Results 101 to 110 of about 11,475 (240)
Uncommon Hepatic Sequelae from an Acute Sickle Cell Crisis [PDF]
, 2013 Background Sickle cell crises are commonly treated at our institution given its large sickle cell patient population and well-established hematology department.
Lim, MD, Kimberly, Walter, MD, James W.
core +2 more sources
Pediatric Blood &Cancer, Volume 73, Issue 5, May 2026.ABSTRACT Background Sickle cell disease (SCD) is an autosomal recessive hemoglobinopathy affecting millions of individuals worldwide. The clinical expression and psychosocial burden of SCD vary widely across geographical, cultural, and healthcare system contexts, underscoring the need for setting‐specific approaches to assessment.
Desiré Fantasia +7 more
wiley +1 more source
Vitamin D and its receptor polymorphisms: New possible prognostic biomarkers in leukemias
Oncology Reviews, 2018 Several factors such as chromosomal translocations, gene mutations, and polymorphisms are involved in the pathogenesis of leukemia/lymphoma. Recently, the role of vitamin D (VD) and vitamin D receptor (VDR) polymorphisms in hematologic malignancies has ...
Seyed Mohammad Sadegh Pezeshki +5 more
doaj +1 more source
Bases moleculares de hemoglobinopatias na Argentina [PDF]
, 2017 Durante el desarrollo de un individuo se expresan distintas cadenas de globina de tipo α y no-α, que se combinan en tetrámeros para formar hemoglobina. Los genes que las codifican se organizan en familias.
Scheps, Karen, Varela, Viviana
core
Pediatric Blood &Cancer, Volume 73, Issue 5, May 2026.ABSTRACT Hemoglobinopathies are prevalent globally; diagnosis is complex in high genetic admixture populations like Brazil. We report, in two pediatric siblings, the first documented cases in Brazil of heterozygosity for hemoglobin (Hb) O‐Arab with coinheritance of α‐thalassemia (αα/−α4.2; −α3.7/−α4.2), resulting in microcytic and hypochromic anemia ...
Elisângela de Souza Miranda Muynarsk +9 more
wiley +1 more source
Complex karyotype in myelodysplastic syndromes: Diagnostic procedure and prognostic susceptibility
Oncology Reviews, 2019 Complex karyotype (CK) is a poor prognosis factor in hematological malignancies. Studies have shown that the presence of CK in myelodysplastic syndrome (MDS) can be associated with MDS progression to acute myeloid leukemia. The goal of this review was to
Mohammad Shahjahani +4 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 5, May 2026.Acute infarcts and microvascular ischemic changes in the brain of a young patient with Sickle‐Cell Disease despite High Fetal Hemoglobin. ABSTRACT Sickle‐cell disease (SCD) is characterized by abnormal hemoglobin (Hb) polymerization, leading to erythrocyte sickling and microvascular obstruction.
Yi Hui Luo +5 more
wiley +1 more source
The impact of N-myc amplification on median survival in children with neuroblastoma [PDF]
, 2013 Background: Neuroblastoma is the most common extracranial malignant solid tumor in children under 5 years, and it is characterized by wide clinical and biological heterogeneity.
Azizi Malamiri, Reza. +5 more
core
Endocrinology, Diabetes &Metabolism, Volume 9, Issue 3, May 2026.Initiation of oral semaglutide in patients with T2D in routine clinical practice in Mexico significantly reduces HbA1c and weight and improves satisfaction with treatment. ABSTRACT Background To investigate the oral semaglutide use among Mexican adults with type 2 diabetes.
Guillermo González‐Gálvez +7 more
wiley +1 more source