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Attainment of the low-density lipoprotein cholesterol treatment target and prognosis of heterozygous familial hypercholesterolemia

Atherosclerosis, 2023-04, Vol.371, p.61-66

2023

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Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery disease

Journal of clinical lipidology, 2018-11, Vol.12 (6), p.1436-1444

2018

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Prognostic impact of cascade screening for familial hypercholesterolemia on cardiovascular events

Journal of clinical lipidology, 2021-03, Vol.15 (2), p.358-365

2021

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Genotypic and phenotypic features in homozygous familial hypercholesterolemia caused by proprotein convertase subtilisin/kexin type 9 ( PCSK9 ) gain-of-function mutation

Atherosclerosis, 2014-09, Vol.236 (1), p.54-61

2014

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Remnant-like particles and coronary artery disease in familial hypercholesterolemia

Clinica chimica acta, 2018-07, Vol.482, p.120-123

2018

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PROGNOSTIC IMPACT OF CASCADE SCREENING FOR FAMILIAL HYPERCHOLESTEROLEMIA ON CARDIOVASCULAR EVENTS

Journal of the American College of Cardiology, 2020-03, Vol.75 (11), p.1921-1921

2020

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A catalog of the pathogenic mutations of LDL receptor gene in Japanese familial hypercholesterolemia

Journal of clinical lipidology, 2020-05, Vol.14 (3), p.346-351.e9

2020

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Impact of evolocumab treatment on low-density lipoprotein cholesterol levels in heterozygous familial hypercholesterolemic patients withdrawing from regular apheresis

Atherosclerosis, 2017-10, Vol.265, p.225-230

2017

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Assessment of Coronary Atherosclerosis in Patients With Familial Hypercholesterolemia by Coronary Computed Tomography Angiography

The American journal of cardiology, 2015-03, Vol.115 (6), p.724-729

2015

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Molecular and functional characterization of familial chylomicronemia syndrome

Atherosclerosis, 2018-02, Vol.269, p.272-278

2018

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Assembly and Disassembly Dynamics of the Cyanobacterial Periodosome

Molecular cell, 2008-03, Vol.29 (6), p.703-716

2008

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Impact of variants of uncertain significance of LDL receptor on phenotypes of familial hypercholesterolemia

Journal of clinical lipidology, 2022-11, Vol.16 (6), p.863-869

2022

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sLR11 as a novel predictor of vascular calcification

Atherosclerosis, 2017-10, Vol.265, p.242-243

Nohara, Atsushi

2017

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The E32K variant of PCSK9 exacerbates the phenotype of familial hypercholesterolaemia by increasing PCSK9 function and concentration in the circulation

Atherosclerosis, 2010-05, Vol.210 (1), p.166-172

2010

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A de novo mutation of the LDL receptor gene as the cause of familial hypercholesterolemia identified using whole exome sequencing

Clinica chimica acta, 2016-01, Vol.453, p.194-196

2016

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Efficacy and Safety of Coadministration of Rosuvastatin , Ezetimibe , and Colestimide in Heterozygous Familial Hypercholesterolemia

The American journal of cardiology, 2012-02, Vol.109 (3), p.364-369

2012

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Reassessment of the cutoff values of waist circumference and visceral fat area for identifying Japanese subjects at risk for the metabolic syndrome

Diabetes research and clinical practice, 2008-03, Vol.79 (3), p.474-481

2008

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A novel type of familial hypercholesterolemia: Double heterozygous mutations in LDL receptor and LDL receptor adaptor protein 1 gene

Atherosclerosis, 2011-12, Vol.219 (2), p.663-666

2011

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A case with familial hypercholesterolemia complicated with severe systemic atherosclerosis intensively treated for more than 30 years

Journal of cardiology cases, 2020-11, Vol.22 (5), p.216-220

2020

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Clinical characteristics of Japanese patients with severe hypertriglyceridemia

Journal of clinical lipidology, 2015-07, Vol.9 (4), p.519-524

2015

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Prevalence, clinical features, and prognosis of patients with extremely low high-density lipoprotein cholesterol

Journal of clinical lipidology, 2016-11, Vol.10 (6), p.1311-1317

2016

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Validation of changes in the cutoff values of Achilles tendon thickness on radiography in the clinical criteria of heterozygous familial hypercholesterolemia in Japan

Atherosclerosis, 2024-08, Vol.395

2024

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Decreased post-prandial triglyceride response and diminished remnant lipoprotein formation in cholesteryl ester transfer protein (CETP) deficiency

Atherosclerosis, 2008-02, Vol.196 (2), p.953-957

2008

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BENEFICIAL EFFECT OF EZETIMIBE-ATORVASTATIN COMBINATION THERAPY IN PATIENTS WITH A MUTATION IN ABCG5 OR ABCG8 GENE

Journal of the American College of Cardiology, 2019-03, Vol.73 (9), p.1736-1736

2019

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Formation of preβ1-HDL during lipolysis of triglyceride-rich lipoprotein

Biochemical and biophysical research communications, 2009-01, Vol.379 (1), p.55-59

2009

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Attainment of the low-density lipoprotein cholesterol treatment target and prognosis of heterozygous familial hypercholesterolemia

Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery disease

Prognostic impact of cascade screening for familial hypercholesterolemia on cardiovascular events

Genotypic and phenotypic features in homozygous familial hypercholesterolemia caused by proprotein convertase subtilisin/kexin type 9 ( PCSK9 ) gain-of-function mutation

Remnant-like particles and coronary artery disease in familial hypercholesterolemia

PROGNOSTIC IMPACT OF CASCADE SCREENING FOR FAMILIAL HYPERCHOLESTEROLEMIA ON CARDIOVASCULAR EVENTS

A catalog of the pathogenic mutations of LDL receptor gene in Japanese familial hypercholesterolemia

Impact of evolocumab treatment on low-density lipoprotein cholesterol levels in heterozygous familial hypercholesterolemic patients withdrawing from regular apheresis

Assessment of Coronary Atherosclerosis in Patients With Familial Hypercholesterolemia by Coronary Computed Tomography Angiography

Molecular and functional characterization of familial chylomicronemia syndrome

Assembly and Disassembly Dynamics of the Cyanobacterial Periodosome

Impact of variants of uncertain significance of LDL receptor on phenotypes of familial hypercholesterolemia

sLR11 as a novel predictor of vascular calcification

The E32K variant of PCSK9 exacerbates the phenotype of familial hypercholesterolaemia by increasing PCSK9 function and concentration in the circulation

A de novo mutation of the LDL receptor gene as the cause of familial hypercholesterolemia identified using whole exome sequencing

Efficacy and Safety of Coadministration of Rosuvastatin , Ezetimibe , and Colestimide in Heterozygous Familial Hypercholesterolemia

Reassessment of the cutoff values of waist circumference and visceral fat area for identifying Japanese subjects at risk for the metabolic syndrome

A novel type of familial hypercholesterolemia: Double heterozygous mutations in LDL receptor and LDL receptor adaptor protein 1 gene

A case with familial hypercholesterolemia complicated with severe systemic atherosclerosis intensively treated for more than 30 years

Clinical characteristics of Japanese patients with severe hypertriglyceridemia

Prevalence, clinical features, and prognosis of patients with extremely low high-density lipoprotein cholesterol

Validation of changes in the cutoff values of Achilles tendon thickness on radiography in the clinical criteria of heterozygous familial hypercholesterolemia in Japan

Decreased post-prandial triglyceride response and diminished remnant lipoprotein formation in cholesteryl ester transfer protein (CETP) deficiency

BENEFICIAL EFFECT OF EZETIMIBE-ATORVASTATIN COMBINATION THERAPY IN PATIENTS WITH A MUTATION IN ABCG5 OR ABCG8 GENE

Formation of preβ1-HDL during lipolysis of triglyceride-rich lipoprotein

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