Molecular and Cellular Pediatrics
ISSN: 2194-7791
Publisher: SpringerOpen
Publications (11)
Sex differences in long-term kidney fibrosis following neonatal nephron loss during ongoing nephrogenesis (2023)
Menendez-Castro C, Cordasic N, Fahlbusch F, Wölfle J, Hilgers KF, Hartner A
Journal article
Modelling human lower urinary tract malformations in zebrafish (2023)
Kolvenbach CM, Dworschak GC, Rieke JM, Woolf AS, Reutter HM, Odermatt B, Hilger AC
Journal article
High-resolution label-free mapping of murine kidney vasculature by raster-scanning optoacoustic mesoscopy: an ex vivo study (2022)
Goebel CA, Brown E, Fahlbusch F, Wagner A, Buehler A, Raupach T, Hohmann M, et al.
Journal article
DMBT1 is upregulated in cystic fibrosis, affects ciliary motility, and is reduced by acetylcysteine (2022)
Kiefer A, Plattner E, Ruppel R, Weiss C, Zhou-Suckow Z, Mall M, Renner M, Müller H
Journal article
DMBT1 expression and neutrophil-to-lymphocyte ratio during necrotizing enterocolitis are influenced by impaired perfusion due to cardiac anomalies. (2022)
Diez S, Besendörfer M, Weyerer V, Hartmann A, Moosmann J, Weiss C, Renner M, Müller H
Journal article
PTEN hamartoma tumor syndrome in childhood and adolescence-a comprehensive review and presentation of the German pediatric guideline. (2022)
Plamper M, Gohlke B, Wölfle J
Journal article, Review article
Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesis. (2021)
Vidic C, Zaniew M, Jurga S, Thiele H, Reutter HM, Hilger AC
Journal article
Evolving pituitary hormone deficits in primarily isolated GHD: a review and experts' consensus. (2020)
Binder G, Schnabel D, Reinehr T, Pfaeffle R, Dörr HG, Bettendorf M, Hauffa BP, Wölfle J
Journal article, Review article
A role for the alpha-8 integrin chain (itga8) in glomerular homeostasis of the kidney. (2020)
Marek I, Hilgers KF, Rascher W, Wölfle J, Hartner A
Journal article, Review article
Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. (2020)
Dörr HG, Schulze N, Bettendorf M, Binder G, Bonfig W, Denzer C, Dunstheimer D, et al.
Journal article