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| Falcão DA, Reis ES, Paixão-Cavalcante D, et al.
Deficiency of the human complement regulatory protein factor h associated with low levels of component c9. [Journal Article]
Scand J Immunol 2008 Oct; 68(4):445-55.
Abstract | Full Citation | Find Related Articles | | Rougier N, Kazatchkine MD, Rougier JP, et al.
Human complement factor H deficiency associated with hemolytic uremic syndrome. [Case Reports, Journal Article]
J Am Soc Nephrol 1998 Dec; 9(12):2318-26.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Stahl AL, Vaziri-Sani F, Heinen S, et al.
Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation. [JOURNAL ARTICLE]
Blood 2008 Feb 11.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Pichette V, Quérin S, Schürch W, et al.
Familial hemolytic-uremic syndrome and homozygous factor H deficiency. [Case Reports, Journal Article]
Am J Kidney Dis 1994 Dec; 24(6):936-41.
Abstract | Full Citation | Find Related Articles | | Kira R, Ihara K, Takada H, et al.
Nonsense mutation in exon 4 of human complement C9 gene is the major cause of Japanese complement C9 deficiency. [Journal Article, Research Support, Non-U.S. Gov't ]
Hum Genet 1998 Jun; 102(6):605-10.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Zoppi M, Weiss M, Nydegger UE, et al.
Recurrent meningitis in a patient with congenital deficiency of the C9 component of complement. First case of C9 deficiency in Europe. [Case Reports, Journal Article, Review]
Arch Intern Med 1990 Nov; 150(11):2395-9.
Abstract | Full Citation | Find Related Articles | | Guc D, Gulati P, Lemercier C, et al.
Expression of the components and regulatory proteins of the alternative complement pathway and the membrane attack complex in normal and diseased synovium. [Journal Article]
Rheumatol Int 1993; 13(4):139-46.
Abstract | Full Citation | Find Related Articles | | Witzel-Schlömp K, Späth PJ, Hobart MJ, et al.
The human complement C9 gene: identification of two mutations causing deficiency and revision of the gene structure. [Journal Article]
J Immunol 1997 May 15; 158(10):5043-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Fijen CA, Kuijper EJ, Te Bulte M, et al.
Heterozygous and homozygous factor H deficiency states in a Dutch family. [Case Reports, Journal Article]
Clin Exp Immunol 1996 Sep; 105(3):511-6.
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