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Clarke, NF, Monnier, N, Smith, RLL, Kornberg, AJ, Farrell, MA, Waddell, L, Cooper, S, Lunardi, J, North, KN.
G.P.1.05 RYR1 is a common cause of congenital fibre type disproportion with ptosis, ophthalmoplegia, scoliosis and pronounced axial muscle weakness.
Neuromuscular Disorders
19(8-9)
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557
2009
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Butler, TL, Egan, JR, Graf, FG, Au, CG, McMahon, AC, North, KN, Winlaw, DS.
Dysfunction induced by ischemia versus edema: does edema matter?.
J Thorac Cardiovasc Surg
138(1)
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141 -147.e1
2009
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Boyd, KP, Korf, BR, Theos, A.
Neurofibromatosis type 1..
61:
1 -14
2009
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Bastiani, M, Liu, L, Hill, MM, Jedrychowski, MP, Nixon, SJ, Lo, HP, Abankwa, D, Luetterforst, R, Fernandez-Rojo, M, Breen, MR, et al.
MURC/Cavin-4 and cavin family members form tissue-specific caveolar complexes..
J Cell Biol
185(7)
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1259 -1273
2009
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Liu, R, Ginn, SL, Lek, M, North, KN, Alexander, IE, Little, DG, Schindeler, A.
Myoblast sensitivity and fibroblast insensitivity to osteogenic conversion by BMP-2 correlates with the expression of Bmpr-1a..
BMC Musculoskelet Disord
10:
51
2009
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