Murphy E - Search Results

1

Mucolipidosis type III, a series of adult patients.

Oussoren E, van Eerd D, Murphy E, Lachmann R, van der Meijden JC, Hoefsloot LH, Verdijk R, Ruijter GJG, Maas M, Hollak CEM, Langendonk JG, van der Ploeg AT, Langeveld M. Oussoren E, et al. Among authors: murphy e. J Inherit Metab Dis. 2018 Sep;41(5):839-848. doi: 10.1007/s10545-018-0186-z. Epub 2018 Apr 27. J Inherit Metab Dis. 2018. PMID: 29704188 Free PMC article.

2

The longest-surviving patient with classical maple syrup urine disease.

le Roux C, Murphy E, Lilburn M, Lee PJ. le Roux C, et al. Among authors: murphy e. J Inherit Metab Dis. 2006 Feb;29(1):190-4. doi: 10.1007/s10545-006-0204-4. J Inherit Metab Dis. 2006. PMID: 16601890

3

Neuropsychometric outcome predictors for adults with maple syrup urine disease.

le Roux C, Murphy E, Hallam P, Lilburn M, Orlowska D, Lee P. le Roux C, et al. Among authors: murphy e. J Inherit Metab Dis. 2006 Feb;29(1):201-2. doi: 10.1007/s10545-006-0223-1. J Inherit Metab Dis. 2006. PMID: 16601892

4

Dietary treatment of phenylketonuria: the effect of phenylalanine on reaction time.

Dawson C, Murphy E, Maritz C, Chan H, Ellerton C, Carpenter RH, Lachmann RH. Dawson C, et al. Among authors: murphy e. J Inherit Metab Dis. 2011 Apr;34(2):449-54. doi: 10.1007/s10545-010-9276-2. Epub 2011 Feb 3. J Inherit Metab Dis. 2011. PMID: 21290182

5

Movement disorders in adult surviving patients with maple syrup urine disease.

Carecchio M, Schneider SA, Chan H, Lachmann R, Lee PJ, Murphy E, Bhatia KP. Carecchio M, et al. Among authors: murphy e. Mov Disord. 2011 Jun;26(7):1324-8. doi: 10.1002/mds.23629. Epub 2011 Apr 11. Mov Disord. 2011. PMID: 21484869 Free PMC article.

6

Incidence and predictors of anti-bradycardia pacing in patients with Anderson-Fabry disease.

O'Mahony C, Coats C, Cardona M, Garcia A, Calcagnino M, Murphy E, Lachmann R, Mehta A, Hughes D, Elliott PM. O'Mahony C, et al. Among authors: murphy e. Europace. 2011 Dec;13(12):1781-8. doi: 10.1093/europace/eur267. Epub 2011 Aug 18. Europace. 2011. PMID: 21856674

7

A series of pregnancies in women with inherited metabolic disease.

Langendonk JG, Roos JC, Angus L, Williams M, Karstens FP, de Klerk JB, Maritz C, Ben-Omran T, Williamson C, Lachmann RH, Murphy E. Langendonk JG, et al. Among authors: murphy e. J Inherit Metab Dis. 2012 May;35(3):419-24. doi: 10.1007/s10545-011-9389-2. Epub 2011 Sep 15. J Inherit Metab Dis. 2012. PMID: 21918856

8

Pregnancy and its management in women with GSD type III - a single centre experience.

Ramachandran R, Wedatilake Y, Coats C, Walker F, Elliott P, Lee PJ, Lachmann RH, Murphy E. Ramachandran R, et al. Among authors: murphy e. J Inherit Metab Dis. 2012 Mar;35(2):245-51. doi: 10.1007/s10545-011-9384-7. Epub 2011 Sep 7. J Inherit Metab Dis. 2012. PMID: 21947574

9

Role of serum N-terminal pro-brain natriuretic peptide measurement in diagnosis of cardiac involvement in patients with anderson-fabry disease.

Coats CJ, Parisi V, Ramos M, Janagarajan K, O'Mahony C, Dawnay A, Lachmann RH, Murphy E, Mehta A, Hughes D, Elliott PM. Coats CJ, et al. Among authors: murphy e. Am J Cardiol. 2013 Jan 1;111(1):111-7. doi: 10.1016/j.amjcard.2012.08.055. Epub 2012 Oct 4. Am J Cardiol. 2013. PMID: 23040658

10

Atypical parkinsonism and cerebrotendinous xanthomatosis: report of a family with corticobasal syndrome and a literature review.

Rubio-Agusti I, Kojovic M, Edwards MJ, Murphy E, Chandrashekar HS, Lachmann RH, Bhatia KP. Rubio-Agusti I, et al. Among authors: murphy e. Mov Disord. 2012 Dec;27(14):1769-74. doi: 10.1002/mds.25229. Epub 2012 Nov 2. Mov Disord. 2012. PMID: 23124517 Review.

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