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Tongue coating microbial communities vary in children with Henoch-Schönlein purpura. [PDF]
Sci RepPang S +7 more
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Purpura Annularis Telangiectodes of Majocchi Following a Booster Dose of the Pfizer-BioNTech COVID-19 Vaccine: Coincidence or Correlation? [PDF]
CureusAl Salmi A, Al Shibli A, Al-Saadi M.
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A Case Report of Severe Thrombocytopenic Purpura during Neoadjuvant Pembrolizumab Administration for Triple-Negative Breast Cancer. [PDF]
Surg Case RepSemba R +6 more
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Henoch-Schönlein Purpura in Children: An Updated Review.
Current pediatric reviews, 2020BACKGROUND Henoch-Schönlein purpura (HSP) is an IgA-mediated systemic small-vessel vasculitis with a predilection for the skin, gastrointestinal tract, joints, and kidneys. It is the most common form of systemic vasculitis in children.
A. Leung, B. Barankin, K. Leong
semanticscholar +1 more source
Transfusion, 2020
The PLASMIC score was developed to identify patients with thrombotic microangiopathy who are most likely to have immune thrombotic thrombocytopenic purpura (TTP) and benefit from therapeutic plasma exchange (TPE).
Koosha Paydary +4 more
semanticscholar +1 more source
The PLASMIC score was developed to identify patients with thrombotic microangiopathy who are most likely to have immune thrombotic thrombocytopenic purpura (TTP) and benefit from therapeutic plasma exchange (TPE).
Koosha Paydary +4 more
semanticscholar +1 more source
Hypergammaglobulinaemic purpura presenting as reticulate purpura
Clinical and Experimental Dermatology, 1999Hypergammaglobulinaemic purpura, first described by Waldenstrom, is a rare skin disease. The essential features are the presence of purpura with polyclonal hypergammaglobulinaemia. We describe a case of hypergammaglobulinaemic purpura occurring in a Chinese man with reticulate purpura and haemorrhagic blisters.
Wong Gc, See Ket Ng, Tan Sh, Eileen Tan
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An update on pathogenesis and diagnosis of thrombotic thrombocytopenic purpura
Expert Review of Hematology, 2019Introduction: Thrombotic thrombocytopenic purpura (TTP) is a rare and life-threatening thrombotic microangiopathy characterized by microangiopathic hemolytic anemia, consumption thrombocytopenia, and organ injury. TTP pathophysiology is based on a severe
B. Joly, P. Coppo, A. Veyradier
semanticscholar +1 more source
Dermatologic Clinics, 1989
Purpura is a cutaneous manifestation of a wide variety of diseases. These include such diverse entities as platelet defects, vasculitides, and disorders of connective tissue. Uncovering the underlying disorder in a patient with purpura is a stimulating challenge to the clinician's diagnostic abilities.
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Purpura is a cutaneous manifestation of a wide variety of diseases. These include such diverse entities as platelet defects, vasculitides, and disorders of connective tissue. Uncovering the underlying disorder in a patient with purpura is a stimulating challenge to the clinician's diagnostic abilities.
openaire +2 more sources