolaryngol. 2012 Aug;76(8):1102-6. doi: 10.1016/j.ijporl.2012.04.008. Epub 2012 May 16.

PMID:
22595461
13.

To tube or not to tube: indications for myringotomy with tube placement.

Smith N, Greinwald J Jr.

Curr Opin Otolaryngol Head Neck Surg. 2011 Oct;19(5):363-6. doi: 10.1097/MOO.0b013e3283499fa8. Review.

PMID:
21804383
14.

Characteristics of children diagnosed as having coagulopathies following posttonsillectomy bleeding.

Sun GH, Harmych BM, Dickson JM, Gonzalez del Rey JA, Myer CM 3rd, Greinwald JH Jr.

Arch Otolaryngol Head Neck Surg. 2011 Jan;137(1):65-8. doi: 10.1001/archoto.2010.227.

PMID:
21242549
15.

Genetic mutations and aminoglycoside-induced ototoxicity in neonates.

Johnson RF, Cohen AP, Guo Y, Schibler K, Greinwald JH.

Otolaryngol Head Neck Surg. 2010 May;142(5):704-7. doi: 10.1016/j.otohns.2010.01.030.

PMID:
20416460
16.

H1N1 influenza A presenting as bacterial tracheitis.

Hopkins BS, Johnson KE, Ksiazek JM, Sun G, Greinwald JH, Rutter M.

Otolaryngol Head Neck Surg. 2010 Apr;142(4):612-4. doi: 10.1016/j.otohns.2010.01.005.

PMID:
20304287
17.

High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays.

Kothiyal P, Cox S, Ebert J, Husami A, Kenna MA, Greinwald JH, Aronow BJ, Rehm HL.

BMC Biotechnol. 2010 Feb 10;10:10. doi: 10.1186/1472-6750-10-10.

18.

Neuroanatomic differences in children with unilateral sensorineural hearing loss detected using functional magnetic resonance imaging.

Propst EJ, Greinwald JH, Schmithorst V.

Arch Otolaryngol Head Neck Surg. 2010 Jan;136(1):22-6. doi: 10.1001/archoto.2009.208.

PMID:
20083773
19.

Hearing loss progression and contralateral involvement in children with unilateral sensorineural hearing loss.

Uwiera TC, DeAlarcon A, Meinzen-Derr J, Cohen AP, Rasmussen B, Shott G, Greinwald J.

Ann Otol Rhinol Laryngol. 2009 Nov;118(11):781-5.

PMID:
19999363
20.

An overview of custom array sequencing.

Kothiyal P, Cox S, Ebert J, Aronow BJ, Greinwald JH, Rehm HL.

Curr Protoc Hum Genet. 2009 Apr;Chapter 7:Unit 7.17. doi: 10.1002/0471142905.hg0717s61.

21.

Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations.

Lee KH, Larson DA, Shott G, Rasmussen B, Cohen AP, Benton C, Halsted M, Choo D, Meinzen-Derr J, Greinwald JH Jr.

Laryngoscope. 2009 Mar;119(3):554-8. doi: 10.1002/lary.20162.

PMID:
19235794
22.

A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness.

Bardien S, Human H, Harris T, Hefke G, Veikondis R, Schaaf HS, van der Merwe L, Greinwald JH, Fagan J, de Jong G.

BMC Med Genet. 2009 Jan 13;10:2. doi: 10.1186/1471-2350-10-2.

23.

Aminoglycoside ototoxicity in Nicaraguan children: patient risk factors and mitochondrial DNA results.

Saunders JE, Greinwald JH, Vaz S, Guo Y.

Otolaryngol Head Neck Surg. 2009 Jan;140(1):103-7. doi: 10.1016/j.otohns.2008.09.027.

PMID:
19130971
24.

Massive lymphatic malformations of the head, neck, and chest.

Greinwald J Jr, Cohen AP, Hemanackah S, Azizkhan RG.

J Otolaryngol Head Neck Surg. 2008 Apr;37(2):169-73.

PMID:
19128607
25.

Macrophage inflammatory proteins in cytomegalovirus-related inner ear injury.

Schraff SA, Schleiss MR, Brown DK, Meinzen-Derr J, Choi KY, Greinwald JH, Choo DI.

Otolaryngol Head Neck Surg. 2007 Oct;137(4):612-8.

PMID:
17903579
26.

Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.

Chen J, Yang L, Yang A, Zhu Y, Zhao J, Sun D, Tao Z, Tang X, Wang J, Wang X, Tsushima A, Lan J, Li W, Wu F, Yuan Q, Ji J, Feng J, Wu C, Liao Z, Li Z, Greinwald JH, Lu J, Guan MX.

Gene. 2007 Oct 15;401(1-2):4-11. Epub 2007 Jun 20.

27.

A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort.

Putcha GV, Bejjani BA, Bleoo S, Booker JK, Carey JC, Carson N, Das S, Dempsey MA, Gastier-Foster JM, Greinwald JH Jr, Hoffmann ML, Jeng LJ, Kenna MA, Khababa I, Lilley M, Mao R, Muralidharan K, Otani IM, Rehm HL, Schaefer F, Seltzer WK, Spector EB, Springer MA, Weck KE, Wenstrup RJ, Withrow S, Wu BL, Zariwala MA, Schrijver I.

Genet Med. 2007 Jul;9(7):413-26.

PMID:
17666888
28.

When is the vestibular aqueduct enlarged? A statistical analysis of the normative distribution of vestibular aqueduct size.

Vijayasekaran S, Halsted MJ, Boston M, Meinzen-Derr J, Bardo DM, Greinwald J, Benton C.

AJNR Am J Neuroradiol. 2007 Jun-Jul;28(6):1133-8.

29.

The role of CMV inflammatory genes in hearing loss.

Schraff SA, Brown DK, Schleiss MR, Meinzen-Derr J, Greinwald JH, Choo DI.

Otol Neurotol. 2007 Oct;28(7):964-9.

PMID:
17558342
30.

The large vestibular aqueduct: a new definition based on audiologic and computed tomography correlation.

Boston M, Halsted M, Meinzen-Derr J, Bean J, Vijayasekaran S, Arjmand E, Choo D, Benton C, Greinwald J.

Otolaryngol Head Neck Surg. 2007 Jun;136(6):972-7.

PMID:
17547990
31.

Prevalence and etiology of hearing loss in rural Nicaraguan children.

Saunders JE, Vaz S, Greinwald JH, Lai J, Morin L, Mojica K.

Laryngoscope. 2007 Mar;117(3):387-98. Review.

PMID:
17334299
32.

The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct.

Madden C, Halsted M, Meinzen-Derr J, Bardo D, Boston M, Arjmand E, Nishimura C, Yang T, Benton C, Das V, Smith R, Choo D, Greinwald J.

Arch Otolaryngol Head Neck Surg. 2007 Feb;133(2):162-8. Erratum in: Arch Otolaryngol Head Neck Surg. 2007 Jun;133(6):607.

PMID:
17309986
33.

Molecular mechanisms underlying inner ear patterning defects in kreisler mutants.

Choo D, Ward J, Reece A, Dou H, Lin Z, Greinwald J.

Dev Biol. 2006 Jan 15;289(2):308-17. Epub 2005 Dec 1.

34.

GJB2 mutations and additional disabilities in a pediatric cochlear implant population.

Wiley S, Choo D, Meinzen-Derr J, Hilbert L, Greinwald J.

Int J Pediatr Otorhinolaryngol. 2006 Mar;70(3):493-500. Epub 2005 Sep 9.

PMID:
16154643
35.

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.

Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX.

Am J Med Genet A. 2005 Oct 1;138A(2):133-40.

36.

Audiometric, clinical and educational outcomes in a pediatric symptomatic congenital cytomegalovirus (CMV) population with sensorineural hearing loss.

Madden C, Wiley S, Schleiss M, Benton C, Meinzen-Derr J, Greinwald J, Choo D.

Int J Pediatr Otorhinolaryngol. 2005 Sep;69(9):1191-8. Epub 2005 Apr 19.

PMID:
16061110
37.

Improved diagnostic effectiveness with a sequential diagnostic paradigm in idiopathic pediatric sensorineural hearing loss.

Preciado DA, Lawson L, Madden C, Myer D, Ngo C, Bradshaw JK, Choo DI, Greinwald JH Jr.

Otol Neurotol. 2005 Jul;26(4):610-5.

PMID:
16015155
38.

Cortical reorganization in children with unilateral sensorineural hearing loss.

Schmithorst VJ, Holland SK, Ret J, Duggins A, Arjmand E, Greinwald J.

Neuroreport. 2005 Apr 4;16(5):463-7.

39.

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.

Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH Jr, Guan MX.

Biochem Biophys Res Commun. 2005 Mar 25;328(4):1244-51.

PMID:
15708009
40.

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.

Wang Q, Li R, Zhao H, Peters JL, Liu Q, Yang L, Han D, Greinwald JH Jr, Young WY, Guan MX.

Am J Med Genet A. 2005 Feb 15;133A(1):27-30.

41.

Bacterial tracheitis reexamined: is there a less severe manifestation?

Salamone FN, Bobbitt DB, Myer CM, Rutter MJ, Greinwald JH Jr.

Otolaryngol Head Neck Surg. 2004 Dec;131(6):871-6.

PMID:
15577783
42.

A diagnostic paradigm for childhood idiopathic sensorineural hearing loss.

Preciado DA, Lim LH, Cohen AP, Madden C, Myer D, Ngo C, Bradshaw JK, Lawson L, Choo DI, Greinwald JH Jr.

Otolaryngol Head Neck Surg. 2004 Dec;131(6):804-9.

PMID:
15577772
43.

Co-expression of pendrin, vacuolar H+-ATPase alpha4-subunit and carbonic anhydrase II in epithelial cells of the murine endolymphatic sac.

Dou H, Xu J, Wang Z, Smith AN, Soleimani M, Karet FE, Greinwald JH Jr, Choo D.

J Histochem Cytochem. 2004 Oct;52(10):1377-84.

PMID:
15385584
44.

Refining the DFNB17 interval in consanguineous Indian families.

Guo Y, Pilipenko V, Lim LH, Dou H, Johnson L, Srisailapathy CR, Ramesh A, Choo DI, Smith RJ, Greinwald JH.

Mol Biol Rep. 2004 Jun;31(2):97-105.

PMID:
15293785
45.

Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss.

Li R, Greinwald JH Jr, Yang L, Choo DI, Wenstrup RJ, Guan MX.

J Med Genet. 2004 Aug;41(8):615-20. No abstract available.

46.

Genomic organization and expression analysis of the murine Fam3c gene.

Pilipenko VV, Reece A, Choo DI, Greinwald JH Jr.

Gene. 2004 Jun 23;335:159-68.

PMID:
15194199
47.

The cochlear cleft.

Chadwell JB, Halsted MJ, Choo DI, Greinwald JH, Benton C.

AJNR Am J Neuroradiol. 2004 Jan;25(1):21-4.

48.

Temporal bone abnormalities associated with hearing loss in Waardenburg syndrome.

Madden C, Halsted MJ, Hopkin RJ, Choo DI, Benton C, Greinwald JH Jr.

Laryngoscope. 2003 Nov;113(11):2035-41.

PMID:
14603070
49.

Expression of aquaporin 1 and 5 in the developing mouse inner ear and audiovestibular assessment of an Aqp5 null mutant.

Merves M, Krane CM, Dou H, Greinwald JH, Menon AG, Choo D.

J Assoc Res Otolaryngol. 2003 Jun;4(2):264-75.

50.

Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United States.

Lim LH, Bradshaw JK, Guo Y, Pilipenko V, Madden C, Ingala D, Keddache M, Choo DI, Wenstrup R, Greinwald JH Jr.

Arch Otolaryngol Head Neck Surg. 2003 Aug;129(8):836-40.

PMID:
12925341

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