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Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference - Kidney International
June 2020 — Molecular Pathology - Insights
Fra klassisk A-hus til moderne villa | Boligmagasinet.dk
Optimal management of atypical hemolytic uremic disease: challenges and solutions. - Document - Gale Academic OneFile
Self‐nonself discrimination by the complement system - Meri - 2016 - FEBS Letters - Wiley Online Library
Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I - Nilsson - 2010 - European Journal of Immunology - Wiley Online Library
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries | Journal of Medical Genetics
Anti-Factor H Antibody Reactivity in Young Adults Vaccinated with a Meningococcal Serogroup B Vaccine Containing Factor H Binding Protein | mSphere
Åhus S:ta Maria kyrka (Ahus, Sverige) - anmeldelser - Tripadvisor
Frontiers | The Relevance of the MCP Risk Polymorphism to the Outcome of aHUS Associated With C3 Mutations. A Case Report | Immunology
Thrombotic microangiopathy after renal transplantation: Current insights in de novo and recurrent disease. - Abstract - Europe PMC
Mutations of Factor H Impair Regulation of Surface-bound C3b by Three Mechanisms in Atypical Hemolytic Uremic Syndrome - ScienceDirect
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference - Kidney International
Thrombotic microangiopathy after renal transplantation: Current insights in de novo and recurrent disease
Mutations of Factor H Impair Regulation of Surface-bound C3b by Three Mechanisms in Atypical Hemolytic Uremic Syndrome - ScienceDirect