Resultats de la cerca - Francesca Mencarelli

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  1. 1
    Expanding Phenotype of Schimke Immuno-Osseous Dysplasia: Congenital Anomalies of the Kidneys and of the Urinary Tract and Alteration of NK Cells

    Expanding Phenotype of Schimke Immuno-Osseous Dysplasia: Congenital Anomalies of the Kidneys and of the Urinary Tract and Alteration of NK Cells per Cristina Bertulli, Antonio Marzollo, Margherita Doria, Silvia Di Cesare, Claudio La Scola, Francesca Mencarelli, Andrea Pasini, Maria Carmen Affinita, Enrico Vidal, Pamela Magini, Paola Dimartino, Riccardo Masetti, Laura Greco, Patrizia Palomba, Francesca Conti, Andrea Pession

    Publicat 2020
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  2. 2
    Best practice guidelines for idiopathic nephrotic syndrome: recommendations versus reality

    Best practice guidelines for idiopathic nephrotic syndrome: recommendations versus reality per Andrea Pasini, Gabriella Aceto, Anita Ammenti, Gianluigi Ardissino, Vitalba Azzolina, Alberto Bettinelli, Elena Cama, Sante Cantatore, Antonella Crisafi, Giovanni Conti, Maria Antonietta D’Agostino, Alessandra Dozza, Alberto Edefonti, Carmelo Fede, Elena Groppali, Chiara Gualeni, Alessandra Lavacchini, Marta Lepore, Silvio Maringhini, Paola Mariotti, Marco Materassi, Francesca Mencarelli, Giovanni Messina, Amata Negri, Marina Piepoli, Fiammetta Ravaglia, Angela Simoni, Laura Spagnoletta, Giovanni Montini

    Publicat 2014
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  3. 3
    Metabolic acidosis is common and associates with disease progression in children with chronic kidney disease

    Metabolic acidosis is common and associates with disease progression in children with chronic kidney disease per Jérôme Harambat, Kevin Kunzmann, Karolis Ažukaitis, Aysun Karabay Bayazıt, Nur Canpolat, Anke Doyon, Ali Düzova, Anna Niemirska, Betül Sözeri, Daniela Thurn‐Valsassina, Ali Anarat, Lucie Bessenay, Cengiz Candan, Amira Peco‐Antić, Alev Yılmaz, Sibylle Tschumi, Sara Testa, Augustina Jankauskiené, Hakan Erdoğan, Alejandra Rosales, Harika Alpay, Francesca Lugani, Klaus Arbeiter, Francesca Mencarelli, Aysel Kıyak, Osman Dönmez, Dorota Drożdż, Anette Melk, Uwe Querfeld, Franz Schaefer

    Publicat 2017
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  4. 4
    Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children

    Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children per Karolis Ažukaitis, Wenjun Ju, Marietta Kirchner, Viji Nair, Michelle R. Smith, Zhiyin Fang, Daniela Thurn‐Valsassina, Aysun Karabay Bayazıt, Anna Niemirska, Nur Canpolat, İpek Kaplan Bulut, Fatoş Yalçınkaya, Dušan Paripović, Jérôme Harambat, Nilgün Çakar, Harika Alpay, Francesca Lugani, Francesca Mencarelli, Mahmut Çivilibal, Hakan Erdoğan, Jutta Gellermann, Enrico Vidal, Yılmaz Tabel, Charlotte Gimpel, Pelin Ertan, Önder Yavaşcan, Anette Melk, Uwe Querfeld, Elke Wühl, Matthias Kretzler, Franz Schaefer, Klaus Arbeiter, Alejandra Rosales, Ladislav Dušek, Ariane Zaloszyc, Uwe Querfeld, Jutta Gellermann, Max C. Liebau, Lutz T. Weber, Evelin Muschiol, Rainer Büscher, Jun Oh, Anette Melk, Daniela Thurn-Valassina, Dieter Haffner, Franz Schaefer, Charlotte Gimpel, Ulrike John, Simone Wygoda, Nikola Jeck, Marianne Wigger, Sara Testa, Luisa Murer, Chiara Matteucci, Augustina Jankauskiené, Karolis Ažukaitis, Dorota Drożdż, Francesca Lugani, Aleksandra Żurowska, Marcin Zaniew, Mieczysław Litwin, Anna Nimierska, Ana Teixeira, Amira Peco‐Antić, Dušan Paripović, Guido F. Laube, Ali Anarat, Aysun Karabay Bayazıt, Ali Düzova, Yelda Bilginer, Salim Çalışkan, Nur Canpolat, Mahmut Çivilibal, Sevgı Mır, Betül Sözeri, Brigitta Kranz, Francesca Mencarelli, Barry C. Dorn, Fatoş Yalçınkaya, Esra Baskın, Nilgün Çakar, Oğuz Söylemezoğlu, Sevinç Emre, Cengiz Candan, Aysel Kıyak, Gül Özçelik, Harika Alpay, Rukshana Shroff, Bruno Rachin, Jérôme Harambat, Maria Szczepańska, Hakan Erdoğan, Osman Dönmez, Ayşe Balat, Nejat Aksu, Yılmaz Tabel, Pelin Ertan, Ebru Yılmaz, Ali Anarat, Ayşı̇n Bakkaloğlu

    Publicat 2019
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  5. 5
    Refining genotype–phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants

    Refining genotype–phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants per Kathrin Burgmaier, Leonie Violetta Brinker, Florian Erger, Bodo B. Beck, Marcus R. Benz, Carsten Bergmann, Olivia Boyer, Laure Collard, Claudia Dafinger, Marc Fila, Claudia Kowalewska, Bärbel Lange-Sperandio, Laura Massella, Antonio Mastrangelo, Djalila Mekahli, Monika Miklaszewska, Nadina Ortiz-Bruechle, Ludwig Patzer, Larisa Prikhodina, Bruno Ranchin, Nadejda Ranguelov, Raphael Schild, Tomáš Seeman, Lale Sever, Przemysław Sikora, Maria Szczepańska, Ana Teixeira, Julia Thumfart, Barbara Uetz, Lutz T. Weber, Elke Wühl, Klaus Zerres, Jörg Dötsch, Franz Schaefer, Max C. Liebau, Loai Eid, Klaus Arbeiter, Nathalie Godefroid, Jacques Lombet, Aurélie De Mul, Markus Feldkoetter, Jakub Zieg, Franziska Grundmann, Matthias Galiano, Bjoern Buchholz, Anja Buescher, Karsten Häffner, Oliver Groß, Ludwig Patzer, Jun Oh, Dieter Haffner, Wanja M. Bernhardt, Susanne Schaefer, Simone Wygoda, Jan Halbritter, Ute Derichs, Günter Klaus, Felix Lechner, Sabine Ponsel, Jens König, Hagen Staude, Donald Wurm, Martin Bald, Michaela Geßner, Neveen A. Soliman, Gema Ariceta, Juan David González-Rodríguez, Francisco de la Cerda Ojeda, Jérôme Harambat, Denis Morin, Claire Dossier, Guillaume Dorval, Rukshana Shroff, Stella Stabouli, Nakysa Hooman, Francesca Mencarelli, William Morello, Germana Longo, Francesco Emma, Augustina Jankauskiené, Katarzyna Taranta‐Janusz, Ilona Zagożdżon, Katarzyna Zachwieja, Małgorzata Stańczyk, Beata Bieniaś, Mieczysław Litwin, Aurelia Morawiec‐Knysak, Alberto Caldas Afonso, Oliver Dunand, Andreea Liana Răchişan, Gordana Miloševski‐Lomić, Svetlana Papizh, Rina Rus, Houweyda Jilani, Bahriye Atmış, Ali Düzova, Alper Soylu, Cengiz Candan, Salim Çalışkan, Alev Yılmaz

    Publicat 2021
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