Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations.
- Published in:
- 2007
- By:
- Publication type:
- Correction Notice
Works matching IS 0931041X AND DT 2007 AND VI 22 AND IP 5
Results: 27
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Genetics of focal segmental glomerulosclerosis.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 638, doi. 10.1007/s00467-007-0445-y
- By:
- Publication type:
- Article
3
In memory of Dr. Johannes Brodehl, born 20 October 1931 and died 2 September 2006.
- Published in:
- 2007
- By:
- Publication type:
- Obituary
4
ACE inhibition in orthostatic proteinuria associated with nutcracker syndrome would be individualized.
- Published in:
- 2007
- By:
- Publication type:
- Letter
5
ACE inhibition in nutcracker syndrome with orthostatic proteinuria: how about a hemodynamic effect?
- Published in:
- 2007
- By:
- Publication type:
- Letter
6
Effects of deflazacort vs. methylprednisone: a randomized study in kidney transplant patients.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 734, doi. 10.1007/s00467-006-0403-0
- By:
- Publication type:
- Article
7
Superior sagittal sinus thrombosis and bilateral sixth-nerve palsy in a child with nephrotic syndrome.
- Published in:
- 2007
- By:
- Publication type:
- Report
8
Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 661, doi. 10.1007/s00467-006-0409-7
- By:
- Publication type:
- Article
9
Effect of carnitine supplementation on lipid profile and anemia in children on chronic dialysis.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 727, doi. 10.1007/s00467-006-0408-8
- By:
- Publication type:
- Article
10
Is mesangial hypercellularity with glomerular immaturity a variant of glomerulosclerosis?
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 674, doi. 10.1007/s00467-006-0407-9
- By:
- Publication type:
- Article
11
Adolescent dialysis patient transition to adult care: a cross-sectional survey.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 720, doi. 10.1007/s00467-006-0404-z
- By:
- Publication type:
- Article
12
Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.
- Published in:
- 2007
- By:
- Publication type:
- Report
13
Darbepoetin, effective treatment of anaemia in paediatric patients with chronic renal failure.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 708, doi. 10.1007/s00467-006-0402-1
- By:
- Publication type:
- Article
14
Ceftriaxone associated nephrolithiasis: a prospective study in 284 children.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 690, doi. 10.1007/s00467-006-0401-2
- By:
- Publication type:
- Article
15
Severe anemia caused by the angiotensin receptor blocker irbesartan after renal transplantation.
- Published in:
- 2007
- By:
- Publication type:
- Letter
16
A multicenter study of the pharmacokinetics of lisinopril in pediatric patients with hypertension.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 695, doi. 10.1007/s00467-006-0399-5
- By:
- Publication type:
- Article
17
How to define anemia in children with chronic kidney disease?
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 702, doi. 10.1007/s00467-006-0397-7
- By:
- Publication type:
- Article
18
Association of isolated preauricular tags and nephrourological anomalies: case-control study.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 658, doi. 10.1007/s00467-006-0395-9
- By:
- Publication type:
- Article
19
Meningococcal disease associated with an acute post-streptococcal complement deficiency.
- Published in:
- 2007
- By:
- Publication type:
- Report
20
Nine novel COL4A3 and COL4A4 mutations and polymorphisms identified in inherited membrane diseases.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 652, doi. 10.1007/s00467-006-0393-y
- By:
- Publication type:
- Article
21
Diagnosis of Alport syndrome without biopsy?
- Published in:
- 2007
- By:
- Publication type:
- Editorial
22
Diagnosis of de novo localized thrombotic microangiopathy by surveillance biopsy.
- Published in:
- 2007
- By:
- Publication type:
- Report
23
A case of nephrogenic diabetes insipidus with a novel missense mutation in the AVPR2 gene.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 670, doi. 10.1007/s00467-006-0388-8
- By:
- Publication type:
- Article
24
Renal scarring sequelae in childhood Kawasaki disease.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 684, doi. 10.1007/s00467-006-0385-y
- By:
- Publication type:
- Article
25
Metabolic disturbances following the use of inadequate solutions for hemofiltration in acute renal failure.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 715, doi. 10.1007/s00467-006-0380-3
- By:
- Publication type:
- Article
26
Do mutations in COL4A1 or COL4A2 cause thin basement membrane nephropathy (TBMN)?
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 645, doi. 10.1007/s00467-006-0391-0
- By:
- Publication type:
- Article
27
Malaria-induced renal damage: facts and myths.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 5, p. 626, doi. 10.1007/s00467-006-0332-y
- By:
- Publication type:
- Article