Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation von Overeem, S, Schelhaas, H.J, Blijham, P.J, Grootscholten, M.I, ter Laak, H.J, Timmermans, J, van den Wijngaard, A, Zwarts, M.J

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Cell loss and shrinkage in the nucleus basalis Meynert complex in Alzheimer's disease von Vogels, O.J.M., Broere, C.A.J., Ter Laak, H.J., Ten Donkelaar, H.J., Nieuwenhuys, R., Schulte, B.P.M.

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Diagnostic value of MHC class I staining in idiopathic inflammatory myopathies von van der Pas, J, Hengstman, G J D, ter Laak, H J, Borm, G F, van Engelen, B G M

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Myositis during long-term interferon-alpha treatment von Hengstman, G J, Vogels, O J, ter Laak, H J, de Witte, T, van Engelen, B G

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A new phenotype of autosomal dominant nemaline myopathy von Gommans, I.M.P., van Engelen, B.G.M., ter Laak, H.J., Brunner, H.G., Kremer, H., Lammens, M., Vogels, O.J.M.

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Familial inclusion body myositis with histologically confirmed sensorimotor axonal neuropathy von Hengstman, G J, van Engelen, B G, ter Laak, H J, Gabreëls-Festen, A A

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Congenital muscular dystrophy: A review of the literature von Leyten, Q.H., Gabreëls, F.J.M., Renier, W.O., ter Laak, H.J.

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Autosomal dominant type of congenital muscular dystrophy von Gabreëls, F.J.M., Leyten, Q.H., ter Laak, H.J., Renier, W.O., Ceulemans, B., Martin, J.J.

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011 Phenotypic variation in merosin-positive congenital muscular dystrophy with cerebellar atrophy: No radiological-clinical correlation von Rooyer, F.A., Gabreëls, F.J.M., Verrips, A., Leyten, Q.H., Ter Laak, H.J.

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Neuromuscular complications in patients given pavulon/sr (pancuronium bromide) during artificial ventilation von de Coul, A.A.W.Op, Lambregts, P.C.L.A., Koeman, J., van Puyenbroek, M.J.E., Ter Laak/, H.J., Gabreëls-Festen, A.A.W.M.

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White matter abnormalities in congenital muscular dystrophy von Leyten, Q.H., Gabreëls, F.J.M., Renier, W.O., van Engelen, B.G.M., ter Laak, H.J., Sengers, R.C.A., Thijssen, H.O.M.

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Laminin- α2 (merosin), β-dystroglycan, α-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: An immunohistochemical study von ter Laak, H.J, Leyten, Q.H, Gabreëls, F.J.M, Kuppen, H, Renier, W.O, Sengers, R.C.A

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Coxsackie B1 virus-induced murine myositis: Relationship of disease severity to virus dose and antiviral antibody response von Jongen, P.J.H., Heessen, F.W.A., ter Laak, H.J., Galama, J.M.D., Gabreëls, F.J.M.

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11. A quantitative morphological study on the human basomedial telencephalic magnocellular celcontinuum (BTMC) in “normal” aging von Vogels, O.J.M., ter Laak, H.J., Nieuwenhuys, R., Schulte, B.P.M.

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Modulation of experimental allergic encephalomyelitis in lewis rats by monoclonal anti-T cell antibodies von Brinkman, C.J.J., Ter Laak, H.J., Hommes, O.R.

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Congenital muscular dystrophy von Leyten, Q.H., Gabreëls, F.J.M., Renier, W.O., Joosten, E.M.G., ter Laak, H.J., Renkawek, K., Sengers, R.C.A., Mullaart, R.A.

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Over de variabiliteit van Molinia caerulea (L.) Moench in Nederland von A.A. Sterk, H.J. ter Laak

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Definition of neural response and incremental sensitivity of retinal ganglion cells in a tree shrew ( Tupaia chinensis) von Ter Laak, H.J., Thijssen, J.M.

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Multiple pterygium syndrome von Kok, J.G., Gabreëls, F.J.M., Renier, W.O., Ter Laak, H.J., Slot, G.H., Bouwsma, G.

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Receptive field properties of optic tract fibres from on-center sustained and transient cells in a tree shrew ( Tupaia chinensis) von Laak, H.J. Ter, Thijssen, J.M

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