Squier W - Search Results

1

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

2

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

3

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.

4

[Pathogenesis of primary inflammatory myopathies].

Benveniste O, Squier W, Boyer O, Hilton-Jones D, Herson S. Benveniste O, et al. Among authors: squier w. Presse Med. 2004 Nov 20;33(20):1444-50. doi: 10.1016/s0755-4982(04)98952-x. Presse Med. 2004. PMID: 15611679 Review. French.

5

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

6

Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal alpha-helical segment.

Dagvadorj A, Goudeau B, Hilton-Jones D, Blancato JK, Shatunov A, Simon-Casteras M, Squier W, Nagle JW, Goldfarb LG, Vicart P. Dagvadorj A, et al. Among authors: squier w. Muscle Nerve. 2003 Jun;27(6):669-75. doi: 10.1002/mus.10370. Muscle Nerve. 2003. PMID: 12766977

7

Periventricular nodular heterotopia with overlying polymicrogyria.

Wieck G, Leventer RJ, Squier WM, Jansen A, Andermann E, Dubeau F, Ramazzotti A, Guerrini R, Dobyns WB. Wieck G, et al. Brain. 2005 Dec;128(Pt 12):2811-21. doi: 10.1093/brain/awh658. Brain. 2005. PMID: 16311271

8

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

9

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.

10

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.

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