Brosnahan D - Search Results

1

Atypical Alstrom syndrome with novel ALMS1 mutations precluded by current diagnostic criteria.

Casey J, McGettigan P, Brosnahan D, Curtis E, Treacy E, Ennis S, Lynch SA. Casey J, et al. Among authors: brosnahan d. Eur J Med Genet. 2014 Feb;57(2-3):55-9. doi: 10.1016/j.ejmg.2014.01.007. Epub 2014 Feb 3. Eur J Med Genet. 2014. PMID: 24503146

2

Septo-optic dysplasia with digital anomalies--a recurrent pattern syndrome.

Harrison IM, Brosnahan D, Phelan E, Fitzgerald RJ, Reardon W. Harrison IM, et al. Among authors: brosnahan d. Am J Med Genet A. 2004 Nov 15;131(1):82-5. doi: 10.1002/ajmg.a.30309. Am J Med Genet A. 2004. PMID: 15368481 Review.

3

Paediatric cataract in the uveitis setting.

O'Rourke M, McCreery K, Kilmartin D, Brosnahan D. O'Rourke M, et al. Among authors: brosnahan d. Eur J Ophthalmol. 2021 Sep;31(5):2651-2658. doi: 10.1177/1120672120962059. Epub 2020 Oct 7. Eur J Ophthalmol. 2021. PMID: 33023329

4

Type VI syndactyly with skeletal dysplasia: a new syndrome?

Sasaki E, Phelan E, Brenner C, Brosnahan D, Reardon W. Sasaki E, et al. Among authors: brosnahan d. Clin Dysmorphol. 2019 Jan;28(1):30-34. doi: 10.1097/MCD.0000000000000238. Clin Dysmorphol. 2019. PMID: 30138139 No abstract available.

5

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in the Irish population.

Dominguez M, Crushell E, Ilmarinen T, McGovern E, Collins S, Chang B, Fleming P, Irvine AD, Brosnahan D, Ulmanen I, Murphy N, Costigan C. Dominguez M, et al. Among authors: brosnahan d. J Pediatr Endocrinol Metab. 2006 Nov;19(11):1343-52. doi: 10.1515/jpem.2006.19.11.1343. J Pediatr Endocrinol Metab. 2006. PMID: 17220063

6

Retinal vasculopathy in autosomal dominant dyskeratosis congenita due to TINF2 mutation.

Gleeson M, O'Marcaigh A, Cotter M, Brosnahan D, Vulliamy T, Smith OP. Gleeson M, et al. Among authors: brosnahan d. Br J Haematol. 2012 Dec;159(5):498. doi: 10.1111/bjh.12088. Epub 2012 Oct 24. Br J Haematol. 2012. PMID: 23094712 Free article. No abstract available.

7

Bilateral optic disk swelling in the 4q34 deletion syndrome.

Connell P, Brosnahan D, Dunlop A, Reardon W. Connell P, et al. Among authors: brosnahan d. J AAPOS. 2007 Oct;11(5):516-8. doi: 10.1016/j.jaapos.2007.05.009. J AAPOS. 2007. PMID: 17933677

8

Oculo-facio-cardio-dental syndrome in a mother and daughter.

McGovern E, Al-Mudaffer M, McMahon C, Brosnahan D, Fleming P, Reardon W. McGovern E, et al. Among authors: brosnahan d. Int J Oral Maxillofac Surg. 2006 Nov;35(11):1060-2. doi: 10.1016/j.ijom.2006.05.001. Epub 2006 Jul 10. Int J Oral Maxillofac Surg. 2006. PMID: 16829040

9

Characterization of optical coherence topography findings in Kenny-Caffey syndrome.

Timoney P, Darcy F, McCreery K, Reardon W, Brosnahan D. Timoney P, et al. Among authors: brosnahan d. J AAPOS. 2007 Jun;11(3):291-3. doi: 10.1016/j.jaapos.2006.09.020. Epub 2007 Mar 13. J AAPOS. 2007. PMID: 17360206

10

Ocular complications of autoimmune polyendocrinopathy syndrome type 1.

Chang B, Brosnahan D, McCreery K, Dominguez M, Costigan C. Chang B, et al. Among authors: brosnahan d. J AAPOS. 2006 Dec;10(6):515-20. doi: 10.1016/j.jaapos.2006.06.018. Epub 2006 Nov 2. J AAPOS. 2006. PMID: 17189144

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