Squier W - Search Results

1

Nemaline myopathy with stiffness and hypertonia associated with an ACTA1 mutation.

Jain RK, Jayawant S, Squier W, Muntoni F, Sewry CA, Manzur A, Quinlivan R, Lillis S, Jungbluth H, Sparrow JC, Ravenscroft G, Nowak KJ, Memo M, Marston SB, Laing NG. Jain RK, et al. Among authors: squier w. Neurology. 2012 Apr 3;78(14):1100-3. doi: 10.1212/WNL.0b013e31824e8ebe. Epub 2012 Mar 21. Neurology. 2012. PMID: 22442437 No abstract available.

2

Nemaline myopathy caused by absence of alpha-skeletal muscle actin.

Nowak KJ, Sewry CA, Navarro C, Squier W, Reina C, Ricoy JR, Jayawant SS, Childs AM, Dobbie JA, Appleton RE, Mountford RC, Walker KR, Clement S, Barois A, Muntoni F, Romero NB, Laing NG. Nowak KJ, et al. Among authors: squier w. Ann Neurol. 2007 Feb;61(2):175-84. doi: 10.1002/ana.21035. Ann Neurol. 2007. PMID: 17187373

3

Congenital myopathies with secondary neuromuscular transmission defects; a case report and review of the literature.

Rodríguez Cruz PM, Sewry C, Beeson D, Jayawant S, Squier W, McWilliam R, Palace J. Rodríguez Cruz PM, et al. Among authors: squier w. Neuromuscul Disord. 2014 Dec;24(12):1103-10. doi: 10.1016/j.nmd.2014.07.005. Epub 2014 Jul 30. Neuromuscul Disord. 2014. PMID: 25127990 Review.

4

A rapid immunohistochemical test to distinguish congenital myotonic dystrophy from X-linked myotubular myopathy.

Sewry CA, Quinlivan RC, Squier W, Morris GE, Holt I. Sewry CA, et al. Among authors: squier w. Neuromuscul Disord. 2012 Mar;22(3):225-30. doi: 10.1016/j.nmd.2011.10.002. Epub 2011 Nov 22. Neuromuscul Disord. 2012. PMID: 22113158

5

H1N1 triggered recurrent acute necrotizing encephalopathy in a family with a T653I mutation in the RANBP2 gene.

Anand G, Visagan R, Chandratre S, Segal S, Nemeth AH, Squier W, Sheerin F, Neilson D, Jayawant S. Anand G, et al. Among authors: squier w. Pediatr Infect Dis J. 2015 Mar;34(3):318-20. doi: 10.1097/INF.0000000000000533. Pediatr Infect Dis J. 2015. PMID: 25170550

6

Clinical assessment determines the diagnosis of inclusion body myositis independently of pathological features.

Brady S, Squier W, Hilton-Jones D. Brady S, et al. Among authors: squier w. J Neurol Neurosurg Psychiatry. 2013 Nov;84(11):1240-6. doi: 10.1136/jnnp-2013-305690. Epub 2013 Jul 16. J Neurol Neurosurg Psychiatry. 2013. PMID: 23864699

7

A retrospective cohort study identifying the principal pathological features useful in the diagnosis of inclusion body myositis.

Brady S, Squier W, Sewry C, Hanna M, Hilton-Jones D, Holton JL. Brady S, et al. Among authors: squier w. BMJ Open. 2014 Apr 28;4(4):e004552. doi: 10.1136/bmjopen-2013-004552. BMJ Open. 2014. PMID: 24776709 Free PMC article.

8

Oculopharyngodistal myopathy--a possible association with cardiomyopathy.

Thevathasan W, Squier W, MacIver DH, Hilton DA, Fathers E, Hilton-Jones D. Thevathasan W, et al. Among authors: squier w. Neuromuscul Disord. 2011 Feb;21(2):121-5. doi: 10.1016/j.nmd.2010.10.002. Epub 2010 Oct 30. Neuromuscul Disord. 2011. PMID: 21041087

9

An investigation of the expression of G1-phase cell cycle proteins in focal cortical dysplasia type IIB.

Thom M, Martinian L, Sen A, Squier W, Harding BN, Cross JH, Harkness W, McEvoy A, Sisodiya SM. Thom M, et al. Among authors: squier w. J Neuropathol Exp Neurol. 2007 Nov;66(11):1045-55. doi: 10.1097/nen.0b013e3181598d23. J Neuropathol Exp Neurol. 2007. PMID: 17984686

10

Long-term observational study of sporadic inclusion body myositis.

Benveniste O, Guiguet M, Freebody J, Dubourg O, Squier W, Maisonobe T, Stojkovic T, Leite MI, Allenbach Y, Herson S, Brady S, Eymard B, Hilton-Jones D. Benveniste O, et al. Among authors: squier w. Brain. 2011 Nov;134(Pt 11):3176-84. doi: 10.1093/brain/awr213. Epub 2011 Oct 12. Brain. 2011. PMID: 21994327

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