Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype

M Noris, J Caprioli, E Bresin, C Mossali… - Clinical Journal of the …, 2010 - journals.lww.com
Background and objectives: Hemolytic uremic syndrome (HUS) is characterized by
microangiopathic hemolytic anemia, thrombocytopenia, and renal impairment. Most …
被引用次数：1244 相关文章
[HTML] nih.gov

[HTML][HTML] Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

M Noris, J Caprioli, E Bresin, C Mossali… - Clinical Journal of the …, 2010 - ncbi.nlm.nih.gov
Background and objectives: Hemolytic uremic syndrome (HUS) is characterized by
microangiopathic hemolytic anemia, thrombocytopenia, and renal impairment. Most …

[引用][C] Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

M Noris, J Caprioli, E Bresin, C Mossali… - Clinical Journal of the …, 2010 - cir.nii.ac.jp
Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their
Impact on Clinical Phenotype | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ …
[PDF] academia.edu

[PDF][PDF] Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

M Noris, J Caprioli, E Bresin, C Mossali… - Clin J Am Soc …, 2010 - academia.edu
Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their
Impact on Clinical Phenotype Page 1 Relative Role of Genetic Complement Abnormalities in …

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype

M Noris, J Caprioli, E Bresin… - Clinical journal of …, 2010 - pubmed.ncbi.nlm.nih.gov
Background and objectives Hemolytic uremic syndrome (HUS) is characterized by
microangiopathic hemolytic anemia, thrombocytopenia, and renal impairment. Most …
[PDF] researchgate.net

[PDF][PDF] Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

M Noris, J Caprioli, E Bresin, C Mossali… - Clin J Am Soc …, 2010 - researchgate.net
Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their
Impact on Clinical Phenotype Page 1 Relative Role of Genetic Complement Abnormalities in …

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.

M Noris, J Caprioli, E Bresin, C Mossali… - Clinical Journal of the …, 2010 - europepmc.org
Results In> 70% of sporadic and familial cases, gene mutations, disease-associated factor H
(CFH) polymorphisms, or anti-CFH autoantibodies were found. Either mutations or CFH …

Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

M Noris, J Caprioli, E Bresin, C Mossali… - Clinical Journal of the …, 2010 - eprints.ncl.ac.uk
Background and objectives: Hemolytic uremic syndrome (HUS) is characterized by
microangiopathic hemolytic anemia, thrombocytopenia, and renal impairment. Most …

[引用][C] Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype

M NORIS - Clin J Am Soc Nephrol, 2010 - cir.nii.ac.jp
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their
impact on clinical phenotype | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ …

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.

M Noris, J Caprioli, E Bresin, C Mossali… - Clinical Journal of the …, 2010 - europepmc.org
Results In> 70% of sporadic and familial cases, gene mutations, disease-associated factor H
(CFH) polymorphisms, or anti-CFH autoantibodies were found. Either mutations or CFH …