Bosley TM[au] - Search Results

Year	Number of Results
1978	1
1979	1
1980	1
1982	1
1983	2
1984	1
1985	8
1986	3
1987	6
1988	7
1989	13
1990	10
1991	5
1992	4
1993	4
1994	5
1995	6
1998	1
1999	1
2000	2
2001	2
2002	2
2003	3
2004	3
2005	5
2006	5
2007	7
2008	8
2009	7
2010	8
2011	10
2012	9
2013	11
2014	6
2015	6
2016	7
2017	3
2018	1
2019	1
2021	2
2022	0

1

Exceptions to the Valsalva doctrine.

Schutta HS, Abu-Amero KK, Bosley TM. Schutta HS, et al. Among authors: bosley tm. Neurology. 2010 Jan 26;74(4):329-35. doi: 10.1212/WNL.0b013e3181cbcd84. Neurology. 2010. PMID: 20101039 Review.

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

Optic Neuritis Associated With Tumor Necrosis Factor-Alpha Inhibitor Certolizumab.

Chen A, Miller NR, Bosley TM. Chen A, et al. Among authors: bosley tm. J Neuroophthalmol. 2021 Dec 1;41(4):e713-e714. doi: 10.1097/WNO.0000000000001150. J Neuroophthalmol. 2021. PMID: 33394638 No abstract available.

4

Congenital cranial dysinnervation disorders: a concept in evolution.

Bosley TM, Abu-Amero KK, Oystreck DT. Bosley TM, et al. Curr Opin Ophthalmol. 2013 Sep;24(5):398-406. doi: 10.1097/ICU.0b013e3283645ad6. Curr Opin Ophthalmol. 2013. PMID: 23872818 Review.

5

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.

6

When straight eyes won't move: phenotypic overlap of genetically distinct ocular motility disturbances.

Oystreck DT, Salih MA, Bosley TM. Oystreck DT, et al. Among authors: bosley tm. Can J Ophthalmol. 2011 Dec;46(6):477-80. doi: 10.1016/j.jcjo.2011.09.009. Can J Ophthalmol. 2011. PMID: 22153632

7

Recent progress in understanding congenital cranial dysinnervation disorders.

Oystreck DT, Engle EC, Bosley TM. Oystreck DT, et al. Among authors: bosley tm. J Neuroophthalmol. 2011 Mar;31(1):69-77. doi: 10.1097/WNO.0b013e31820d0756. J Neuroophthalmol. 2011. PMID: 21317732 Free PMC article. Review.

8

Retrospective review of visual outcome in operated lens subluxation.

Alzuhairy SA, Bosley TM, Alotaibi AG. Alzuhairy SA, et al. Among authors: bosley tm. Saudi Med J. 2013 Oct;34(10):1030-4. Saudi Med J. 2013. PMID: 24145937 Review.

9

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. Among authors: bosley tm. 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

10

The results of radiotherapy for orbital pseudotumor.

Lanciano R, Fowble B, Sergott RC, Atlas S, Savino PJ, Bosley TM, Rubenstein J. Lanciano R, et al. Among authors: bosley tm. Int J Radiat Oncol Biol Phys. 1990 Feb;18(2):407-11. doi: 10.1016/0360-3016(90)90108-v. Int J Radiat Oncol Biol Phys. 1990. PMID: 2406229 Review.

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