Zobrazeno 1 - 10 of 83 pro vyhledávání: '"M, van Meegen"'
1
Akademický článek
Erector spinae plane block improves postoperative recovery after laminectomy and discectomy surgery: a retrospective cohort study
Autor: Renee J. C. van den Broek, Valerie M. M. van Meegen, Hazem Al Khawaja, R. Arthur Bouwman, Barbara Versyck
Publikováno v: BMC Anesthesiology, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background There is still room for improvement of pain management after spinal surgery. The goal of this study was to evaluate adding the erector spinae block to the standard analgesia regimen. Our hypothesis was that the erector spinae plan
Externí odkaz: https://doaj.org/article/08d32643a5034f0dbab4fb165b08c58e
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2
Akademický článek
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3
A novel gamma-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy
Autor: Frans G. I. Jennekens, M van Meegen, M. de Visser, A. J. van der Kooi, Peter Joseph Jongen, N. J. Leschot, Pieter A. Bolhuis, H.B. Ginjaar, A. J. van Essen
Publikováno v: Neuromuscular disorders, 8(5), 305-308. PERGAMON-ELSEVIER SCIENCE LTD
Neuromuscular disorders, 8(5), 305-308. Elsevier Limited
Limb girdle muscular dystrophy is a heterogeneous group of disorders. One autosomal recessive subtype, LGMD2C, has been linked to chromosome 13, and is caused by gamma-sarcoglycan deficiency in muscle. This report describes a novel missense mutation
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d35e38d2c868e6c5872a37d6a0ed409
https://doi.org/10.1016/s0960-8966(98)00040-6
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4
Molecular Heterogeneity of Second and Fourth Components of Complement and Their Genes in Systemic Sclerosis and Association of HLA Alleles A1, B8 and DR3 with Limited and DR5 with Diffuse Systemic Sclerosis
Autor: R. F. H. J. Hulsmans, L.P. de Waal, F. H. J. Van Den Hoogen, Jan D. Bos, A. M. T. Boerbooms, Syed S. Asghar, M. de Kok-Nazaruk, G.T. Venneker, M. van Meegen
Publikováno v: Experimental and clinical immunogenetics, 15(2), 90-99. S. Karger AG
Experimental and Clinical Immunogenetics, 15, 90-99
Experimental and Clinical Immunogenetics, 15, pp. 90-99
Deficiency of the complement component C4 at the functional, protein and gene level and deficiency of complement component C2 at the functional level were investigated and HLA analysis was performed on patients with limited and diffuse systemic scler
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e69ef1837fdb3d174d99a6639f75297b
https://hdl.handle.net/2066/138828
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5
[Clinical algorithm for cerebrospinal fluid test of 14-3-3 protein in diagnosis of Creutzfeldt-Jacob disease]
Autor: A W, Lemstra, M, van Meegen, F, Baas, W A, van Gool
Publikováno v: Nederlands tijdschrift voor geneeskunde. 145(30)
To study whether an algorithm that includes additional diagnostic information could increase the specificity of the 14-3-3 protein testing in patients suspected to suffer from Creutzfeldt-Jakob disease (CJD).The development of a diagnostic algorithm.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::61382749da956c8f6f0bc153e8947d95
https://pubmed.ncbi.nlm.nih.gov/11503317
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6
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy
Autor: Egbert Bakker, L.V.B. Anderson, H.B. Ginjaar, M. Jeanpierre, Peter G. Barth, John H. J. Wokke, A. L. J. Kneppers, Pieter A. Bolhuis, H.F.M. Busch, H. Ceelie, M van Meegen, Carsten G. Bönnemann, A. J. van der Kooi, A. F. M. Moorman, M. de Visser, Gert-Jan B. van Ommen
Publikováno v: Journal of neurology, 247(7), 524-529. D. Steinkopff-Verlag
Journal of Neurology, 247, 524-529. D. Steinkopff-Verlag
Within a group of 76 sporadic/autosomal recessive limb girdle muscular dystrophy (LGMD) patients we tried to identify those with LGMD type 2C-E. Muscle biopsy specimens of 40 index patients, who had 22 affected sibs, were analyzed immuno-histochemica
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5db66c330a7b08c15102f5aa888fb7c
https://pure.amc.nl/en/publications/sarcoglycanopathies-in-dutch-patients-with-autosomal-recessive-limb-girdle-muscular-dystrophy(974e841d-5077-46b0-b498-4f90672de52d).html
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7
Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21
Autor: A J, van der Kooi, M, van Meegen, T M, Ledderhof, E M, McNally, M, de Visser, P A, Bolhuis
Publikováno v: American journal of human genetics. 60(4)
Limb-girdle muscular dystrophy (LGMD) constitutes a clinically and genetically heterogeneous group of myogenic disorders with a limb-girdle distribution of weakness. One autosomal dominant family, LGMD1A, has been linked to chromosome 5q, whereas in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dbe6a76f519e9b1e7b47169cfb914845
https://pubmed.ncbi.nlm.nih.gov/9106535
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8
Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system
Autor: G T, Venneker, M, van Meegen, M, de Kok-Nazaruk, R F, Hulsmans, L P, de Waall, J D, Bos, S S, Asghar
Publikováno v: Experimental and clinical immunogenetics. 13(2)
In a previous study, a patient suffering from linear frontoparietal scleroderma and some of his family members were found to have an incomplete functional deficiency of the second component (C2) of complement (C). In this study, the proband and the r
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4ccd227230c52fa9e8528fa3440b661b
https://pubmed.ncbi.nlm.nih.gov/9063702
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10
Conference
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