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The British Journal of Dermatology
|
December 1, 1991
Atypical facial porokeratosis of Mibelli
A Enk, K Bork, N Hoede, et al.
Allergy
|
May 9, 2015
Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations
K 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 systems
G Witzke, K Bork, P Benes, et al.
Biology of the Cell
|
January 1, 1986
Immunological detection of actin in isolated cilia from quail oviduct
B 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 autoantibodies
J Alsenz, J D Lambris, K Bork, et al.
Archives of Dermatological Research
|
January 1, 1985
Effects of ethanol and acetaldehyde on phagocytic functions
R E Schopf, M Trompeter, K Bork, et al.
Lancet (London, England)
|
August 30, 2000
Hereditary angioedema with normal C1-inhibitor activity in women
K Bork, S E Barnstedt, P Koch, et al.
Page
of 16
Search research articles
Search
Showing results (111-120 of 159) with videos related to
Sort By:
Page
of 16
The British Journal of Dermatology
|
December 1, 1991
Atypical facial porokeratosis of Mibelli
A Enk, K Bork, N Hoede, et al.
Allergy
|
May 9, 2015
Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations
K 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 systems
G Witzke, K Bork, P Benes, et al.
Biology of the Cell
|
January 1, 1986
Immunological detection of actin in isolated cilia from quail oviduct
B 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 autoantibodies
J Alsenz, J D Lambris, K Bork, et al.
Archives of Dermatological Research
|
January 1, 1985
Effects of ethanol and acetaldehyde on phagocytic functions
R E Schopf, M Trompeter, K Bork, et al.
Lancet (London, England)
|
August 30, 2000
Hereditary angioedema with normal C1-inhibitor activity in women
K Bork, S E Barnstedt, P Koch, et al.
Page
of 16