Cargando…

Deficiency of complement factor H-related proteins and autoantibody-positive hemolytic uremic syndrome in an infant with combined partial deficiencies and autoantibodies to complement factor H and ADAMTS13

Mostrar otras versiones (1)

Detalles Bibliográficos
Autores principales:	Michael, Mini, Turner, Nancy, Elenberg, Ewa, Shaffer, Linda G, Teruya, Jun, Arar, Mazen, Hui, Shiu-Ki, Smith, Richard J, Moake, Joel
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2018
Materias:	Errata
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467586/ https://www.ncbi.nlm.nih.gov/pubmed/32905169 http://dx.doi.org/10.1093/ckj/sfy028

Ejemplares similares

Deficiency of complement factor H-related proteins and autoantibody-positive hemolytic uremic syndrome in an infant with combined partial deficiencies and autoantibodies to complement factor H and ADAMTS13
por: Michael, Mini, et al.
Publicado: (2018)

Association among Complement Factor H Autoantibodies, Deletions of CFHR, and the Risk of Atypical Hemolytic Uremic Syndrome
por: Jiang, Hong, et al.
Publicado: (2016)

Complement factor H and the hemolytic uremic syndrome
por: Atkinson, John P., et al.
Publicado: (2007)

Factor H autoantibodies and deletion of Complement Factor H-Related protein-1 in rheumatic diseases in comparison to atypical hemolytic uremic syndrome
por: Foltyn Zadura, Anna, et al.
Publicado: (2012)

Factor H Autoantibodies and Complement-Mediated Diseases
por: Zhang, Yuzhou, et al.
Publicado: (2020)

Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation
por: Kim, Sejin, et al.
Publicado: (2017)

Idiopathic combined, autoantibody-mediated ADAMTS-13/factor H deficiency in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome in a 17-year-old woman: a case report
por: Patschan, Daniel, et al.
Publicado: (2011)

Anesthetic management of living donor liver transplantation for complement factor H deficiency hemolytic uremic syndrome: a case report
por: Park, Suk-Hee, et al.
Publicado: (2014)

Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland
por: Brocklebank, Vicky, et al.
Publicado: (2017)

Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains
por: Pickering, Matthew C., et al.
Publicado: (2007)

ATYPICAL HEMOLYTIC UREMIC SYNDROME AND GENETIC ABERRATIONS IN THE COMPLEMENT FACTOR H RELATED 5 GENE
por: Westra, Dineke, et al.
Publicado: (2012)

Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome
por: Oymak, Yeşim, et al.
Publicado: (2015)

Complement Factor H Modulates Splenic B Cell Development and Limits Autoantibody Production
por: Kiss, Máté G., et al.
Publicado: (2019)

Complement and the atypical hemolytic uremic syndrome in children
por: Loirat, Chantal, et al.
Publicado: (2008)

Atypical hemolytic-uremic syndrome due to complement factor I mutation
por: Almalki, Abdullah H, et al.
Publicado: (2017)

Autoantibodies against complement factor B in rheumatoid arthritis
por: Matola, Alexandra T., et al.
Publicado: (2023)

Autoantibodies Against the Complement Regulator Factor H in the Serum of Patients With Neuromyelitis Optica Spectrum Disorder
por: Uzonyi, Barbara, et al.
Publicado: (2021)

Anti-complement factor H (CFH) autoantibodies could delay pristane-induced lupus nephritis
por: Li, Lin-Lin, et al.
Publicado: (2023)

Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome
por: Zipfel, Peter F, et al.
Publicado: (2007)

Antibody recognition of complement factor H reveals a flexible loop involved in atypical hemolytic uremic syndrome pathogenesis
por: Yokoo, Takanori, et al.
Publicado: (2022)

Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndrome
por: Westra, Dineke, et al.
Publicado: (2016)

Complement Factor H Inhibits Anti-Neutrophil Cytoplasmic Autoantibody-Induced Neutrophil Activation by Interacting With Neutrophils
por: Chen, Su-Fang, et al.
Publicado: (2018)

Regulatory Components of the Alternative Complement Pathway in Endothelial Cell Cytoplasm, Factor H and Factor I, Are Not Packaged in Weibel-Palade Bodies
por: Turner, Nancy A., et al.
Publicado: (2015)

Atypical Hemolytic Uremic Syndrome Caused by a Rare Complement Factor B Mutation
por: Bandaru, Sai Samyuktha
Publicado: (2022)

Complements Spurned: Our Experience with Atypical Hemolytic Uremic Syndrome
por: Nagar, Vidya S., et al.
Publicado: (2017)

Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies
por: Zhou, Danlei, et al.
Publicado: (2023)

Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics
por: Geerdink, Lianne M., et al.
Publicado: (2012)

Evaluation of complement regulatory components in patients with atypical hemolytic uremic syndrome
por: Soudabeh, Hosseini, et al.
Publicado: (2014)

Complement activation in children with Streptococcus pneumoniae associated hemolytic uremic syndrome
por: Holle, Johannes, et al.
Publicado: (2021)

Case report: Autoimmune hemolytic anemia caused by warm and cold autoantibodies with complement activation—etiological and therapeutic issues
por: Turudic, Daniel, et al.
Publicado: (2023)

High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3*B
por: Pouw, Richard B., et al.
Publicado: (2018)

Newer Antigens, Controls and Types in Complement, in the Serology of Syphilis, and Associated Considerations
Publicado: (1951)

Postoperative Atypical Hemolytic Uremic Syndrome Associated with Complement C3 Mutation
por: Matsukuma, Eiji, et al.
Publicado: (2014)

Acute Systolic Heart Failure Associated with Complement-Mediated Hemolytic Uremic Syndrome
por: Vaughn, John L., et al.
Publicado: (2015)

Complement Activation Contributes to the Pathophysiology of Shiga Toxin-Associated Hemolytic Uremic Syndrome
por: Buelli, Simona, et al.
Publicado: (2019)

ADAMTS13 Gene Mutations in Children with Hemolytic Uremic Syndrome
por: Choi, Hyoung Soo, et al.
Publicado: (2011)

Efficacy of rituximab and plasmapharesis in an adult patient with antifactor H autoantibody-associated hemolytic uremic syndrome: A case report and literature review
por: Deville, Clemence, et al.
Publicado: (2016)

Blockade of the Terminal Complement Cascade Using Ravulizumab in a Pediatric Patient With Anti-complement Factor H Autoantibody-Associated aHUS: A Case Report and Literature Review
por: Wu, Xiaoyan, et al.
Publicado: (2021)

Corrigendum: High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3(*)B
por: Pouw, Richard B., et al.
Publicado: (2020)

MOGAD patient autoantibodies induce complement, phagocytosis, and cellular cytotoxicity
por: Yandamuri, Soumya S., et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_fsb215dvkve19pjhqpucpvplrt