McClelland V - Search Results

1

Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy.

Cullup T, Kho AL, Dionisi-Vici C, Brandmeier B, Smith F, Urry Z, Simpson MA, Yau S, Bertini E, McClelland V, Al-Owain M, Koelker S, Koerner C, Hoffmann GF, Wijburg FA, ten Hoedt AE, Rogers RC, Manchester D, Miyata R, Hayashi M, Said E, Soler D, Kroisel PM, Windpassinger C, Filloux FM, Al-Kaabi S, Hertecant J, Del Campo M, Buk S, Bodi I, Goebel HH, Sewry CA, Abbs S, Mohammed S, Josifova D, Gautel M, Jungbluth H. Cullup T, et al. Among authors: mcclelland v. Nat Genet. 2013 Jan;45(1):83-7. doi: 10.1038/ng.2497. Epub 2012 Dec 9. Nat Genet. 2013. PMID: 23222957 Free PMC article.

2

Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy.

McClelland V, Cullup T, Bodi I, Ruddy D, Buj-Bello A, Biancalana V, Boehm J, Bitoun M, Miller O, Jan W, Menson E, Amaya L, Trounce J, Laporte J, Mohammed S, Sewry C, Raiman J, Jungbluth H. McClelland V, et al. Am J Med Genet A. 2010 Mar;152A(3):741-7. doi: 10.1002/ajmg.a.33296. Am J Med Genet A. 2010. PMID: 20186778

3

Glutaric aciduria type 1 presenting with epilepsy.

McClelland VM, Bakalinova DB, Hendriksz C, Singh RP. McClelland VM, et al. Dev Med Child Neurol. 2009 Mar;51(3):235-9. doi: 10.1111/j.1469-8749.2008.03240.x. Dev Med Child Neurol. 2009. PMID: 19260933 Free article.

4

Abnormal patterns of corticomuscular and intermuscular coherence in childhood dystonia.

McClelland VM, Cvetkovic Z, Lin JP, Mills KR, Brown P. McClelland VM, et al. Clin Neurophysiol. 2020 Apr;131(4):967-977. doi: 10.1016/j.clinph.2020.01.012. Epub 2020 Feb 4. Clin Neurophysiol. 2020. PMID: 32067914 Free PMC article.

5

"Spastic Dystonia", "Dystonia with Spasticity" or "Dystonia accompanying the Upper Motor Neuron Complex"? A reconciliation of nomenclature is needed.

Lumsden DE, Barkey S, McClelland V, Lin JP. Lumsden DE, et al. Among authors: mcclelland v. Clin Neurophysiol. 2019 Jun;130(6):1074-1075. doi: 10.1016/j.clinph.2019.03.010. Epub 2019 Mar 27. Clin Neurophysiol. 2019. PMID: 30935823 No abstract available.

6

Disease-specific patterns of basal ganglia neuronal activity in Neurodegeneration with Brain Iron Accumulation type I (NBIA-1).

McClelland VM, Lumsden DE, Lin JP. McClelland VM, et al. Clin Neurophysiol. 2019 Jun;130(6):877-878. doi: 10.1016/j.clinph.2019.03.005. Epub 2019 Mar 26. Clin Neurophysiol. 2019. PMID: 30978626 No abstract available.

7

Glutaryl-CoA dehydrogenase deficiency.

McClelland VM, Gissen P, Hendriksz C, Chakrapani A. McClelland VM, et al. Pediatr Res. 2007 Jan;61(1):134; author reply 134-5. doi: 10.1203/01.pdr.0b013e31802d9ab4. Pediatr Res. 2007. PMID: 17211155 No abstract available.

8

Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) as a cause of liver disease in infants in the UK.

Hutchin T, Preece MA, Hendriksz C, Chakrapani A, McClelland V, Okumura F, Song YZ, Iijima M, Kobayashi K, Saheki T, McKiernan P, Baumann U. Hutchin T, et al. Among authors: mcclelland v. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S151-5. doi: 10.1007/s10545-009-1116-x. Epub 2009 Jun 11. J Inherit Metab Dis. 2009. PMID: 19517266

9

Central motor conduction studies and diagnostic magnetic resonance imaging in children with severe primary and secondary dystonia.

McClelland V, Mills K, Siddiqui A, Selway R, Lin JP. McClelland V, et al. Dev Med Child Neurol. 2011 Aug;53(8):757-63. doi: 10.1111/j.1469-8749.2011.03981.x. Epub 2011 Jun 27. Dev Med Child Neurol. 2011. PMID: 21707595 Free article.

10

Rectification of the EMG is an unnecessary and inappropriate step in the calculation of Corticomuscular coherence.

McClelland VM, Cvetkovic Z, Mills KR. McClelland VM, et al. J Neurosci Methods. 2012 Mar 30;205(1):190-201. doi: 10.1016/j.jneumeth.2011.11.001. Epub 2011 Nov 17. J Neurosci Methods. 2012. PMID: 22120690

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