Nele Kanzelmeyer
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Explore the profile of Nele Kanzelmeyer including associated specialties, affiliations and a list of published articles.
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28
Citations
96
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Recent Articles
1.
Holle J, Reitmeir R, Behrens F, Singh D, Schindler D, Potapenko O, et al.
Am J Transplant
. 2025 Feb;
PMID: 39978595
Kidney transplantation (KT) is the best treatment for end-stage kidney disease, with graft survival critically affected by the recipient's immune response. The role of the gut microbiome in modulating this...
2.
Saffe S, Doerry K, Buscher A, Hansen M, Rohmann M, Kanzelmeyer N, et al.
Pediatr Nephrol
. 2025 Jan;
PMID: 39869204
Background: Primary hyperoxaluria type 1 (PH 1) is a rare genetic condition due to mutations in the AGXT gene. This leads to an overproduction of oxalate in the liver. Hyperoxaluria...
3.
Prytula A, Reynders D, Goetghebeur E, Krupka K, Bacchetta J, Kanzelmeyer N, et al.
Pediatr Nephrol
. 2025 Jan;
PMID: 39865159
Background: We investigated factors associated with post-transplant growth in pediatric kidney transplant (KTx) recipients with a focus on plasma bicarbonate (HCO3) and estimated the effect of alkali treatment on growth....
4.
Ubenauf T, von der Born J, Sugianto R, Grabitz C, Lehmann E, Memaran N, et al.
J Cardiovasc Magn Reson
. 2025 Jan;
27(1):101839.
PMID: 39814266
Background: Patients after kidney transplantation (KTx) in childhood show a high prevalence of cardiac complications, but the underlying mechanism is still poorly understood. In adults, myocardial fibrosis detected in cardiovascular...
5.
Cappoli A, Kersnik-Levart T, Silecchia V, Ariceta G, Gjerstad A, Ghiggeri G, et al.
Pediatr Nephrol
. 2024 Nov;
40(4):979-986.
PMID: 39589481
Background: C3 glomerulopathy is a rare clinical entity characterized by dysregulation of the alternative complement pathway in glomerular disease. Studies defining the natural history of C3G in the pediatric population...
6.
Brunkhorst L, Terhardt M, Bulitta B, Gutting M, Janzen N, Haffner D, et al.
Kidney Int Rep
. 2024 Nov;
9(11):3236-3249.
PMID: 39534197
Introduction: Monitoring kidney function and immunosuppressant levels in children post-kidney transplantation or those with glomerulopathies is challenging due to frequent venipunctures and clinic visits. Capillary dried blood spot sampling (DBS)...
7.
Klaus R, Kanzelmeyer N, Haffner D, Lange-Sperandio B
Pediatr Nephrol
. 2024 Sep;
40(2):423-430.
PMID: 39320552
Background: Anti-GBM disease is a rare vasculitis mediated by pathogenic antibodies against collagen IV. Anti-GBM disease presents with rapid progressive glomerulonephritis and leads to kidney failure if untreated. KDIGO recommends...
8.
Patry C, Webb N, Feisst M, Krupka K, Becker J, Bald M, et al.
Pediatr Nephrol
. 2024 Aug;
39(12):3569-3580.
PMID: 39110227
Background: Complement 3 glomerulopathy (C3G) and immune complex membranoproliferative glomerulonephritis (IC-MPGN) are ultra-rare chronic kidney diseases with an overall poor prognosis, with approximately 40-50% of patients progressing to kidney failure...
9.
Prytula A, Shroff R, van Gremberghe I, Krupka K, Bacchetta J, Benetti E, et al.
Kidney Int Rep
. 2024 Jun;
9(6):1684-1693.
PMID: 38899185
Introduction: We investigated the relationship between metabolic acidosis over time and allograft outcome in pediatric kidney transplantation (KTx). Methods: This registry study collected data up to 10 years posttransplant. Survival...
10.
Brugelmann M, Muller S, Bohlen A, Hohenfellner K, Buscher A, Kemper M, et al.
Pediatr Nephrol
. 2024 Jun;
39(10):3067-3077.
PMID: 38850407
Background: Infantile nephropathic cystinosis (INC) is a rare lysosomal storage disorder, mostly and often firstly affecting the kidneys, together with impaired disharmonious growth and rickets, eventually resulting in progressive chronic...