Abu-Amero KK - Search Results

1

Assessing mitochondrial DNA nucleotide changes in spontaneous optic neuropathies.

Bosley TM, Abu-Amero KK. Bosley TM, et al. Ophthalmic Genet. 2010 Dec;31(4):163-72. doi: 10.3109/13816810.2010.514015. Ophthalmic Genet. 2010. PMID: 21067478

2

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.

3

Increased relative mitochondrial DNA content in leucocytes of patients with NAION.

Abu-Amero KK, Bosley TM. Abu-Amero KK, et al. Br J Ophthalmol. 2006 Jul;90(7):823-5. doi: 10.1136/bjo.2006.090332. Epub 2006 Mar 15. Br J Ophthalmol. 2006. PMID: 16540486 Free PMC article.

4

GSTM1 and GSTT1 deletion genotypes in various spontaneous optic neuropathies in Arabs.

Abu-Amero KK, Milcarek B, Bosley TM. Abu-Amero KK, et al. Br J Ophthalmol. 2009 Aug;93(8):1101-4. doi: 10.1136/bjo.2008.152983. Epub 2009 Mar 13. Br J Ophthalmol. 2009. PMID: 19286687

5

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

6

The role of mitochondrial haplogroups in non-arteritic anterior ischemic optic neuropathy.

Abu-Amero KK, Larruga JM, González AM, Bosley TM. Abu-Amero KK, et al. Ophthalmic Genet. 2008 Sep;29(3):111-6. doi: 10.1080/13816810802183748. Ophthalmic Genet. 2008. PMID: 18766989

7

Genome-wide expression profile of LHON patients with the 11778 mutation.

Abu-Amero KK, Jaber M, Hellani A, Bosley TM. Abu-Amero KK, et al. Br J Ophthalmol. 2010 Feb;94(2):256-9. doi: 10.1136/bjo.2009.165571. Epub 2009 Sep 1. Br J Ophthalmol. 2010. PMID: 19726426

8

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. Ophthalmic Genet. 2010 Mar;31(1):1-11. doi: 10.3109/13816810903312535. Ophthalmic Genet. 2010. PMID: 20141352

9

Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy.

Abu-Amero KK, Hellani A, Salih MA, Alorainy IA, Zidan G, Kern KC, Sicotte NL, Bosley TM. Abu-Amero KK, et al. Ophthalmic Genet. 2010 Sep;31(3):147-54. doi: 10.3109/13816810.2010.492817. Ophthalmic Genet. 2010. PMID: 20565246

10

Horizontal gaze palsy and progressive scoliosis without ROBO3 mutations.

Abu-Amero KK, Faletra F, Gasparini P, Parentin F, Pensiero S, Alorainy IA, Hellani AM, Catalano D, Bosley TM. Abu-Amero KK, et al. Ophthalmic Genet. 2011 Nov;32(4):212-6. doi: 10.3109/13816810.2011.574186. Epub 2011 Apr 21. Ophthalmic Genet. 2011. PMID: 21510772

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