Detalhe da pesquisa
1.
Relationship between age at initiation of cysteamine treatment, adherence with therapy, and glomerular kidney function in infantile nephropathic cystinosis.
Mol Genet Metab
; 136(4): 268-273, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35835062
2.
Timing of reconstruction of the lower urinary tract in pediatric kidney transplant recipients: A CERTAIN multicenter analysis of current practice.
Pediatr Transplant
; 26(6): e14328, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35689820
3.
Prevalence and potential relevance of hyperuricemia in pediatric kidney transplant recipients-a CERTAIN registry analysis.
Pediatr Transplant
; 26(4): e14265, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35263498
4.
Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis.
Pediatr Nephrol
; 36(2): 463-471, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32715379
5.
Sex and age as determinants for high blood pressure in pediatric renal transplant recipients: a longitudinal analysis of the CERTAIN Registry.
Pediatr Nephrol
; 35(3): 415-426, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31811541
6.
Clinical course of hantavirus-induced nephropathia epidemica in children compared to adults in Germany-analysis of 317 patients.
Pediatr Nephrol
; 34(7): 1247-1252, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30874941
7.
Vaccination titres pre- and post-transplant in paediatric renal transplant recipients and the impact of immunosuppressive therapy.
Pediatr Nephrol
; 33(5): 897-910, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29322328
8.
Incomplete vaccination coverage in European children with end-stage kidney disease prior to renal transplantation.
Pediatr Nephrol
; 33(2): 341-350, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28983694
9.
Presentation of pediatric Henoch-Schönlein purpura nephritis changes with age and renal histology depends on biopsy timing.
Pediatr Nephrol
; 33(2): 277-286, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28983704
10.
Dyslipidemia after pediatric renal transplantation-The impact of immunosuppressive regimens.
Pediatr Transplant
; 21(3)2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28370750
11.
Correction to: Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis.
Pediatr Nephrol
; 36(12): 4015, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34553238
12.
Automated Greulich-Pyle bone age determination in children with chronic kidney disease.
Pediatr Nephrol
; 30(7): 1173-9, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25787071
13.
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease.
Hum Mutat
; 34(5): 714-24, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23418020
14.
Expanding the Phenotypic Spectrum of Kenny-Caffey Syndrome.
J Clin Endocrinol Metab
; 108(9): e754-e768, 2023 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36916904
15.
Withdrawn as duplicate: Expanding the phenotypic spectrum of Kenny-Caffey syndrome: a case series and systematic literature review.
J Clin Endocrinol Metab
; 108(7): e501, 2023 Jun 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36919775
16.
Working Towards a Treat-to-Target Protocol in Juvenile Proliferative Lupus Nephritis - A Survey of Pediatric Rheumatologists and Nephrologists in Germany and Austria.
Front Pediatr
; 10: 851998, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35529329
17.
Refining Kidney Survival in 383 Genetically Characterized Patients With Nephronophthisis.
Kidney Int Rep
; 7(9): 2016-2028, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36090483
18.
Renal and Skeletal Anomalies in a Cohort of Individuals With Clinically Presumed Hereditary Nephropathy Analyzed by Molecular Genetic Testing.
Front Genet
; 12: 642849, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34122504
19.
Cardiac Phenotype and Tissue Sodium Content in Adolescents With Defects in the Melanocortin System.
J Clin Endocrinol Metab
; 106(9): 2606-2616, 2021 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34036349
20.
Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD).
Sci Rep
; 10(1): 16025, 2020 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32994492