Zobrazeno 1 - 10
of 432
pro vyhledávání: '"Deufel T"'
Publikováno v:
59. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie e.V. (DGNC), 3. Joint Meeting mit der Italienischen Gesellschaft für Neurochirurgie (SINch); 20080601-20080604; Würzburg; DOCP 004 /20080530/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1175::30dbcfd00fb539dafc38d029637a9218
http://www.egms.de/en/meetings/dgnc2008/08dgnc272.shtml
http://www.egms.de/en/meetings/dgnc2008/08dgnc272.shtml
Autor:
Reinhart, K, Brunkhorst, F M, Engel, C, Bloos, F, Meier-Hellmann, A, Ragaller, M, Weiler, N, Moerer, O, Gruendling, M, Oppert, M, Grond, S, Olthoff, D, Jaschinski, U, John, S, Rossaint, R, Welte, T, Schaefer, M, Kern, P, Kuhnt, E, Kiehntopf, M, Deufel, T, Hartog, C, Gerlach, H, Stüber, F, Volk, H-D, Quintel, M, Loeffler, M
Publikováno v:
Reinhart, K; Brunkhorst, F M; Engel, C; Bloos, F; Meier-Hellmann, A; Ragaller, M; Weiler, N; Moerer, O; Gruendling, M; Oppert, M; Grond, S; Olthoff, D; Jaschinski, U; John, S; Rossaint, R; Welte, T; Schaefer, M; Kern, P; Kuhnt, E; Kiehntopf, M; ... (2008). [Study protocol of the VISEP study. Response of the SepNet study group]. Anaesthesist, 57(7), pp. 723-8. Heidelberg: Springer-Medizin-Verlag 10.1007/s00101-008-1391-1
In the commentary by Zander et al. the authors appear concerned about the methods and results of our, at that time, unpublished sepsis trial evaluating hydroxyethyl starch (HES) and insulin therapy. Unfortunately, the authors' concerns are based on f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a82b9b5b3cc49947c1eaada1a4a30842
https://boris.unibe.ch/27299/1/Reinhart2008_Article_StudienprotokollDerVISEP-Studi.pdf
https://boris.unibe.ch/27299/1/Reinhart2008_Article_StudienprotokollDerVISEP-Studi.pdf
Publikováno v:
58. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie e.V. (DGNC); 20070426-20070429; Leipzig; DOCDO.02.05 /20070411/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1175::ce0a90df6b63df9e8b7d7c4d231636c0
http://www.egms.de/en/meetings/dgnc2007/07dgnc015.shtml
http://www.egms.de/en/meetings/dgnc2007/07dgnc015.shtml
Publikováno v:
20. Wissenschaftliche Jahrestagung der DGPP; 20030912-20030914; Rostock; DOCV39 /20030912/
Bei einer großen Familie (MS-DFN 0001) mit nicht-syndromaler Hörstörung und autosomal-dominantem Erbgang wurde eine genetische Kopplungsanalyse durchgeführt. Dabei wurden alle bisher für diese Erkrankung bekannten autosomal dominanten Loci (DFNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1175::25ddb27f6929a8ca42a0dbea3a62ed12
http://www.egms.de/en/meetings/dgpp2003/03dgpp087.shtml
http://www.egms.de/en/meetings/dgpp2003/03dgpp087.shtml
Autor:
Seidel, J., Streck, S., Bellstedt, K., Vianey-Saban, C., Pedersen, Christina Bak, Vockley, J., Korall, H., Roskos, M., Deufel, T., Trefz, F.K., Sewell, A.C., Lehnert, W., Gregersen, N.
Publikováno v:
Seidel, J, Streck, S, Bellstedt, K, Vianey-Saban, C, Pedersen, C B, Vockley, J, Korall, H, Roskos, M, Deufel, T, Trefz, F K, Sewell, A C, Lehnert, W & Gregersen, N 2003, ' Recurrent vomiting and ethylmalonic aciduria associated with rare mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene ', J. Inher. Metab. Dis, vol. 26, no. 1, pp. 37-42 .
We report identification of short-chain acyl-CoA dehydrogenase (SCAD) deficiency in a 12-year-old boy who suffered from recurrent attacks of vomiting once or twice a year from infancy. Growth and development were normal and there were no muscular sym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::f6b7ef8328b812f148b085990fec2c8e
https://pure.au.dk/portal/da/publications/recurrent-vomiting-and-ethylmalonic-aciduria-associated-with-rare-mutations-in-the-shortchain-acylcoa-dehydrogenase-scad-gene(0702eae0-bea3-11db-bee9-02004c4f4f50).html
https://pure.au.dk/portal/da/publications/recurrent-vomiting-and-ethylmalonic-aciduria-associated-with-rare-mutations-in-the-shortchain-acylcoa-dehydrogenase-scad-gene(0702eae0-bea3-11db-bee9-02004c4f4f50).html
Akademický článek
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Autor:
Deufel, T., Sudbrak, R., Feist, Y., Rübsam, B., Chesne, I. Du, Schäfer, K.-L., Roewer, N., Grimm, T., Lehmann-Horn, F., Hartung, E. J., Müller, C. R.
A point mutation in the gene encoding the skeletal muscle calcium release channel (RYR1) has been proposed as the probable cause of malignant hyperthermia (MH) in swine, where it segregates with the disease in all MH-prone strains investigated. The s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d41aabb3773b75397d0e1789cd4eb713
https://europepmc.org/articles/PMC1801094/
https://europepmc.org/articles/PMC1801094/
Autor:
Sudbrak, R., Procaccio, V., Klausnitzer, M., Curran, J. L., Koenraad Monsieurs, Vanbroeckhoven, C., Ellis, R., Heyetens, L., Hartung, E. J., Kozakribbens, G., Heilinger, D., Weissenbach, J., Lehmanhorn, F., Mueller, C. R., Deufel, T., Stewart, A. D., Lunardi, J.
Publikováno v:
Web of Science
ResearcherID
ResearcherID
Malignant hyperthermia (MH) is a potentially lethal pharmacogenetic disease for which MH susceptibility (MHS) is transmitted as an autosomal dominant trait. A potentially life-threatening MH crisis is triggered by exposure to commonly used inhalation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::66efe1b71f4718c0b38194fa5c7d51a3
https://europepmc.org/articles/PMC1801161/
https://europepmc.org/articles/PMC1801161/
Autor:
Sudbrak, R., Procaccio, V., Klausnitzer, M., Curran, J.L., Monsieurs, Koen, Van Broeckhoven, Christine, Ellis, R., Heytens, Luc, Hartung, E.J., Kozak-Ribbens, G., Heilinger, D., Weissenbach, J., Lehmann-Horn, F., Mueller, C.R., Deufel, T., Stewart, A.D., Lunardi, J.
Publikováno v:
The American journal of human genetics