1.
Eculizumab in atypical hemolytic uremic syndrome: strategies toward restrictive use
by Wijnsma, Kioa L
Pediatric nephrology (Berlin, West), 2018-11-06, Vol.34 (11), p.2261-2277
2.
The role of properdin in complement-mediated renal diseases: a new player in complement-inhibiting therapy?
by Michels, M.A.H.M
Pediatric nephrology (Berlin, West), 2019, Vol.34 (8), p.1349-1367
3.
An international consensus approach to the management of atypical hemolytic uremic syndrome in children
by Loirat, C
Pediatric Nephrology, 2016, Vol.31 (1), p.15-39
4.
Glyco-iELISA: a highly sensitive and unambiguous serological method to diagnose STEC-HUS caused by serotype O157
by Wijnsma, K.L
Pediatric nephrology (Berlin, West), 2019, Vol.34 (4), p.631-639
5.
Unusual severe case of hemolytic uremic syndrome due to Shiga toxin 2d-producing E. coli O80:H2
by Wijnsma, K.L
Pediatric nephrology (Berlin, West), 2017, Vol.32 (7), p.1263-1268
6.
Fecal diagnostics in combination with serology: best test to establish STEC-HUS
by Wijnsma, K.L
Pediatric nephrology (Berlin, West), 2016, Vol.31 (11), p.2163-2170
7.
Correction to: Eculizumab in atypical hemolytic uremic syndrome: strategies toward restrictive use
by Wijnsma, Kioa L
Pediatric nephrology (Berlin, West), 2019-01-15, Vol.34 (4), p.741-742
8.
Eculizumab as rescue therapy for atypical hemolytic uremic syndrome with normal platelet count
by Dorresteijn, E.M
Pediatric nephrology (Berlin, West), 2012, Vol.27 (7), p.1193-1195
9.
A young girl with an unusual cause of acute kidney injury: Questions
by Binkhorst, M
Pediatric nephrology (Berlin, West), 2016, Vol.31 (11), p.2071-3
10.
A young girl with an unusual cause of acute kidney injury: Answers
by Binkhorst, M
Pediatric nephrology (Berlin, West), 2016, Vol.31 (11), p.2075-2078
11.
Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics
by Geerdink, Lianne M
Pediatric nephrology (Berlin, West), 2012, Vol.27 (8), p.1283-1291
12.
Severe infantile Bordetella pertussis pneumonia in monozygotic twins with a congenital C3 deficiency
by Kurvers, R.A.J
European journal of pediatrics, 2014, Vol.173 (12), p.1591-1594
13.
Unexplained hypothermia and bradycardia in two pediatric patients with Wegener's granulomatosis
by Geerdink, L.M
Pediatric nephrology (Berlin, West), 2011, Vol.26 (2), p.325-326
14.
Cardiovascular disease as a late complication of end-stage renal disease in children
by Groothoff, Jaap W
Pediatric nephrology (Berlin, West), 2005, Vol.20 (3), p.374-379
15.
Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndrome
by Westra, Dineke
Pediatric nephrology (Berlin, West), 2017, Vol.32 (2), p.297-309
16.
The challenge of managing hemophilia A and STEC-induced hemolytic uremic syndrome
by Westra, D
Pediatric nephrology (Berlin, West), 2013, Vol.28 (2), p.349-352
17.
Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy
by Stokman, Marijn F
Pediatric nephrology (Berlin, West), 2018, Vol.33 (10), p.1701-1712
18.
Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene
by Westra, D
Journal of human genetics, 2012, Vol.57 (7), p.459-464
19.
Eculizumab in atypical hemolytic uremic syndrome: strategies toward restrictive use
by Wijnsma, K.L
Pediatric nephrology (Berlin, West), 2019, Vol.34, p.741-742
20.
Unusual severe case of hemolytic uremic syndrome due to Shiga toxin 2d-producing E. coli O80:H2
by Wijnsma, Kioa L
Pediatric nephrology (Berlin, West), 2017-07, Vol.32 (7), p.1263-1268
