Výsledky vyhledávání - "Controlled nerve expansion in rabbits"

Peripheral nerve elongation by laser Doppler flowmetry controlled expansion: morphological aspects

Autor: Wey, L.P. van der, Gabreëls-Festen, A.A.W.M., Merks, M.H.J.H., Polder, T.W., Stegeman, D.F., Spauwen, P.H.M., Gabreëls, F.J.M.

Publikováno v: Acta Neuropathologica, 89, 166-171
Acta Neuropathologica, 89, pp. 166-171
Acta Neuropathologica, 89, 2, pp. 166-171

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Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::39b7354928a84b0018846dfb92bafb09
https://hdl.handle.net/2066/20840

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Immunophenotyping of congenital myopathies: disorganization of sarcomeric, cytoskeletal and extracellular matrix proteins

Autor: Rob C.A. Sengers, Ad M. Stadhouders, Frans C. S. Ramaekers, Peter G. Barth, Henk J. ter Laak, Paul H.K. Jap, Peter F.M. van der Ven, Ikuya Nonaka

Publikováno v: The Journal of Neuroscience, 129, 199-213
The Journal of Neuroscience, 129, pp. 199-213
Journal of the neurological sciences, 129(2), 199-213. Elsevier
Journal of the Neurological Sciences, 129, 199-213
Journal of the Neurological Sciences, 129, 2, pp. 199-213

We have studied the expression and distribution patterns of the intermediate filament proteins desmin and vimentin, the sarcomere components titin, nebulin and myosin, the basement membrane constituents collagen type IV and laminin, and the reticular

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74a7836507da0416a1ca9fad20429dd3
http://hdl.handle.net/2066/22265

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Peripheral nerve elongation by laser doppler flowmetry controlled expansion

Autor: Wey, L.P. van der

Item does not contain fulltext Katholieke Universiteit Nijmegen, 25 april 1995 Promotores : Gabreëls, F.J.M., Spauwen, P.H.M., Gabreëls-Festen, A.A.W.M., Stegeman, D.F. 1-136 p.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3962ef485898ed5d0ef2ee700f83e67f
https://hdl.handle.net/2066/255611

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Congenital muscular dystrophy and severe central nervous system atrophy in two siblings

Autor: A.A.W.M. Gabreëls-Festen, Peter G. Barth, W. O. Renier, H.J. ter Laak, K. Renkawek, Q.H. Leyten, M. G. Smits, Fons J. M. Gabreëls

Publikováno v: Acta Neuropathologica, 90, 650-656
Acta Neuropathologica, 90, pp. 650-656
Acta Neuropathologica, 90, 6, pp. 650-656
Acta neuropathologica, 90(6), 650-656. Springer Verlag

Severe degenerative features of the nervous system of a hitherto unknown kind, associated with a neuromuscular disorder with histopathological features of congenital muscular dystrophy, are reported in two female siblings. The clinical profile was ch

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23162e01707c0aeb1adc49383f3256f4
http://hdl.handle.net/2066/264544

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Human diseases with defects in oxidative phophorylation 1. Decreased amounts of assembled oxidative phosporylation complexes in mitochondrial encephalomyopathies

Autor: Kathy Pfeiffer, Wim Ruitenbeek, I.F.M. de Coo, W. Schlote, H.A.C.M. Bentlage, Simonida Gencic, H.J. ter Laak, J. M. F. Trijbels, G. von Jagow, R. C. A. Sengers, H. Schägger

Publikováno v: European Journal of Biochemistry, 227, pp. 909-915
European Journal of Biochemistry, 227, 909-915
European Journal of Biochemistry, 227, 3, pp. 909-915

The amount of oxidative phosphorylation enzymes in mitochondrial encephalomyopathy patients has been studied by two-dimensional electrophoresis (blue native PAGE/Tricine-SDS-PAGE). Only 20 mg muscle was required to identify and analyse complexes I, I

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e900987348e6ace52e02befa8b3b0a10
https://hdl.handle.net/2066/188470

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White matter abnormalities in congenital muscular dystrophy

Autor: H.J. ter Laak, F.J.M. Gabreëls, Willy O. Renier, Rob C.A. Sengers, B.G.M. van Engelen, Q.H. Leyten, H.O.M. Thijssen

Publikováno v: Journal of the Neurological Sciences, 129, 162-169
The Journal of Neuroscience, 129, pp. 162-169
The Journal of Neuroscience, 129, 162-169
Journal of the Neurological Sciences, 129, 2, pp. 162-169

Central nervous system (CNS) characteristics were examined in seventeen patients with autosomal recessive classic or “pure” congenital muscular dystrophy (CMD). In three patients, neuroradiological examination (CT/MRI) indicated hypodense white m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afab8bb130335ae8572b15d4291848ea
https://doi.org/10.1016/0022-510X(94)00264-O

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