Issue 1/2021
Content (21 Articles)
Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortality
Claudia Dafinger, Thomas Benzing, Jörg Dötsch, Bernhard Schermer, Max C. Liebau
Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT)
Stefan Kohl, Sandra Habbig, Lutz T. Weber, Max C. Liebau
Relationship between adiponectin, TNFα, and SHBG in prepubertal children with obesity
Marta Ramon-Krauel, María Jesús Leal-Witt, Óscar Osorio-Conles, Montse Amat-Bou, Carles Lerin, David M. Selva
Combined RT-qPCR and pyrosequencing of a Spike glycoprotein polybasic cleavage motif can uncover pediatric SARS-CoV-2 infections associated with heterogeneous presentation
Patrick Philipp Weil, Jacqueline Hentschel, Frank Schult, Anton Pembaur, Beniam Ghebremedhin, Olivier Mboma, Andreas Heusch, Anna-Christin Reuter, Daniel Müller, Stefan Wirth, Malik Aydin, Andreas C. W. Jenke, Jan Postberg
Daratumumab therapy for post-HSCT immune-mediated cytopenia: experiences from two pediatric cases and review of literature
Lina Driouk, Robert Schmitt, Anke Peters, Sabine Heine, Hermann Josef Girschick, Brigitte Strahm, Charlotte M. Niemeyer, Carsten Speckmann
Identification of a novel MICU1 nonsense variant causes myopathy with extrapyramidal signs in an Iranian consanguineous family
Fatemeh Bitarafan, Mehrnoosh Khodaeian, Elham Amjadi Sardehaei, Fatemeh Zahra Darvishi, Navid Almadani, Yalda Nilipour, Masoud Garshasbi
Aggressive infantile myofibromatosis with intestinal involvement
Tristan Römer, Norbert Wagner, Till Braunschweig, Robert Meyer, Miriam Elbracht, Udo Kontny, Olga Moser
Novel ways to monitor immunosuppression in pediatric kidney transplant recipients—underlying concepts and emerging data
Thurid Ahlenstiel-Grunow, Lars Pape
A fresh look to the phenotype in mono-allelic likely pathogenic variants of the leptin and the leptin receptor gene
Ingrid Koerber-Rosso, Stephanie Brandt, Julia von Schnurbein, Pamela Fischer-Posovszky, Josef Hoegel, Hannah Rabenstein, Reiner Siebert, Martin Wabitsch
ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give?
Hannah von Lukowicz, Paul-Gerhardt Schlegel, Christoph Härtel, Henner Morbach, Imme Haubitz, Verena Wiegering
How FGF23 shapes multiple organs in chronic kidney disease
Maren Leifheit-Nestler, Dieter Haffner
Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesis
Clara Vidic, Marcin Zaniew, Szymon Jurga, Holger Thiele, Heiko Reutter, Alina C. Hilger
Correction to: Novel ways to monitor immunosuppression in pediatric kidney transplant recipients—underlying concepts and emerging data
Thurid Ahlenstiel-Grunow, Lars Pape
Does allogeneic stem cell transplantation in survivors of pediatric leukemia impact regular physical activity, pulmonary function, and exercise capacity?
Katharina Ruf, Alaa Badran, Céline Siauw, Imme Haubitz, Paul-Gerhardt Schlegel, Helge Hebestreit, Christoph Härtel, Verena Wiegering
Bacterial metabolites and cardiovascular risk in children with chronic kidney disease
Julia Schlender, Felix Behrens, Victoria McParland, Dominik Müller, Nicola Wilck, Hendrik Bartolomaeus, Johannes Holle
The role of the immune system in idiopathic nephrotic syndrome
Agnes Hackl, Seif El Din Abo Zed, Paul Diefenhardt, Julia Binz-Lotter, Rasmus Ehren, Lutz Thorsten Weber
Imaging of peripheral vascular malformations — current concepts and future perspectives
Vanessa F. Schmidt, Max Masthoff, Michael Czihal, Beatrix Cucuruz, Beate Häberle, Richard Brill, Walter A. Wohlgemuth, Moritz Wildgruber
Translational research approaches to study pediatric polycystic kidney disease
Max Christoph Liebau, Djalila Mekahli
Patho-mechanisms of the origins of bronchopulmonary dysplasia
Mitali Sahni, Vineet Bhandari