Nuala Murphy - Search Results

Year	Number of Results
2002	2
2003	2
2004	4
2005	1
2006	2
2009	3
2010	1
2011	1
2012	4
2013	4
2014	3
2015	4
2016	3
2017	3
2018	7
2019	4
2021	2
2022	4
2023	3
2024	3

1

Children and young people's experiences and perceptions of self-management of type 1 diabetes: A qualitative meta-synthesis.

Tuohy E, Rawdon C, Gallagher P, Glacken M, Murphy N, Swallow V, Lambert V. Tuohy E, et al. Among authors: murphy n. Health Psychol Open. 2019 Sep 18;6(2):2055102919877105. doi: 10.1177/2055102919877105. eCollection 2019 Jul-Dec. Health Psychol Open. 2019. PMID: 31555459 Free PMC article. Review.

2

Towards evidence based medicine for paediatricians. Question 2. What is the ideal dose of vitamin D supplementation for term neonates?

Onwuneme C, Carroll A, McCarthy R, Kilbane M, McKenna M, Murphy N, Molloy EJ. Onwuneme C, et al. Among authors: murphy n. Arch Dis Child. 2012 Apr;97(4):387-9. doi: 10.1136/archdischild-2011-301764. Arch Dis Child. 2012. PMID: 22448000 Review. No abstract available.

3

An overview of the nursing issues involved in caring for a child with adrenal insufficiency.

Moloney S, Murphy N, Collin J. Moloney S, et al. Among authors: murphy n. Nurs Child Young People. 2015 Sep;27(7):28-36. doi: 10.7748/ncyp.27.7.28.e609. Nurs Child Young People. 2015. PMID: 26360180 Review.

4

The presentation of congenital adrenal hyperplasia in an unscreened population.

Conlon TA, Hawkes CP, Brady JJ, Murphy NP. Conlon TA, et al. Among authors: murphy np. J Pediatr Endocrinol Metab. 2021 Jun 25;34(9):1123-1129. doi: 10.1515/jpem-2021-0123. Print 2021 Sep 27. J Pediatr Endocrinol Metab. 2021. PMID: 34167176

5

A realist synthesis of multicentre comparative audit implementation: exploring what works and in which healthcare contexts.

McGlacken-Byrne SM, Murphy NP, Barry S. McGlacken-Byrne SM, et al. Among authors: murphy np. BMJ Open Qual. 2024 Mar 5;13(1):e002629. doi: 10.1136/bmjoq-2023-002629. BMJ Open Qual. 2024. PMID: 38448042 Free PMC article. Review.

6

Parents' perspectives of factors affecting parent-adolescent communication about type 1 diabetes and negotiation of self-management responsibilities.

Rawdon C, Kilcullen SM, Murphy N, Swallow V, Gallagher P, Lambert V. Rawdon C, et al. Among authors: murphy n. J Child Health Care. 2022 Dec 18:13674935221146009. doi: 10.1177/13674935221146009. Online ahead of print. J Child Health Care. 2022. PMID: 36529483 Free article.

7

Secondary Hyperparathyroidism in Children with Mucolipidosis Type II (I-Cell Disease): Irish Experience.

Boruah R, Monavari AA, Conlon T, Murphy N, Stroiescu A, Ryan S, Hughes J, Knerr I, McDonnell C, Crushell E. Boruah R, et al. Among authors: murphy n. J Clin Med. 2022 Mar 2;11(5):1366. doi: 10.3390/jcm11051366. J Clin Med. 2022. PMID: 35268460 Free PMC article.

8

DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency.

Logan CV, Murray JE, Parry DA, Robertson A, Bellelli R, Tarnauskaitė Ž, Challis R, Cleal L, Borel V, Fluteau A, Santoyo-Lopez J; SGP Consortium; Aitman T, Barroso I, Basel D, Bicknell LS, Goel H, Hu H, Huff C, Hutchison M, Joyce C, Knox R, Lacroix AE, Langlois S, McCandless S, McCarrier J, Metcalfe KA, Morrissey R, Murphy N, Netchine I, O'Connell SM, Olney AH, Paria N, Rosenfeld JA, Sherlock M, Syverson E, White PC, Wise C, Yu Y, Zacharin M, Banerjee I, Reijns M, Bober MB, Semple RK, Boulton SJ, Rios JJ, Jackson AP. Logan CV, et al. Among authors: murphy n. Am J Hum Genet. 2018 Dec 6;103(6):1038-1044. doi: 10.1016/j.ajhg.2018.10.024. Epub 2018 Nov 29. Am J Hum Genet. 2018. PMID: 30503519 Free PMC article.

9

Incidence of Congenital Hypothyroidism Over 37 Years in Ireland.

McGrath N, Hawkes CP, McDonnell CM, Cody D, O'Connell SM, Mayne PD, Murphy NP. McGrath N, et al. Among authors: murphy np. Pediatrics. 2018 Oct;142(4):e20181199. doi: 10.1542/peds.2018-1199. Pediatrics. 2018. PMID: 30242075

10

Catalogue of inherited disorders found among the Irish Traveller population.

Lynch SA, Crushell E, Lambert DM, Byrne N, Gorman K, King MD, Green A, O'Sullivan S, Browne F, Hughes J, Knerr I, Monavari AA, Cotter M, McConnell VPM, Kerr B, Jones SA, Keenan C, Murphy N, Cody D, Ennis S, Turner J, Irvine AD, Casey J. Lynch SA, et al. Among authors: murphy n. J Med Genet. 2018 Apr;55(4):233-239. doi: 10.1136/jmedgenet-2017-104974. Epub 2018 Jan 22. J Med Genet. 2018. PMID: 29358271

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