Ryan MM - Search Results

1

'A short time but a lovely little short time': Bereaved parents' experiences of having a child with spinal muscular atrophy type 1.

Higgs EJ, McClaren BJ, Sahhar MA, Ryan MM, Forbes R. Higgs EJ, et al. Among authors: ryan mm. J Paediatr Child Health. 2016 Jan;52(1):40-6. doi: 10.1111/jpc.12993. Epub 2015 Sep 10. J Paediatr Child Health. 2016. PMID: 26437687

2

Spinal muscular atrophy type 1: is long-term mechanical ventilation ethical?

Ryan MM, Kilham H, Jacobe S, Tobin B, Isaacs D. Ryan MM, et al. J Paediatr Child Health. 2007 Apr;43(4):237-42. doi: 10.1111/j.1440-1754.2007.01052.x. J Paediatr Child Health. 2007. PMID: 17444824

3

Physician attitudes towards ventilatory support for spinal muscular atrophy type 1 in Australasia.

Geevasinga N, Ryan MM. Geevasinga N, et al. Among authors: ryan mm. J Paediatr Child Health. 2007 Dec;43(12):790-4. doi: 10.1111/j.1440-1754.2007.01197.x. Epub 2007 Sep 4. J Paediatr Child Health. 2007. PMID: 17803671

4

The use of invasive ventilation is appropriate in children with genetically proven spinal muscular atrophy type 1: the motion against.

Ryan MM. Ryan MM. Paediatr Respir Rev. 2008 Mar;9(1):51-4; discussion 55-6. doi: 10.1016/j.prrv.2007.10.002. Epub 2008 Feb 1. Paediatr Respir Rev. 2008. PMID: 18280980 Review.

5

Adolescent spinal muscular atrophy with calf hypertrophy and a deletion in the SMN gene.

Yiu EM, Ravat S, Ryan MM, Shield LK, Smith LJ, Kornberg AJ. Yiu EM, et al. Among authors: ryan mm. Muscle Nerve. 2008 Jul;38(1):930-2. doi: 10.1002/mus.21013. Muscle Nerve. 2008. PMID: 18508340

6

High resolution chromosomal microarray in undiagnosed neurological disorders.

Howell KB, Kornberg AJ, Harvey AS, Ryan MM, Mackay MT, Freeman JL, Rodriguez Casero MV, Collins KJ, Hayman M, Mohamed A, Ware TL, Clark D, Bruno DL, Burgess T, Slater H, McGillivray G, Leventer RJ. Howell KB, et al. Among authors: ryan mm. J Paediatr Child Health. 2013 Sep;49(9):716-24. doi: 10.1111/jpc.12256. Epub 2013 Jun 3. J Paediatr Child Health. 2013. PMID: 23731025 Clinical Trial.

7

A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy.

Wong SH, McClaren BJ, Archibald AD, Weeks A, Langmaid T, Ryan MM, Kornberg A, Metcalfe SA. Wong SH, et al. Among authors: ryan mm. Eur J Hum Genet. 2015 Oct;23(10):1294-300. doi: 10.1038/ejhg.2014.301. Epub 2015 Jan 28. Eur J Hum Genet. 2015. PMID: 25626706 Free PMC article.

8

Describing nutrition in spinal muscular atrophy: A systematic review.

Moore GE, Lindenmayer AW, McConchie GA, Ryan MM, Davidson ZE. Moore GE, et al. Among authors: ryan mm. Neuromuscul Disord. 2016 Jul;26(7):395-404. doi: 10.1016/j.nmd.2016.05.005. Epub 2016 May 10. Neuromuscul Disord. 2016. PMID: 27241822 Review.

9

Cerebral palsy is not a diagnosis: A case report of a novel atlastin-1 mutation.

Andersen EW, Leventer RJ, Reddihough DS, Davis MR, Ryan MM. Andersen EW, et al. Among authors: ryan mm. J Paediatr Child Health. 2016 Jun;52(6):669-71. doi: 10.1111/jpc.13200. J Paediatr Child Health. 2016. PMID: 27333849 No abstract available.

10

Fifty years of paediatric neurology in Australasia.

Shield LK, Riney K, Antony JH, Ouvrier RA, Ryan MM. Shield LK, et al. Among authors: ryan mm. J Paediatr Child Health. 2016 Sep;52(9):861-4. doi: 10.1111/jpc.13286. J Paediatr Child Health. 2016. PMID: 27650142 No abstract available.

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