Articles with "hhd" as a keyword



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Progressive impairment of atrial myocyte function during left ventricular hypertrophy and heart failure.

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Published in 2018 at "Journal of molecular and cellular cardiology"

DOI: 10.1016/j.yjmcc.2017.11.020

Abstract: Hypertensive heart disease (HHD) can cause left ventricular (LV) hypertrophy and heart failure (HF). It is unclear, though, which factors may contribute to the transition from compensated LV hypertrophy to HF in HHD. We hypothesized… read more here.

Keywords: heart; atrial myocyte; heart failure; hypertrophy ... See more keywords
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The role of fibroblast - Cardiomyocyte interaction for atrial dysfunction in HFpEF and hypertensive heart disease.

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Published in 2019 at "Journal of molecular and cellular cardiology"

DOI: 10.1016/j.yjmcc.2019.04.016

Abstract: AIMS Atrial contractile dysfunction is associated with increased mortality in heart failure (HF). We have shown previously that a metabolic syndrome-based model of HFpEF and a model of hypertensive heart disease (HHD) have impaired left… read more here.

Keywords: heart; dysfunction; disease; hfpef ... See more keywords
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P150 Hand-held dynamometry may provide a valid and objective method of muscle strength quantification in adult inflammatory myopathy: results from clinical practice in a tertiary centre

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Published in 2021 at "Rheumatology"

DOI: 10.1093/rheumatology/keab247.146

Abstract: Background/Aims  Accurate methods of muscle strength assessment are vital in the care of patients with idiopathic inflammatory myopathy (IIM). Manual muscle testing (MMT) is limited in quantification of strength and has a demonstrated 'ceiling effect'.… read more here.

Keywords: patient; hand held; muscle; strength ... See more keywords
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Acitretin as a successful treatment for Hailey–Hailey disease

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Published in 2019 at "Clinical and Experimental Dermatology"

DOI: 10.1111/ced.13762

Abstract: Hailey–Hailey disease (HHD) is a rare, autosomal dominant disorder caused by a mutation in one copy of the ATP2C1 gene, which encodes an ATP-dependent calcium pump, thus mutations result in defects in calcium ion binding… read more here.

Keywords: treatment; hailey disease; hailey; hhd ... See more keywords
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Concurrent Validity of Lower Limb Muscle Strength by Handheld Dynamometry in Children 7 to 11 Years Old.

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Published in 2022 at "Journal of sport rehabilitation"

DOI: 10.1123/jsr.2021-0273

Abstract: CONTEXT The assessment of pediatric muscle strength is necessary in a range of applications, including rehabilitation programs. Handheld dynamometry (HHD) is considered easy to use, portable, and low cost, but validity to measure lower limb… read more here.

Keywords: strength; hhd; concurrent validity; lower limb ... See more keywords
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Sensitive marker for evaluation of hypertensive heart disease: extracellular volume and myocardial strain

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Published in 2020 at "BMC Cardiovascular Disorders"

DOI: 10.1186/s12872-020-01553-7

Abstract: Background Evaluation of tissue fibrosis and myocardial hypertrophy in left ventricular (LV) remodeling is the basis of post-treatment evaluation of hypertensive heart disease (HHD). Extracellular volume (ECV) and myocardial strain parameters can indirectly reflect the… read more here.

Keywords: hhd; evaluation hypertensive; treatment; myocardial strain ... See more keywords
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Home hemodialysis treatment and outcomes: retrospective analysis of the Knowledge to Improve Home Dialysis Network in Europe (KIHDNEy) cohort

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Published in 2018 at "BMC Nephrology"

DOI: 10.1186/s12882-018-1059-2

Abstract: BackgroundUtilization of home hemodialysis (HHD) is low in Europe. The Knowledge to Improve Home Dialysis Network in Europe (KIHDNEy) is a multi-center study of HHD patients who have used a transportable hemodialysis machine that employs… read more here.

Keywords: biochemistry; hemodialysis; home; use ... See more keywords

Structure and Membrane Targeting of the PDZD7 Harmonin Homology Domain (HHD) Associated With Hearing Loss

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Published in 2021 at "Frontiers in Cell and Developmental Biology"

DOI: 10.3389/fcell.2021.642666

Abstract: Usher syndrome (USH) is the leading cause of hereditary hearing–vision loss in humans. PDZ domain-containing 7 (PDZD7) has been reported to be a modifier of and contributor to USH. PDZD7 co-localizes with USH2 proteins in… read more here.

Keywords: harmonin; hhd; pdzd7 hhd; domain ... See more keywords
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Tungsten Promoted Ni/Al2O3 as a Noble-Metal-Free Catalyst for the Conversion of 5-Hydroxymethylfurfural to 1-Hydroxy-2,5-Hexanedione

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Published in 2022 at "Frontiers in Chemistry"

DOI: 10.3389/fchem.2022.857199

Abstract: The conversion of 5-hydroxymethylfurfural (HMF) to 1-hydroxy-2,5-hexanedione (HHD) represented a typical route for high-value utilization of biomass. However, this reaction was often catalyzed by the noble metal catalyst. In this manuscript, W promoted Ni/Al2O3 was… read more here.

Keywords: catalyst; noble metal; hhd; promoted al2o3 ... See more keywords
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Can Adverse Childhood Experiences Heighten Risk for Problematic Internet and Smartphone Use? Findings from a College Sample

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Published in 2021 at "International Journal of Environmental Research and Public Health"

DOI: 10.3390/ijerph18115978

Abstract: Background: College students are among the heaviest users of smartphones and the Internet, and there is growing concern regarding problematic Internet (PIU) and smartphone use (PSU). A subset of adverse childhood experiences, household dysfunction [(HHD)… read more here.

Keywords: hhd; problematic internet; smartphone use; internet ... See more keywords