Results 171 to 180 of about 206,651 (343)

Suction purpura

open access: yesIndian Dermatology Online Journal, 2014
Lalit Kumar Gupta   +3 more
openaire   +3 more sources

A Case Report of Acute Hemorrhagic Edema of Infancy

open access: yesپزشکی بالینی ابن سینا, 2005
Introduction: Acute hemorrhagic edema of infancy is an acute and rare cutaneous disorder that affects children between 4 months to 2 years of age and characterized by cutaneous purpuric lesions with millimeters to centimeters diameter.
Mozhgan Safari   +2 more
doaj  

Salicylamide purpura.

open access: yesSouth African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 2003
The purpose of tills article is to draw attention to a thrombocytopenic purpura which has resulted from the taking of salicylamide.This drug is advertised in the lay press as 'R12' and claims are made for it as a drug which 'not only relieves the pain of rheumatism but actually reduces swelling by dispersing the uric acid accumulation ... Locked joints
openaire   +2 more sources

Idiopathic thrombocytopenic purpura: a practice guideline developed by explicit methods for the American Society of Hematology.

open access: yesBlood, 1996
J. George   +14 more
semanticscholar   +1 more source

Clinical progress note: Rubella

open access: yesJournal of Hospital Medicine, Volume 21, Issue 2, Page 179-182, February 2026.
Visual Abstract Abstract Rates of rubella infection and congenital rubella syndrome decreased significantly since the introduction of the rubella vaccine in 1969. Endemic rubella was declared eliminated in the United States in 2004, and since 2012, all rubella cases in the United States have been associated with infections acquired abroad. With vaccine
Adam E. Gailani   +2 more
wiley   +1 more source

IKAROS Associated Immunodeficiency and Thrombotic Thrombocytopenic Purpura

open access: yesPediatric Blood &Cancer, Volume 73, Issue 2, February 2026.
ABSTRACT Pathogenic variants in IKZF1 (IKAROS) are linked to immunodeficiency, malignancy, and immune dysregulation. We describe a family with a rare IKZF1 variant presenting with humoral immunodeficiency and thrombotic thrombocytopenic purpura (TTP). A non‐consanguineous family was clinically monitored; clinical, immunological, and genetic data (exome
Ilia Spivak   +7 more
wiley   +1 more source

Postictal hemifacial purpura

open access: bronze, 1998
J. Reis, Peter W. Kaplan
openalex   +1 more source

von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome.

open access: yesNew England Journal of Medicine, 1998
M. Furlan   +11 more
semanticscholar   +1 more source

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