Sanne W. Van Kraaij
Nijmegen, GE, Netherlands
Last Updated: 09/26/2026
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Found 8 publications
Different Aspects of Classical Pathway Overactivation in Patients With C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis.
Journal: Frontiers in immunology
Published: May 27, 2021
Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa.
Journal: American journal of human genetics
Published: August 09, 2020
The complement component C5 is not responsible for the alternative pathway activity in rabbit erythrocyte hemolytic assays during eculizumab treatment.
Journal: Cellular & molecular immunology
Published: February 27, 2020
Novel defect in phosphatidylinositol 4-kinase type 2-alpha (PI4K2A) at the membrane-enzyme interface is associated with metabolic cutis laxa.
Journal: Journal of inherited metabolic disease
Published: December 30, 2019
Novel Assays to Distinguish Between Properdin-Dependent and Properdin-Independent C3 Nephritic Factors Provide Insight Into Properdin-Inhibiting Therapy.
Journal: Frontiers in immunology
Published: November 30, 2018
Overactivity of Alternative Pathway Convertases in Patients With Complement-Mediated Renal Diseases.
Overactivity of Alternative Pathway Convertases in Patients With Complement-Mediated Renal Diseases.
Journal: Frontiers in immunology
Published: December 16, 2017
Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies.
Journal: American journal of human genetics
Published: October 31, 2017
Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa.
Journal: American journal of human genetics
Published: September 21, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026