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H W Kreth

Showing results (71-80 of 78) with videos related to

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Immunogenetics|January 1, 1984
Partial C4 deficiency in subacute sclerosing panencephalitisC Rittner, E M Meier, B Stradmann, et al.
The American Journal of Surgical Pathology|July 14, 1999
Reversible monoclonal lymphadenopathy in autoimmune lymphoproliferative syndrome with functional FAS (CD95/APO-1) deficiencyP Ströbel, R Nanan, S Gattenlöhner, et al.
European Journal of Haematology|November 28, 2001
Periodic fever (TRAPS) caused by mutations in the TNFalpha receptor 1 (TNFRSF1A) gene of three German patientsA Rösen-Wolff, H W Kreth, S Hofmann, et al.
Annals of Neurology|April 1, 1992
Human immunodeficiency virus infection in microglia: correlation between cells infected in the brain and cells cultured from infectious brain tissueR Brinkmann, A Schwinn, O Narayan, et al.
Experimental Hematology|March 25, 1999
Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous diseaseJ Roesler, S Heyden, M Burdelski, et al.
Thrombosis and Haemostasis|July 4, 2001
Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitisV Schuster, P Zeitler, S Seregard, et al.
European Journal of Pediatrics|November 1, 1990
Epstein-Barr virus infection rapidly progressing to monoclonal lymphoproliferative disease in a child with selective immunodeficiencyV Schuster, H W Kreth, H K Müller-Hermelink, et al.
Blood|May 11, 1999
Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitisV Schuster, S Seidenspinner, P Zeitler, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Immunogenetics|January 1, 1984
Partial C4 deficiency in subacute sclerosing panencephalitisC Rittner, E M Meier, B Stradmann, et al.
The American Journal of Surgical Pathology|July 14, 1999
Reversible monoclonal lymphadenopathy in autoimmune lymphoproliferative syndrome with functional FAS (CD95/APO-1) deficiencyP Ströbel, R Nanan, S Gattenlöhner, et al.
European Journal of Haematology|November 28, 2001
Periodic fever (TRAPS) caused by mutations in the TNFalpha receptor 1 (TNFRSF1A) gene of three German patientsA Rösen-Wolff, H W Kreth, S Hofmann, et al.
Annals of Neurology|April 1, 1992
Human immunodeficiency virus infection in microglia: correlation between cells infected in the brain and cells cultured from infectious brain tissueR Brinkmann, A Schwinn, O Narayan, et al.
Experimental Hematology|March 25, 1999
Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous diseaseJ Roesler, S Heyden, M Burdelski, et al.
Thrombosis and Haemostasis|July 4, 2001
Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitisV Schuster, P Zeitler, S Seregard, et al.
European Journal of Pediatrics|November 1, 1990
Epstein-Barr virus infection rapidly progressing to monoclonal lymphoproliferative disease in a child with selective immunodeficiencyV Schuster, H W Kreth, H K Müller-Hermelink, et al.
Blood|May 11, 1999
Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitisV Schuster, S Seidenspinner, P Zeitler, et al.
Pageof 8