| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An atypical case of a 2-year-old boy with acute kidney injury: a race against time. Answers
|
Keenswijk, Werner
|
|
2016
|
32 |
7 |
p. 1177-1179
|
artikel
|
| 2 |
An atypical case of a 2-year-old boy with acute kidney injury: a race against time. Questions
|
Keenswijk, Werner
|
|
2016
|
32 |
7 |
p. 1175-1176
|
artikel
|
| 3 |
Association among prematurity (<30 weeks’ gestational age), blood pressure, urinary albumin, calcium, and phosphate in early childhood
|
Vashishta, Namrata
|
|
2017
|
32 |
7 |
p. 1243-1250
|
artikel
|
| 4 |
C4d deposits in IgA nephropathy: where does complement activation come from?
|
Coppo, Rosanna
|
|
2017
|
32 |
7 |
p. 1097-1101
|
artikel
|
| 5 |
Challenges in establishing genotype–phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations
|
Ebner, Kathrin
|
|
2017
|
32 |
7 |
p. 1269-1273
|
artikel
|
| 6 |
Children with Henoch–Schönlein purpura with low complement levels: follow-up for >6 years
|
Lin, Qiang
|
|
2017
|
32 |
7 |
p. 1279
|
artikel
|
| 7 |
Clinical outcomes in children with Henoch–Schönlein purpura nephritis without crescents
|
Delbet, Jean Daniel
|
|
2017
|
32 |
7 |
p. 1193-1199
|
artikel
|
| 8 |
Congenital eyelid ptosis, decreased glomerular filtration, and orthostatic hypotension: Answers
|
Wassenberg, Tessa
|
|
2016
|
32 |
7 |
p. 1171-1174
|
artikel
|
| 9 |
Congenital eyelid ptosis, decreased glomerular filtration, and orthostatic hypotension: Questions
|
Wassenberg, Tessa
|
|
2016
|
32 |
7 |
p. 1169-1170
|
artikel
|
| 10 |
Conversion from immediate- to extended-release cysteamine may decrease disease control and increase additional side effects
|
Bäumner, Sören
|
|
2017
|
32 |
7 |
p. 1281-1282
|
artikel
|
| 11 |
Delayed graft function and its management in children
|
Grenda, Ryszard
|
|
2016
|
32 |
7 |
p. 1157-1167
|
artikel
|
| 12 |
Dietary sources of energy and nutrient intake among children and adolescents with chronic kidney disease
|
Chen, Wen
|
|
2017
|
32 |
7 |
p. 1233-1241
|
artikel
|
| 13 |
Efficacy and safety of paricalcitol in children with stages 3 to 5 chronic kidney disease
|
Webb, Nicholas J. A.
|
|
2017
|
32 |
7 |
p. 1221-1232
|
artikel
|
| 14 |
Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability
|
Crawford, Brendan D.
|
|
2017
|
32 |
7 |
p. 1285
|
artikel
|
| 15 |
Erratum to: mesangial C4d deposition may predict progression of kidney disease in pediatric patients with IgA nephropathy
|
Fabiano, Rafaela Cabral Gonçalves
|
|
2017
|
32 |
7 |
p. 1283
|
artikel
|
| 16 |
Genetic causes of hypomagnesemia, a clinical overview
|
Viering, Daan H. H. M
|
|
2016
|
32 |
7 |
p. 1123-1135
|
artikel
|
| 17 |
Membrane pressures predict clotting of pediatric continuous renal replacement therapy circuits
|
Kakajiwala, Aadil
|
|
2017
|
32 |
7 |
p. 1251-1261
|
artikel
|
| 18 |
Mesangial C4d deposition may predict progression of kidney disease in pediatric patients with IgA nephropathy
|
Fabiano, Rafaela Cabral Gonçalves
|
|
2017
|
32 |
7 |
p. 1211-1220
|
artikel
|
| 19 |
Oral paricalcitol: expanding therapeutic options for pediatric chronic kidney disease patients
|
Freundlich, Michael
|
|
2017
|
32 |
7 |
p. 1103-1108
|
artikel
|
| 20 |
Peritoneal dialysis for the management of pediatric patients with acute kidney injury
|
Vasudevan, Anil
|
|
2016
|
32 |
7 |
p. 1145-1156
|
artikel
|
| 21 |
Peritoneal dialysis for the management of pediatric patients with acute kidney injury
|
Vasudevan, Anil
|
|
|
32 |
7 |
p. 1145-1156
|
artikel
|
| 22 |
Polycythemia, capillary rarefaction, and focal glomerulosclerosis in two adolescents born extremely low birth weight and premature
|
Asada, Nariaki
|
|
2017
|
32 |
7 |
p. 1275-1278
|
artikel
|
| 23 |
Potassium: friend or foe?
|
Rodan, Aylin R.
|
|
2016
|
32 |
7 |
p. 1109-1121
|
artikel
|
| 24 |
Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome
|
Wang, Fang
|
|
2017
|
32 |
7 |
p. 1181-1192
|
artikel
|
| 25 |
The ISKDC classification and a new semiquantitative classification for predicting outcomes of Henoch–Schönlein purpura nephritis
|
Koskela, Mikael
|
|
2017
|
32 |
7 |
p. 1201-1209
|
artikel
|
| 26 |
Treatment of renal angiomyolipoma in tuberous sclerosis complex (TSC) patients
|
Brakemeier, S.
|
|
2016
|
32 |
7 |
p. 1137-1144
|
artikel
|
| 27 |
Unusual severe case of hemolytic uremic syndrome due to Shiga toxin 2d-producing E. coli O80:H2
|
Wijnsma, Kioa L.
|
|
2017
|
32 |
7 |
p. 1263-1268
|
artikel
|
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