Search Results - Riedhammer, Korbinian M.

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  1. 1
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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 by Drovandi, Stefania (Author) , Lipska-Ziętkiewicz, Beata S. (Author) , Ozaltin, Fatih (Author) , Emma, Francesco (Author) , Gulhan, Bora (Author) , Boyer, Olivia (Author) , Trautmann, Agnes (Author) , Xu, Hong (Author) , Shen, Qian (Author) , Rao, Jia (Author) , Riedhammer, Korbinian M. (Author) , Heemann, Uwe (Author) , Hoefele, Julia (Author) , Stenton, Sarah L. (Author) , Tsygin, Alexey N. (Author) , Ng, Kar-Hui (Author) , Fomina, Svitlana (Author) , Benetti, Elisa (Author) , Aurelle, Manon (Author) , Prikhodina, Larisa (Author) , Schreuder, Michiel F. (Author) , Tabatabaeifar, Mansoureh (Author) , Jankowski, Maciej (Author) , Baiko, Sergey (Author) , Mao, Jianhua (Author) , Feng, Chunyue (Author) , Liu, Cuihua (Author) , Sun, Shuzhen (Author) , Deng, Fang (Author) , Wang, Xiaowen (Author) , Clavé, Stéphanie (Author) , Stańczyk, Małgorzata (Author) , Bałasz-Chmielewska, Irena (Author) , Fila, Marc (Author) , Durkan, Anne M. (Author) , Levart, Tanja Kersnik (Author) , Dursun, Ismail (Author) , Esfandiar, Nasrin (Author) , Haas, Dorothea (Author) , Bjerre, Anna (Author) , Anarat, Ali (Author) , Benz, Marcus R. (Author) , Talebi, Saeed (Author) , Hooman, Nakysa (Author) , Ariceta, Gema (Author) , Serna Higuita, Lina Maria (Author) , Schaefer, Franz (Author) , Gheissari, Alaleh (Author) , Nigmatullina, Nazym (Author) , Tkaczyk, Marcin (Author) , Borzecka, Halina (Author) , Bogdanovic, Radovan (Author) , Mir, Sevgi (Author) , Klopstock, Thomas (Author) , Prokisch, Holger (Author) , Kornblum, Cornelia (Author) , Liu, Cui-Hua (Author) , Sun, Shu-Zhen (Author) , Dong, Yang (Author) , Wang, Xiao-Wen (Author) , Luan, Jiang-Wei (Author) ,


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  2. 2
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    Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy by Drovandi, Stefania (Author) , Lipska-Ziętkiewicz, Beata S. (Author) , Ozaltin, Fatih (Author) , Emma, Francesco (Author) , Gulhan, Bora (Author) , Boyer, Olivia (Author) , Trautmann, Agnes (Author) , Ziętkiewicz, Szymon (Author) , Xu, Hong (Author) , Shen, Qian (Author) , Rao, Jia (Author) , Riedhammer, Korbinian M. (Author) , Heemann, Uwe (Author) , Hoefele, Julia (Author) , Stenton, Sarah L. (Author) , Tsygin, Alexey N. (Author) , Ng, Kar-Hui (Author) , Fomina, Svitlana (Author) , Benetti, Elisa (Author) , Aurelle, Manon (Author) , Prikhodina, Larisa (Author) , Schijvens, Anne M. (Author) , Tabatabaeifar, Mansoureh (Author) , Jankowski, Maciej (Author) , Baiko, Sergey (Author) , Mao, Jianhua (Author) , Feng, Chunyue (Author) , Deng, Fang (Author) , Rousset-Rouviere, Caroline (Author) , Stańczyk, Małgorzata (Author) , Bałasz-Chmielewska, Irena (Author) , Fila, Marc (Author) , Durkan, Anne M. (Author) , Levart, Tanja Kersnik (Author) , Dursun, Ismail (Author) , Esfandiar, Nasrin (Author) , Haas, Dorothea (Author) , Bjerre, Anna (Author) , Anarat, Ali (Author) , Benz, Marcus R. (Author) , Talebi, Saeed (Author) , Hooman, Nakysa (Author) , Ariceta, Gema (Author) , Schaefer, Franz (Author) ,


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  3. 3
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    Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age by Günthner, Roman (Author) , Knipping, Lea (Author) , Jeruschke, Stefanie (Author) , Satanoskij, Robin (Author) , Lorenz-Depiereux, Bettina (Author) , Hemmer, Clara (Author) , Braunisch, Matthias C. (Author) , Riedhammer, Korbinian M. (Author) , Ćomić, Jasmina (Author) , Tönshoff, Burkhard (Author) , Tasic, Velibor (Author) , Abazi-Emini, Nora (Author) , Nushi-Stavileci, Valbona (Author) , Buiting, Karin (Author) , Gjorgjievski, Nikola (Author) , Momirovska, Ana (Author) , Patzer, Ludwig (Author) , Kirschstein, Martin (Author) , Gross, Oliver (Author) , Lungu, Adrian (Author) , Weber, Stefanie (Author) , Renders, Lutz (Author) , Heemann, Uwe (Author) , Meitinger, Thomas (Author) , Büscher, Anja K. (Author) , Hoefele, Julia (Author) ,


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  4. 4
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    New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics by Begemann, Anaïs (Author) , Sticht, Heinrich (Author) , Begtrup, Amber (Author) , Vitobello, Antonio (Author) , Faivre, Laurence (Author) , Banka, Siddharth (Author) , Alhaddad, Bader (Author) , Asadollahi, Reza (Author) , Becker, Jessica (Author) , Bierhals, Tatjana (Author) , Brown, Kathleen E. (Author) , Bruel, Ange-Line (Author) , Brunet, Theresa (Author) , Carneiro, Maryline (Author) , Cremer, Kirsten (Author) , Day, Robert (Author) , Denommé-Pichon, Anne-Sophie (Author) , Dyment, Dave A. (Author) , Engels, Hartmut (Author) , Fisher, Rachel (Author) , Goh, Elaine S. (Author) , Hajianpour, M. J. (Author) , Haertel, Lucia Ribeiro Machado (Author) , Hauer, Nadine (Author) , Hempel, Maja (Author) , Herget, Theresia (Author) , Johannsen, Jessika (Author) , Kraus, Cornelia (Author) , Le Guyader, Gwenaël (Author) , Lesca, Gaetan (Author) , Mau-Them, Frédéric Tran (Author) , McDermott, John Henry (Author) , McWalter, Kirsty (Author) , Meyer, Pierre (Author) , Õunap, Katrin (Author) , Popp, Bernt (Author) , Reimand, Tiia (Author) , Riedhammer, Korbinian M. (Author) , Russo, Martina (Author) , Sadleir, Lynette G. (Author) , Saenz, Margarita (Author) , Schiff, Manuel (Author) , Schuler, Elisabeth (Author) , Syrbe, Steffen (Author) , Van der Ven, Amelie Theresa (Author) , Verloes, Alain (Author) , Willems, Marjolaine (Author) , Zweier, Christiane (Author) , Steindl, Katharina (Author) , Zweier, Markus (Author) , Rauch, Anita (Author) ,


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  5. 5
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    Precise variant interpretation, phenotype ascertainment, and genotype-phenotype correlation of children in the EARLY PRO-TECT Alport trial by Böckhaus, Jan Simon (Author) , Höfele, Julia (Author) , Riedhammer, Korbinian M. (Author) , Tönshoff, Burkhard (Author) , Ehren, Rasmus (Author) , Pape, Lars (Author) , Latta, Kay (Author) , Fehrenbach, Henry (Author) , Lange-Sperandio, Bärbel (Author) , Kettwig, Matthias (Author) , Hoyer, Peter (Author) , Staude, Hagen (Author) , Konrad, Martin (Author) , John-Kroegel, Ulrike (Author) , Gellermann, Jutta (Author) , Hoppe, Bernd (Author) , Galiano, Matthias (Author) , Gessner, Michaela (Author) , Pohl, Michael (Author) , Bergmann, Carsten (Author) , Friede, Tim (Author) , Gross, Oliver (Author) ,


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  6. 6
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    Biotinidase deficiency: a treatable cause of hereditary spastic paraparesis by Radelfahr, Florentine (Author) , Riedhammer, Korbinian M. (Author) , Keidel, Leonie F. (Author) , Gramer, Gwendolyn (Author) , Meitinger, Thomas (Author) , Klopstock, Thomas (Author) , Wagner, Matias (Author) ,


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