Thalassemias: An Overview

por Angastiniotis, Michael, Lobitz, Stephan
Publicado 2019

A Medication Adherence App for Children With Sickle Cell Disease: Qualitative Study

por Curtis, Kristina, Lebedev, Anastasiya, Aguirre, Elisa, Lobitz, Stephan
Publicado 2019

Editorial for Special Issue “Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies”

por Colombatti, Raffaella, Cela, Elena, Elion, Jacques, Lobitz, Stephan
Publicado 2019

Remote sensing and human health: new sensors and new opportunities.

por Beck, L R, Lobitz, B M, Wood, B L
Publicado 2000

Newborn Screening for Sickle Cell Disease: Technical and Legal Aspects of a German Pilot Study with 38,220 Participants

por Frömmel, Claudia, Brose, Annemarie, Klein, Jeannette, Blankenstein, Oliver, Lobitz, Stephan
Publicado 2014

HIF-1α determines the metastatic potential of gastric cancer cells

por Rohwer, N, Lobitz, S, Daskalow, K, Jöns, T, Vieth, M, Schlag, P M, Kemmner, W, Wiedenmann, B, Cramer, T, Höcker, M
Publicado 2009

Introduction of Universal Newborn Screening for Sickle Cell Disease in Germany—A Brief Narrative Review

por Lobitz, Stephan, Kunz, Joachim B., Cario, Holger, Hakimeh, Dani, Jarisch, Andrea, Kulozik, Andreas E., Oevermann, Lena, Grosse, Regine
Publicado 2021

Biosocial medicine: Biology, biography, and the tailored care of the patient

por Horwitz, Ralph I., Lobitz, Gabriella, Mawn, McKayla, Conroy, Allison Hayes, Cullen, Mark R., Sim, Ida, Singer, Burton H.
Publicado 2021

Viral Preservation with Protein-Supplemented Nebulizing Media in Aerosols

por Humphrey, Brittany, Tezak, Matthew, Lobitz, Mia, Hendricks, Anastasia, Sanchez, Andres, Zenker, Jake, Storch, Steven, Davis, Ryan D., Ricken, Bryce, Cahill, Jesse
Publicado 2023

P1480: SPLENIC SEQUESTRATION IS MORE COMMON IN SCD-S/Β0-THAL THAN IN SCD-S/S PATIENTS: RESULTS FROM THE GERMAN SCD REGISTRY

por Allard, P., Tagliaferri, L., Lobitz, S., Cario, H., Jarisch, A., Grosse, R., Ebert, S., Bleeke, M., Oevermann, L., Hakimeh, D., Kulozik, A., Kunz, J.
Publicado 2022

Conditional gene expression in the mouse using a Sleeping Beauty gene-trap transposon

por Geurts, Aron M, Wilber, Andrew, Carlson, Corey M, Lobitz, Paul D, Clark, Karl J, Hackett, Perry B, McIvor, R Scott, Largaespada, David A
Publicado 2006

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...

por Kunz, Joachim B., Schlotmann, Andreas, Daubenbüchel, Andrea, Lobitz, Stephan, Jarisch, Andrea, Grosse, Regine, Cario, Holger, Oevermann, Lena, Hakimeh, Dani, Tagliaferri, Laura, Kulozik, Andreas E.
Publicado 2021

Biotic countermeasures that rescue Nannochloropsis gaditana from a Bacillus safensis infection

por Humphrey, Brittany, Mackenzie, Morgan, Lobitz, Mia, Schambach, Jenna Y., Lasley, Greyson, Kolker, Stephanie, Ricken, Bryce, Bennett, Haley, Williams, Kelly P., Smallwood, Chuck R., Cahill, Jesse
Publicado 2023

Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea

por 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.
Publicado 2021

Newborn Screening for Sickle Cell Disease in Europe

por 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
Publicado 2019

5613004 NEWBORN SCREENING FOR SICKLE CELL DISEASE IN GERMANY - THE FIRST YEAR

por Lobitz, S., Kunz, J.B., Ceglarek, U., Grosse, R., Hakimeh, D., Holtkamp, U., Jarisch, A., Klein, J., Kulozik, A.E., Mirtschink, P., Murko, S., Neisse, T., Nennstiel-Ratzel, U., Oevermann, L., Rödel, M., Rönicke, S., Sinemus, N., Winter, T., Cario, H.
Publicado 2023

5612617 EFFICACY AND SAFETY OF A SINGLE DOSE OF EXAGAMGLOGENE AUTOTEMCEL FOR TRANSFUSION-DEPENDENT-THALASSEMIA AND SEVERE SICKLE CELL DISEASE

por de la Fuente, J., Locatelli, F., Frangoul, H., Corbacioglu, S., Wall, D., Cappellini, M., de Montalembert, M., Kattamis, A., Lobitz, S., Rondelli, D., Sheth, S., Steinberg, M., Walters, M., Bobruff, Y., Simard, C., Song, Y., Zhang, L., Sharma, A., Imren, S., Hobbs, B., Grupp, S.
Publicado 2023

High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers

por 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
Publicado 2020

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes

por 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
Publicado 2019