Stephan Lobitz
Koblenz, RP, Germany
Last Updated: 09/26/2026
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Found 30 publications
Exa-cel in Children with Transfusion-Dependent β-Thalassemia or Sickle Cell Disease.
Journal: The New England journal of medicine
Published: June 11, 2026
Progressive short stature in Pearson syndrome and the impact of organ failure.
Journal: Molecular genetics and metabolism
Published: February 03, 2026
Approaches to Invasive Fungal Diseases in Paediatric Cancer Centres: An Analysis of Current Practices and Challenges in Germany, Austria and Switzerland.
Journal: Mycoses
Published: April 01, 2025
Exagamglogene Autotemcel for Severe Sickle Cell Disease.
Journal: The New England journal of medicine
Published: April 25, 2024
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.
Journal: European journal of haematology
Published: March 13, 2024
Sickle cell disease landscape and challenges in the EU: the ERN-EuroBloodNet perspective.
Journal: The Lancet. Haematology
Published: May 31, 2023
Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency.
Journal: Gastroenterology
Published: September 08, 2022
Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol.
Journal: Annals of hematology
Published: November 04, 2021
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.
Journal: Journal of clinical medicine
Published: August 31, 2021
Last Updated: 09/26/2026