Хайлтын үр дүнгүүд - Paraskevas Iatropoulos

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  1. 1
    Unraveling the Molecular Mechanisms Underlying Complement Dysregulation by Nephritic Factors in C3G and IC-MPGN

    Unraveling the Molecular Mechanisms Underlying Complement Dysregulation by Nephritic Factors in C3G and IC-MPGN -н Roberta Donadelli, Patrizia Pulieri, Rossella Piras, Paraskevas Iatropoulos, Elisabetta Valoti, Ariela Benigni, Giuseppe Remuzzi, Marina Noris

    Хэвлэсэн 2018
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    Artigo
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  2. 2
    Variations of the angiotensin II type 1 receptor gene are associated with extreme human longevity

    Variations of the angiotensin II type 1 receptor gene are associated with extreme human longevity -н Ariela Benigni, Silvia Orisio, Marina Noris, Paraskevas Iatropoulos, Davide Castaldi, Kei Kamide, Hiromi Rakugi, Yasumichi Arai, Marta Todeschini, Giulia Ogliari, Enyu Imai, Yasuyuki Gondo, Nobuyoshi Hirose, Daniela Mari, Giuseppe Remuzzi

    Хэвлэсэн 2012
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    Artigo
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  3. 3
    Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome

    Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome -н Fatih Özaltın, Tulin Ibsirlioglu, Ekim Z. Taşkıran, Dilek Ertoy Baydar, Figen Kaymaz, Mithat Büyükçelik, Beltinge Demircioğlu Kılıç, Ayşe Balat, Paraskevas Iatropoulos, Esin Aşan, Nurten Akarsu, Franz Schaefer, Engin Yılmaz, Ayşı̇n Bakkaloğlu

    Хэвлэсэн 2011
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    Artigo
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  4. 4
    Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex–Mediated Membranoproliferative GN

    Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex–Mediated Membranoproliferative GN -н Paraskevas Iatropoulos, Erica Daina, Manuela Curreri, Rossella Piras, Elisabetta Valoti, Caterina Mele, Elena Bresin, Sara Gamba, Marta Alberti, Matteo Breno, Annalisa Perna, Serena Bettoni, Ettore Sabadini, Luisa Murer, Marina Vivarelli, Marina Noris, Giuseppe Remuzzi

    Хэвлэсэн 2017
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    Artigo
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  5. 5
    Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome

    Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome -н Caterina Mele, Mathieu Lemaire, Paraskevas Iatropoulos, Rossella Piras, Elena Bresin, Serena Bettoni, David Bick, Daniel Helbling, Regan Veith, Elisabetta Valoti, Roberta Donadelli, Luisa Murer, Maria Neunhäuserer, Matteo Breno, Véronique Frémeaux‐Bacchi, Richard P. Lifton, Giuseppe Remuzzi, Marina Noris

    Хэвлэсэн 2015
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    Artigo
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  6. 6
    Profiling cancer gene mutations in longitudinal epithelial ovarian cancer biopsies by targeted next-generation sequencing: a retrospective study

    Profiling cancer gene mutations in longitudinal epithelial ovarian cancer biopsies by targeted next-generation sequencing: a retrospective study -н Luca Beltrame, Mariacristina Di Marino, Robert Fruscio, Enrica Calura, Brad Chapman, Luca Clivio, Federica Sina, Caterina Mele, Paraskevas Iatropoulos, Tommaso Grassi, Vittoria Fotia, Chiara Romualdi, Paolo Martini, Marina Noris, Lara Paracchini, Ilaria Craparotta, Marco Petrillo, Rodolfo Milani, Patrizia Perego, Antonella Ravaggi, Alberto Zambelli, E Ronchetti, Maurizio D’Incalci, Sergio Marchini

    Хэвлэсэн 2015
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    Artigo
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  7. 7
    <i>MYO1E</i>Mutations and Childhood Familial Focal Segmental Glomerulosclerosis

    <i>MYO1E</i>Mutations and Childhood Familial Focal Segmental Glomerulosclerosis -н Caterina Mele, Paraskevas Iatropoulos, Roberta Donadelli, Andrea Calabria, Ramona Maranta, Paola Cassis, Simona Buelli, Susanna Tomasoni, Rossella Piras, Mira Krendel, Serena Bettoni, Marina Morigi, Massimo Delledonne, Carmine Pecoraro, Isabella Abbate, Maria Rosaria Capobianchi, Friedhelm Hildebrandt, Edgar A. Otto, Franz Schaefer, Fabìo Macciardi, Fatih Özaltın, Sevinç Emre, Tulin Ibsirlioglu, Ariela Benigni, Giuseppe Remuzzi, Marina Noris

    Хэвлэсэн 2011
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    Artigo
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  8. 8
    Genotype–phenotype associations in WT1 glomerulopathy

    Genotype–phenotype associations in WT1 glomerulopathy -н Beata S. Lipska‐Ziętkiewicz, Bruno Ranchin, Paraskevas Iatropoulos, Jutta Gellermann, Anette Melk, Fatih Özaltın, Gianluca Caridi, Tomáš Seeman, Kálmán Tory, Augustina Jankauskiené, Aleksandra Żurowska, Maria Szczepańska, Anna Wasilewska, Jérôme Harambat, Agnes Trautmann, Amira Peco‐Antić, Halina Borzęcka, Anna Moczulska, Bassam Saeed, Radovan Bogdanović, Mukaddes Kalyoncu, Eva Šimková, Özlem Erdoğan, Kristina Vrljičak, Ana Teixeira, Marta Azócar, Franz Schaefer

    Хэвлэсэн 2014
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    Artigo
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  9. 9
    Genetic screening in adolescents with steroid-resistant nephrotic syndrome

    Genetic screening in adolescents with steroid-resistant nephrotic syndrome -н Beata S. Lipska‐Ziętkiewicz, Paraskevas Iatropoulos, Ramona Maranta, Gianluca Caridi, Fatih Özaltın, Ali Anarat, Ayşe Balat, Jutta Gellermann, Agnes Trautmann, Özlem Erdoğan, Bassam Saeed, Sevinç Emre, Radovan Bogdanović, Marta Azócar, Irena Bałasz–Chmielewska, Elisa Benetti, Salim Çalışkan, Sevgı Mır, Anette Melk, Pelin Ertan, Esra Baskın, Helena Jardim, Tinatin Davitaia, Anna Wasilewska, Dorota Drożdż, Maria Szczepańska, Augustina Jankauskiené, Lina María Serna‐Higuita, Gianluigi Ardissino, Ozan Özkaya, Elżbieta Kuźma-Mroczkowska, Oğuz Söylemezoğlu, Bruno Ranchin, Anna Medyńska, Marcin Tkaczyk, Amira Peco‐Antić, İpek Akil, Tomasz Jarmoliński, Piotr Adamczyk, Ladislav Dušek, Giacomo D. Simonetti, Faysal Gök, Alaleh Gheissari, Francesco Emma, Rafael T. Krmar, Michel Fischbach, Nikoleta Printza, Eva Šimková, Caterina Mele, Gian Marco Ghiggeri, Franz Schaefer

    Хэвлэсэн 2013
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