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North, K, Hyman, S, Barton, B.
Review Article : Cognitive Deficits in Neurofibromatosis 1.
Journal of Child Neurology
17(8)
:
605 -612
2002
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Bönnemann, CG, Wong, J, Jones, KJ, Lidov, HGW, Feener, CA, Shapiro, F, Darras, BT, Kunkel, LM, North, KN.
Primary γ-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile.
Neuromuscular Disorders
12(3)
:
273 -280
2002
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He, Y, Jones, KJ, Vignier, N, Morgan, G, Chevallay, M, Barois, A, Estournet–Mathiaud, B, Hori, H, Mizuta, T, Tomé, FMS, et al.
Congenital muscular dystrophy with primary partial laminin &agr;2 chain deficiency: Molecular study.
Neurology
57(7)
:
1319 -1322
2001
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Jones, KJ, Morgan, G, Johnston, H, Tobias, V, Ouvrier, RA, Wilkinson, I, North, KN.
The expanding phenotype of laminin α2 chain (merosin) abnormalities: case series and review.
Journal of Medical Genetics
38(10)
:
649
2001
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Ryan, MM, Schnell, C, Strickland, CD, Shield, LK, Morgan, G, Iannaccone, ST, Laing, NG, Beggs, AH, North, KN.
Nemaline myopathy: A clinical study of 143 cases.
Annals of Neurology
50(3)
:
312 -320
2001
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