Results 141 to 150 of about 57,162 (316)
Acta Paediatrica, Volume 114, Issue 8, Page 1857-1867, August 2025.ABSTRACT Aim To assess the prevalence of endocrine disorders and investigate growth patterns in single large‐scale mitochondrial DNA deletion syndromes (SLSMDs). Methods A retrospective study of all children with SLSMD who attended Sheba Medical Center, Israel, from February 2017 to September 2024.
Ayman Daka +7 more
wiley +1 more source
Persistent Fever and Pancytopenia: Lupus Flare vs Macrophage Activation Syndrome [PDF]
, 2015 Introduction Macrophage activation syndrome (MAS), first named in 1993, is a subcategory of hemophagocytic lymphohistiocytosis (HLH), characterized by prolonged fever, hepatosplenomegaly, pancytopenia, liver dysfunction, and most notably ...
McGhee, MD, Amy
core +2 more sources
Clinical Study of Pancytopenia
International Journal of Medical Research and Review, 2016 Introduction: Pancytopenia is a common and alarming condition encountered by clinicians. We had studied the clinical presentation, laboratory investigations and various etiologies of Pancytopenia. Material and Methods: Study was carried out in a tertiary care centre in western India.
Vishal Gupta +2 more
openaire +3 more sources
Acute Myeloid Leukemia as the Main Cause of Pancytopenia in Iranian Population
Iranian Journal of Pathology, 2017 Background & objective: Pancytopenia is the reduction in the number of all 3 major cellular elements of blood and leads to anemia, leukopenia, and thrombocytopenia.
H. Jalaeikhoo +7 more
semanticscholar +1 more source
European Journal of Haematology, Volume 115, Issue 2, Page 185-192, August 2025.ABSTRACT The evolution of acute myeloid leukemia (AML) classifications has progressively shifted the diagnostic focus toward genetic criteria. Nevertheless, morphology remains a key element in clinical practice, often serving as the initial trigger for additional molecular investigations. The diagnosis of acute erythroleukemia (AEML), initially defined
Laurène Fenwarth +23 more
wiley +1 more source
Targeting inflammatory pathways in axial spondyloarthritis. [PDF]
, 2019 The triggers and pathogenesis of axial spondyloarthritis (axSpA) are not yet completely understood. However, therapeutic agents targeting tumor necrosis factor-α and interleukin-17 inflammatory pathways have proven successful in suppressing many of the ...
Furst, Daniel E, Louie, James S
core
Gaucher Disease and Myelofibrosis: A Combined Disease or a Misdiagnosis? [PDF]
, 2018 Background: Gaucher disease (GD) and primary myelofibrosis (PMF) share similar clinical and laboratory features, such as cytopenia, hepatosplenomegaly, and marrow fibrosis, often resulting in a misdiagnosis.
Cardarelli, L +5 more
core +1 more source
Pediatric Transplantation, Volume 29, Issue 5, August 2025.ABSTRACT Background Hematopoietic stem cell transplantation (HSCT) in solid organ transplant recipients has been reported in adults. However, data on children are scarce. We report a case of an allogeneic HSCT in a 14‐year‐old girl to treat idiopathic very severe aplastic anemia (SAA). Case Presentation The girl developed end‐stage renal disease at the
Gintarė Mierkienė +4 more
wiley +1 more source
Management of aplastic anemia in a woman during pregnancy: A case report [PDF]
, 2011 Introduction. Aplastic anemia is a rare disease caused by destruction of pluripotent stem cells in bone marrow. During pregnancy it could be life-threatening for both mother and child.
Lugtenburg, P.J. +2 more
core +3 more sources
Clinical Case Reports, Volume 13, Issue 7, July 2025.ABSTRACT Auto‐inflammatory diseases can exhibit a wide variety of clinical symptoms, which often result in delays in diagnosis and treatment for patients. Intestinal inflammation is a clinical symptom frequently observed in auto‐inflammatory syndromes.
Maryam Khalesi +5 more
wiley +1 more source