Normal Haemostasis, Inherited Bleeding Disorders and Surgery: What Does the Anaesthesiologist Need to Know? [PDF]
Ștefan M+5 more
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ABSTRACT Idiopathic multicentric Castleman disease (iMCD) is a rare lymphoproliferative disorder classified into three recognized clinical subtypes—idiopathic plasmacytic lymphadenopathy (IPL), TAFRO, and NOS. Although clinical criteria are available for subtyping, diagnostically challenging cases with overlapping histopathological features highlight ...
Midori Filiz Nishimura+14 more
wiley +1 more source
Pregnancy in May-Hegglin Anomaly: Diagnostic Challenges and Management Considerations. [PDF]
Mastanzade M, Koç A.
europepmc +1 more source
Diagnosis of Inherited Platelet Disorders: Clinical Evaluation and Functional and Molecular Assays. [PDF]
Sánchez-Fuentes A+3 more
europepmc +1 more source
41 Validation of Thromboxane A2 Analogue U46619 in Whole Blood Platelet Aggregation to Diagnose Platelet Disorders [PDF]
Xi Zhang, Morayma Reyes‐Gil
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Coagulation profiles and platelet parameters among preeclampsia, eclampsia, and normotensive pregnant women attending Comprehensive Specialized Hospital maternity wards, Northwest Ethiopia. [PDF]
Alemu N+5 more
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ABSTRACT Cardiovascular complications are the leading cause of mortality in sickle cell anemia (SCA) patients. While extensive data have identified diastolic dysfunction (DD) to increase morbidity and mortality, the unique hemodynamic conditions inherent to SCA challenge the current recommendations to assess diastolic function. Thus, there is an urgent
Théo Simon+20 more
wiley +1 more source
Automated Quantitative Immunofluorescence Microscopy Approach for Diagnosis of Hereditary Thrombopathies: A Proof of Concept Using Bernard-Soulier Syndrome and Glanzmann Thrombasthenia. [PDF]
Loos K+6 more
europepmc +1 more source