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K Bork

Showing results (111-120 of 159) with videos related to

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The British Journal of Dermatology|December 1, 1991
Atypical facial porokeratosis of MibelliA Enk, K Bork, N Hoede, et al.
Allergy|May 9, 2015
Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutationsK Bork, K Wulff, G Witzke, et al.
Deutsche Medizinische Wochenschrift (1946)|December 31, 1997
[Ascites and suspected acute abdomen in hereditary angioedema due to C1 inhibitor deficiency]K Bork, H Bindewald, M Böckers, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 1, 1977
[Diffuse melanosis in malignant melanoma]K Bork, G W Korting, H J Rumpelt
Klinische Wochenschrift|November 15, 1983
Hereditary angioneurotic oedema and blood-coagulation: interaction between C1-esterase-inhibitor and the activation factors of the proteolytic enzyme systemsG Witzke, K Bork, P Benes, et al.
Biology of the Cell|January 1, 1986
Immunological detection of actin in isolated cilia from quail oviductB Chailley, K Bork, P Gounon, et al.
Allergy|December 2, 2016
Treatment for hereditary angioedema with normal C1-INH and specific mutations in the F12 gene (HAE-FXII)K Bork, K Wulff, G Witzke, et al.
The Journal of Clinical Investigation|June 1, 1989
Acquired C1 inhibitor (C1-INH) deficiency type II. Replacement therapy with C1-INH and analysis of patients' C1-INH and anti-C1-INH autoantibodiesJ Alsenz, J D Lambris, K Bork, et al.
Archives of Dermatological Research|January 1, 1985
Effects of ethanol and acetaldehyde on phagocytic functionsR E Schopf, M Trompeter, K Bork, et al.
Lancet (London, England)|August 30, 2000
Hereditary angioedema with normal C1-inhibitor activity in womenK Bork, S E Barnstedt, P Koch, et al.
Pageof 16

Showing results (111-120 of 159) with videos related to

Sort By:
Pageof 16
The British Journal of Dermatology|December 1, 1991
Atypical facial porokeratosis of MibelliA Enk, K Bork, N Hoede, et al.
Allergy|May 9, 2015
Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutationsK Bork, K Wulff, G Witzke, et al.
Deutsche Medizinische Wochenschrift (1946)|December 31, 1997
[Ascites and suspected acute abdomen in hereditary angioedema due to C1 inhibitor deficiency]K Bork, H Bindewald, M Böckers, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 1, 1977
[Diffuse melanosis in malignant melanoma]K Bork, G W Korting, H J Rumpelt
Klinische Wochenschrift|November 15, 1983
Hereditary angioneurotic oedema and blood-coagulation: interaction between C1-esterase-inhibitor and the activation factors of the proteolytic enzyme systemsG Witzke, K Bork, P Benes, et al.
Biology of the Cell|January 1, 1986
Immunological detection of actin in isolated cilia from quail oviductB Chailley, K Bork, P Gounon, et al.
Allergy|December 2, 2016
Treatment for hereditary angioedema with normal C1-INH and specific mutations in the F12 gene (HAE-FXII)K Bork, K Wulff, G Witzke, et al.
The Journal of Clinical Investigation|June 1, 1989
Acquired C1 inhibitor (C1-INH) deficiency type II. Replacement therapy with C1-INH and analysis of patients' C1-INH and anti-C1-INH autoantibodiesJ Alsenz, J D Lambris, K Bork, et al.
Archives of Dermatological Research|January 1, 1985
Effects of ethanol and acetaldehyde on phagocytic functionsR E Schopf, M Trompeter, K Bork, et al.
Lancet (London, England)|August 30, 2000
Hereditary angioedema with normal C1-inhibitor activity in womenK Bork, S E Barnstedt, P Koch, et al.
Pageof 16