Results 101 to 110 of about 33,029 (292)
Thrombotic microangiopathies: thrombotic thrombocytopenic purpura / hemolytic uremic syndrome [PDF]
, 2010 Thrombotic microangiopathies (TMAs) are pathological conditions characterized by generalized microvascular occlusion by platelet thrombi, thrombocytopenia, and microangiopathic hemolytic anemia.
Mastroianni Kirsztajn, Gianna +1 more
core +2 more sources
Comorbidities in Mild WAS/XLT Require Lifelong Follow‐Up and Consideration of Definitive Treatment
American Journal of Hematology, Volume 100, Issue 11, Page 2004-2016, November 2025.Our study followed the clinical and biological course of 261 WAS/XLT patients, including 170 with a mild form of the disease. The occurrence of late complications even in mild patients confirms the importance of offering lifelong follow‐up and considering definitive treatment (HSCT/gene therapy) for all patients.
Coralie Mallebranche +16 more
wiley +1 more source
Autoimmune Hemolytic Anemia Induced by Levofloxacin
Case Reports in Infectious Diseases, 2014 Drug-induced autoimmune hemolytic anemia is a rare condition. We report the case of a 32-year-old white female who presented to the emergency department with generalized fatigue, fever, and jaundice. The patient reported using levofloxacin few days prior
Marwan Sheikh-Taha, Pascale Frenn
doaj +1 more source
Marked efficacy of Rituximab in multifocal motor neuropathy associated with chronic lymphocytic leukemia [PDF]
, 2016 The authors describe a patient who presented a multifocal motor neuropathy (MMN) associated with a high anti-ganglioside antibody (anti-GM1 and anti-GD1) titer at the clinical onset of a B-cell chronic lymphocytic leukemia (B-CLL). Immunomodulation (IVIg
Antonella Di, Pasquale +6 more
core
Clinical Genetics, Volume 108, Issue 5, Page 495-510, November 2025.A growing number of genetic variants linking non‐autoimmune diabetes to NDDs across different ages offer key insights about a common background of these phenotypes. These findings call for multidisciplinary approaches to care that integrate metabolic and neurological management in affected children.
Gabriele Di Pasquale +6 more
wiley +1 more source
Ask a specialist : Ask a pathologist [PDF]
, 2014 Question: I ordered a type and screen on my patient, and the blood bank reported that her direct Coombs test was positive.
Coberly, Emily
core
HematologyBackground Urgent splenectomy is recommended for the management of highly transfusion-dependent life-threatening warm autoimmune hemolytic anemia, while for individuals unfit for surgery, splenic embolization is an alternative treatment option.
Aya Egbaria, Naiel Bisharat
doaj +1 more source
Molecular and cellular basis for pathogenicity of autoantibodies: lessons from murine monoclonal autoantibodies [PDF]
, 2018 The pathogenesis of autoantibody-mediated cellular and tissue lesions in autoimmune diseases is most straightforwardly attributable to the combined action of self-antigen binding properties and effector functions associated with the Fc regions of the ...
Azeredo da Silveira, Samareh +3 more
core
Misdiagnoses of Hair and Scalp Disorders in Adult Patients With Skin of Color
International Journal of Dermatology, EarlyView.
Eric McMullen +10 more
wiley +1 more source
Cancer, Volume 131, Issue 20, 15 October 2025.Abstract Background Only 30%–40% of high‐grade sarcomas respond to initial chemotherapy, which can have significant toxicities. Computed tomography imaging alone has limitations in evaluating treatment response. Imaging with 5‐fluoro‐deoxyglucose–positron emission tomography/computed tomography (FDG‐PET/CT), which evaluates tumor metabolism, offers an ...
Edward Y. Cheng +10 more
wiley +1 more source