Results 161 to 170 of about 59,669 (311)

Hydroxychloroquine directly reduces the binding of antiphospholipid antibody–β2-glycoprotein I complexes to phospholipid bilayers [PDF]

open access: bronze, 2008
Jacob H. Rand   +5 more
openalex   +1 more source

Rilzabrutinib for the Treatment of Immune Thrombocytopenia

open access: yesEuropean Journal of Haematology, EarlyView.
ABSTRACT Advancements in the understanding of ITP pathogenesis have led to significant improvements in disease management through the use of both traditional immunosuppressive strategies and novel targeted therapies. However, a subset of patients remains refractory to treatment or achieves only transient benefits, underscoring the need for alternative ...
Caterina Labanca   +12 more
wiley   +1 more source

From reliability to pragmatism: Hospital management in the context of radical uncertainty

open access: yesEuropean Management Review, EarlyView.
Abstract The COVID‐19 pandemic presented a scenario of radical uncertainty that hospitals had to manage. Two strands of research can illuminate this management. The first puts forward the high‐reliability organization (HRO) principles that the hospital sector has applied for two decades.
Hervé Dumez, Etienne Minvielle
wiley   +1 more source

IgG4-Related Disease (IgG4-RD) Autoimmune Pancreatitis (AIP) as an Initial Presentation of Systemic Lupus Erythematosus (SLE). [PDF]

open access: yesClin Case Rep
ABSTRACT Acute pancreatitis stemming from IgG4‐Related Disease (IgG4‐RD) seldom coincides with Systemic Lupus Erythematosus (SLE), highlighting the importance of investigating autoimmune conditions in patients with IgG4‐RD. We present the case of a 57‐year‐old male with a medical history notable for hypertension, photosensitivity, arthritis, and malar ...
Kothandaraman S, Terala R.
europepmc   +2 more sources

SAT0130 Toxic psychosis related with hydroxychloroquine

open access: bronze, 2001
Paulo José Bastos Barbosa   +4 more
openalex   +1 more source

Dermatologic manifestations of hereditary hemochromatosis: A systematic review

open access: yesJournal of the European Academy of Dermatology and Venereology, EarlyView.
Abstract Hereditary hemochromatosis (HH) is a genetic disorder leading to excessive iron absorption, impacting multiple organs, notably the skin, nails and mucosae. The objective of this study is to elucidate the dermatologic manifestations, associated symptoms, pathophysiology and management recommendations of HH.
Hossein Akbarialiabad   +3 more
wiley   +1 more source

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