Results 181 to 190 of about 150,260 (318)

MERCURIAL PURGATIVES IN PURPURA HÆMORRHAGICA. [PDF]

Thomas Head
openalex   +1 more source

A skin lesion after cardiac catheterization [PDF]

, 2012
Alaminos, Miguel, Aneiros-Fernández, José, Arias-Santiago, Salvador, Buendía-Eisman, Aguistin, Carriel Araya, Víctor Sebastián, González-Andrades, Miguel, Orgaz-Molina, Jacinto   +6 more
core   +2 more sources

Steroid‐Induced Takotsubo Cardiomyopathy in a Patient With Immune Thrombocytopenic Purpura

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT This case report highlights a temporal relationship between dexamethasone administration and the onset of Takotsubo cardiomyopathy, underscoring the importance of recognizing pharmacologic agents as potential non‐traditional triggers, particularly in patients with underlying cardiovascular disease and no identifiable emotional or physical ...
Qutaiba Qafisheh, Roaa Aljunaidi, Abdalhakim Shubietah, Mohammed AbuBaha, Hossam Salameh, Muath Baniowda, Mohanad Qwaider, Mohammad Alqadi, Imad Hariri   +8 more
wiley   +1 more source

A case of Henoch-Schönlein purpura associated with tick exposure. [PDF]

Oxf Med Case Reports
Randrianarisoa RMF, Nachet FZ, Truta V, Letrillard C.   +3 more
europepmc   +1 more source

A Metabolic Study of a Patient with Idiopathic Cyclical Thrombocytopenic Purpura [PDF]

, 1957
William A. Skoog, J. S. Lawrence, W. Stirk Adams   +2 more
openalex   +1 more source

Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom [PDF]

, 2010
,, Goodship, Tim H J, Machin, Sam, Taylor, C Mark, Wigmore, Stephen J   +4 more
core   +1 more source

A Novel Homozygous GFI1B Mutation in Siblings With Thrombocytopenia and Bleeding Tendency

Clinical Case Reports, Volume 13, Issue 10, October 2025.
Pedigree chart showing affected siblings. ABSTRACT Platelet type bleeding disorder 17 (OMIM #187900) is a type of “gray platelet syndrome” and occurs due to a mutation in the GFI1B gene on chromosome 9q34.13. Patients usually present with a history of easy bleeding tendencies, recurrent epistaxis or gum bleeding, and rarely with severe hemorrhage, and ...
Shova Aryal, Surabhi Aryal, Sangit Adhikari, Punam Adhikari   +3 more
wiley   +1 more source

IgA Vasculitis Across the Ages: Is It Time for a Precision Medicine Approach? [PDF]

ACR Open Rheumatol
Gage A, Pepper RJ, Marro J, Salama AD, Oni L.   +4 more
europepmc   +1 more source

Thrombocytopenic Purpura in the Newborn [PDF]

, 1954
Michael B. Morris
openalex   +1 more source

Management of Gaucher Disease Type 1 in a Resource‐Limited Setting: A Pediatric Case Study

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT This case report depicts the management of an 8‐year‐old male with Gaucher Disease Type 1, manifesting as massive splenomegaly, anemia, and skeletal involvement in a resource‐constrained environment. Treated with splenectomy due to the absence of enzyme replacement therapy, it underscores the necessity for enhanced therapeutic access and ...
Bipesh Kumar Shah, Diwakar Koirala, Bivek Mishra, Ramesh Sapkota, Manjil Basnet   +4 more
wiley   +1 more source