Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Henk Veldman"'
Autor:
Marianne de Visser, I. M. Bronner, Marius A. van den Bergh Weerman, Jessica E. Hoogendijk, Marja Ramkema, Annemieke J M Rozemuller, Henk Veldman
Publikováno v:
Ultrastructural Pathology, 32(4), 123-126. Informa Healthcare
Ultrastructural pathology, 32(4), 123-126. Informa Healthcare
Bronner, I M, Hoogendijk, J E, Veldman, H, Ramkema, M, Weerman, M A V, Rozemuller, A J M & Visser, M 2008, ' Tubuloreticular structures in different types of myositis: Implications for pathogenesis ', Ultrastructural Pathology, vol. 32, no. 4, pp. 123-126 . https://doi.org/10.1080/01913120802209379
Ultrastructural pathology, 32(4), 123-126. Informa Healthcare
Bronner, I M, Hoogendijk, J E, Veldman, H, Ramkema, M, Weerman, M A V, Rozemuller, A J M & Visser, M 2008, ' Tubuloreticular structures in different types of myositis: Implications for pathogenesis ', Ultrastructural Pathology, vol. 32, no. 4, pp. 123-126 . https://doi.org/10.1080/01913120802209379
In dermatomyositis (DM) there is strong histopathological evidence of a microvascular pathogenesis, including endothelial microtubular inclusions. In nonspecific myositis, perimysial and perivascular infiltrates in the muscle biopsy similar to DM are
Autor:
John H. J. Wokke, Henk Veldman, Jessica E. Hoogendijk, Umesh A. Badrising, K Moons, Marjon F. G. van der Meulen
Publikováno v:
Neuromuscular Disorders. 11:447-451
Problems in diagnosing sporadic inclusion body myositis may arise if all clinical features fit a diagnosis of polymyositis, but the muscle biopsy shows some rimmed vacuoles. Recently, immunohistochemistry with an antibody directed against phosphoryla
Autor:
A.A.W.M. Gabreëls-Festen, I. Zorn, P.H.S. Meijerink, M. de Visser, Frank Baas, Henk Veldman, Pieter A. Bolhuis, Jessica E. Hoogendijk
Publikováno v:
Annals of Neurology. 40:672-675
Mutations in the major peripheral myelin protein zero (P0) gene on chromosome 1q21-q23 have been found with the hereditary demyelinating polyneuropathy Charcot-Marie-Tooth type 1B. Here, we describe 2 patients with distinct neurological characteristi
Publikováno v:
Brain. 118:533-545
We have used histological and histochemical techniques at the light microscopical level, and electron microscopy to examine the myopathological changes in rat muscle up to 30 weeks following botulinum toxin injection. Apart from muscle fibre atrophy
Publikováno v:
Neuromuscular Disorders. 4:489-496
Changes in calcitonin gene-related peptide-like immunoreactivity (CGRP-LI) at the motor endplates of botulinum toxin-paralysed rat muscles were investigated using immunohistochemistry. One day following toxin injection, a dramatic increase in CGRP-LI
Publikováno v:
Muscle & Nerve. 17:623-631
In order to determine the fate of the superfluous neuromuscular junctions (NMJs) formed during the course of botulinum toxin (BoTx)-induced paralysis, we have quantified the change in the total length of the nerve muscle contact area(s) following BoT
Publikováno v:
Acta neuropathologica, 87(4), 405-410. Springer Verlag
We have used immunohistochemistry and electron microscopy to investigate the distribution of basic fibroblast growth factor (bFGF) in the peripheral motor system of the adult rat. In the lumbar segments of the spinal cord, bFGF immunoreactivity (bFGF
Publikováno v:
Muscle & Nerve. 13:516-527
In a new, typical case of Schwartz-Jampel syndrome (SJS) the origin of the disorder was found to be purely myogenic. Concentric needle EMG showed abundant and persistent spontaneous activity, maximal at insertion, and uninfluenced by local curarizati
Autor:
Peter M. Frederik, Marc H. De Baets, Frank Spaans, Henk Veldman, John H. J. Wokke, Angela Vincent, Hans Duimel, Mario Losen, Maurice H. W. Stassen, Pilar Martinez-Martinez, Barbie M. Machiels
Publikováno v:
Brain : a journal of neurology. 128(Pt 10)
Myasthenia gravis is usually caused by autoantibodies to the acetylcholine receptor (AChR). The AChR is clustered and anchored in the postsynaptic membrane of the neuromuscular junction (NMJ) by a cytoplasmic protein called rapsyn. We previously show
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 64(3)
According to recently published criteria a diagnosis of definite sporadic inclusion body myositis is made if the typical histopathological abnormalities (rimmed vacuoles and abnormal accumulations of proteins, in addition to mononuclear cell infiltra