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G Hauptmann

Showing results (111-120 of 172) with videos related to

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La Nouvelle Presse Medicale|April 3, 1976
[Angioneurotic hereditary edema. 3 faimilial cases]A Jaeger, M Hammann, G Hauptmann, et al.
Le Poumon Et Le Coeur|January 1, 1981
[Pleural effusion as the presenting feature of rheumatoid disease. The value of the level of complement in the pleural fluid. A propos of 2 cases]G Pauli, J L Pasquali, A Jory, et al.
Clinical Immunology (Orlando, Fla.)|September 22, 2006
Which complement assays and typings are necessary for the diagnosis of complement deficiency in patients with lupus erythematosus? A study of 25 patientsP Boeckler, A Meyer, B Uring-Lambert, et al.
DNA and Cell Biology|June 1, 1993
Synthesis and regulation of complement components by human monocytes/macrophages and by acute monocytic leukemiaF Vincent, H de la Salle, A Bohbot, et al.
IEEE Transactions on Image Processing : a Publication of the IEEE Signal Processing Society|March 21, 2015
Event oriented dictionary learning for complex event detectionYan Yan, Yi Yang, Deyu Meng, et al.
The American Journal of Medicine|August 1, 1983
Genetic deficiency of C4 presenting with recurrent infections and a SLE-like disease. Genetic and immunologic studiesF Mascart-Lemone, G Hauptmann, J Goetz, et al.
Scandinavian Journal of Haematology|August 1, 1975
Lymphosarcoma, cold urticaria, IgG1 monoclonal cryoglobulin and complement abnormalitiesG Hauptmann, J M Lang, M L North, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|December 1, 1994
Genomic analysis of the F subtypes of human complement factor BI Jahn, J E Mejía, M Thomas, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|November 25, 2010
Towards automated assistance for operating home medical devicesZan Gao, Marcin Detyniecki, Ming-Yu Chen, et al.
FEBS Letters|June 8, 1987
Heterogeneity in the structural basis of the human complement C4A null allele (C4A Q0) as revealed by HindIII restriction fragment length polymorphism analysisB Uring-Lambert, N Vegnaduzzi, M C Carroll, et al.
Pageof 18

Showing results (111-120 of 172) with videos related to

Sort By:
Pageof 18
La Nouvelle Presse Medicale|April 3, 1976
[Angioneurotic hereditary edema. 3 faimilial cases]A Jaeger, M Hammann, G Hauptmann, et al.
Le Poumon Et Le Coeur|January 1, 1981
[Pleural effusion as the presenting feature of rheumatoid disease. The value of the level of complement in the pleural fluid. A propos of 2 cases]G Pauli, J L Pasquali, A Jory, et al.
Clinical Immunology (Orlando, Fla.)|September 22, 2006
Which complement assays and typings are necessary for the diagnosis of complement deficiency in patients with lupus erythematosus? A study of 25 patientsP Boeckler, A Meyer, B Uring-Lambert, et al.
DNA and Cell Biology|June 1, 1993
Synthesis and regulation of complement components by human monocytes/macrophages and by acute monocytic leukemiaF Vincent, H de la Salle, A Bohbot, et al.
IEEE Transactions on Image Processing : a Publication of the IEEE Signal Processing Society|March 21, 2015
Event oriented dictionary learning for complex event detectionYan Yan, Yi Yang, Deyu Meng, et al.
The American Journal of Medicine|August 1, 1983
Genetic deficiency of C4 presenting with recurrent infections and a SLE-like disease. Genetic and immunologic studiesF Mascart-Lemone, G Hauptmann, J Goetz, et al.
Scandinavian Journal of Haematology|August 1, 1975
Lymphosarcoma, cold urticaria, IgG1 monoclonal cryoglobulin and complement abnormalitiesG Hauptmann, J M Lang, M L North, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|December 1, 1994
Genomic analysis of the F subtypes of human complement factor BI Jahn, J E Mejía, M Thomas, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|November 25, 2010
Towards automated assistance for operating home medical devicesZan Gao, Marcin Detyniecki, Ming-Yu Chen, et al.
FEBS Letters|June 8, 1987
Heterogeneity in the structural basis of the human complement C4A null allele (C4A Q0) as revealed by HindIII restriction fragment length polymorphism analysisB Uring-Lambert, N Vegnaduzzi, M C Carroll, et al.
Pageof 18