419 research outputs found

    Video_1_Case report: Spontaneous coronary artery dissection in a man with Ehlers–Danlos syndrome.MOV

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    BackgroundSpontaneous coronary artery dissection (SCAD), as a medical emergency, represents one of the non-atherosclerotic causes of an acute coronary syndrome (ACS). It often occurs in young and middle-aged females and is a rarity among male patients. Yet, it is easily misdiagnosed or missed even though it has one of the highest in-hospital mortality rates.Case summaryHere, we present a young male patient admitted to the emergency department of our hospital due to a complaint of acute chest pain. During his hospitalization, we utilized several tools, including imaging modalities, genetic analyses, and clinical strategies, to ensure a proper diagnosis and management of the patient. The results indicated that the patient suffered from SCAD, as well as vascular Ehlers–Danlos syndrome (vEDS). Unfortunately, the patient died of SCAD-related sudden cardiac death (SCD) on the ninth day before the DNA analysis results were obtained. Despite a global effort and huge progress in the clinical characterization of SCAD, as well as patients’ assessments, its pathophysiology remains poorly understood, with a significant recurrence risk and no specific disease-modifying therapy.ConclusionVascular Ehlers–Danlos syndrome, as an inherited connective tissue disorder characterized by congenital connective tissue dysplasia, is a rare and particularly challenging monogenetic disease. It can cause life-threatening changes, including arterial dissections and ruptures, and lead to early death due to COL3A1 pathogenic variants. It is also a rare cause of SCAD. Currently, the gold standard for SCAD diagnosis is coronary angiography (CAG).</p

    Video_2_Case report: Spontaneous coronary artery dissection in a man with Ehlers–Danlos syndrome.MOV

    No full text
    BackgroundSpontaneous coronary artery dissection (SCAD), as a medical emergency, represents one of the non-atherosclerotic causes of an acute coronary syndrome (ACS). It often occurs in young and middle-aged females and is a rarity among male patients. Yet, it is easily misdiagnosed or missed even though it has one of the highest in-hospital mortality rates.Case summaryHere, we present a young male patient admitted to the emergency department of our hospital due to a complaint of acute chest pain. During his hospitalization, we utilized several tools, including imaging modalities, genetic analyses, and clinical strategies, to ensure a proper diagnosis and management of the patient. The results indicated that the patient suffered from SCAD, as well as vascular Ehlers–Danlos syndrome (vEDS). Unfortunately, the patient died of SCAD-related sudden cardiac death (SCD) on the ninth day before the DNA analysis results were obtained. Despite a global effort and huge progress in the clinical characterization of SCAD, as well as patients’ assessments, its pathophysiology remains poorly understood, with a significant recurrence risk and no specific disease-modifying therapy.ConclusionVascular Ehlers–Danlos syndrome, as an inherited connective tissue disorder characterized by congenital connective tissue dysplasia, is a rare and particularly challenging monogenetic disease. It can cause life-threatening changes, including arterial dissections and ruptures, and lead to early death due to COL3A1 pathogenic variants. It is also a rare cause of SCAD. Currently, the gold standard for SCAD diagnosis is coronary angiography (CAG).</p

    Distributed Learning for Principal Eigenspaces without Moment Constraints

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    Distributed Principal Component Analysis (PCA) has been studied to deal with the case when data are stored across multiple machines and communication cost or privacy concerns prohibit the computation of PCA in a central location. However, the sub-Gaussian assumption in the related literature is restrictive in real application where outliers or heavy-tailed data are common in areas such as finance and macroeconomics. In this article, we propose a distributed algorithm for estimating the principal eigenspaces without any moment constraints on the underlying distribution. We study the problem under the elliptical family framework and adopt the sample multivariate Kendall’s tau matrix to extract eigenspace estimators from all submachines, which can be viewed as points in the Grassmann manifold. We then find the “center” of these points as the final distributed estimator of the principal eigenspace. We investigate the bias and variance for the distributed estimator and derive its convergence rate which depends on the effective rank, eigengap of the scatter matrix and the number of submachines. We show that the distributed estimator performs as if we have full access to the whole data. Simulation studies show that the distributed algorithm performs comparably with the existing one for light-tailed data, while showing great advantages for heavy-tailed data. We also extend the distributed algorithm to cases with limited communication constraints and with elliptical factor structure. Thorough simulation studies and a real application to a macroeconomic dataset verify the advantages of the proposed distributed algorithms. Supplementary materials for this article are available online.</p

    Video_3_Case report: Spontaneous coronary artery dissection in a man with Ehlers–Danlos syndrome.MOV

    No full text
    BackgroundSpontaneous coronary artery dissection (SCAD), as a medical emergency, represents one of the non-atherosclerotic causes of an acute coronary syndrome (ACS). It often occurs in young and middle-aged females and is a rarity among male patients. Yet, it is easily misdiagnosed or missed even though it has one of the highest in-hospital mortality rates.Case summaryHere, we present a young male patient admitted to the emergency department of our hospital due to a complaint of acute chest pain. During his hospitalization, we utilized several tools, including imaging modalities, genetic analyses, and clinical strategies, to ensure a proper diagnosis and management of the patient. The results indicated that the patient suffered from SCAD, as well as vascular Ehlers–Danlos syndrome (vEDS). Unfortunately, the patient died of SCAD-related sudden cardiac death (SCD) on the ninth day before the DNA analysis results were obtained. Despite a global effort and huge progress in the clinical characterization of SCAD, as well as patients’ assessments, its pathophysiology remains poorly understood, with a significant recurrence risk and no specific disease-modifying therapy.ConclusionVascular Ehlers–Danlos syndrome, as an inherited connective tissue disorder characterized by congenital connective tissue dysplasia, is a rare and particularly challenging monogenetic disease. It can cause life-threatening changes, including arterial dissections and ruptures, and lead to early death due to COL3A1 pathogenic variants. It is also a rare cause of SCAD. Currently, the gold standard for SCAD diagnosis is coronary angiography (CAG).</p

    Video_9_Case report: Spontaneous coronary artery dissection in a man with Ehlers–Danlos syndrome.MP4

    No full text
    BackgroundSpontaneous coronary artery dissection (SCAD), as a medical emergency, represents one of the non-atherosclerotic causes of an acute coronary syndrome (ACS). It often occurs in young and middle-aged females and is a rarity among male patients. Yet, it is easily misdiagnosed or missed even though it has one of the highest in-hospital mortality rates.Case summaryHere, we present a young male patient admitted to the emergency department of our hospital due to a complaint of acute chest pain. During his hospitalization, we utilized several tools, including imaging modalities, genetic analyses, and clinical strategies, to ensure a proper diagnosis and management of the patient. The results indicated that the patient suffered from SCAD, as well as vascular Ehlers–Danlos syndrome (vEDS). Unfortunately, the patient died of SCAD-related sudden cardiac death (SCD) on the ninth day before the DNA analysis results were obtained. Despite a global effort and huge progress in the clinical characterization of SCAD, as well as patients’ assessments, its pathophysiology remains poorly understood, with a significant recurrence risk and no specific disease-modifying therapy.ConclusionVascular Ehlers–Danlos syndrome, as an inherited connective tissue disorder characterized by congenital connective tissue dysplasia, is a rare and particularly challenging monogenetic disease. It can cause life-threatening changes, including arterial dissections and ruptures, and lead to early death due to COL3A1 pathogenic variants. It is also a rare cause of SCAD. Currently, the gold standard for SCAD diagnosis is coronary angiography (CAG).</p

    Video_6_Case report: Spontaneous coronary artery dissection in a man with Ehlers–Danlos syndrome.MP4

    No full text
    BackgroundSpontaneous coronary artery dissection (SCAD), as a medical emergency, represents one of the non-atherosclerotic causes of an acute coronary syndrome (ACS). It often occurs in young and middle-aged females and is a rarity among male patients. Yet, it is easily misdiagnosed or missed even though it has one of the highest in-hospital mortality rates.Case summaryHere, we present a young male patient admitted to the emergency department of our hospital due to a complaint of acute chest pain. During his hospitalization, we utilized several tools, including imaging modalities, genetic analyses, and clinical strategies, to ensure a proper diagnosis and management of the patient. The results indicated that the patient suffered from SCAD, as well as vascular Ehlers–Danlos syndrome (vEDS). Unfortunately, the patient died of SCAD-related sudden cardiac death (SCD) on the ninth day before the DNA analysis results were obtained. Despite a global effort and huge progress in the clinical characterization of SCAD, as well as patients’ assessments, its pathophysiology remains poorly understood, with a significant recurrence risk and no specific disease-modifying therapy.ConclusionVascular Ehlers–Danlos syndrome, as an inherited connective tissue disorder characterized by congenital connective tissue dysplasia, is a rare and particularly challenging monogenetic disease. It can cause life-threatening changes, including arterial dissections and ruptures, and lead to early death due to COL3A1 pathogenic variants. It is also a rare cause of SCAD. Currently, the gold standard for SCAD diagnosis is coronary angiography (CAG).</p

    Video_10_Case report: Spontaneous coronary artery dissection in a man with Ehlers–Danlos syndrome.MP4

    No full text
    BackgroundSpontaneous coronary artery dissection (SCAD), as a medical emergency, represents one of the non-atherosclerotic causes of an acute coronary syndrome (ACS). It often occurs in young and middle-aged females and is a rarity among male patients. Yet, it is easily misdiagnosed or missed even though it has one of the highest in-hospital mortality rates.Case summaryHere, we present a young male patient admitted to the emergency department of our hospital due to a complaint of acute chest pain. During his hospitalization, we utilized several tools, including imaging modalities, genetic analyses, and clinical strategies, to ensure a proper diagnosis and management of the patient. The results indicated that the patient suffered from SCAD, as well as vascular Ehlers–Danlos syndrome (vEDS). Unfortunately, the patient died of SCAD-related sudden cardiac death (SCD) on the ninth day before the DNA analysis results were obtained. Despite a global effort and huge progress in the clinical characterization of SCAD, as well as patients’ assessments, its pathophysiology remains poorly understood, with a significant recurrence risk and no specific disease-modifying therapy.ConclusionVascular Ehlers–Danlos syndrome, as an inherited connective tissue disorder characterized by congenital connective tissue dysplasia, is a rare and particularly challenging monogenetic disease. It can cause life-threatening changes, including arterial dissections and ruptures, and lead to early death due to COL3A1 pathogenic variants. It is also a rare cause of SCAD. Currently, the gold standard for SCAD diagnosis is coronary angiography (CAG).</p

    Statistical information of calibration and prediction sets.

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    <p>Statistical information of calibration and prediction sets.</p

    Summary of neuroscience networks tools.

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    <p>Abbreviations: PANDA, Pipeline for Analyzing braiN Diffusion imAges; BCT, Brain Connectivity Toolbox; GAT, Graph-Analysis Toolbox; GRETNA, Graph-theoRETical Network Analysis toolkit; Caret, Computerized Anatomical Reconstruction and Editing Toolkit; CPT, Connectivity Pattern Tables; NA, not available.</p

    Effective wavelengths selected by <i>x</i>-LW.

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    <p>Effective wavelengths selected by <i>x</i>-LW.</p
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