Search Results - "Raedler, Johannes"

Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency by Raedler, Johannes, Magg, Thomas, Rohlfs, Meino, Klein, Christoph, Vallée, Tanja, Hauck, Fabian, Albert, Michael H.

“…Bi-allelic variants in the dedicator of cytokinesis 8 ( DOCK8 ) gene cause a combined immunodeficiency, characterized by recurrent sinopulmonary and skin…”
Get full text

Rubella Virus Infected Macrophages and Neutrophils Define Patterns of Granulomatous Inflammation in Inborn and Acquired Errors of Immunity by Perelygina, Ludmila, Faisthalab, Raeesa, Abernathy, Emily, Chen, Min-Hsin, Hao, LiJuan, Bercovitch, Lionel, Bayer, Diana K, Noroski, Lenora M, Lam, Michael T, Cicalese, Maria Pia, Al-Herz, Waleed, Nanda, Arti, Hajjar, Joud, Vanden Driessche, Koen, Schroven, Shari, Leysen, Julie, Rosenbach, Misha, Peters, Philipp, Raedler, Johannes, Albert, Michael H, Abraham, Roshini S, Rangarjan, Hemalatha G, Buchbinder, David, Kobrynski, Lisa, Pham-Huy, Anne, Dhossche, Julie, Cunningham Rundles, Charlotte, Meyer, Anna K, Theos, Amy, Atkinson, T Prescott, Musiek, Amy, Adeli, Mehdi, Derichs, Ute, Walz, Christoph, Krüger, Renate, von Bernuth, Horst, Klein, Christoph, Icenogle, Joseph, Hauck, Fabian, Sullivan, Kathleen E

“…Rubella virus (RuV) has recently been found in association with granulomatous inflammation of the skin and several internal organs in patients with inborn…”
Get full text

Defective Interfering Genomes and the Full-Length Viral Genome Trigger RIG-I After Infection With Vesicular Stomatitis Virus in a Replication Dependent Manner by Linder, Andreas, Bothe, Viktoria, Linder, Nicolas, Schwarzlmueller, Paul, Dahlström, Frank, Bartenhagen, Christoph, Dugas, Martin, Pandey, Dharmendra, Thorn-Seshold, Julia, Boehmer, Daniel F R, Koenig, Lars M, Kobold, Sebastian, Schnurr, Max, Raedler, Johannes, Spielmann, Giulia, Karimzadeh, Hadi, Schmidt, Andreas, Endres, Stefan, Rothenfusser, Simon

“…Replication competent vesicular stomatitis virus (VSV) is the basis of a vaccine against Ebola and VSV strains are developed as oncolytic viruses. Both…”
Get full text

Do Not Miss Acute Diffuse Panbronchiolitis for Tree-in-Bud: Case Series of a Rare Lung Disease by Raedler, Johannes, Hoelz, Hannes, Zschocke, Anna, Loeffler-Ragg, Judith, Paolini, Marco, Ley-Zaporozhan, Julia, Griese, Matthias

“…Acute bronchiolitis is a common disease of infants affecting the small airways. Rarely, acute bronchiolitis may occur in adolescents and adults. Here, we…”
Get full text

Leukemia escape in immune desert: intraocular relapse of pediatric pro-B-ALL during systemic control by CD19-CAR T cells by Willier, Semjon, Raedler, Johannes, Blaeschke, Franziska, Stenger, Dana, Pazos Escudero, Montserrat, Jurgeleit, Florian, Grünewald, Thomas G P, Binder, Vera, Schmid, Irene, Albert, Michael H, Wolf, Armin, Feuchtinger, Tobias

“…BackgroundRelapsed/refractory B-precursor acute lymphoblastic leukemia (BCP-ALL) remains a major therapeutic challenge in pediatric hematology. Chimeric…”
Get full text

Venetoclax and decitabine for relapsed paediatric myelodysplastic syndrome‐related acute myeloid leukaemia with complex aberrant karyotype after second stem cell transplantation by Raedler, Johannes, Heyde, Sita, Kolokythas, Marie, Eichinger, Anna, Binder, Vera, Schmid, Irene, Klein, Christoph, Feuchtinger, Tobias, Albert, Michael H.

Get full text

Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency by Lévy, Romain, Gothe, Florian, Momenilandi, Mana, Magg, Thomas, Materna, Marie, Peters, Philipp, Raedler, Johannes, Philippot, Quentin, Rack-Hoch, Anita Lena, Langlais, David, Bourgey, Mathieu, Lanz, Anna-Lisa, Ogishi, Masato, Rosain, Jérémie, Martin, Emmanuel, Latour, Sylvain, Vladikine, Natasha, Distefano, Marco, Khan, Taushif, Rapaport, Franck, Schulz, Marian S, Holzer, Ursula, Fasth, Anders, Sogkas, Georgios, Speckmann, Carsten, Troilo, Arianna, Bigley, Venetia, Roppelt, Anna, Dinur-Schejter, Yael, Toker, Ori, Bronken Martinsen, Karen Helene, Sherkat, Roya, Somekh, Ido, Somech, Raz, Shouval, Dror S, Kühl, Jörn-Sven, Ip, Winnie, McDermott, Elizabeth M, Cliffe, Lucy, Ozen, Ahmet, Baris, Safa, Rangarajan, Hemalatha G, Jouanguy, Emmanuelle, Puel, Anne, Bustamante, Jacinta, Alyanakian, Marie-Alexandra, Fusaro, Mathieu, Wang, Yi, Kong, Xiao-Fei, Cobat, Aurélie, Boutboul, David, Castelle, Martin, Aguilar, Claire, Hermine, Olivier, Cheminant, Morgane, Suarez, Felipe, Yildiran, Alisan, Bousfiha, Aziz, Al-Mousa, Hamoud, Alsohime, Fahad, Cagdas, Deniz, Abraham, Roshini S, Knutsen, Alan P, Fevang, Borre, Bhattad, Sagar, Kiykim, Ayca, Erman, Baran, Arikoglu, Tugba, Unal, Ekrem, Kumar, Ashish, Geier, Christoph B, Baumann, Ulrich, Neven, Bénédicte, Rohlfs, Meino, Walz, Christoph, Abel, Laurent, Malissen, Bernard, Marr, Nico, Klein, Christoph, Casanova, Jean-Laurent, Hauck, Fabian, Béziat, Vivien

“…Patients with inherited CARMIL2 or CD28 deficiency have defective T cell CD28 signaling, but their immunological and clinical phenotypes remain largely…”
Get full text

Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency by Lévy, Romain, Gothe, Florian, Momenilandi, Mana, Magg, Thomas, Materna, Marie, Peters, Philipp, Raedler, Johannes, Philippot, Quentin, Rack-Hoch, Anita Lena, Langlais, David, Bourgey, Mathieu, Lanz, Anna-Lisa, Ogishi, Masato, Rosain, Jérémie, Martin, Emmanuel, Latour, Sylvain, Vladikine, Natasha, Distefano, Marco, Khan, Taushif, Rapaport, Franck, Schulz, Marian, Holzer, Ursula, Fasth, Anders, Sogkas, Georgios, Speckmann, Carsten, Troilo, Arianna, Bigley, Venetia, Roppelt, Anna, Dinur-Schejter, Yael, Toker, Ori, Bronken Martinsen, Karen Helene, Sherkat, Roya, Somekh, Ido, Somech, Raz, Shouval, Dror, Kühl, Jörn-Sven, Ip, Winnie, Mcdermott, Elizabeth, Cliffe, Lucy, Ozen, Ahmet, Baris, Safa, Rangarajan, Hemalatha, Jouanguy, Emmanuelle, Puel, Anne, Bustamante, Jacinta, Alyanakian, Marie-Alexandra, Fusaro, Mathieu, Wang, Yi, Kong, Xiao-Fei, Cobat, Aurélie, Boutboul, David, Castelle, Martin, Aguilar, Claire, Hermine, Olivier, Cheminant, Morgane, Suarez, Felipe, Yildiran, Alisan, Bousfiha, Aziz, Al-Mousa, Hamoud, Alsohime, Fahad, Cagdas, Deniz, Abraham, Roshini, Knutsen, Alan, Fevang, Borre, Bhattad, Sagar, Kiykim, Ayca, Erman, Baran, Arikoglu, Tugba, Unal, Ekrem, Kumar, Ashish, Geier, Christoph, Baumann, Ulrich, Neven, Bénédicte, Calas, Julie, Feuille, Elizabeth, Chan, Angela, Yesil, Gozde, Nammour, Justine, Bandet, Élise, Picard, Capucine, Benhsaien, Ibtihal, Lang, Peter, Atschekzei, Faranaz, Warnatz, Klaus, Hambleton, Sophie, Desai, Mukesh, Karakoc-Aydiner, Elif, Kolukisa, Burcu, Al-Muhsen, Saleh, Alosaimi, Mohammed, Cipe, Funda, Alazami, Anas, Hancioglu, Gonca, Can Meydan, Bilge, Sorte, Hanne, Stray-Pedersen, Asbjørg, Mammayil, Geetha, Tökmeci, Nazan, Shcherbina, Anna, Stepensky, Polina

“…Patients with inherited CARMIL2 or CD28 deficiency have defective T cell CD28 signaling, but their immunological and clinical phenotypes remain largely…”
Get full text

Autoantibodies against type I IFNs in humans with alternative NF- K B pathway deficiency by Le Voyer, Tom, Liu, Xian, Gervais, Adrian, Rosain, Jeremie, Lorenzo, Malena Perez, Zhang, Peng, Bizien, Lucy, Charuel, Jean-Luc, Philippot, Quentin, Renkilaraj, Majistor Raj Luxman Maglorius, Ogishi, Masato, Migaud, Melanie, Rozenberg, Flore, Momenilandi, Mana, Riller, Quentin, Imberti, Luisa, Mueller, Gabriele, Keller, Baerbel, Gallego, William Alexander Franco, Rubin, Tamar, Emiroglu, Melike, Parvaneh, Nima, Eriksson, Daniel, Aranda-Guillen, Maribel, Berrios, David I., Vong, Linda, Mustillo, Peter, Raedler, Johannes, Bohlen, Jonathan, Astudillo, Camila, Winter, Sarah, DeRisi, Joseph L., Yu, David, Feng, Yi, Guichard, Audrey, Zhang, Yu, Rosen, Lindsey B., Holland, Steve M., Bosticardo, Marita, Kenney, Heather, Castagnoli, Riccardo, Slade, Charlotte A., Boztug, Kaan, Mahlaoui, Nizar, Abraham, Roshini S., Lougaris, Vassilios, Hauck, Fabian, Sediva, Anna, Sogkas, Georgios, Poli, M. Cecilia, Slatter, Mary A., Palterer, Boaz, Keller, Michael D., Pinzon-Charry, Alberto, Sullivan, Anna, Wong, Melanie, Ma, Cindy, Grombirikova, Hana, Dalal, Ilan, Aladjidi, Nathalie, Lazaro, Estibaliz, Keles, Sevgi, Malphettes, Marion, Maccari, Maria Elena, Meinhardt, Andrea, Shahrooei, Mohammad, Celmeli, Fatih, Frosk, Patrick, Goodnow, Christopher C., Gray, Paul E., Belot, Alexandre, Kuehn, Hye Sun, Rosenzweig, Sergio D., Miyara, Makoto, Servettaz, Amelie, Barlogis, Vincent, Le Guenno, Guillaume, Herrmann, Vera-Maria, Kuijpers, Taco, Schuetz, Catharina, Cunningham-Rundles, Charlotte, Rieux-Laucat, Frederic, Tangye, Stuart G., Warnatz, Klaus, Grimbacher, Bodo, Fieschi, Claire, Berteloot, Laureline, Bryant, Vanessa L., Assant, Sophie Trouillet, Su, Helen, Neven, Benedicte, Zhang, Qian, Boisson, Bertrand, Jouanguy, Emmanuelle, Bastard, Paul, Landegren, Nils, Notarangelo, Luigi D., Anderson, Mark S., Casanova, Jean-Laurent, Puel, Anne

“…Patients with autoimmune polyendocrinopathy syndrome type 1 (APS-1) caused by autosomal recessive AIRE deficiency produce autoantibodies that neutralize type I…”
Get full text