Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Haematologica|August 16, 2023
Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndromeMiriam Erlacher, Felicia Andresen, Martina Sukova, et al.
Blood Advances|January 20, 2026
Comparable outcomes of HSCT upfront and after failure of IST in pediatric aplastic anemia in recent yearsFelicia Andresen, Ayami Yoshimi, Peter Bader, et al.
European Journal of Human Genetics : EJHG|June 6, 2025
Biallelic SH2B3 germline variants are associated with a neonatal myeloproliferative disease and multisystemic involvementDavide Leardini, Elisabetta Flex, Elliot Stieglitz, et al.
Clinical Chemistry and Laboratory Medicine|February 10, 2021
High-resolution pediatric reference intervals for 15 biochemical analytes described using fractional polynomialsJakob Zierk, Hannsjörg Baum, Alexander Bertram, et al.
Haematologica|January 2, 2015
Criteria for evaluating response and outcome in clinical trials for children with juvenile myelomonocytic leukemiaCharlotte M Niemeyer, Mignon L Loh, Annamaria Cseh, et al.
British Journal of Haematology|November 9, 2023
Biallelic inactivation of the NF1 tumour suppressor gene in juvenile myelomonocytic leukaemia: Genetic evidence of driver function and implications for diagnostic workupSenthilkumar Ramamoorthy, Dirk Lebrecht, Denny Schanze, et al.
Bone Marrow Transplantation|July 10, 2021
Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndromeRachel Bortnick, Marcin Wlodarski, Valerie de Haas, et al.
Haematologica|October 29, 2013
Comparison of horse and rabbit antithymocyte globulin in immunosuppressive therapy for refractory cytopenia of childhoodAyami Yoshimi, Marry M van den Heuvel-Eibrink, Irith Baumann, et al.
Human Mutation|July 23, 2021
SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literatureMatthew M Heeney, Simon Berhe, Dean R Campagna, et al.
Clinical Immunology (Orlando, Fla.)|September 23, 2023
C-terminal variants in CDC42 drive type I interferon-dependent autoinflammation in NOCARH syndrome reversible by ruxolitinibFriedrich G Kapp, Stefanie Kretschmer, Cora C A Beckmann, et al.
Pageof 7