Ryan MM - Search Results

1

Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy.

Billich N, Bray P, Truby H, Evans M, Ryan MM, Carroll K, de Valle K, Villano D, Kornberg A, Sowerby B, Farrar MA, Menezes MP, Holland S, Lindeback R, Cairns A, Davidson ZE. Billich N, et al. Among authors: ryan mm. Muscle Nerve. 2024 Apr;69(4):448-458. doi: 10.1002/mus.28062. Epub 2024 Feb 14. Muscle Nerve. 2024. PMID: 38353293

2

The association between dietary factors and body weight and composition in boys with Duchenne muscular dystrophy.

Billich N, Evans M, Truby H, Ryan MM, Davidson ZE. Billich N, et al. Among authors: ryan mm. J Hum Nutr Diet. 2022 Oct;35(5):804-815. doi: 10.1111/jhn.12987. Epub 2022 Feb 1. J Hum Nutr Diet. 2022. PMID: 34936149

3

Pilot study of a virtual weight management program for Duchenne muscular dystrophy.

Billich N, Bray P, Truby H, Evans M, Carroll K, de Valle K, Adams J, Kennedy RA, Villano D, Kornberg AJ, Yiu EM, Ryan MM, Davidson ZE. Billich N, et al. Among authors: ryan mm. Muscle Nerve. 2024 Apr;69(4):459-466. doi: 10.1002/mus.28065. Epub 2024 Feb 14. Muscle Nerve. 2024. PMID: 38353295

4

Evaluation of Serial Casting for Boys with Duchenne Muscular Dystrophy: A Case Report.

Carroll K, de Valle K, Kornberg A, Ryan M, Kennedy R. Carroll K, et al. Phys Occup Ther Pediatr. 2018 Feb;38(1):88-96. doi: 10.1080/01942638.2017.1280874. Epub 2017 Mar 16. Phys Occup Ther Pediatr. 2018. PMID: 28300461

5

Characterising gait in paediatric neuromuscular disorders: an observational study of spatio-temporal gait in a clinical cohort.

Kennedy RA, de Valle K, Adams J, Ryan MM, Fitzgerald AK, Carroll K. Kennedy RA, et al. Among authors: ryan mm. Disabil Rehabil. 2022 Nov;44(23):7023-7029. doi: 10.1080/09638288.2021.1977399. Epub 2021 Sep 21. Disabil Rehabil. 2022. PMID: 34546805

6

Correlation between whole body muscle MRI and functional measures in paediatric patients with facioscapulohumeral muscular dystrophy.

Woodcock IR, de Valle K, Varma N, Kean M, Ryan MM. Woodcock IR, et al. Among authors: ryan mm. Neuromuscul Disord. 2023 Jan;33(1):15-23. doi: 10.1016/j.nmd.2022.11.006. Epub 2022 Nov 25. Neuromuscul Disord. 2023. PMID: 36522253

7

Connective tissue presentation in two families expands the phenotypic spectrum of PYROXD1 disorders.

Evesson FJ, Dziaduch G, Bryen SJ, Moore F, Pittman S, Devanapalli B, Waddell LB, Ryan MM, Menezes MP, Weihl CC, Tolun AA, Zaidman C, Young H, Adès LC, Cooper ST. Evesson FJ, et al. Among authors: ryan mm. Hum Mol Genet. 2023 Jun 5;32(12):2084-2092. doi: 10.1093/hmg/ddad035. Hum Mol Genet. 2023. PMID: 36920481 Free PMC article.

8

Pathogenic deep intronic MTM1 variant activates a pseudo-exon encoding a nonsense codon resulting in severe X-linked myotubular myopathy.

Bryen SJ, Oates EC, Evesson FJ, Lu JK, Waddell LB, Joshi H, Ryan MM, Cummings BB, McLean CA, MacArthur DG, Kornberg AJ, Cooper ST. Bryen SJ, et al. Among authors: ryan mm. Eur J Hum Genet. 2021 Jan;29(1):61-66. doi: 10.1038/s41431-020-00715-7. Epub 2020 Aug 29. Eur J Hum Genet. 2021. PMID: 32862205 Free PMC article.

9

Carpal tunnel syndrome secondary to ganglion cyst in a child.

Mohamed A, Rosalie S, Taylor K, Fink M, Coombs C, Ryan M, Kornberg A. Mohamed A, et al. J Child Neurol. 2011 May;26(5):630-3. doi: 10.1177/0883073810387299. Epub 2011 Jan 31. J Child Neurol. 2011. PMID: 21285036

10

Characterization of the human myelin oligodendrocyte glycoprotein antibody response in demyelination.

Tea F, Lopez JA, Ramanathan S, Merheb V, Lee FXZ, Zou A, Pilli D, Patrick E, van der Walt A, Monif M, Tantsis EM, Yiu EM, Vucic S, Henderson APD, Fok A, Fraser CL, Lechner-Scott J, Reddel SW, Broadley S, Barnett MH, Brown DA, Lunemann JD, Dale RC, Brilot F; Australasian and New Zealand MOG Study Group. Tea F, et al. Acta Neuropathol Commun. 2019 Sep 3;7(1):145. doi: 10.1186/s40478-019-0786-3. Acta Neuropathol Commun. 2019. PMID: 31481127 Free PMC article.

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