Dieter Haffner
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Explore the profile of Dieter Haffner including associated specialties, affiliations and a list of published articles.
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204
Citations
3600
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Recent Articles
1.
Burgmaier K, Kilian S, Arbeiter K, Atmis B, Boyer O, Buescher A, et al.
Kidney Int
. 2025 Feb;
PMID: 39922379
Autosomal recessive polycystic kidney disease (ARPKD) is a severe hepatorenal fibrocystic disorder. Its rareness and the variability of disease courses have been major obstacles for the establishment of clinical trials...
2.
Haffner D, Emma F, Seefried L, Hogler W, Javaid K, Bockenhauer D, et al.
Nat Rev Nephrol
. 2025 Feb;
PMID: 39905262
No abstract available.
3.
Boeckhaus J, Tonshoff B, Weber L, Pape L, Latta K, Fehrenbach H, et al.
Pediatr Nephrol
. 2025 Feb;
PMID: 39904897
Background: Chronic kidney disease (CKD) seriously affects the well-being and shortens the life expectancy of children and adolescents, but its progression is challenging to predict. Therefore, there is an urgent...
4.
Haffner D, Emma F, Seefried L, Hogler W, Javaid K, Bockenhauer D, et al.
Nat Rev Nephrol
. 2025 Jan;
PMID: 39814982
X-linked hypophosphataemia (XLH) is a rare metabolic bone disorder caused by pathogenic variants in the PHEX gene, which is predominantly expressed in osteoblasts, osteocytes and odontoblasts. XLH is characterized by...
5.
Ehrich J, Tasic V, Edvardsson V, Preka E, Prikhodina L, Stefanidis C, et al.
Front Pediatr
. 2025 Jan;
12:1458003.
PMID: 39759883
Background: There is a lack of information on the current healthcare systems for children with kidney diseases across Europe. The aim of this study was to explore the different national...
6.
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...
7.
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)...
8.
Brunkhorst M, Brunkhorst L, Martens H, Papizh S, Besouw M, Grasemann C, et al.
Kidney Int
. 2024 Oct;
107(1):116-129.
PMID: 39461557
Pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter 2a and 2c are rare causes of phosphate wasting. Since data on presentation and outcomes are scarce, we collected clinical, biochemical...
9.
Kesdiren E, Martens H, Brand F, Werfel L, Wedekind L, Trowe M, et al.
Eur J Hum Genet
. 2024 Oct;
33(1):44-55.
PMID: 39420202
Around 180 genes have been associated with congenital anomalies of the kidney and urinary tract (CAKUT) in mice, and represent promising novel candidate genes for human CAKUT. In whole-exome sequencing...
10.
Vivarelli M, Samuel S, Coppo R, Barratt J, Bonilla-Felix M, Haffner D, et al.
Pediatr Nephrol
. 2024 Sep;
40(2):533-569.
PMID: 39331079
IgA nephropathy and IgA vasculitis with nephritis, albeit rare, represent two relatively frequent glomerular conditions in childhood. Compared to adults, pediatric IgA nephropathy has a more acute presentation, most frequently...