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J Forristal

Showing results (1-10 of 39) with videos related to

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Pediatric Nephrology (Berlin, Germany)|April 1, 1994
Serum complement levels before and after the onset of acute post-streptococcal glomerulonephritis. A case reportC F Strife, T J Forristal, J Forristal
The Journal of Laboratory and Clinical Medicine|October 1, 1980
Partial properdin deficiencyC A Davis, J Forristal
The Journal of Laboratory and Clinical Medicine|June 1, 1986
Relationship between the component and regulatory proteins of the classical pathway C3 convertaseT R Welch, J Forristal, L Beischel
Pediatric Research|September 1, 1979
Serum complement levels in infancy: age related changesC A Davis, E H Vallota, J Forristal
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 1, 1990
Patterns of complement activation in idiopathic membranoproliferative glomerulonephritis, types I, II, and IIIW S Varade, J Forristal, C D West
Pediatric Research|April 1, 1977
Alternative pathway of complement in sickle cell diseaseR G Strauss, T Asbrock, J Forristal, et al.
The Journal of Rheumatology|February 1, 1987
C4 binding protein deficiency in a patient with atypical Behçet's diseaseR G Trapp, M Fletcher, J Forristal, et al.
Kidney International|November 1, 1983
Inherited complement component deficiencies in membranoproliferative glomerulonephritisT H Coleman, J Forristal, T Kosaka, et al.
Clinical and Experimental Immunology|April 1, 1977
Correlations between serum factor B and C3b inactivator levels in normal subjects and in patients with infections, nephrosis and hypocomplementaemic glomerulonephritisJ Forristal, K Iitaka, E H Vallota, et al.
The Journal of Clinical Investigation|June 1, 1985
A circulating inhibitor of fluid-phase amplification. C3 convertase formation in systemic lupus erythematosusF B Waldo, J Forristal, L Beischel, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Pediatric Nephrology (Berlin, Germany)|April 1, 1994
Serum complement levels before and after the onset of acute post-streptococcal glomerulonephritis. A case reportC F Strife, T J Forristal, J Forristal
The Journal of Laboratory and Clinical Medicine|October 1, 1980
Partial properdin deficiencyC A Davis, J Forristal
The Journal of Laboratory and Clinical Medicine|June 1, 1986
Relationship between the component and regulatory proteins of the classical pathway C3 convertaseT R Welch, J Forristal, L Beischel
Pediatric Research|September 1, 1979
Serum complement levels in infancy: age related changesC A Davis, E H Vallota, J Forristal
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 1, 1990
Patterns of complement activation in idiopathic membranoproliferative glomerulonephritis, types I, II, and IIIW S Varade, J Forristal, C D West
Pediatric Research|April 1, 1977
Alternative pathway of complement in sickle cell diseaseR G Strauss, T Asbrock, J Forristal, et al.
The Journal of Rheumatology|February 1, 1987
C4 binding protein deficiency in a patient with atypical Behçet's diseaseR G Trapp, M Fletcher, J Forristal, et al.
Kidney International|November 1, 1983
Inherited complement component deficiencies in membranoproliferative glomerulonephritisT H Coleman, J Forristal, T Kosaka, et al.
Clinical and Experimental Immunology|April 1, 1977
Correlations between serum factor B and C3b inactivator levels in normal subjects and in patients with infections, nephrosis and hypocomplementaemic glomerulonephritisJ Forristal, K Iitaka, E H Vallota, et al.
The Journal of Clinical Investigation|June 1, 1985
A circulating inhibitor of fluid-phase amplification. C3 convertase formation in systemic lupus erythematosusF B Waldo, J Forristal, L Beischel, et al.
Pageof 4