Featured Publications
Histiocytic Neoplasms, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.
Go RS, Jacobsen E, Baiocchi R, Buhtoiarov I, Butler EB, Campbell PK, Coulter DW, Diamond E, Flagg A, Goodman AM, Goyal G, Gratzinger D, Hendrie PC, Higman M, Hogarty MD, Janku F, Karmali R, Morgan D, Raldow AC, Stefanovic A, Tantravahi SK, Walkovich K, Zhang L, Bergman MA, Darlow SD. Histiocytic Neoplasms, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology. Journal Of The National Comprehensive Cancer Network 2021, 19: 1277-1303. PMID: 34781268, DOI: 10.6004/jnccn.2021.0053.Peer-Reviewed Reviews, Practice Guidelines, Standards, and Consensus StatementsConceptsHistiocytic neoplasmsNCCN Clinical Practice GuidelinesCommon histiocytic disorderRare hematologic disorderRosai-Dorfman diseaseTreatment of adultsClinical practice guidelinesErdheim-Chester diseaseLangerhans cell histiocytosisNCCN guidelinesSelect patientsSystemic therapyLymph nodesClinical presentationMild diseaseCell histiocytosisHematologic disordersHistiocytic disorderPractice guidelinesOptimal managementPatientsNeoplasmsSoft tissueDiseaseDisordersInfectious diseases in pediatric transplantation: Literature review 2006–2007
Flagg A, Danziger‐Isakov L. Infectious diseases in pediatric transplantation: Literature review 2006–2007. Pediatric Transplantation 2008, 12: 729-736. DOI: 10.1111/j.1399-3046.2008.00985.x.Peer-Reviewed Reviews, Practice Guidelines, Standards, and Consensus Statements
2023
384 Vaso-Occlusive Pain Requiring Hospitalization or Treatment Is Rare Following Successful Hematopoietic Cell Transplantation for Sickle Cell Disease
Krishnamurti L, He Z, Deng Y, Hamidi R, Flagg A, Shah N. 384 Vaso-Occlusive Pain Requiring Hospitalization or Treatment Is Rare Following Successful Hematopoietic Cell Transplantation for Sickle Cell Disease. Transplantation And Cellular Therapy 2023, 29: s291. DOI: 10.1016/s2666-6367(23)00453-0.Peer-Reviewed Original Research
2020
Severe megaloblastic anemia: Vitamin deficiency and other causes
Socha DS, DeSouza SI, Flagg A, Sekeres M, Rogers HJ. Severe megaloblastic anemia: Vitamin deficiency and other causes. Cleveland Clinic Journal Of Medicine 2020, 87: 153-164. PMID: 32127439, DOI: 10.3949/ccjm.87a.19072.Peer-Reviewed Reviews, Practice Guidelines, Standards, and Consensus StatementsConceptsMegaloblastic anemiaRed blood cell productionVitamin supplementationLaboratory findingsVitamin deficiencyBlood cell productionIntramedullary hemolysisCobalamin deficiencyMacrocytic anemiaCommon causeCase of deficiencySevere casesNeoplastic diseaseCharacteristic morphologicFolate deficiencyUnderlying causeAnemiaCell productionCauseDeficiencyDiscontinuationMedicationsTherapyDiseaseSupplementation