Young HK - Search Results

1

Outcome of noninvasive ventilation in children with neuromuscular disease.

Young HK, Lowe A, Fitzgerald DA, Seton C, Waters KA, Kenny E, Hynan LS, Iannaccone ST, North KN, Ryan MM. Young HK, et al. Neurology. 2007 Jan 16;68(3):198-201. doi: 10.1212/01.wnl.0000251299.54608.13. Neurology. 2007. PMID: 17224573 Clinical Trial.

2

Neurofibromatosis 1: clinical review and exceptions to the rules.

Young H, Hyman S, North K. Young H, et al. J Child Neurol. 2002 Aug;17(8):613-21; discussion 627-9, 646-51. doi: 10.1177/088307380201700812. J Child Neurol. 2002. PMID: 12403560

3

Intracranial tumors in infants.

Young HK, Johnston H. Young HK, et al. J Child Neurol. 2004 Jun;19(6):424-30. doi: 10.1177/088307380401900605. J Child Neurol. 2004. PMID: 15446390

4

Cognitive and psychological profile of males with Becker muscular dystrophy.

Young HK, Barton BA, Waisbren S, Portales Dale L, Ryan MM, Webster RI, North KN. Young HK, et al. J Child Neurol. 2008 Feb;23(2):155-62. doi: 10.1177/0883073807307975. Epub 2007 Dec 3. J Child Neurol. 2008. PMID: 18056690

5

Sniff nasal inspiratory pressure and sleep disordered breathing in childhood neuromuscular disorders.

Anderson VB, McKenzie JA, Seton C, Fitzgerald DA, Webster RI, North KN, Joffe DA, Young HK. Anderson VB, et al. Among authors: young hk. Neuromuscul Disord. 2012 Jun;22(6):528-33. doi: 10.1016/j.nmd.2012.02.002. Epub 2012 Mar 3. Neuromuscul Disord. 2012. PMID: 22386707

6

Can daytime measures of lung function predict respiratory failure in children with neuromuscular disease?

Pandit CA, Waters K, Jones KJ, Young H, Fitzgerald DA. Pandit CA, et al. Paediatr Respir Rev. 2015 Sep;16(4):241-5. doi: 10.1016/j.prrv.2015.08.001. Epub 2015 Aug 12. Paediatr Respir Rev. 2015. PMID: 26563514 Review.

7

Prominent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related disease.

O'Grady GL, Ma A, Sival D, Wong MT, Peduto T, Menezes MP, Young H, Waddell L, Ghaoui R, Needham M, Lek M, North KN, MacArthur DG, van Ravenswaaij-Arts CM, Clarke NF. O'Grady GL, et al. Eur J Hum Genet. 2016 Aug;24(8):1216-9. doi: 10.1038/ejhg.2015.276. Epub 2016 Jan 27. Eur J Hum Genet. 2016. PMID: 26813943 Free PMC article.

8

Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3.

Brewer MH, Chaudhry R, Qi J, Kidambi A, Drew AP, Menezes MP, Ryan MM, Farrar MA, Mowat D, Subramanian GM, Young HK, Zuchner S, Reddel SW, Nicholson GA, Kennerson ML. Brewer MH, et al. Among authors: young hk. PLoS Genet. 2016 Jul 20;12(7):e1006177. doi: 10.1371/journal.pgen.1006177. eCollection 2016 Jul. PLoS Genet. 2016. PMID: 27438001 Free PMC article.

9

Unique clinical and neurophysiologic profile of a cohort of children with CMTX3.

Kanhangad M, Cornett K, Brewer MH, Nicholson GA, Ryan MM, Smith RL, Subramanian GM, Young HK, Züchner S, Kennerson ML, Burns J, Menezes MP. Kanhangad M, et al. Among authors: young hk. Neurology. 2018 May 8;90(19):e1706-e1710. doi: 10.1212/WNL.0000000000005479. Epub 2018 Apr 6. Neurology. 2018. PMID: 29626178 Free PMC article.

10

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. Hum Mol Genet. 2023 Jun 5;32(12):2084-2092. doi: 10.1093/hmg/ddad035. Hum Mol Genet. 2023. PMID: 36920481 Free PMC article.

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