An atypical case of a 2-year-old boy with acute kidney injury: a race against time. Questions.
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- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1175, doi. 10.1007/s00467-016-3497-z
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- Publication type:
- Article
Works matching IS 0931041X AND DT 2017 AND VI 32 AND IP 7
Results: 26
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Congenital eyelid ptosis, decreased glomerular filtration, and orthostatic hypotension: Answers.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1171, doi. 10.1007/s00467-016-3515-1
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- Publication type:
- Article
3
An atypical case of a 2-year-old boy with acute kidney injury: a race against time. Answers.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1177, doi. 10.1007/s00467-016-3516-0
- By:
- Publication type:
- Article
4
Delayed graft function and its management in children.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1157, doi. 10.1007/s00467-016-3528-9
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- Publication type:
- Article
5
C4d deposits in IgA nephropathy: where does complement activation come from?
- Published in:
- 2017
- By:
- Publication type:
- Editorial
6
Efficacy and safety of paricalcitol in children with stages 3 to 5 chronic kidney disease.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1221, doi. 10.1007/s00467-017-3579-6
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- Publication type:
- Article
7
Dietary sources of energy and nutrient intake among children and adolescents with chronic kidney disease.
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- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1233, doi. 10.1007/s00467-017-3580-0
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- Publication type:
- Article
8
Association among prematurity (<30 weeks' gestational age), blood pressure, urinary albumin, calcium, and phosphate in early childhood.
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- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1243, doi. 10.1007/s00467-017-3581-z
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- Publication type:
- Article
9
Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1181, doi. 10.1007/s00467-017-3590-y
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- Publication type:
- Article
10
Membrane pressures predict clotting of pediatric continuous renal replacement therapy circuits.
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- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1251, doi. 10.1007/s00467-017-3601-z
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- Publication type:
- Article
11
Clinical outcomes in children with Henoch-Schönlein purpura nephritis without crescents.
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- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1193, doi. 10.1007/s00467-017-3604-9
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- Publication type:
- Article
12
The ISKDC classification and a new semiquantitative classification for predicting outcomes of Henoch-Schönlein purpura nephritis.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1201, doi. 10.1007/s00467-017-3608-5
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- Publication type:
- Article
13
Mesangial C4d deposition may predict progression of kidney disease in pediatric patients with IgA nephropathy.
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- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1211, doi. 10.1007/s00467-017-3610-y
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- Publication type:
- Article
14
Conversion from immediate- to extended-release cysteamine may decrease disease control and increase additional side effects.
- Published in:
- 2017
- By:
- Publication type:
- Letter
15
Children with Henoch-Schönlein purpura with low complement levels: follow-up for >6 years.
- Published in:
- 2017
- By:
- Publication type:
- Letter
16
Unusual severe case of hemolytic uremic syndrome due to Shiga toxin 2d-producing E. coli O80:H2.
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- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1263, doi. 10.1007/s00467-017-3642-3
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- Publication type:
- Article
17
Erratum to: mesangial C4d deposition may predict progression of kidney disease in pediatric patients with IgA nephropathy.
- Published in:
- 2017
- By:
- Publication type:
- Erratum
18
Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1269, doi. 10.1007/s00467-017-3648-x
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- Publication type:
- Article
19
Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.
- Published in:
- 2017
- By:
- Publication type:
- Erratum
20
Polycythemia, capillary rarefaction, and focal glomerulosclerosis in two adolescents born extremely low birth weight and premature.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1275, doi. 10.1007/s00467-017-3654-z
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- Publication type:
- Article
21
Oral paricalcitol: expanding therapeutic options for pediatric chronic kidney disease patients.
- Published in:
- 2017
- By:
- Publication type:
- Editorial
22
Potassium: friend or foe?
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1109, doi. 10.1007/s00467-016-3411-8
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- Publication type:
- Article
23
Genetic causes of hypomagnesemia, a clinical overview.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1123, doi. 10.1007/s00467-016-3416-3
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- Publication type:
- Article
24
Treatment of renal angiomyolipoma in tuberous sclerosis complex (TSC) patients.
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- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1137, doi. 10.1007/s00467-016-3474-6
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- Publication type:
- Article
25
Peritoneal dialysis for the management of pediatric patients with acute kidney injury.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1145, doi. 10.1007/s00467-016-3482-6
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- Publication type:
- Article
26
Congenital eyelid ptosis, decreased glomerular filtration, and orthostatic hypotension: Questions.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 7, p. 1169, doi. 10.1007/s00467-016-3494-2
- By:
- Publication type:
- Article