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Publications by Nicholas Medjeral-Thomas
A Novel CFHR5 Fusion Protein Causes C3 Glomerulopathy in a Family Without Cypriot Ancestry
Kidney International
Nephrology
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Familial C3 Glomerulopathy Associated With CFHR5 Mutations: Clinical Characteristics of 91 Patients in 16 Pedigrees
Clinical Journal of the American Society of Nephrology
Epidemiology
Nephrology
Critical Care
Transplantation
Intensive Care Medicine
C3 Glomerulopathy
F1000Research
Genetics
Molecular Biology
Pharmacology
Biochemistry
Microbiology
Immunology
Medicine
Toxicology
Pharmaceutics
Effectiveness of Cyclosporine in a 10-Year-Old Girl With C3 Glomerulopathy
Childhood Kidney Diseases
Factor B and C4b2a Autoantibodies in C3 Glomerulopathy
Frontiers in Immunology
Allergy
Immunology
Efficacy of Targeted Complement Inhibition in Experimental C3 Glomerulopathy
Journal of the American Society of Nephrology : JASN
Medicine
Nephrology
Membranoproliferative Glomerulonephritis and C3 Glomerulopathy: Resolving the Confusion
Yearbook of Pathology and Laboratory Medicine
A Novel Nonsense ATP2C1 Mutation Causes Hailey-Hailey Disease in a Tunisian Family
Our Dermatology Online
a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family
G3: Genes, Genomes, Genetics
Medicine
Genetics
Molecular Biology
An Engineered Complement Factor H Construct for Treatment of C3 Glomerulopathy
Journal of the American Society of Nephrology : JASN
Medicine
Nephrology