Results 81 to 90 of about 10,512 (289)
An Overview: Embryonic and Fetal Mammalian Haematopoiesis
, 2022 P.B.Rathod . P.I.Sindhi .
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Therapy-related leukaemias with balanced translocations can arise from pre-existing clonal haematopoiesis [PDF]
, 2021 Richard Dillon +14 more
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective This study aims to identify both fluid and neuroimaging biomarkers for CSF1R‐RD that can inform the optimal timing of treatment administration to maximize therapeutic benefit, while also providing sensitive quantitative measurements to monitor disease progression.
Tomasz Chmiela +13 more
wiley +1 more source
Clonal haematopoiesis and cardiovascular diseases: A growing relationship
, 2021 Sami Fawaz +8 more
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Use of Symptomatic Drug Treatment for Fatigue in Multiple Sclerosis and Patterns of Work Loss
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To describe the use of central stimulants and amantadine for fatigue in MS and evaluate a potential association with reduced work loss in people with MS. Methods We conducted a nationwide, matched, register‐based cohort study in Sweden (2006 to 2023) using national registers with prospective data collection.
Simon Englund +3 more
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Modelling acute myeloid leukaemia in a continuum of differentiation states
Letters in Biomathematics, 2018 Here we present a mathematical model of movement in an abstract space representing states of cellular differentiation. We motivate this work with recent examples that demonstrate a continuum of cellular differentiation using single-cell RNA-sequencing ...
H. Cho +6 more
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Chronic sympathetic driven hypertension promotes atherosclerosis by enhancing hematopoiesis
Haematologica, 2019 Hypertension is a major, independent risk factor for atherosclerotic cardiovascular disease. However, this pathology can arise through multiple pathways, which could influence vascular disease through distinct mechanisms.
Annas Al-Sharea +17 more
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Meningeal extramedullar haematopoiesis [PDF]
British Journal of Haematology, 2004 Hakan, Ozdogu, Can, Boga
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Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan +3 more
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