Results 211 to 220 of about 333,295 (341)

Prolonged Activated Partial Thromboplastin Time

open access: yesClinical and applied thrombosis/hemostasis, 2015
P. Ames   +4 more
semanticscholar   +1 more source

Anti-factor Xa and activated partial thromboplastin time measurements for heparin monitoring in mechanical circulatory support.

open access: yesJACC. Heart failure, 2015
S. Adatya   +9 more
semanticscholar   +1 more source

Acute Non‐Hemorrhagic Adrenal Infarction in a Diabetic Patient: A Rare but Critical Consideration in Acute Abdominal Pain

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Acute non‐hemorrhagic adrenal infarction (ANHAI), though rare, should be taken into account in the differential diagnosis of patients presenting with unexplained abdominal pain, especially those with underlying hypercoagulable conditions or risk factors for thrombosis.
Parvaneh Layegh   +2 more
wiley   +1 more source

Anti-Factor Xa Assay Is a Superior Correlate of Heparin Dose Than Activated Partial Thromboplastin Time or Activated Clotting Time in Pediatric Extracorporeal Membrane Oxygenation*

open access: yesPediatric Critical Care Medicine, 2014
Anna Liveris   +7 more
semanticscholar   +1 more source

Essential Thrombocythemia's Role in the Complex Landscape of Vasculitis: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Peripheral gangrenes have been sporadically documented as the initial presentation of essential thrombocythemia (ET), as exemplified in the preceding case reports. Nevertheless, the prevalence of vasculitis‐induced skin problems as the primary indication of ET has not been extensively examined.
Mohammad Reza Jafari Nakhjavani   +8 more
wiley   +1 more source

Clinical and Genetic Analysis of Dehydrated Hereditary Stomatocytosis: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Dehydrated hereditary stomatocytosis (DHS) is a rare autosomal dominant hemolytic anemia caused by abnormal erythrocyte ion permeability, most often due to PIEZO1 mutations. We report the case of a 15‐year‐old male with elevated indirect bilirubin and mild anemia.
Chen Ming, Shiyuan Wu, Rui Pan
wiley   +1 more source

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