D. Hakimeh

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

A. Kopp-Schneider, A. Kulozik, H. Cario, 2021, Haematologica.

"Default" versus "pre-atopic" IgG responses to foodborne and airborne pathogenesis-related group 10 protein molecules in birch-sensitized and nonatopic children.

T. Keil, S. Lau, U. Wahn, 2015, Journal of Allergy and Clinical Immunology.

Recent advances on diagnosis and management of childhood asthma and food allergies

D. Hakimeh, S. Tripodi, 2013, Italian Journal of Pediatrics.

Sickle cell disease in Germany: Results from a national registry

A. Kulozik, H. Cario, M. Erlacher, 2019, Pediatric blood & cancer.

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

A. Kulozik, H. Cario, S. Lobitz, 2021, Journal of clinical medicine.

HLA-haploidentical hematopoietic stem cell transplantation in pediatric patients with hemoglobinopathies: current practice and new approaches

J. Schulte, A. Eggert, L. Oevermann, 2019, Bone Marrow Transplantation.

Allogeneic hematopoietic stem cell transplantation from sibling and unrelated donors in pediatric patients with sickle cell disease—A single center experience

J. Schulte, A. Eggert, P. Hundsdoerfer, 2020, Pediatric transplantation.

Parental hay fever reinforces IgE to pollen as pre‐clinical biomarker of hay fever in childhood

T. Keil, S. Lau, U. Wahn, 2014, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

A. Kulozik, H. Cario, S. Lobitz, 2021, International journal of neonatal screening.