Results 191 to 200 of about 414,209 (326)

Common Hematologic Emergencies—Acute Promyelocytic Leukemia and Microangiopathic Hemolytic Anemias—A Pivotal Role of Clinical Laboratory

open access: yesInternational Journal of Laboratory Hematology, EarlyView.
ABSTRACT Hematologic emergencies are urgent health conditions which result in significant mortality and morbidity unless timely therapeutic measures are taken. Therapeutic success depends on their timely and accurate recognition by hematology laboratory services.
Ganna Shestakova   +2 more
wiley   +1 more source

A systematic review of ABCG8 mutation and sitosterolemia. [PDF]

open access: yesAm J Blood Res
Parekh D   +4 more
europepmc   +1 more source

Upadacitinib-Induced Hemolysis in a Patient With Glucose-6-Phosphate Dehydrogenase Deficiency-A Possible Adverse Drug Reaction. [PDF]

open access: yesPharmacol Res Perspect
ABSTRACT Glucose‐6‐phosphate‐dehydrogenase (G6PD) deficiency is a heterogenous disorder that may lead to severe hemolytic events with the ingestion of fava beans and exposure to certain drugs. We report the first case of a 65‐year‐old male with Crohn's disease who developed a hemolytic crisis leading to hospitalization shortly after commencement of ...
Patanè L   +5 more
europepmc   +2 more sources

Mixed Autoimmune Hemolytic Anemia: A Systematic Review of Epidemiology, Clinical Characteristics, Therapies, and Outcomes. [PDF]

open access: yesAm J Hematol
Mixed autoimmune hemolytic anemia (AIHA) is a rare condition characterized by the presence of both warm and cold autoantibodies, often leading to severe, treatment‐resistant hemolysis. In this systematic review of 81 patients across 35 studies, the median age was 45 years with a notable female predominance.
Jacobs JW   +12 more
europepmc   +2 more sources

A new unstable haemoglobin, Hb Alger, causes a transfusion‐dependent anaemia in early childhood

open access: yes
British Journal of Haematology, EarlyView.
Syrine Bouazizi   +6 more
wiley   +1 more source

Gaucher disease, state of the art and perspectives

open access: yesJournal of Internal Medicine, EarlyView.
Abstract Knowledge about Gaucher disease (GD), considered a model for rare diseases, has considerably increased since its discovery. The pathophysiology of this lysosomal disorder is better known, and specific therapies that can control many aspects of the disease have been developed, particularly for the most common form, Type 1 GD.
Fabrice Camou, Marc G. Berger
wiley   +1 more source

Immune hemolytic anemia associated with the use of immune checkpoint inhibitors: a scoping review. [PDF]

open access: yesFront Immunol
Hernandez-Martinez JM   +3 more
europepmc   +1 more source

Parvovirus B19 infection causing pure red cell aplasia in a recipient of pediatric donor kidneys [PDF]

open access: yes, 1993
Corral, DA   +8 more
core   +1 more source

Neonatal Hemolytic Jaundice: Causes, Diagnostic Approach, and Management. [PDF]

open access: yesChildren (Basel)
Parastatidou S   +5 more
europepmc   +1 more source

Systemic, Lifestyle and Environmental Modifying Factors in the Pathogenesis of Periodontitis

open access: yesJournal of Periodontal Research, EarlyView.
A variety of impacting factors in the pathogenesis of periodontitis exist, including systemic, lifestyle, and environmental factors. This review highlights the manifold mechanistic aspects of the link between the pathogenesis of periodontitis, addressing these numerous factors to supplement the long‐standing knowledge of the progression of the disease.
Groeger Sabine Elisabeth   +5 more
wiley   +1 more source

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