Neonatal Innate Immunity to Infectious Agents

بواسطة Maródi, László
منشور في 2006

Survival of Group B Streptococcus Type III in Mononuclear Phagocytes: Differential Regulation of Bacterial Killing in Cord Macrophages by Human Recombinant Gamma Interferon and Gra...

بواسطة Maródi, László, Káposzta, Rita, Nemes, Éva
منشور في 2000

Characteristics of Invasive Candidiasis in Gamma Interferon- and Interleukin-4-Deficient Mice: Role of Macrophages in Host Defense against Candida albicans

بواسطة Káposzta, Rita, Tree, Peter, Maródi, László, Gordon, Siamon
منشور في 1998

Editorial: Advances in Primary Immunodeficiency in Central-Eastern Europe

بواسطة Pac, Malgorzata, Casanova, Jean-Laurent, Reisli, Ismail, Maródi, László
الحاوية / القاعدة Front Immunol (2021)

Augmentation of Human Macrophage Candidacidal Capacity by Recombinant Human Myeloperoxidase and GranulocyteMacrophage Colony-Stimulating Factor

بواسطة Maródi, László, Tournay, Christophe, Káposzta, Rita, Johnston, Richard B., Moguilevsky, Nicole
منشور في 1998

Immunity to infection in IL-17-deficient mice and humans

بواسطة Cypowyj, Sophie, Picard, Capucine, Marodi, Laszlo, Casanova, Jean-Laurent, Puel, Anne
منشور في 2012

Inborn errors of human IL-17 immunity underlie chronic mucocutaneous candidiasis

بواسطة Puel, Anne, Cypowyj, Sophie, Maródi, László, Abel, Laurent, Picard, Capucine, Casanova, Jean-Laurent
منشور في 2012

Molecular mechanisms of mucocutaneous immunity against Candida and Staphylococci

بواسطة Maródi, László, Cypowyj, Sophie, Tóth, Beáta, Chernyshova, Liudmyla, Puel, Anne, Casanova, Jean-Laurent
منشور في 2012

Recurrent, Severe Aphthous Stomatitis and Mucosal Ulcers as Primary Manifestations of a Novel STAT1 Gain-of-Function Mutation

بواسطة Erdős, Melinda, Jakobicz, Eszter, Soltész, Beáta, Tóth, Beáta, Bata-Csörgő, Zsuzsanna, Maródi, László
الحاوية / القاعدة Front Immunol (2020)

Molecular Genetic Characterization of Novel Sphingomyelin Phosphodiesterase 1 Mutations Causing Niemann–Pick Disease

بواسطة Tóth, Beata, Erdős, Melinda, Székely, Annamária, Ritli, László, Bagossi, Péter, Sümegi, János, Maródi, László
منشور في 2011

Analysis of Lyso-Globotriaosylsphingosine in Dried Blood Spots

بواسطة Johnson, Britt, Mascher, Hermann, Mascher, Daniel, Legnini, Elisa, Hung, Christina Y, Dajnoki, Angela, Chien, Yin-Hsiu, Maródi, László, Hwu, Wuh-Liang, Bodamer, Olaf A
منشور في 2013

A primary immunodeficiency characterized by defective immunoglobulin class switch recombination and impaired DNA repair

بواسطة Péron, Sophie, Pan-Hammarström, Qiang, Imai, Kohsuke, Du, Likun, Taubenheim, Nadine, Sanal, Ozden, Marodi, Laszlo, Bergelin-Besançon, Anne, Benkerrou, Malika, de Villartay, Jean-Pierre, Fischer, Alain, Revy, Patrick, Durandy, Anne
منشور في 2007

IRAK4 and NEMO mutations in otherwise healthy children with recurrent invasive pneumococcal disease

بواسطة Ku, Cheng‐Lung, Picard, Capucine, Erdős, Melinda, Jeurissen, Axel, Bustamante, Jacinta, Puel, Anne, von Bernuth, Horst, Filipe‐Santos, Orchidée, Chang, Huey‐Hsuan, Lawrence, Tatiana, Raes, Marc, Maródi, László, Bossuyt, Xavier
منشور في 2007

Hyper-IgM syndrome type 4 with a B lymphocyte–intrinsic selective deficiency in Ig class-switch recombination

بواسطة Imai, Kohsuke, Catalan, Nadia, Plebani, Alessandro, Maródi, László, Sanal, Özden, Kumaki, Satoru, Nagendran, Vasantha, Wood, Philip, Glastre, Catherine, Sarrot-Reynauld, Françoise, Hermine, Olivier, Forveille, Monique, Revy, Patrick, Fischer, Alain, Durandy, Anne
منشور في 2003

The cognitive profile of type 1 Gaucher disease patients

بواسطة Biegstraaten, Marieke, Wesnes, Keith A., Luzy, Cécile, Petakov, Milan, Mrsic, Mirando, Niederau, Claus, Giraldo, Pilar, Hughes, Derralynn, Mehta, Atul, Mengel, Karl-Eugen, Hollak, Carla E. M, Maródi, László, van Schaik, Ivo N.
منشور في 2012

Prognostic Indicators of Renal Disease Progression in Adults with Fabry Disease: Natural History Data from the Fabry Registry

بواسطة Wanner, Christoph, Oliveira, João P., Ortiz, Alberto, Mauer, Michael, Germain, Dominique P., Linthorst, Gabor E., Serra, Andreas L., Maródi, László, Mignani, Renzo, Cianciaruso, Bruno, Vujkovac, Bojan, Lemay, Roberta, Beitner-Johnson, Dana, Waldek, Stephen, Warnock, David G.
منشور في 2010

Phenotypic characteristics of the p.Asn215Ser (p.N215S) GLA mutation in male and female patients with Fabry disease: A multicenter Fabry Registry study

بواسطة Germain, Dominique P., Brand, Eva, Burlina, Alessandro, Cecchi, Franco, Garman, Scott C., Kempf, Judy, Laney, Dawn A., Linhart, Aleš, Maródi, László, Nicholls, Kathy, Ortiz, Alberto, Pieruzzi, Federico, Shankar, Suma P., Waldek, Stephen, Wanner, Christoph, Jovanovic, Ana
الحاوية / القاعدة Mol Genet Genomic Med (2018)

The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and function

بواسطة Locci, Michela, Draghici, Elena, Marangoni, Francesco, Bosticardo, Marita, Catucci, Marco, Aiuti, Alessandro, Cancrini, Caterina, Marodi, Laszlo, Espanol, Teresa, Bredius, Robbert G.M., Thrasher, Adrian J., Schulz, Ansgar, Litzman, Jiri, Roncarolo, Maria Grazia, Casorati, Giulia, Dellabona, Paolo, Villa, Anna
منشور في 2009

Renal outcomes of agalsidase beta treatment for Fabry disease: role of proteinuria and timing of treatment initiation

بواسطة Warnock, David G., Ortiz, Alberto, Mauer, Michael, Linthorst, Gabor E., Oliveira, João P., Serra, Andreas L., Maródi, László, Mignani, Renzo, Vujkovac, Bojan, Beitner-Johnson, Dana, Lemay, Roberta, Cole, J.Alexander, Svarstad, Einar, Waldek, Stephen, Germain, Dominique P., Wanner, Christoph
منشور في 2012

Stem-Cell Gene Therapy for the Wiskott–Aldrich Syndrome

بواسطة Boztug, Kaan, Schmidt, Manfred, Schwarzer, Adrian, Banerjee, Pinaki P., Díez, Inés Avedillo, Dewey, Ricardo A., Böhm, Marie, Nowrouzi, Ali, Ball, Claudia R., Glimm, Hanno, Naundorf, Sonja, Kühlcke, Klaus, Blasczyk, Rainer, Kondratenko, Irina, Maródi, László, Orange, Jordan S., von Kalle, Christof, Klein, Christoph
منشور في 2010