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Blood|October 26, 2021
Perturbed NK-cell homeostasis associated with disease severity in chronic neutropeniaEbba Sohlberg, Aline Pfefferle, Eivind Heggernes Ask, et al.
Reproductive Biomedicine Online|August 21, 2023
Reference standards for follicular density in ovarian cortex from birth to sexual maturityJasmin Hassan, Katri Knuus, Atte Lahtinen, et al.
Bone Marrow Transplantation|October 22, 2020
Vitamin D levels and busulphan kinetics in patients undergoing hematopoietic stem cell transplantation, a multicenter studyAhmed El-Serafi, Rui He, Wenyi Zheng, et al.
British Journal of Haematology|May 29, 2024
Decreased spermatogonial numbers in boys with severe haematological diseasesAtte K Lahtinen, Miriam Funke, Claudia Krallmann, et al.
Frontiers in Pediatrics|April 1, 2022
A Phase II Trial of a Personalized, Dose-Intense Administration Schedule of <sup>177</sup>Lutetium-DOTATATE in Children With Primary Refractory or Relapsed High-Risk Neuroblastoma-LuDO-NFredrik Sundquist, Kleopatra Georgantzi, Kirsten Brunsvig Jarvis, et al.
Haematologica|September 11, 2016
Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosisAmanda J Walne, Laura Collopy, Shirleny Cardoso, et al.
Human Reproduction (Oxford, England)|June 7, 2025
Early transcriptional states of spermatogonia and marker expressions in the prepubertal human testis following chemotherapy-induced depletionHajar Ba Omar, Justine Stevens, Anu Haavisto, et al.
Transplantation and Cellular Therapy|May 9, 2021
Outcomes of Unmanipulated Haploidentical Transplantation Using Post-Transplant Cyclophosphamide (PT-Cy) in Pediatric Patients With Acute Lymphoblastic LeukemiaAnnalisa Ruggeri, Jacques-Emmanuel Galimard, Olesya Paina, et al.
Cells|January 30, 2021
Spermatogonia Loss Correlates with LAMA 1 Expression in Human Prepubertal Testes Stored for Fertility PreservationMagdalena Kurek, Elisabet Åkesson, Masahito Yoshihara, et al.
British Journal of Haematology|October 5, 2023
Busulfan-fludarabine- or treosulfan-fludarabine-based conditioning before allogeneic HSCT from matched sibling donors in paediatric patients with sickle cell disease: A study on behalf of the EBMT Paediatric Diseases and Inborn Errors Working PartiesAnnamária Cseh, Jacques-Emmanuel Galimard, Josu de la Fuente, et al.
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