Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation
Overeem, S, Schelhaas, H.J, Blijham, P.J, Grootscholten, M.I, ter Laak, H.J, Timmermans, J, van den Wijngaard, A, Zwarts, M.J
Published in Neuromuscular disorders : NMD (01.06.2007)
Published in Neuromuscular disorders : NMD (01.06.2007)
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Myositis during long-term interferon-alpha treatment
Hengstman, G J, Vogels, O J, ter Laak, H J, de Witte, T, van Engelen, B G
Published in Neurology (13.06.2000)
Published in Neurology (13.06.2000)
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Journal Article
A new phenotype of autosomal dominant nemaline myopathy
Gommans, I.M.P., van Engelen, B.G.M., ter Laak, H.J., Brunner, H.G., Kremer, H., Lammens, M., Vogels, O.J.M.
Published in Neuromuscular disorders : NMD (2002)
Published in Neuromuscular disorders : NMD (2002)
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Journal Article
Familial inclusion body myositis with histologically confirmed sensorimotor axonal neuropathy
Hengstman, G J, van Engelen, B G, ter Laak, H J, Gabreëls-Festen, A A
Published in Journal of neurology (01.11.2000)
Published in Journal of neurology (01.11.2000)
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Journal Article
Autosomal dominant type of congenital muscular dystrophy
Gabreëls, F.J.M., Leyten, Q.H., ter Laak, H.J., Renier, W.O., Ceulemans, B., Martin, J.J.
Published in Neuromuscular disorders : NMD (01.09.1997)
Published in Neuromuscular disorders : NMD (01.09.1997)
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Journal Article
011 Phenotypic variation in merosin-positive congenital muscular dystrophy with cerebellar atrophy: No radiological-clinical correlation
Rooyer, F.A., Gabreëls, F.J.M., Verrips, A., Leyten, Q.H., Ter Laak, H.J.
Published in European journal of paediatric neurology (1999)
Published in European journal of paediatric neurology (1999)
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Journal Article
Neuromuscular complications in patients given pavulon/sr (pancuronium bromide) during artificial ventilation
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.
Published in Clinical neurology and neurosurgery (1985)
Published in Clinical neurology and neurosurgery (1985)
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Journal Article
Congenital muscular dystrophy: A review of the literature
Leyten, Q.H., Gabreëls, F.J.M., Renier, W.O., ter Laak, H.J.
Published in Clinical Neurology and Neurosurgery (01.11.1996)
Published in Clinical Neurology and Neurosurgery (01.11.1996)
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Book Review
Conference Proceeding
Journal Article
White matter abnormalities in congenital muscular dystrophy
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.
Published in Journal of the neurological sciences (01.04.1995)
Published in Journal of the neurological sciences (01.04.1995)
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Journal Article
Laminin- α2 (merosin), β-dystroglycan, α-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: An immunohistochemical study
ter Laak, H.J, Leyten, Q.H, Gabreëls, F.J.M, Kuppen, H, Renier, W.O, Sengers, R.C.A
Published in Clinical neurology and neurosurgery (01.03.1998)
Published in Clinical neurology and neurosurgery (01.03.1998)
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Journal Article
Congenital muscular dystrophy
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.
Published in Clinical neurology and neurosurgery (1990)
Published in Clinical neurology and neurosurgery (1990)
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Journal Article
Multiple pterygium syndrome
Kok, J.G., Gabreëls, F.J.M., Renier, W.O., Ter Laak, H.J., Slot, G.H., Bouwsma, G.
Published in Clinical neurology and neurosurgery (01.01.1984)
Published in Clinical neurology and neurosurgery (01.01.1984)
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