Publications by authors named "Stephan Lobitz"

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Approaches to Invasive Fungal Diseases in Paediatric Cancer Centres: An Analysis of Current Practices and Challenges in Germany, Austria and Switzerland.
Danila Seidel, Zoi Dorothea Pana, Daniel Ebrahimi-Fakhari, Sarina K Butzer, Katrin Mehler, Stephan Lobitz

Mycoses· June 2025

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Selecting patients with sickle cell disease for gene addition or gene editing-based therapeutic approaches: Report on behalf of a joint EHA Specialized Working Group and EBMT Hemoglobinopathies Working Party consensus conference.
Lucia de Franceschi, Franco Locatelli, David Rees, Christian Chabannon, Jean-Hugues Dalle, Stephan Lobitz

Hemasphere· March 2025

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Gene therapy in transfusion-dependent non-β0/β0 genotype β-thalassemia: first real-world experience of beti-cel.
Adil Mirza, Mona-Lisa Ritsert, Gloria Tao, Himal Thakar, Stephan Lobitz

Blood Adv· January 2025

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The German sickle cell disease registry reveals a surprising risk of acute splenic sequestration and an increased transfusion requirement in patients with compound heterozygous sickle cell disease HbS/β-thalassaemia and no or low HbA expression.
Pierre Allard, Laura Tagliaferri, Vivienn Weru, Holger Cario, Stephan Lobitz

Eur J Haematol· October 2024

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Sickle cell disease landscape and challenges in the EU: the ERN-EuroBloodNet perspective.
María Del Mar Mañú Pereira, Raffaella Colombatti, Federico Alvarez, Pablo Bartolucci, Celeste Bento, Stephan Lobitz

Lancet Haematol· August 2023

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Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency.
Richard Gallon, Rachel Phelps, Christine Hayes, Laurence Brugieres, Léa Guerrini-Rousseau, Stephan Lobitz

Gastroenterology· April 2023

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Complete Tracheal Ring Deformity, Recurrent Pneumothoraces and Pleuropulmonary Blastoma in a Child: Coincidence or Common Genetic Cause?
Inga Thiemann, Thomas Hoppen, Martin Laur, Manuel Ohlert, Stephan Lobitz

Klin Padiatr· September 2022

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Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol.
Stephan Lobitz, Claudia Frömmel, Annemarie Brose, Oliver Blankenstein, Charles Turner

Ann Hematol· August 2022

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Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea.
Pierre Allard, Nareen Alhaj, Stephan Lobitz, Holger Cario, Andreas Jarisch

Haematologica· July 2022

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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.
Joachim B Kunz, Andreas Schlotmann, Andrea Daubenbüchel, Stephan Lobitz, Andrea Jarisch

J Clin Med· September 2021

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Haematological characteristics and spontaneous haematological recovery in Pearson syndrome.
Ayami Yoshimi, Sarah C Grünert, Holger Cario, Aron Fisch, Ute Gross-Wieltsch, Stephan Lobitz

Br J Haematol· June 2021

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Introduction of Universal Newborn Screening for Sickle Cell Disease in Germany-A Brief Narrative Review.
Stephan Lobitz, Joachim B Kunz, Holger Cario, Dani Hakimeh, Andrea Jarisch

Int J Neonatal Screen· January 2021

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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.
Maribel González-Acosta, Fátima Marín, Benjamin Puliafito, Nuria Bonifaci, Anna Fernández, Stephan Lobitz

J Med Genet· April 2020

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Sickle cell disease in Germany: Results from a national registry.
Joachim B Kunz, Stephan Lobitz, Regine Grosse, Lena Oevermann, Dani Hakimeh

Pediatr Blood Cancer· April 2020

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Transmission of chromosomally integrated human herpes virus-6A via haploidentical stem cell transplantation poses a risk for virus reactivation and associated complications.
Lena Oevermann, Cosima Zimmermann, Sebastian Voigt, Annette Künkele, Stephan Lobitz

Bone Marrow Transplant· January 2020

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Editorial for Special Issue "Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies".
Raffaella Colombatti, Elena Cela, Jacques Elion, Stephan Lobitz

Int J Neonatal Screen· December 2019

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[What's new in diagnostics and treatment of hemoglobinopathies?].
Holger Cario, Stephan Lobitz

Dtsch Med Wochenschr· June 2019

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A Medication Adherence App for Children With Sickle Cell Disease: Qualitative Study.
Kristina Curtis, Anastasiya Lebedev, Elisa Aguirre, Stephan Lobitz

JMIR Mhealth Uhealth· June 2019

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A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes.
Richard Gallon, Barbara Mühlegger, Sören-Sebastian Wenzel, Harsh Sheth, Christine Hayes, Stephan Lobitz

Hum Mutat· May 2019

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Newborn Screening for Sickle Cell Disease in Europe.
Yvonne Daniel, Jacques Elion, Bichr Allaf, Catherine Badens, Marelle J Bouva, Stephan Lobitz

Int J Neonatal Screen· March 2019

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Thalassemias: An Overview.
Michael Angastiniotis, Stephan Lobitz

Int J Neonatal Screen· March 2019

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Newborn screening by tandem mass spectrometry confirms the high prevalence of sickle cell disease among German newborns.
Stephan Lobitz, Jeannette Klein, Annemarie Brose, Oliver Blankenstein, Claudia Frömmel

Ann Hematol· January 2019

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Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference.
Stephan Lobitz, Paul Telfer, Elena Cela, Bichr Allaf, Michael Angastiniotis

Br J Haematol· November 2018

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The epidemiology of sickle cell disease in Germany following recent large-scale immigration.
Joachim B Kunz, Holger Cario, Regine Grosse, Andrea Jarisch, Stephan Lobitz

Pediatr Blood Cancer· July 2017

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