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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 13

Zeitschriftenartikel

Seeman, Tomáš ORCID logoORCID: https://orcid.org/0000-0003-1371-3096; Blahova, Kveta; Fencl, Filip; Klaus, Richard; Lange-Sperandio, Baerbel; Hrckova, Gabriela und Podracka, Ludmila (2022): Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension. In: Pediatric Nephrology, Bd. 38, Nr. 7: S. 2093-2100 [PDF, 768kB]

Klaus, Richard und Lange-Sperandio, Baerbel (2022): Chronic Kidney Disease in Boys with Posterior Urethral Valves-Pathogenesis, Prognosis and Management. In: Biomedicines, Bd. 10, Nr. 8, 1894

Burgmaier, Kathrin; Brinker, Leonie; Erger, Florian; Beck, Bodo B.; Benz, Marcus R.; Bergmann, Carsten; Boyer, Olivia; Collard, Laure; Dafinger, Claudia; Fila, Marc; Kowalewska, Claudia; Lange-Sperandio, Baerbel; Massella, Laura; Mastrangelo, Antonio; Mekahli, Djalila; Miklaszewska, Monika; Ortiz-Bruechle, Nadina; Patzer, Ludwig; Prikhodina, Larisa; Ranchin, Bruno; Ranguelov, Nadejda; Schild, Raphael; Seeman, Tomas; Sever, Lale; Sikora, Przemyslaw; Szczepanska, Maria; Teixeira, Ana; Thumfart, Julia; Uetz, Barbara; Weber, Lutz Thorsten; Wuehl, Elke; Zerres, Klaus; Doetsch, Joerg; Schaefer, Franz und Liebau, Max Christoph (2021): Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants. In: Kidney International, Bd. 100, Nr. 3: S. 650-659

Kameritsch, Petra; Singer, Miriam; Nuernbergk, Christoph; Rios, Natalia; Reyes, Anibal M.; Schmidt, Kjestine; Kirsch, Julian; Schneider, Holger; Mueller, Susanna; Pogoda, Kristin; Cui, Ruicen; Kirchner, Thomas; de Wit, Cor; Lange-Sperandio, Baerbel; Pohl, Ulrich; Conrad, Marcus; Radi, Rafael und Beck, Heike (2021): The mitochondrial thioredoxin reductase system (TrxR2) in vascular endothelium controls peroxynitrite levels and tissue integrity. In: Proceedings of the National Academy of Sciences of the United States of America, Bd. 118, Nr. 7, e1921828118

Suhlrie, Adriana; Hennies, Imke; Gellermann, Jutta; Buescher, Anja; Hoyer, Peter; Waldegger, Siegfried; Wygoda, Simone; Beetz, Rolf; Lange-Sperandio, Baerbel; Klaus, Guenter; Konrad, Martin; Holder, Martin; Staude, Hagen; Rascher, Wolfgang; Oh, Jun; Pape, Lars; Toenshoff, Burkhard und Haffner, Dieter (2020): Twelve-month outcome in juvenile proliferative lupus nephritis: results of the German registry study. In: Pediatric Nephrology, Bd. 35, Nr. 7: S. 1235-1246

Gross, Oliver; Toenshoff, Burkhard; Weber, Lutz T.; Pape, Lars; Latta, Kay; Fehrenbach, Henry; Lange-Sperandio, Baerbel; Zappel, Hildegard; Hoyer, Peter; Staude, Hagen; König, Sabine; John, Ulrike; Gellermann, Jutta; Hoppe, Bernd; Galiano, Matthias; Hoecker, Britta; Ehren, Rasmus; Lerch, Christian; Kashtan, Clifford E.; Harden, Markus; Boeckhaus, Jan und Friede, Tim (2020): A multicenter, randomized, placebo -controlled, double-blind phase 3 trial with open -arm comparison indicates safety and ef fi cacy of nephroprotective therapy with ramipril in children with Alport ? s syndrome see commentary. In: Kidney International, Bd. 97, Nr. 6: S. 1275-1286

Boeckhaus, Jan; Hoefele, Julia; Riedhammer, Korbinian M.; Tonshoff, Burkhard; Ehren, Rasmus; Pape, Lars; Latta, Kay; Fehrenbach, Henry; Lange-Sperandio, Baerbel; Kettwig, Matthias; Hoyer, Peter; Staude, Hagen; Konrad, Martin; John, Ulrike; Gellermann, Jutta; Hoppe, Bernd; Galiano, Matthias; Gessner, Michaela; Pohl, Michael; Bergmann, Carsten; Friede, Tim und Gross, Oliver (2020): Precise variant interpretation, phenotype ascertainment, and genotype-phenotype correlation of children in the EARLY PRO-TECT Alport trial. In: Clinical Genetics, Bd. 99, Nr. 1: S. 143-156

Lorenz, Robin; Ahting, Uwe; Betzler, Cornelia; Heimering, Sigrid; Borggraefe, Ingo und Lange-Sperandio, Baerbel (2020): Homoplasmy of the Mitochondrial DNA Mutation m.616T>C Leads to Mitochondrial Tubulointerstitial Kidney Disease and Encephalopathia. In: Nephron, Bd. 144, Nr. 3: S. 156-160

Riedhammer, Korbinian M.; Braunisch, Matthias C.; Guenthner, Roman; Wagner, Matias; Hemmer, Clara; Strom, Tim M.; Schmaderer, Christoph; Renders, Lutz; Tasic, Velibor; Gucev, Zoran; Nushi-Stavileci, Valbona; Putnik, Jovana; Stajic, Natasa; Weidenbusch, Marc; Uetz, Barbara; Montoya, Carmen; Strotmann, Peter; Ponsel, Sabine; Lange-Sperandio, Baerbel und Hoefele, Julia (2020): Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies. In: American Journal of Kidney Diseases, Bd. 76, Nr. 4: S. 460-470

Eichinger, Anna; Ponsel, Sabine; Bergmann, Carsten; Günthner, Roman; Hoefele, Julia; Amann, Kerstin und Lange-Sperandio, Baerbel (2018): Cyclosporine A responsive congenital nephrotic syndrome with single heterozygous variants in NPHS1, NPHS2, and PLCE1. In: Pediatric Nephrology, Bd. 33, Nr. 7: S. 1269-1272

Günthner, Roman; Wagner, Matias; Thurm, Tobias; Ponsel, Sabine; Hoefele, Julia und Lange-Sperandio, Baerbel (2018): Identification of co-occurrence in a patient with Dent's disease and ADA2-deficiency by exome sequencing. In: Gene, Bd. 649: S. 23-26

Nussbaum, Claudia; Bannenberg, Sarah; Keul, Petra; Gräler, Markus H.; Goncalves-de-Albuquerque, Cassiano F.; Korhonen, Hanna; Lipinski, Karin von Wnuck; Heusch, Gerd; Castro Faria Neto, Hugo C. de; Rohwedder, Ina; Göthert, Joachim R.; Prasad, Vysakh Pushpa; Haufe, Günter; Lange-Sperandio, Baerbel; Offermanns, Stefan; Sperandio, Markus und Levkau, Bodo (2015): Sphingosine-1-phosphate receptor 3 promotes leukocyte rolling by mobilizing endothelial P-selectin. In: Nature Communications, Bd. 6, 6416 [PDF, 1MB]

Frommhold, David; Kamphues, Anna; Dannenberg, Susanne; Buschmann, Kirsten; Zablotskaya, Victoria; Tschada, Raphaela; Lange-Sperandio, Baerbel; Nawroth, Peter P.; Poeschl, Johannes; Bierhaus, Angelika und Sperandio, Markus (2011): RAGE and ICAM-1 differentially control leukocyte recruitment during acute inflammation in a stimulus-dependent manner. In: BMC Immunology 12:56 [PDF, 810kB]

Diese Liste wurde am Sat Apr 13 21:23:13 2024 CEST erstellt.