Хайлтын үр дүнгүүд - Laura Massella
- 21-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
-
1
Minimal Change Disease -н Marina Vivarelli, Laura Massella, Barbara Ruggiero, Francesco Emma
Хэвлэсэн 2016Revisão -
2
Risk Factors for Cyclosporin A Nephrotoxicity in Children with Steroid-Dependant Nephrotic Syndrome -н Severin-Wafo Kengne, Laura Massella, Francesca Diomedi‐Camassei, Alessandra Gianviti, Marina Vivarelli, Marcella Greco, Gilda Stringini Rita, Francesco Emma
Хэвлэсэн 2009Artigo -
3
Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group -н Clifford E. Kashtan, Jie Ding, Guido Garosi, Laurence Heidet, Laura Massella, Koichi Nakanishi, Kandai Nozu, Alessandra Renieri, Michelle N. Rheault, Fang Wang, Oliver Groß
Хэвлэсэн 2018Artigo -
4
Advances in Alport syndrome diagnosis using next-generation sequencing -н 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
Хэвлэсэн 2011Artigo -
5
Prolonged Impairment of Immunological Memory After Anti-CD20 Treatment in Pediatric Idiopathic Nephrotic Syndrome -н 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
Хэвлэсэн 2019Artigo -
6
Rituximab in Children with Resistant Idiopathic Nephrotic Syndrome -н 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
Хэвлэсэн 2012Artigo -
7
TRPC6 Mutations in Children with Steroid-Resistant Nephrotic Syndrome and Atypical Phenotype -н 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
Хэвлэсэн 2011Artigo -
8
Broadening the Spectrum of Diseases Related to Podocin Mutations -н 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
Хэвлэсэн 2003Artigo -
9
Impact of COVID-19 Pandemic in Children with CKD or Immunosuppression -н 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
Хэвлэсэн 2020Carta -
10
Rituximab in Steroid-Dependent or Frequently Relapsing Idiopathic Nephrotic Syndrome -н 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
Хэвлэсэн 2014Artigo -
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... -н 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
Хэвлэсэн 2017Revisão -
12
COL4A3/COL4A4 mutations: From familial hematuria to autosomal-dominant or recessive Alport syndrome -н 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
Хэвлэсэн 2002Artigo -
13
A randomized clinical trial indicates that levamisole increases the time to relapse in children with steroid-sensitive idiopathic nephrotic syndrome -н 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
Хэвлэсэн 2017Artigo -
14
The 2019 and 2021 International Workshops on Alport Syndrome -н 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
Хэвлэсэн 2022Artigo -
15
Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia? -н 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
Хэвлэсэн 2016Artigo -
16
Prevalence of Hypertension in Children with Early-Stage ADPKD -н 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
Хэвлэсэн 2018Artigo -
17
Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria -н 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
Хэвлэсэн 2021Artigo -
18
Guidelines for Genetic Testing and Management of Alport Syndrome -н 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
Хэвлэсэн 2021Artigo -
19
Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease -н 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
Хэвлэсэн 2018Artigo -
20
ADPedKD: A Global Online Platform on the Management of Children With ADPKD -н 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
Хэвлэсэн 2019Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Medicine
Internal medicine
Kidney
Nephrotic syndrome
Biology
Genetics
Glomerulonephritis
Proteinuria
Alport syndrome
Disease
Focal segmental glomerulosclerosis
Gene
Gastroenterology
Pediatrics
Autosomal dominant polycystic kidney disease
Immunosuppression
Intensive care medicine
Kidney disease
Minimal change disease
Pathology
Prednisone
Compound heterozygosity
Endocrinology
Environmental health
Family medicine
Mutation
Nephrology
Phenotype
Population
Surgery