Bosley TM - Search Results

1

A newly recognized autosomal recessive syndrome affecting neurologic function and vision.

Salih MA, Tzschach A, Oystreck DT, Hassan HH, AlDrees A, Elmalik SA, El Khashab HY, Wienker TF, Abu-Amero KK, Bosley TM. Salih MA, et al. Among authors: bosley tm. Am J Med Genet A. 2013 Jun;161A(6):1207-13. doi: 10.1002/ajmg.a.35850. Epub 2013 Apr 30. Am J Med Genet A. 2013. PMID: 23633300

2

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.

3

Molecular and neurological characterizations of three Saudi families with lipoid proteinosis.

Salih MA, Abu-Amero KK, Alrasheed S, Alorainy IA, Liu L, McGrath JA, Van Maldergem L, Al-Faky YH, AlSuhaibani AH, Oystreck DT, Bosley TM. Salih MA, et al. Among authors: bosley tm. BMC Med Genet. 2011 Feb 24;12:31. doi: 10.1186/1471-2350-12-31. BMC Med Genet. 2011. PMID: 21349189 Free PMC article.

4

Retinal Dysfunction in Patients with Congenital Fibrosis of the Extraocular Muscles Type 2.

Khan AO, Almutlaq M, Oystreck DT, Engle EC, Abu-Amero K, Bosley T. Khan AO, et al. Ophthalmic Genet. 2016 Jun;37(2):130-6. doi: 10.3109/13816810.2014.926942. Epub 2014 Jun 18. Ophthalmic Genet. 2016. PMID: 24940936 Free PMC article.

5

Duane retraction syndrome in a patient with Duchenne muscular dystrophy.

Bosley TM, Salih MA, Alkhalidi H, Oystreck DT, El Khashab HY, Kondkar AA, Abu-Amero KK. Bosley TM, et al. Ophthalmic Genet. 2016 Sep;37(3):276-80. doi: 10.3109/13816810.2015.1039139. Epub 2016 Feb 5. Ophthalmic Genet. 2016. PMID: 26849454

6

The genetics of nonsyndromic bilateral Duane retraction syndrome.

Abu-Amero KK, Khan AO, Oystreck DT, Kondkar AA, Bosley TM. Abu-Amero KK, et al. Among authors: bosley tm. J AAPOS. 2016 Oct;20(5):396-400.e2. doi: 10.1016/j.jaapos.2016.06.008. Epub 2016 Sep 20. J AAPOS. 2016. PMID: 27658539

7

Mitochondrial abnormalities in patients with LHON-like optic neuropathies.

Abu-Amero KK, Bosley TM. Abu-Amero KK, et al. Among authors: bosley tm. Invest Ophthalmol Vis Sci. 2006 Oct;47(10):4211-20. doi: 10.1167/iovs.06-0295. Invest Ophthalmol Vis Sci. 2006. PMID: 17003408

8

Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities.

Bosley TM, Brodsky MC, Glasier CM, Abu-Amero KK. Bosley TM, et al. Invest Ophthalmol Vis Sci. 2008 Dec;49(12):5250-6. doi: 10.1167/iovs.08-2193. Epub 2008 Aug 1. Invest Ophthalmol Vis Sci. 2008. PMID: 18676632

9

Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations.

Abu-Amero KK, al Dhalaan H, al Zayed Z, Hellani A, Bosley TM. Abu-Amero KK, et al. Among authors: bosley tm. J Neurol Sci. 2009 Jan 15;276(1-2):22-6. doi: 10.1016/j.jns.2008.08.026. Epub 2008 Oct 1. J Neurol Sci. 2009. PMID: 18829051

10

Ophthalmologic abnormalities in a de novo terminal 6q deletion.

Abu-Amero KK, Hellani A, Salih MA, Al Hussain A, al Obailan M, Zidan G, Alorainy IA, Bosley TM. Abu-Amero KK, et al. Among authors: bosley tm. Ophthalmic Genet. 2010 Mar;31(1):1-11. doi: 10.3109/13816810903312535. Ophthalmic Genet. 2010. PMID: 20141352

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