Výsledky vyhledávání - Laura Massella

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  1. 1
    Minimal Change Disease

    Minimal Change Disease Autor Marina Vivarelli, Laura Massella, Barbara Ruggiero, Francesco Emma

    Vydáno 2016
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  2. 2
    Risk Factors for Cyclosporin A Nephrotoxicity in Children with Steroid-Dependant Nephrotic Syndrome

    Risk Factors for Cyclosporin A Nephrotoxicity in Children with Steroid-Dependant Nephrotic Syndrome Autor Severin-Wafo Kengne, Laura Massella, Francesca Diomedi‐Camassei, Alessandra Gianviti, Marina Vivarelli, Marcella Greco, Gilda Stringini Rita, Francesco Emma

    Vydáno 2009
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  3. 3
    Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group

    Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group Autor Clifford E. Kashtan, Jie Ding, Guido Garosi, Laurence Heidet, Laura Massella, Koichi Nakanishi, Kandai Nozu, Alessandra Renieri, Michelle N. Rheault, Fang Wang, Oliver Groß

    Vydáno 2018
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  4. 4
    Advances in Alport syndrome diagnosis using next-generation sequencing

    Advances in Alport syndrome diagnosis using next-generation sequencing Autor Rosangela Artuso, Chiara Fallerini, Laura Dosa, Francesca Scionti, Maurizio Clementi, Guido Garosi, Laura Massella, Maria Carmela Epistolato, Roberta Mancini, Francesca Mari, Ilaria Longo, Francesca Ariani, Alessandra Renieri, Mirella Bruttini

    Vydáno 2011
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  5. 5
    Prolonged Impairment of Immunological Memory After Anti-CD20 Treatment in Pediatric Idiopathic Nephrotic Syndrome

    Prolonged Impairment of Immunological Memory After Anti-CD20 Treatment in Pediatric Idiopathic Nephrotic Syndrome Autor Manuela Colucci, Rita Carsetti, Jessica Serafinelli, Salvatore Rocca, Laura Massella, Antonio Gargiulo, Anna Lo Russo, Claudia Capponi, Nicola Cotugno, Ottavia Porzio, Andrea Onetti Muda, Paolo Palma, Francesco Emma, Marina Vivarelli

    Vydáno 2019
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  6. 6
    Rituximab in Children with Resistant Idiopathic Nephrotic Syndrome

    Rituximab in Children with Resistant Idiopathic Nephrotic Syndrome Autor Alberto Magnasco, Pietro Ravani, Alberto Edefonti, Luisa Murer, Luciana Ghio, Mirco Belingheri, Elisa Benetti, Corrado Murtas, Giovanni Messina, Laura Massella, Maria Gabriella Porcellini, Michela Montagna, Mario Regazzi, Francesco Scolari, Gian Marco Ghiggeri

    Vydáno 2012
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  7. 7
    TRPC6 Mutations in Children with Steroid-Resistant Nephrotic Syndrome and Atypical Phenotype

    TRPC6 Mutations in Children with Steroid-Resistant Nephrotic Syndrome and Atypical Phenotype Autor Maddalena Gigante, Gianluca Caridi, Eustacchio Montemurno, Mario Soccio, Maria D’Apolito, Giuseppina Cerullo, Filippo Aucella, Annalisa Schirinzi, Francesco Emma, Laura Massella, Giovanni Messina, Tommaso De Palo, Elena Ranieri, Gian Marco Ghiggeri, Loreto Gesualdo

    Vydáno 2011
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  8. 8
    Broadening the Spectrum of Diseases Related to Podocin Mutations

    Broadening the Spectrum of Diseases Related to Podocin Mutations Autor Gianluca Caridi, Roberta Bertelli, Marco Di Duca, Monica Dagnino, Francesco Emma, Andrea Onetti Muda, Francesco Scolari, Nunzia Miglietti, Gianna Mazzucco, Luisa Murer, Alba Carrea, Laura Massella, Gianfranco Rizzoni, Francesco Perfumo, Gian Marco Ghiggeri

    Vydáno 2003
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  9. 9
    Impact of COVID-19 Pandemic in Children with CKD or Immunosuppression

    Impact of COVID-19 Pandemic in Children with CKD or Immunosuppression Autor Antonio Mastrangelo, William Morello, Enrico Vidal, Isabella Guzzo, Luigi Annicchiarico Petruzzelli, Elisa Benetti, Marco Materassi, Mario Giordano, Andrea Pasini, Ciro Corrado, Giuseppe Puccio, Roberto Chimenz, Carmine Pecoraro, Laura Massella, Licia Peruzzi, Giovanni Montini

    Vydáno 2020
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  10. 10
    Rituximab in Steroid-Dependent or Frequently Relapsing Idiopathic Nephrotic Syndrome

    Rituximab in Steroid-Dependent or Frequently Relapsing Idiopathic Nephrotic Syndrome Autor Piero Ruggenenti, Barbara Ruggiero, Paolo Cravedi, Marina Vivarelli, Laura Massella, Maddalena Marasà, Antonietta Chianca, Nadia Rubis, Bogdan Ene‐Iordache, Michael Rudnicki, Rosa Maria Pollastro, Giovambattista Capasso, Antonio Pisani, Marco Pennesi, Francesco Emma, Giuseppe Remuzzi

    Vydáno 2014
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  11. 11
    The Italian Society for Pediatric Nephrology (SINePe) consensus document on the management of nephrotic syndrome in children: Part I - Diagnosis and treatment of the first episode and the first relapse

    The Italian Society for Pediatric Nephrology (SINePe) consensus document on the management of nephrotic syndrome in children: Part I - Diagnosis and treatment of the first episode... Autor Andrea Pasini, Elisa Benetti, Giovanni Conti, Luciana Ghio, Marta Lepore, Laura Massella, Daniela Molino, Licia Peruzzi, Francesco Emma, Carmelo Fede, Antonella Trivelli, Silvio Maringhini, Marco Materassi, Giovanni Messina, Giovanni Montini, Luisa Murer, Carmine Pecoraro, Marco Pennesi

    Vydáno 2017
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  12. 12
    COL4A3/COL4A4 mutations: From familial hematuria to autosomal-dominant or recessive Alport syndrome

    COL4A3/COL4A4 mutations: From familial hematuria to autosomal-dominant or recessive Alport syndrome Autor Ilaria Longo, Paola Porcedda, Francesca Mari, Daniela Giachino, Ilaria Meloni, Carla Deplano, Alfredo Brusco, Maurizio Bosio, Laura Massella, Giancarlo Lavoratti, Dario Roccatello, Giovanni M. Frascà, Gianna Mazzucco, Andrea Onetti Muda, M I Bonanno Conti, F Fasciolo, Christelle Arrondel, Laurence Heidet, Alessandra Renieri, Mario Marchi

    Vydáno 2002
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  13. 13
    A randomized clinical trial indicates that levamisole increases the time to relapse in children with steroid-sensitive idiopathic nephrotic syndrome

    A randomized clinical trial indicates that levamisole increases the time to relapse in children with steroid-sensitive idiopathic nephrotic syndrome Autor Mariken Gruppen, Antonia H. Bouts, Marijke C. Jansen‐van der Weide, Maruschka P. Merkus, Aleksandra Żurowska, Michał Maternik, Laura Massella, Francesco Emma, Patrick Niaudet, Marlies Cornelissen, Thierry Schurmans, Ann Raes, Johan Van de Walle, Mieke van Dyck, Ashima Gulati, Arvind Bagga, Jean‐Claude Davin

    Vydáno 2017
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  14. 14
    The 2019 and 2021 International Workshops on Alport Syndrome

    The 2019 and 2021 International Workshops on Alport Syndrome Autor Sergio Daga, Jie Ding, Constantinos Deltas, Judy Savige, Beata S. Lipska‐Ziętkiewicz, Julia Hoefele, Frances Flinter, Daniel P. Gale, Marina Aksenova, Hirofumi Kai, Laura Perin, Moumita Barua, Roser Torrá, Jeff H. Miner, Laura Massella, Danica Galešić Ljubanović, Rachel Lennon, André Weinstock, Bertrand Knebelmann, Agnė Čerkauskaitė, Susie Gear, Oliver Groß, Neil Turner, Margherita Baldassarri, Anna Maria Pinto, Alessandra Renieri

    Vydáno 2022
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  15. 15
    Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?

    Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia? Autor Marie Morimoto, Clara Myung, Kimberly Beirnes, Kunho Choi, Yumi Asakura, Arend Bökenkamp, Dominique Bonneau, Milena Brugnara, Joel Charrow, Estelle Colin, Amira Davis, Georges Deschênes, Mattia Gentile, Mario Giordano, Andrew K. Gormley, Rajeshree Govender, Mark Joseph, Kory Keller, Evelyne Lerut, Elena Levtchenko, Laura Massella, Christy Mayfield, Behzad Najafian, David M. Parham, Jürgen W. Spranger, Peter Stenzel, Uluç Yiş, Zhongxin Yu, Jonathan Zonana, Glenda Hendson, Cornelius F. Boerkoel

    Vydáno 2016
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  16. 16
    Prevalence of Hypertension in Children with Early-Stage ADPKD

    Prevalence of Hypertension in Children with Early-Stage ADPKD Autor Laura Massella, Djalila Mekahli, Dušan Paripović, Larisa Prikhodina, Nathalie Godefroid, Anna Niemirska, Ayşe Ağbaş, Karolina Kalicka, Augustina Jankauskiené, Małgorzata Mizerska-Wasiak, Alberto Caldas Afonso, Rémi Salomon, Georges Deschênes, Gema Ariceta, Zeynep Birsin Özçakar, Ana Teixeira, Ali Düzova, Jérôme Harambat, Tomáš Seeman, Gabriela Hrčková, Adrian Lungu, Svetlana Papizh, Amira Peco‐Antić, Stéphanie De Rechter, Ugo Giordano, Marietta Kirchner, Teresa Lutz, Franz Schaefer, Olivier Devuyst, Elke Wühl, Francesco Emma

    Vydáno 2018
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  17. 17
    Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

    Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria Autor Judy Savige, Helen Storey, E. Watson, Jens Michael Hertz, Constantinos Deltas, Alessandra Renieri, Francesca Mari, Pascale Hilbert, Pavlína Plevová, Peter H. Byers, Agnė Čerkauskaitė, Martin C. Gregory, Rimantė Čerkauskienė, Danica Galešić Ljubanović, Francesca Becherucci, Carmela Errichiello, Laura Massella, Valeria Aiello, Rachel Lennon, Louise Hopkinson, Ania Koziell, Adrian Lungu, H. Rothe, Julia Hoefele, Miriam Zacchia, Tamara Nikuševa Martić, Asheeta Gupta, Albertien M. van Eerde, Susie Gear, Samuela Landini, Viviana Palazzo, Laith Al‐Rabadi, Kathleen Claes, Anniek Corveleyn, Elke Van Hoof, Micheel van Geel, Maggie Williams, Emma Ashton, Hendica Belge, Elisabet Ars, Agnieszka Bierżyńska, Concetta Gangemi, Beata S. Lipska‐Ziętkiewicz

    Vydáno 2021
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  18. 18
    Guidelines for Genetic Testing and Management of Alport Syndrome

    Guidelines for Genetic Testing and Management of Alport Syndrome Autor Judy Savige, Beata S. Lipska‐Ziętkiewicz, E. Watson, Jens Michael Hertz, Constantinos Deltas, Francesca Mari, Pascale Hilbert, Pavlína Plevová, Peter H. Byers, Agnė Čerkauskaitė, Martin C. Gregory, Rimantė Čerkauskienė, Danica Galešić Ljubanović, Francesca Becherucci, Carmela Errichiello, Laura Massella, Valeria Aiello, Rachel Lennon, Louise Hopkinson, Ania Koziell, Adrian Lungu, H. Rothe, Julia Hoefele, Miriam Zacchia, Tamara Nikuševa Martić, Asheeta Gupta, Albertien M. van Eerde, Susie Gear, Samuela Landini, Viviana Palazzo, Laith Al‐Rabadi, Kathleen Claes, Anniek Corveleyn, Elke Van Hoof, Micheel van Geel, Maggie Williams, Emma Ashton, Hendica Belge, Elisabet Ars, Agnieszka Bierżyńska, Concetta Gangemi, Alessandra Renieri, Helen Storey, Frances Flinter

    Vydáno 2021
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  19. 19
    Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease

    Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease Autor Kathrin Burgmaier, Kevin Kunzmann, Gema Ariceta, Carsten Bergmann, Anja Buescher, Mathias Burgmaier, İsmail Dursun, Ali Düzova, Loai Eid, Florian Erger, Markus Feldkoetter, Matthias Galiano, Michaela Geßner, Heike Goebel, İbrahim Gökçe, Dieter Haffner, Nakysa Hooman, Bernd Höppe, Augustina Jankauskiené, Günter Klaus, Jens König, Mieczysław Litwin, Laura Massella, Djalila Mekahli, Engin Melek, Sevgı Mır, Lars Pape, Larisa Prikhodina, Bruno Ranchin, Raphael Schild, Tomáš Seeman, Lale Sever, Rukshana Shroff, Neveen A. Soliman, Stella Stabouli, Małgorzata Stańczyk, Yılmaz Tabel, Katarzyna Taranta‐Janusz, Sara Testa, Julia Thumfart, Rezan Topaloĝlu, Lutz T. Weber, Dorota Wicher, Elke Wühl, Simone Wygoda, Alev Yılmaz, Katarzyna Zachwieja, Ilona Zagożdżon, Klaus Zerres, Jörg Dötsch, Franz Schaefer, Max C. Liebau, Nadejda Ranguelov, Nathalie Godefroid, Laure Collard, Jacques Lombet, Julie Maquet, Gesa Schalk, Uwe Querfeld, Bodo B. Beck, Thomas Benzing, Reinhard Buettner, Franziska Grundmann, Christine Kurschat, Kerstin Benz, Anja Tzschoppe, Bjoern Buchholz, Rainer Buescher, Karsten Häffner, Martin Pöhl, Oliver Groß, Jenny Krügel, Johanna Stock, Ludwig Patzer, Jun Oh, Wanja M. Bernhardt, Anke Doyon, Tobias Vinke, Anja Sander, Michael Henn, Ute Derichs, Rolf Beetz, Nikola Jeck, Bärbel Lange-Sperandio, Sabine Ponsel, Franziska Kusser, Barbara Uetz, Marcus R. Benz, Silke Schmidt, C. J. Huppertz-Kessler, Birgitta Kranz, Andrea Titieni, Donald Wurm, Heinz E. Leichter, Martin Bald, Heiko Billing, Marwa M. Nabhan, Luis Enrique Lara, Fotiοs Papachristou, Francesco Emma

    Vydáno 2018
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  20. 20
    ADPedKD: A Global Online Platform on the Management of Children With ADPKD

    ADPedKD: A Global Online Platform on the Management of Children With ADPKD Autor Stéphanie De Rechter, Detlef Böckenhauer, Lisa M. Guay‐Woodford, Isaac Liu, Andrew Mallett, Neveen A. Soliman, Lucimary C. Sylvestre, Franz Schaefer, Max C. Liebau, Djalila Mekahli, Piotr Adamczyk, Nurver Akıncı, Harika Alpay, Carmen Ardelean, Nadia Ayasreh, Zeki Aydın, A. Bael, Véronique Baudouin, US Bayrakci, A Bensman, Hanna Bialkevich, A. Biebuyck, Olivia Boyer, Omar Bjanid, Olivia Boyer, A. Bryłka, Salim Çalışkan, Alexandra Cambier, A. Camelio, Vincenza Carbone, Marina Charbit, Benedetta Chiodini, A. Chirita, Neslihan Çiçek, Rimantė Čerkauskienė, Laure Collard, Magda S. da Conceição, Ileana Constantinescu, Anne‐Laure Couderc, B. Crapella, Mirjana Cvetković, B. Dima, F. Diomeda, M. Docx, Nancy C. Dolan, Claire Dossier, Dorota Drożdż, Jens Drube, Oliver Dunand, Dušan Paripović, Loai Eid, Francesco Emma, M. Espino Hernández, Marc Fila, Mónica Furlano, Mihai Gafencu, M.S. Ghuysen, Mauro Giani, Mario Giordano, I. Girisgen, Nathalie Godefroid, Astrid Godron-Dubrasquet, I. Gojkovic, Elizabeth M. Gonzalez, İbrahim Gökçe, Jaap W. Groothoff, Stefano Guarino, Anne Guffens, P. R. Hansen, Jérôme Harambat, Sara Kretzschmar Haumann, Guanheng He, Laurence Heidet, Remon Helmy, F. Hémery, Nakysa Hooman, Brigitte Llanas, Augustina Jankauskiené, Peter Janssens, S. Karamaria, I. A. Kazyra, Julian Koenig, Saoussen Krid, Penny Krug, V. Kwon, Angela La Manna, V. Leroy, Mieczysław Litwin, Jacques Lombet, Germana Longo, Adrian Lungu, Amali Mallawaarachchi, Anna Marín, P. Marzuillo, Laura Massella, Antonio Mastrangelo, Helen McCarthy, Monika Miklaszewska, Anna Moczulska, Giovanni Montini

    Vydáno 2019
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