TLR2 mediates renal apoptosis in neonatal mice subjected experimentally to obstructive nephropathy von Wyczanska, Maja, Rohling, Jana, Keller, Ursula, Benz, Marcus R, Kirschning, Carsten, Lange-Sperandio, Bärbel

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Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease von BERGMANN, Carsten, VON BOTHMER, Jennifer, SARIOGLU, Nanette, SANTOS, Antónia, FERREIRA, Jose Carlos, BECKER, Jan U, CREAMER, Reinhold, HOEFELE, Julia, BENZ, Marcus R, WEBER, Lutz T, BUETTNER, Reinhard, ZERRES, Klaus, ORTIZ BRÜCHLE, Nadina, VENGHAUS, Andreas, FRANK, Valeska, FEHRENBACH, Henry, HAMPEL, Tobias, PAPE, Lars, BUSKE, Annegret, JONSSON, Jon

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Not all farming environments protect against the development of asthma and wheeze in children von Ege, Markus Johannes, MD, Frei, Remo, MSc, Bieli, Christian, MD, Schram-Bijkerk, Dieneke, PhD, Waser, Marco, PhD, Benz, Marcus R., MD, Weiss, Gertraud, MPH, Nyberg, Fredrik, MD, PhD, van Hage, Marianne, MD, PhD, Pershagen, Göran, MD, PhD, Brunekreef, Bert, PhD, Riedler, Josef, MD, Lauener, Roger, MD, Braun-Fahrländer, Charlotte, MD, von Mutius, Erika, MD

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Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency von Drovandi, Stefania, Lipska-Ziętkiewicz, Beata S., Ozaltin, Fatih, Emma, Francesco, Gulhan, Bora, Boyer, Olivia, Trautmann, Agnes, Xu, Hong, Shen, Qian, Rao, Jia, Riedhammer, Korbinian M., Heemann, Uwe, Hoefele, Julia, Stenton, Sarah L., Tsygin, Alexey N., Ng, Kar-Hui, Fomina, Svitlana, Benetti, Elisa, Aurelle, Manon, Prikhodina, Larisa, Schreuder, Michiel F., Tabatabaeifar, Mansoureh, Jankowski, Maciej, Baiko, Sergey, Mao, Jianhua, Feng, Chunyue, Liu, Cuihua, Sun, Shuzhen, Deng, Fang, Wang, Xiaowen, Clavé, Stéphanie, Stańczyk, Małgorzata, Bałasz-Chmielewska, Irena, Fila, Marc, Durkan, Anne M., Levart, Tanja Kersnik, Dursun, Ismail, Esfandiar, Nasrin, Haas, Dorothea, Bjerre, Anna, Anarat, Ali, Benz, Marcus R., Talebi, Saeed, Hooman, Nakysa, Ariceta, Gema, Baiko, Sergey, Serna Higuita, Lina Maria, Schaefer, Franz, Trautmann, Agnes, Tabatabaeifar, Mansoureh, Gheissari, Alaleh, Hooman, Nakysa, Benetti, Elisa, Emma, Francesco, Nigmatullina, Nazym, Lipska-Ziętkiewicz, Beata S., Bałasz-Chmielewska, Irena, Tkaczyk, Marcin, Stańczyk, Małgorzata, Borzecka, Halina, Tsygin, Alexey N., Prikhodina, Larisa, Bogdanovic, Radovan, Anarat, Ali, Ozaltin, Fatih, Mir, Sevgi, Fomina, Svitlana, Klopstock, Thomas, Prokisch, Holger, Kornblum, Cornelia, Xu, Hong, Shen, Qian, Rao, Jia, Liu, Cui-Hua, Sun, Shu-Zhen, Deng, Fang, Dong, Yang, Wang, Xiao-Wen, Luan, Jiang-Wei, Schaefer, Franz

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Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy von Drovandi, Stefania, Lipska-Ziętkiewicz, Beata S., Ozaltin, Fatih, Emma, Francesco, Gulhan, Bora, Boyer, Olivia, Trautmann, Agnes, Ziętkiewicz, Szymon, Xu, Hong, Shen, Qian, Rao, Jia, Riedhammer, Korbinian M., Heemann, Uwe, Hoefele, Julia, Stenton, Sarah L., Tsygin, Alexey N., Ng, Kar-Hui, Fomina, Svitlana, Benetti, Elisa, Aurelle, Manon, Prikhodina, Larisa, Schijvens, Anne M., Tabatabaeifar, Mansoureh, Jankowski, Maciej, Baiko, Sergey, Mao, Jianhua, Feng, Chunyue, Deng, Fang, Rousset-Rouviere, Caroline, Stańczyk, Małgorzata, Bałasz-Chmielewska, Irena, Fila, Marc, Durkan, Anne M., Levart, Tanja Kersnik, Dursun, Ismail, Esfandiar, Nasrin, Haas, Dorothea, Bjerre, Anna, Anarat, Ali, Benz, Marcus R., Talebi, Saeed, Hooman, Nakysa, Ariceta, Gema, Baiko, Sergey, Serna Higuita, Lina Maria, Schaefer, Franz, Trautmann, Agnes, Tabatabaeifar, Mansoureh, Gheissari, Alaleh, Hooman, Nakysa, Benetti, Elisa, Emma, Francesco, Nigmatullina, Nazym, Lipska-Ziętkiewicz, Beata S., Bałasz-Chmielewska, Irena, Tkaczyk, Marcin, Stańczyk, Małgorzata, Borzecka, Halina, Tsygin, Alexey N., Prikhodina, Larisa, Bogdanovic, Radovan, Anarat, Ali, Ozaltin, Fatih, Mir, Sevgi, Fomina, Svitlana, Klopstock, Thomas, Prokisch, Holger, Kornblum, Cornelia, Xu, Hong, Shen, Qian, Rao, Jia, Liu, Cui-Hua, Sun, Shu-Zhen, Deng, Fang, Dong, Yang, Wang, Xiao-Wen, Luan, Jiang-Wei, Schaefer, Franz

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Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy —short version of the updated German best practice guideline (S2e) — AWMF register no. 166-001, 6/2... von Ehren, Rasmus, Benz, Marcus R., Brinkkötter, Paul T., Dötsch, Jörg, Eberl, Wolfgang R., Gellermann, Jutta, Hoyer, Peter F., Jordans, Isabelle, Kamrath, Clemens, Kemper, Markus J., Latta, Kay, Müller, Dominik, Oh, Jun, Tönshoff, Burkhard, Weber, Stefanie, Weber, Lutz T.

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Prenatal farm exposure is related to the expression of receptors of the innate immunity and to atopic sensitization in school-age children von Ege, Markus Johannes, Bieli, Christian, Frei, Remo, van Strien, Robert Theodoor, Riedler, Josef, Üblagger, Ellen, Schram-Bijkerk, Dieneke, Brunekreef, Bert, van Hage, Marianne, Scheynius, Annika, Pershagen, Göran, Benz, Marcus R., Lauener, Roger, von Mutius, Erika, Braun-Fahrländer, Charlotte, the PARSIFAL Study team

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Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1 von Lehnhardt, Anja, Karnatz, Claartje, Ahlenstiel-Grunow, Thurid, Benz, Kerstin, Benz, Marcus R, Budde, Klemens, Büscher, Anja K, Fehr, Thomas, Feldkötter, Markus, Graf, Norbert, Höcker, Britta, Jungraithmayr, Therese, Klaus, Günter, Koehler, Birgit, Konrad, Martin, Kranz, Birgitta, Montoya, Carmen R, Müller, Dominik, Neuhaus, Thomas J, Oh, Jun, Pape, Lars, Pohl, Martin, Royer-Pokora, Brigitte, Querfeld, Uwe, Schneppenheim, Reinhard, Staude, Hagen, Spartà, Giuseppina, Timmermann, Kirsten, Wilkening, Frauke, Wygoda, Simone, Bergmann, Carsten, Kemper, Markus J

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Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy von Weber, Stefanie, Strasser, Katja, Rath, Sabine, Kittke, Achim, Beicht, Sonja, Alberer, Martin, Lange-Sperandio, Bärbel, Hoyer, Peter F., Benz, Marcus R., Ponsel, Sabine, Weber, Lutz T., Klein, Hanns-Georg, Hoefele, Julia

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Commentary on “Pediatric Idiopathic Steroid-sensitive Nephrotic Syndrome Diagnosis and Therapy - Short version of the updated German Best Practice Guideline (S2e)” von Ehren, Rasmus, Benz, Marcus R., Brinkkötter, Paul T., Dötsch, Jörg, Eberl, Wolfgang R., Gellermann, Jutta, Hoyer, Peter F., Jordans, Isabelle, Kamrath, Clemens, Kemper, Markus J., Latta, Kay, Müller, Dominik, Oh, Jun, Tönshoff, Burkhard, Weber, Stefanie, Weber, Lutz T.

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Initial treatment of steroid-sensitive idiopathic nephrotic syndrome in children with mycophenolate mofetil versus prednisone: protocol for a randomised, controlled, multicentre tr... von Ehren, Rasmus, Benz, Marcus R, Doetsch, Jorg, Fichtner, Alexander, Gellermann, Jutta, Haffner, Dieter, Höcker, Britta, Hoyer, Peter F, Kästner, Bärbel, Kemper, Markus J, Konrad, Martin, Luntz, Steffen, Querfeld, Uwe, Sander, Anja, Toenshoff, Burkhard, Weber, Lutz T

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Reply to correspondence letter by A. Costa et al.: pediatric mercury poisoning, brain MRI, and white matter hyperintensities von Benz, Marcus R.

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Hyperintense lesions in brain MRI after exposure to a mercuric chloride-containing skin whitening cream von Benz, Marcus R., Lee, Seung-Hee, Kellner, Lars, Döhlemann, Christoph, Berweck, Steffen

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Novel OCRL1 Mutations in Patients With the Phenotype of Dent Disease von Utsch, Boris, Bökenkamp, Arend, Benz, Marcus R., Besbas, Nesrin, Dötsch, Jörg, Franke, Ingo, Fründ, Stefan, Gok, Faysal, Hoppe, Bernd, Karle, Stephanie, Kuwertz-Bröking, Eberhard, Laube, Guido, Neb, Margarita, Nuutinen, Matti, Ozaltin, Fatih, Rascher, Wolfgang, Ring, Troels, Tasic, Velibor, van Wijk, Joanna A.E., Ludwig, Michael

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No Impact of the Analytical Method Used for Determining Cystatin C on Estimating Glomerular Filtration Rate in Children von Alberer, Martin, Hoefele, Julia, Benz, Marcus R, Bökenkamp, Arend, Weber, Lutz T

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Novel heterozygous COL4A3 mutation in a family with late-onset ESRD von Hoefele, Julia, Lange-Sperandio, Bärbel, Ruessmann, Despina, Glöckner-Pagel, Judith, Alberer, Martin, Benz, Marcus R., Nagel, Mato, Weber, Lutz T.

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Different factor H-related protein patterns in siblings with typical hemolytic uremic syndrome von Benz, Marcus R., Schmid, Holger, Heinen, Stefan, Lange-Sperandio, Bärbel, Hoefele, Julia, Sitter, Thomas, Zipfel, Peter F., Weber, Lutz T.

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Idiopathisches nephrotisches Syndrom im Kindesalter von Benz, Marcus R.

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Reduced methotrexate clearance and renal impairment in a boy with osteosarcoma and earlier undetected autosomal dominant polycystic kidney disease (ADPKD) von Alberer, Martin, Hoefele, Julia, Bergmann, Carsten, Hartrampf, Steffen, Hilberath, Jutta, Pawlita, Ingo, Albert, Michael H, Benz, Marcus R, Weber, Lutz T, Schmid, Irene

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Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy -short version of the updated German best practice guideline von Hoyer, Peter F, Ehren, Rasmus, Brinkkötter, Paul T, Eberl, Wolfgang R, Dötsch, Jörg, Benz, Marcus R, Gellermann, Jutta

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