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Nature Genetics|August 18, 2016
Patterns of genic intolerance of rare copy number variation in 59,898 human exomesDouglas M Ruderfer, Tymor Hamamsy, Monkol Lek, et al.
Molecular Immunology|August 3, 2006
Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndromeAnna Richards, M Kathryn Liszewski, David Kavanagh, et al.
Immunobiology|June 9, 2016
Chromosomal rearrangement-A rare cause of complement factor I associated atypical haemolytic uraemic syndromePatrick J Gleeson, Valerie Wilson, Thomas E Cox, et al.
Journal of Medical Case Reports|May 1, 2015
Plasma resistant atypical hemolytic uremic syndrome associated with a CFH mutation treated with eculizumab: a case reportMustafa Sevinc, Taner Basturk, Tuncay Sahutoglu, et al.
Journal of the American Society of Nephrology : JASN|May 27, 2005
Mutations in complement factor I predispose to development of atypical hemolytic uremic syndromeDavid Kavanagh, Elizabeth J Kemp, Elizabeth Mayland, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 21, 2009
The binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndromeViviana P Ferreira, Andrew P Herbert, Claudio Cortés, et al.
Kidney Medicine|April 20, 2026
C3 Glomerulonephritis Associated With Anti-complement Factor B Antibodies Following Anti-cancer Treatment With PembrolizumabPersia Stroppou, Lucia Asaelof, Alexia Panayides, et al.
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