Výsledky vyhledávání - Lobitz, Stephan
- Zobrazuji výsledky 1 - 12 z 12
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Thalassemias: An Overview Autor Angastiniotis, Michael, Lobitz, Stephan
Vydáno 2019Text -
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Introduction of Universal Newborn Screening for Sickle Cell Disease in Germany—A Brief Narrative Review Autor Lobitz, Stephan, Kunz, Joachim B., Cario, Holger, Hakimeh, Dani, Jarisch, Andrea, Kulozik, Andreas E., Oevermann, Lena, Grosse, Regine
Vydáno 2021Text -
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Benefits of a Disease Management Program for Sickle Cell Disease in Germany 2011–2019: The Increased Use of Hydroxyurea Correlates with a Reduced Frequency of Acute Chest Syndrome... Autor Kunz, Joachim B., Schlotmann, Andreas, Daubenbüchel, Andrea, Lobitz, Stephan, Jarisch, Andrea, Grosse, Regine, Cario, Holger, Oevermann, Lena, Hakimeh, Dani, Tagliaferri, Laura, Kulozik, Andreas E.
Vydáno 2021Text -
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Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea Autor Allard, Pierre, Alhaj, Nareen, Lobitz, Stephan, Cario, Holger, Jarisch, Andreas, Grosse, Regine, Oevermann, Lena, Hakimeh, Dani, Tagliaferri, Laura, Kohne, Elisabeth, Kopp-Schneider, Annette, Kulozik, Andreas E., Kunz, Joachim B.
Vydáno 2021Text -
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Newborn Screening for Sickle Cell Disease in Europe Autor Daniel, Yvonne, Elion, Jacques, Allaf, Bichr, Badens, Catherine, Bouva, Marelle J., Brincat, Ian, Cela, Elena, Coppinger, Cathy, de Montalembert, Mariane, Gulbis, Béatrice, Henthorn, Joan, Ketelslegers, Olivier, McMahon, Corrina, Streetly, Allison, Colombatti, Raffaella, Lobitz, Stephan
Vydáno 2019Text -
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A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network Autor Casado, José Antonio, Callén, Elsa, Jacome, Ariana, Río, Paula, Castella, Maria, Lobitz, Stephan, Ferro, Teresa, Muñoz, Arturo, Sevilla, Julián, Cantalejo, Ángeles, Cela, Elena, Cervera, José, Sánchez‐Calero, Jesús, Badell, Isabel, Estella, Jesús, Dasí, Ángeles, Olivé, Teresa, Ortega, Juan José, Rodriguez‐Villa, Antonia, Tapia, María, Molinés, Antonio, Madero, Luis, Segovia, José C, Neveling, Kornelia, Kalb, Reinhard, Schindler, Detlev, Hanenberg, Helmut, Surrallés, Jordi, Bueren, Juan A
Vydáno 2007Text -
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High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers Autor González-Acosta, Maribel, Marín, Fátima, Puliafito, Benjamin, Bonifaci, Nuria, Fernández, Anna, Navarro, Matilde, Salvador, Hector, Balaguer, Francesc, Iglesias, Silvia, Velasco, Angela, Grau Garces, Elia, Moreno, Victor, Gonzalez-Granado, Luis Ignacio, Guerra-García, Pilar, Ayala, Rosa, Florkin, Benoît, Kratz, Christian, Ripperger, Tim, Rosenbaum, Thorsten, Januszkiewicz-Lewandowska, Danuta, Azizi, Amedeo A, Ragab, Iman, Nathrath, Michaela, Pander, Hans-Jürgen, Lobitz, Stephan, Suerink, Manon, Dahan, Karin, Imschweiler, Thomas, Demirsoy, Ugur, Brunet, Joan, Lázaro, Conxi, Rueda, Daniel, Wimmer, Katharina, Capellá, Gabriel, Pineda, Marta
Vydáno 2020Text -
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A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes Autor Gallon, Richard, Mühlegger, Barbara, Wenzel, Sören‐Sebastian, Sheth, Harsh, Hayes, Christine, Aretz, Stefan, Dahan, Karin, Foulkes, William, Kratz, Christian P., Ripperger, Tim, Azizi, Amedeo A., Baris Feldman, Hagit, Chong, Anne‐Laure, Demirsoy, Ugur, Florkin, Benoît, Imschweiler, Thomas, Januszkiewicz‐Lewandowska, Danuta, Lobitz, Stephan, Nathrath, Michaela, Pander, Hans‐Jürgen, Perez‐Alonso, Vanesa, Perne, Claudia, Ragab, Iman, Rosenbaum, Thorsten, Rueda, Daniel, Seidel, Markus G., Suerink, Manon, Taeubner, Julia, Zimmermann, Stefanie‐Yvonne, Zschocke, Johannes, Borthwick, Gillian M., Burn, John, Jackson, Michael S., Santibanez‐Koref, Mauro, Wimmer, Katharina
Vydáno 2019Text