Lynch T - Search Results

1

Fatal presentation of ornithine transcarbamylase deficiency in a 62-year-old man and family studies.

Rohininath T, Costello DJ, Lynch T, Monavari A, Tuchman M, Treacy EP. Rohininath T, et al. Among authors: lynch t. J Inherit Metab Dis. 2004;27(2):285-8. doi: 10.1023/b:boli.0000028840.97261.c6. J Inherit Metab Dis. 2004. PMID: 15243986

2

Audit of an inpatient neurology consultation service in a tertiary referral centre: value of the consulting neurologist.

Costello DJ, Renganathan R, O'Hare A, Murray B, Lynch T. Costello DJ, et al. Among authors: lynch t. Ir Med J. 2005 May;98(5):134-7. Ir Med J. 2005. PMID: 16010778

3

Asymmetrical leg atrophy in levodopa-responsive dystonia due to a novel GTP cyclohydrolase mutation.

Mulroy E, McCarthy A, Lynch T, Costello D, Ross OA. Mulroy E, et al. Among authors: lynch t. Mov Disord. 2014 Mar;29(3):425-6. doi: 10.1002/mds.25813. Epub 2014 Jan 28. Mov Disord. 2014. PMID: 24474670 Free PMC article. No abstract available.

4

Age at onset as a factor in determining the phenotype of primary torsion dystonia.

O'Riordan S, Raymond D, Lynch T, Saunders-Pullman R, Bressman SB, Daly L, Hutchinson M. O'Riordan S, et al. Among authors: lynch t. Neurology. 2004 Oct 26;63(8):1423-6. doi: 10.1212/01.wnl.0000142035.26034.c2. Neurology. 2004. PMID: 15505159

5

Primary torsion dystonia due to the Tor1A GAG deletion in an Irish family.

O'Riordan S, Cockburn D, Barton D, Lynch T, Hutchinson M. O'Riordan S, et al. Among authors: lynch t. Ir J Med Sci. 2002 Jan-Mar;171(1):31-2. doi: 10.1007/BF03168938. Ir J Med Sci. 2002. PMID: 11993591

6

Inherited myoclonus-dystonia and epilepsy: further evidence of an association?

O'Riordan S, Ozelius LJ, de Carvalho Aguiar P, Hutchinson M, King M, Lynch T. O'Riordan S, et al. Among authors: lynch t. Mov Disord. 2004 Dec;19(12):1456-9. doi: 10.1002/mds.20224. Mov Disord. 2004. PMID: 15389977

7

Closing the tau loop: the missing tau mutation.

McCarthy A, Lonergan R, Olszewska DA, O'Dowd S, Cummins G, Magennis B, Fallon EM, Pender N, Huey ED, Cosentino S, O'Rourke K, Kelly BD, O'Connell M, Delon I, Farrell M, Spillantini MG, Rowland LP, Fahn S, Craig P, Hutton M, Lynch T. McCarthy A, et al. Among authors: lynch t. Brain. 2015 Oct;138(Pt 10):3100-9. doi: 10.1093/brain/awv234. Epub 2015 Aug 21. Brain. 2015. PMID: 26297556 Free PMC article.

8

Clinicopathological features of the tauopathies.

Murray B, Lynch T, Farrell M. Murray B, et al. Among authors: lynch t. Biochem Soc Trans. 2005 Aug;33(Pt 4):595-9. doi: 10.1042/BST0330595. Biochem Soc Trans. 2005. PMID: 16042552 Review.

9

Is PARK10 a Locus for Familial PD? Yes or No?

Olszewska DA, Lynch T. Olszewska DA, et al. Among authors: lynch t. Mov Disord. 2016 Jul;31(7):970. doi: 10.1002/mds.26612. Epub 2016 Apr 19. Mov Disord. 2016. PMID: 27090980 No abstract available.

10

MUL1-A new potential for a therapeutic target for Parkinson's disease a commentary on "MUL1 acts in parallel to the PINK1/parkin pathway in regulating mitofusin and compensates for loss of PINK1/parkin" by Yun and colleagues (eLife 2014; 3: 1-26).

Olszewska DA, Lynch T. Olszewska DA, et al. Among authors: lynch t. Mov Disord. 2016 Jul;31(7):1037. doi: 10.1002/mds.26652. Epub 2016 Apr 29. Mov Disord. 2016. PMID: 27126246 No abstract available.

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