Search Results - "Leyten, Q.H"

Autosomal dominant type of congenital muscular dystrophy by 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 by Rooyer, F.A., Gabreëls, F.J.M., Verrips, A., Leyten, Q.H., Ter Laak, H.J.

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

“…Congenital muscular dystrophy (CMD) is a condition in which there are already at birth, marked hypotonia, generalized muscle weakness and frequently multiple…”
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Cerebral hemorrhage complicating exertional heat stroke by Boersma, L.V.A, Leyten, Q.H, Meijer, J.W.R, Strubbe, E.J, Bosch, F.H

“…Exertional heat stroke may be complicated by mild neurological deficits, usually with complete convalescence. This may be associated with metabolic disorders…”
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White matter abnormalities in congenital muscular dystrophy by 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.

“…Central nervous system (CNS) characteristics were examined in seventeen patients with autosomal recessive classic or “pure” congenital muscular dystrophy…”
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Laminin- α2 (merosin), β-dystroglycan, α-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: An immunohistochemical study by ter Laak, H.J, Leyten, Q.H, Gabreëls, F.J.M, Kuppen, H, Renier, W.O, Sengers, R.C.A

“…Muscle biopsies of 13 congenital muscular dystrophy (CMD) patients were investigated for the expression of laminin- α 2 (merosin), β-dystroglycan,…”
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