Similar articles for PMID: 32409310

Year	Number of Results
1980	1
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1995	3
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2024	0

1

A Case Series of X-Linked Deafness-2 with Sensorineural Hearing Loss, Stapes Fixation, and Perilymphatic Gusher: MR Imaging and Clinical Features of Hypothalamic Malformations.

Prat Matifoll JA, Wilson M, Goetti R, Birman C, Bennett B, Peadon E, Prats-Uribe A, Prelog K. Prat Matifoll JA, et al. AJNR Am J Neuroradiol. 2020 Jun;41(6):1087-1093. doi: 10.3174/ajnr.A6541. Epub 2020 May 14. AJNR Am J Neuroradiol. 2020. PMID: 32409310 Free PMC article.

2

New Imaging Findings of Incomplete Partition Type III Inner Ear Malformation and Literature Review.

Hong R, Du Q, Pan Y. Hong R, et al. AJNR Am J Neuroradiol. 2020 Jun;41(6):1076-1080. doi: 10.3174/ajnr.A6576. Epub 2020 May 28. AJNR Am J Neuroradiol. 2020. PMID: 32467182 Free PMC article. Review.

3

Association Between Incomplete Partition Type III and Abnormal Hypothalamic Morphology: Further Imaging Evidence.

Oztunali C, Saylisoy S, Toprak U, Incesulu A. Oztunali C, et al. J Comput Assist Tomogr. 2020 Sep/Oct;44(5):704-707. doi: 10.1097/RCT.0000000000001050. J Comput Assist Tomogr. 2020. PMID: 32842072

4

Preoperative computed tomography scan may fail to predict perilymphatic gusher.

Krouchi L, Callonnec F, Bouchetemblé P, Tollard E, Dehesdin D, Marie JP. Krouchi L, et al. Ann Otol Rhinol Laryngol. 2013 Jun;122(6):374-7. doi: 10.1177/000348941312200605. Ann Otol Rhinol Laryngol. 2013. PMID: 23837389

5

Study of complex structural variations of X-linked deafness-2 based on single-molecule sequencing.

Jiang Y, Wu L, Huang S, Li P, Gao B, Yuan Y, Zhang S, Yu G, Gao Y, Wu H, Dai P. Jiang Y, et al. Biosci Rep. 2021 Jun 25;41(6):BSR20203740. doi: 10.1042/BSR20203740. Biosci Rep. 2021. PMID: 33860785 Free PMC article.

6

Hypothalamic malformations in patients with X-linked deafness and incomplete partition type 3.

Siddiqui A, D'Amico A, Colafati GS, Cicala D, Talenti G, Rajput K, Pinelli L, D'Arco F. Siddiqui A, et al. Neuroradiology. 2019 Aug;61(8):949-952. doi: 10.1007/s00234-019-02230-z. Epub 2019 Jun 8. Neuroradiology. 2019. PMID: 31177298

7

Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families.

Su Y, Gao X, Huang SS, Mao JN, Huang BQ, Zhao JD, Kang DY, Zhang X, Dai P. Su Y, et al. BMC Med Genet. 2018 Sep 4;19(1):157. doi: 10.1186/s12881-018-0630-9. BMC Med Genet. 2018. PMID: 30176854 Free PMC article.

8

Hypothalamic hamartomas and inner ear diverticula with X-linked stapes gusher syndrome - new associations?

Anderson EA, Özütemiz C, Miller BS, Moss TJ, Nascene DR. Anderson EA, et al. Pediatr Radiol. 2020 Jan;50(1):142-145. doi: 10.1007/s00247-019-04497-z. Epub 2019 Aug 22. Pediatr Radiol. 2020. PMID: 31440883

9

A novel pathogenic variant c.975G>A (p.Trp325*) in the POU3F4 gene in Yakut family (Eastern Siberia, Russia) with the X-linked deafness-2 (DFNX2).

Barashkov NA, Klarov LA, Teryutin FM, Solovyev AV, Pshennikova VG, Konnikova EE, Romanov GP, Tobokhov AV, Morozov IV, Bondar AA, Posukh OL, Dzhemileva LU, Tomsky MI, Khusnutdinova EK, Fedorova SA. Barashkov NA, et al. Int J Pediatr Otorhinolaryngol. 2018 Jan;104:94-97. doi: 10.1016/j.ijporl.2017.11.001. Epub 2017 Nov 6. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29287890

10

X-linked deafness-2 (DFNX2) phenotype associated with a paracentric inversion upstream of POU3F4.

Anger GJ, Crocker S, McKenzie K, Brown KK, Morton CC, Harrison K, MacKenzie JJ. Anger GJ, et al. Am J Audiol. 2014 Mar;23(1):1-6. doi: 10.1044/1059-0889(2013/13-0018). Am J Audiol. 2014. PMID: 24096866 Free PMC article.

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