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UnknownFrequency of allogeneic hematopoietic cell transplantation among patients with high- or intermediate-risk acute myeloid leukemia in first complete remission.
Not available
S-EPMC3805928 | biostudies-literature
UnknownBrain system integration and message consistent health behavior change.
Not available
S-EPMC10152515 | biostudies-literature
UnknownSomatic instability of the FGF14-SCA27B GAA•TTC repeat reveals a marked expansion bias in the cerebellum.
Not available
S-EPMC11969470 | biostudies-literature
UnknownValidating the predictive ability of the 2MACE score for major adverse cardiovascular events in patients with atrial fibrillation: results from phase II/III of the GLORIA-AF registry.
Not available
S-EPMC10830583 | biostudies-literature
UnknownMissense variants in <i>TUBA4A</i> cause myo-tubulinopathies.
Not available
S-EPMC12262762 | biostudies-literature
UnknownPatterns of oral anticoagulant use and outcomes in Asian patients with atrial fibrillation: a post-hoc analysis from the GLORIA-AF Registry.
Not available
S-EPMC10518516 | biostudies-literature
UnknownThe UK-PBC risk scores: Derivation and validation of a scoring system for long-term prediction of end-stage liver disease in primary biliary cholangitis.
Not available
S-EPMC6984963 | biostudies-literature
UnknownGenome Sequencing for Diagnosing Rare Diseases.
Not available
S-EPMC11350637 | biostudies-literature
UnknownRecurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome.
Not available
S-EPMC9069069 | biostudies-literature
UnknownAn ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.
Not available
S-EPMC8263055 | biostudies-literature
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