Similar articles for PMID: 20075099

Year	Number of Results
1978	1
1997	1
1998	1
1999	2
2001	3
2002	3
2003	5
2004	2
2005	6
2006	3
2007	6
2008	9
2009	4
2010	7
2011	2
2012	5
2013	5
2014	9
2015	6
2016	6
2017	6
2018	3
2019	4
2020	6
2021	2
2024	0

1

Bilateral complete labyrinthine aplasia with bilateral internal carotid artery aplasia, developmental delay, and gaze abnormalities: a presumptive case of a rare HOXA1 mutation syndrome.

Higley MJ, Walkiewicz TW, Miller JH, Curran JG, Towbin RB. Higley MJ, et al. AJNR Am J Neuroradiol. 2011 Feb;32(2):E23-5. doi: 10.3174/ajnr.A1969. Epub 2010 Jan 14. AJNR Am J Neuroradiol. 2011. PMID: 20075099 Free PMC article.

2

Clinical characterization of the HOXA1 syndrome BSAS variant.

Bosley TM, Salih MA, Alorainy IA, Oystreck DT, Nester M, Abu-Amero KK, Tischfield MA, Engle EC. Bosley TM, et al. Neurology. 2007 Sep 18;69(12):1245-53. doi: 10.1212/01.wnl.0000276947.59704.cf. Neurology. 2007. PMID: 17875913 Free PMC article.

3

Bosley-Salih-Alorainy syndrome in patients from India.

Patil SJ, Karthik GA, Bhavani GS, Bhat V, Matalia J, Shah J, Shukla A, Girisha KM. Patil SJ, et al. Am J Med Genet A. 2020 Nov;182(11):2699-2703. doi: 10.1002/ajmg.a.61809. Epub 2020 Aug 31. Am J Med Genet A. 2020. PMID: 32864817

4

Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder.

Abu-Amero KK, Kondkar AA, Salih MA, Alorainy IA, Khan AO, Oystreck DT, Bosley TM. Abu-Amero KK, et al. Ophthalmic Genet. 2013 Mar-Jun;34(1-2):90-6. doi: 10.3109/13816810.2012.718850. Epub 2012 Sep 6. Ophthalmic Genet. 2013. PMID: 22950449

5

Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development.

Tischfield MA, Bosley TM, Salih MA, Alorainy IA, Sener EC, Nester MJ, Oystreck DT, Chan WM, Andrews C, Erickson RP, Engle EC. Tischfield MA, et al. Nat Genet. 2005 Oct;37(10):1035-7. doi: 10.1038/ng1636. Epub 2005 Sep 11. Nat Genet. 2005. PMID: 16155570

6

The clinical spectrum of homozygous HOXA1 mutations.

Bosley TM, Alorainy IA, Salih MA, Aldhalaan HM, Abu-Amero KK, Oystreck DT, Tischfield MA, Engle EC, Erickson RP. Bosley TM, et al. Am J Med Genet A. 2008 May 15;146A(10):1235-40. doi: 10.1002/ajmg.a.32262. Am J Med Genet A. 2008. PMID: 18412118 Free PMC article.

7

Athabascan brainstem dysgenesis syndrome.

Holve S, Friedman B, Hoyme HE, Tarby TJ, Johnstone SJ, Erickson RP, Clericuzio CL, Cunniff C. Holve S, et al. Am J Med Genet A. 2003 Jul 15;120A(2):169-73. doi: 10.1002/ajmg.a.20087. Am J Med Genet A. 2003. PMID: 12833395

8

Wildervanck's syndrome with severe inner ear dysplasia and agenesis of the right internal carotid artery.

Hernando M, Urbasos M, Amarillo VE, Herrera MT, García-Peces V, Plaza G. Hernando M, et al. Int J Pediatr Otorhinolaryngol. 2014 Apr;78(4):704-6. doi: 10.1016/j.ijporl.2014.01.036. Epub 2014 Feb 7. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24576452

9

Complete labyrinthine aplasia: clinical and radiologic findings with review of the literature.

Ozgen B, Oguz KK, Atas A, Sennaroglu L. Ozgen B, et al. AJNR Am J Neuroradiol. 2009 Apr;30(4):774-80. doi: 10.3174/ajnr.A1426. Epub 2009 Jan 15. AJNR Am J Neuroradiol. 2009. PMID: 19147720 Free PMC article. Review.

10

HOXA1 Mutations are Not Commonly Associated with Non-Syndromic Deafness.

Abu-Amero KK, Hagr Aa, Almomani MO, Azad TA, Alorainy IA, Oystreck DT, Bosley TM. Abu-Amero KK, et al. Can J Neurol Sci. 2014 Jul;41(4):448-51. doi: 10.1017/s0317167100018473. Can J Neurol Sci. 2014. PMID: 24878468

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