Disease‐related thrombocytopenia in myelofibrosis is defined by distinct genetic etiologies and is associated with unique prognostic correlates
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DOI: 10.1002/cncr.34414
Abstract: Thrombocytopenia in patients with myelofibrosis (MF) is prognostically detrimental and poses a therapeutic challenge. MF patients with thrombocytopenia are considered high‐risk by most prognostic models and their distinct phenotype has given rise to the emerging… read more here.
Keywords: related thrombocytopenia; distinct genetic; disease related; thrombocytopenia myelofibrosis ... See more keywords
Distinct genetic basis of common epilepsies and structural magnetic resonance imaging measures
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DOI: 10.1111/epi.17529
Abstract: Focal and generalized epilepsies are associated with robust differences in magnetic resonance imaging (MRI) measures of subcortical structures, gray matter, and white matter. However, it is unknown whether such structural brain differences reflect the cause… read more here.
Keywords: magnetic resonance; distinct genetic; resonance imaging; structural brain ... See more keywords
Long QTc in hypertrophic cardiomyopathy: A consequence of structural myocardial damage or a distinct genetic disease?
Sign Up to like & getrecommendations! Published in 2023 at "Frontiers in Cardiovascular Medicine"
DOI: 10.3389/fcvm.2023.1112759
Abstract: Hypertrophic cardiomyopathy (HCM) is an autosomal dominant disease, characterized by the presence of unexplained left ventricular hypertrophy. This condition is often associated with electrocardiographic abnormalities including QTc prolongation occurring in 13% of patients. The main… read more here.
Keywords: hypertrophic cardiomyopathy; distinct genetic; disease; hcm ... See more keywords