Ryan F - Search Results

1

Ret-proto-oncogene analysis in medullary thyroid carcinoma.

O'Keeffe DA, Hill AD, Sheahan K, Ryan F, Barton D, Fitzgerald RJ, McDermott EW, O'Higgins NJ. O'Keeffe DA, et al. Among authors: ryan f. Ir J Med Sci. 1998 Oct-Dec;167(4):226-30. doi: 10.1007/BF02937418. Ir J Med Sci. 1998. PMID: 9868860

2

Detection of five common CFTR mutations by rapid-cycle real-time amplification refractory mutation system PCR.

Dempsey E, Barton DE, Ryan F. Dempsey E, et al. Among authors: ryan f. Clin Chem. 2004 Apr;50(4):773-5. doi: 10.1373/clinchem.2003.030445. Clin Chem. 2004. PMID: 15044340 No abstract available.

3

Mosaicism for trisomy 3q arising from an unbalanced, de novo t(3;15).

Stallings R, Vaughn D, Hall K, Joyce C, Ryan F, Barton D, Geraghty M. Stallings R, et al. Among authors: ryan f. J Med Genet. 1997 Jun;34(6):512-4. doi: 10.1136/jmg.34.6.512. J Med Genet. 1997. PMID: 9192276 Free PMC article.

4

Typical Friedreich's ataxia without GAA expansions and GAA expansion without typical Friedreich's ataxia.

McCabe DJ, Ryan F, Moore DP, McQuaid S, King MD, Kelly A, Daly K, Barton DE, Murphy RP. McCabe DJ, et al. Among authors: ryan f. J Neurol. 2000 May;247(5):346-55. doi: 10.1007/s004150050601. J Neurol. 2000. PMID: 10896266

5

Development and validation of a novel PCR-RFLP based method for the detection of 3 primary mitochondrial mutations in Leber's hereditary optic neuropathy patients.

Eustace Ryan S, Ryan F, Barton D, O'Dwyer V, Neylan D. Eustace Ryan S, et al. Among authors: ryan f. Eye Vis (Lond). 2015 Oct 25;2:18. doi: 10.1186/s40662-015-0028-0. eCollection 2015. Eye Vis (Lond). 2015. PMID: 26605371 Free PMC article.

6

Hyperinsulinism: molecular aetiology of focal disease.

Ryan F, Devaney D, Joyce C, Nestorowicz A, Permutt MA, Glaser B, Barton DE, Thornton PS. Ryan F, et al. Arch Dis Child. 1998 Nov;79(5):445-7. doi: 10.1136/adc.79.5.445. Arch Dis Child. 1998. PMID: 10193261 Free PMC article.

7

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.

Glaser B, Ryan F, Donath M, Landau H, Stanley CA, Baker L, Barton DE, Thornton PS. Glaser B, et al. Among authors: ryan f. Diabetes. 1999 Aug;48(8):1652-7. doi: 10.2337/diabetes.48.8.1652. Diabetes. 1999. PMID: 10426386

8

Intrafamilial phenotypic variability in Friedreich ataxia associated with a G130V mutation in the FRDA gene.

McCabe DJ, Wood NW, Ryan F, Hanna MG, Connolly S, Moore DP, Redmond J, Barton DE, Murphy RP. McCabe DJ, et al. Among authors: ryan f. Arch Neurol. 2002 Feb;59(2):296-300. doi: 10.1001/archneur.59.2.296. Arch Neurol. 2002. PMID: 11843702

9

Haemochromatosis mutation analysis in a normal Irish population.

Ryan F, Vaughan J. Ryan F, et al. Br J Biomed Sci. 2000;57(4):315-6. Br J Biomed Sci. 2000. PMID: 11204863 No abstract available.

10

A real-time ARMS PCR/high-resolution melt curve assay for the detection of the three primary mitochondrial mutations in Leber's hereditary optic neuropathy.

Ryan SE, Ryan F, O'Dwyer V, Neylan D. Ryan SE, et al. Among authors: ryan f. Mol Vis. 2016 Oct 12;22:1169-1175. eCollection 2016. Mol Vis. 2016. PMID: 27746671 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

400 results

Search Page

Filters