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Burkhard Toenshoff

Explore the profile of Burkhard Toenshoff including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 12
Citations 473
Followers 0
Related Specialties
General Medicine
Genetics
General Surgery
Top 10 Co-Authors
Henry Fehrenbach
Christoph Mache
Bernd Hoppe
Lars Pape
Hanno J Bolz
Lothar B Zimmerhackl
Dirk E Muller-Wiefel
Valeska Frank
Britta Hocker
Martin Pohl
Published In
BMJ Open
Am J Hum Genet
Transplantation
Eur J Hum Genet
Ther Drug Monit
Affiliations
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Recent Articles
1.
The gut microbiome in solid organ transplantation
Baghai Arassi M, Zeller G, Karcher N, Zimmermann M, Toenshoff B
Pediatr Transplant . 2020 Sep; 24(7):e13866. PMID: 32997434
Despite ground-breaking advances in allogeneic transplantation, allograft rejection and immunosuppressant-specific complications remain a major challenge in transplant medicine. Growing evidence suggests the human gut microbiome as a potential contributor to...
2.
Cross-sectional analysis on publication status and age representation of clinical studies addressing mechanical ventilation and ventilator-induced lung injury in infants and children
Patry C, Kranig S, Rafat N, Schaible T, Toenshoff B, Hoffmann G, et al.
BMJ Open . 2018 Nov; 8(11):e023524. PMID: 30455388
Objectives: We determined the number and time-to-public availability of study results of published and unpublished clinical studies in paediatric mechanical ventilation (MV) and ventilator-induced lung injury (VILI), which were registered...
3.
Initial treatment of steroid-sensitive idiopathic nephrotic syndrome in children with mycophenolate mofetil prednisone: protocol for a randomised, controlled, multicentre trial (INTENT study)
Ehren R, Benz M, Doetsch J, Fichtner A, Gellermann J, Haffner D, et al.
BMJ Open . 2018 Oct; 8(10):e024882. PMID: 30309995
Introduction: Idiopathic nephrotic syndrome is the most common glomerular disease in childhood with an incidence of 1.8 cases per 100 000 children in Germany. The treatment of the first episode...
4.
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease
Eisenberger T, Decker C, Hiersche M, Hamann R, Decker E, Neuber S, et al.
PLoS One . 2015 Feb; 10(2):e0116680. PMID: 25646624
Renal cysts are clinically and genetically heterogeneous conditions. Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent life-threatening genetic disease and mainly caused by mutations in PKD1. The presence...
5.
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease
Schmidts M, Frank V, Eisenberger T, Al Turki S, Bizet A, Antony D, et al.
Hum Mutat . 2013 Feb; 34(5):714-24. PMID: 23418020
Ciliopathies are genetically heterogeneous disorders characterized by variable expressivity and overlaps between different disease entities. This is exemplified by the short rib-polydactyly syndromes, Jeune, Sensenbrenner, and Mainzer-Saldino chondrodysplasia syndromes. These...
6.
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies
Beck B, Baasner A, Buescher A, Habbig S, Reintjes N, Kemper M, et al.
Eur J Hum Genet . 2012 Jul; 21(2):162-72. PMID: 22781098
Identification of mutations in the HOGA1 gene as the cause of autosomal recessive primary hyperoxaluria (PH) type III has revitalized research in the field of PH and related stone disease....
7.
Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation
Jungraithmayr T, Hofer K, Cochat P, Chernin G, Cortina G, Fargue S, et al.
J Am Soc Nephrol . 2011 Mar; 22(3):579-85. PMID: 21355056
Steroid-resistant focal segmental glomerulosclerosis (FSGS) often recurs after renal transplantation. In this international survey, we sought to identify genotype-phenotype correlations of recurrent FSGS. We surveyed 83 patients with childhood-onset primary...
8.
Intestinal reconstruction of the lower urinary tract as a prerequisite for renal transplantation
Djakovic N, Wagener N, Adams J, Gilfrich C, Haferkamp A, Pfitzenmaier J, et al.
BJU Int . 2008 Dec; 103(11):1555-60. PMID: 19076129
OBJECTIVE To report a two-stage protocol for children in whom bladder reconstruction was followed by kidney transplantation, as about a quarter of children requiring a kidney transplantation show significant lower...
9.
Efficacy and safety of basiliximab in pediatric renal transplant patients receiving cyclosporine, mycophenolate mofetil, and steroids
Offner G, Toenshoff B, Hocker B, Krauss M, Bulla M, Cochat P, et al.
Transplantation . 2008 Nov; 86(9):1241-8. PMID: 19005406
Background: Basiliximab, a monoclonal CD25 antibody has proofed effective in reducing acute rejection episodes in adults in various immunosuppressive regimens. The effect of basiliximab in the pediatric population is controversial....
10.
CNS or bone marrow involvement as risk factors for poor survival in post-transplantation lymphoproliferative disorders in children after solid organ transplantation
Maecker B, Jack T, Zimmermann M, Abdul-Khaliq H, Burdelski M, Fuchs A, et al.
J Clin Oncol . 2007 Nov; 25(31):4902-8. PMID: 17971586
Purpose: To identify prognostic factors of survival in pediatric post-transplantation lymphoproliferative disorder (PTLD) after solid organ transplantation. Patients And Methods: A multicenter, retrospective case analysis of 55 pediatric solid organ...