Peripheral T-Cell Lymphoma in Children and Adolescents: A Single Institution Case Series [0.03%]
儿童和青少年周围T细胞淋巴瘤的病例系列研究
Kaitlin J Devine,Laura Lenzi,Moe Takeda et al.
Kaitlin J Devine et al.
These findings emphasize the need for a better understanding of disease biology for this complex group of malignancies to refine treatment approaches. ...
A Rare Case of Homozygous HbE With Coinherited Alpha-Thalassemia and Hb Constant Spring in a Neonate Reveals a Mild Hematologic Phenotype [0.03%]
一个新生儿的罕见纯合HbE合并α-地中海贫血和Hb恒春型病例显示出了较轻的血液学表型
Victor Bobée,Maïssa Souissi,Cécile Dumesnil et al.
Victor Bobée et al.
Background: Neonatal microcytosis may reveal complex hemoglobinopathy combinations requiring molecular clarification. Observation: We d...
Knowledge Translation of Pharmacogenomics for Pain Management in Patients With Sickle Cell Disease-A Qualitative Study [0.03%]
血红蛋白SC病患者镇痛管理的药物基因组学知识转化定性研究
Audrey Rosenblatt,Vanessa Williams,Nathan Lamb et al.
Audrey Rosenblatt et al.
Background: Health care providers (HCPs) currently prescribe analgesics based on clinical experience, placing Black Americans with sickle cell disease (SCD) at risk for poorly controlled pain, adverse drug effects, and bi...
Bleeding Phenotypes in Inherited Platelet Function Disorders: Insights From the ATHNdataset [0.03%]
inherited platelet function障碍的出血表型：来自ATHN数据集的见解
Divyaswathi Citla-Sridhar,Jianzhong Hu,Robert F Sidonio Jr et al.
Divyaswathi Citla-Sridhar et al.
Background: Inherited platelet function disorders (IPFDs) are rare, heterogeneous conditions that pose diagnostic and management challenges. While bleeding in Glanzmann thrombasthenia (GT) and Bernard-Soulier syndrome (BS...
Beacon Bootcamp: A Near-Peer, Experiential Approach to Chemotherapy Prescribing Education in Pediatric Hematology/Oncology Fellowship [0.03%]
儿科血液肿瘤专业化疗开方能力的近-peer经验式教学项目 Beacon 训练营
Paula Sulikowski,Jennifer C Yu
Paula Sulikowski
Pediatric hematology/oncology fellows at our institution lacked formal training in prescribing chemotherapy and supportive care. This pilot study aimed to assess the feasibility of implementing a structured curriculum in a fellowship progra...
The Clinico-Therapeutic Challenge of Tuberculosis in Pediatric Acute Leukemia and Stem Cell Transplant Patients: An Experience From a Tertiary Care Center Over 5 Years [0.03%]
三级医疗中心5年来儿科急性白血病和干细胞移植患者的结核临床治疗挑战及经验总结
Swati Bhayana,Anil Sachdev,Dhiren Gupta et al.
Swati Bhayana et al.
Despite the high prevalence of tuberculosis (TB) in developing countries, tubercular reactivation or new infections are rarely observed in patients with acute leukemia or after hematopoietic stem cell transplant (HSCT). We describe 9 pediat...
A Survey of Provider Practices for Diagnosis and Treatment of Pediatric Moderate Aplastic Anemia From the North American Pediatric Aplastic Anemia Consortium [0.03%]
北美地区儿童中度再生障碍性贫血诊疗实践的调查研究——来自北美儿科再障联盟的数据
Linah Omer,Nicholas J Gloude,Catherine McGuinn et al.
Linah Omer et al.
Pediatric moderate aplastic anemia (MAA) lacks defined diagnostic criteria and a clear standard of care due to limited understanding of its pathophysiology and natural history. To understand current diagnostic and management practices for p...
COVID-19 and Influenza Vaccine Acceptance and Hesitancy Among Caregivers of Children With Cancer [0.03%]
儿童癌症患者的看护者接受新型冠状病毒和流感疫苗及犹豫的研究
Alastair Murray,Palcah Shibale,Jennifer Wilkes et al.
Alastair Murray et al.
Introduction: Children with cancer are immunocompromised and at increased risk for severe outcomes from infections such as COVID-19 and influenza. Vaccination is recommended, but caregiver perceptions in this high-risk gr...
Process Analysis of Time to Antibiotics in Pediatric Patients With Fever in Neutropenia During Chemotherapy for Cancer [0.03%]
发热性中性粒细胞减少症儿童癌症化疗患者的抗生素使用时机分析流程研究
Christa Koenig,Claudia E Kuehni,Nicole Bodmer et al.
Christa Koenig et al.
For fever in neutropenia (FN) during chemotherapy timely start of antibiotics is recommended. We analyzed time to antibiotics (TTA) and sub-timespans between detection of fever and start of antibiotics in children undergoing chemotherapy fo...
Ghosal Hematodiaphyseal Dysplasia: A Case Report with Review of Genetically Confirmed Cases [0.03%]
戈萨尔骨髓发育不良综合征1型：1例报告及文献复习
Gürcan Dikme,Mutlu Karkucak,Feyza Sönmez Topçu et al.
Gürcan Dikme et al.
Background: Ghosal hematodiaphyseal dysplasia syndrome (GHDS) is a rare disorder caused by loss-of-function mutations in thromboxane A synthase 1 (TBXAS1). ...