UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 37

Sortiert nach

Fabry Disease and/or Hypertrophic Cardiomyopathy: Only One Mutation in a Family?

International Heart Journal, 2017, Vol.58(3), pp.305-306

Anan, Ryuichiro

2017

Volltextzugriff (PDF)

Ventricular tachycardia in patients undergoing 24-h Holter monitoring as preoperative evaluation for noncardiac surgery

Heart and vessels, 2021-07, Vol.36 (7), p.1047-1055

2021

Volltextzugriff (PDF)

Concentric hypertrophy geometry is a significant determinant of impaired global longitudinal strain in patients with normal cardiac structure and function

Heliyon, 2023-06, Vol.9 (6), p.e16252-e16252, Article e16252

2023

Volltextzugriff (PDF)

Guidelines for Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy (JCS 2012)　– Digest Version

Circulation Journal, 2016/02/25, Vol.80(3), pp.753-774

Group, JCS Joint Working

2016

Volltextzugriff (PDF)

Terminal stage cardiac findings in patients with cardiac Fabry disease: An electrocardiographic, echocardiographic, and autopsy study

Journal of cardiology, 2008-02, Vol.51 (1), p.50-59

2008

Volltextzugriff (PDF)

Editorial: Cibenzoline for left ventricular outflow tract obstruction in tako-tsubo cardiomyopathy and hypertrophic cardiomyopathy

Journal of cardiology cases, 2015-06, Vol.11 (6), p.158-159

Anan, Ryuichiro, MD, PhD, FJCC

2015

Volltextzugriff (PDF)

Sarcomere Gene Mutations Are Associated With Increased Cardiovascular Events in Left Ventricular Hypertrophy

JACC. Heart failure, 2013-12, Vol.1 (6), p.459-466

2013

Volltextzugriff (PDF)

Mutations in the Genes for Sarcomeric Proteins in Japanese Patients With Onset Sporadic Hypertrophic Cardiomyopathy After Age 40 Years

The American journal of cardiology, 2007-06, Vol.99 (12), p.1750-1754

2007

Volltextzugriff (PDF)

Cardiac involvement in mitochondrial diseases : a study on 17 patients with documented mitochondrial DNA defects

Circulation (New York, N.Y.), 1995-02, Vol.91 (4), p.955-961

1995

Volltextzugriff (PDF)

Intracardiac thrombus, superior vena cava syndrome, and pulmonary embolism in a patient with Behçet's disease: a case report and literature review

Heart and vessels, 2007-07, Vol.22 (4), p.278-283

2007

Volltextzugriff (PDF)

Prevalence and time of appearance of Brugada electrocardiographic pattern in young male adolescents from a three-year follow-up study

The American journal of cardiology, 2004-11, Vol.94 (9), p.1186-1189

2004

Volltextzugriff (PDF)

Disease entity of ischemic cardiomyopathy

Nihon rinshō, 2011-11, Vol.69 Suppl 9, p.347

Anan, Ryuichiro

2011

Volltextzugriff (PDF)

Limitation of Angiography to Identify the Culprit Plaque in Acute Myocardial Infarction With Coronary Total Occlusion

Journal of the American College of Cardiology, 2007-12, Vol.50 (23), p.2197-2203

2007

Volltextzugriff (PDF)

Usefulness and Cost Effectiveness of Cardiovascular Screening of Young Adolescents

Medicine and science in sports and exercise, 2006-01, Vol.38 (1), p.2-6

2006

Volltextzugriff (PDF)

A novel deletion mutation in the cardiac myosin-binding protein C gene as a cause of Maron’s type IV hypertrophic cardiomyopathy

The American journal of cardiology, 2002-02, Vol.89 (4), p.487-488

2002

Volltextzugriff (PDF)

Usefulness and cost effectiveness of cardiovascular screening of young adolescents

Medicine and science in sports and exercise, 2006, Vol.38 (1), p.2-6

2006

Volltextzugriff (PDF)

Fabry Disease and/or Hypertrophic Cardiomyopathy

International heart journal, 2017-05, Vol.58 (3), p.305

Anan, Ryuichiro

2017

Volltextzugriff (PDF)

Sarcomere gene mutations are associated with increased cardiovascular events in left ventricular hypertrophy: results from multicenter registration in Japan

JACC. Heart failure, 2013-12, Vol.1 (6), p.459-466

2013

Volltextzugriff (PDF)

Limitation of angiography to identify the culprit plaque in acute myocardial infarction with coronary total occlusion utility of coronary plaque temperature measurement to identify the culprit plaque

Journal of the American College of Cardiology, 2007-12, Vol.50 (23), p.2197-2203

2007

Volltextzugriff (PDF)

Mutations in the Genes for Cardiac Troponin T and α-Tropomyosin in Hypertrophic Cardiomyopathy

The New England journal of medicine, 1995-04, Vol.332 (16), p.1058-1065

1995

Volltextzugriff (PDF)

Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis

Circulation (New York, N.Y.), 1998-08, Vol.98 (5), p.391-397

1998

Volltextzugriff (PDF)

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3

The Journal of clinical investigation, 1995-09, Vol.96 (3), p.1216-1220

1995

Volltextzugriff (PDF)

Prognostic implications of novel β cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy

The Journal of clinical investigation, 1994, Vol.93 (1), p.280-285

1994

Volltextzugriff (PDF)

Limitation of Angiography to Identify the Culprit Plaque in Acute Myocardial Infarction With Coronary Total Occlusion : Utility of Coronary Plaque Temperature Measurement to Identify the Culprit Plaque. Commentary

Journal of the American College of Cardiology, 2007, Vol.50 (23), p.2197-2206

2007

Volltextzugriff (PDF)

Novel cardiac ?-myosin heavy chain gene missense mutations (R869C and R870C) that cause familial hypertrophic cardiomyopathy

Human mutation, 2000-06, Vol.15 (6), p.584-584

2000

Volltextzugriff (PDF)

1 – 25 von 37

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(34)
Mit Volltextzugriff
(35)

Publikationsform

Artikel
(37)

Sprache

Englisch
(36)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

Humans
(22)
Science & Technology
(21)
Life Sciences & Biomedicine
(20)
Male
(17)
Female
(15)
Cardiac & Cardiovascular Systems
(13)
Cardiovascular System & Cardiology
(13)
Biological And Medical Sciences
(12)
Adult
(11)
Heart
(11)
Medical Sciences
(11)
Middle Aged
(11)
Cardiomyopathy, Hypertrophic - Genetics
(10)
Cardiology. Vascular System
(9)
Mutation
(8)
Adolescent
(7)
Aged
(7)
Cardiology
(7)
Myocarditis. Cardiomyopathies
(7)
Pedigree
(7)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Fabry Disease and/or Hypertrophic Cardiomyopathy: Only One Mutation in a Family?

Ventricular tachycardia in patients undergoing 24-h Holter monitoring as preoperative evaluation for noncardiac surgery

Concentric hypertrophy geometry is a significant determinant of impaired global longitudinal strain in patients with normal cardiac structure and function

Guidelines for Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy (JCS 2012)　– Digest Version

Terminal stage cardiac findings in patients with cardiac Fabry disease: An electrocardiographic, echocardiographic, and autopsy study

Editorial: Cibenzoline for left ventricular outflow tract obstruction in tako-tsubo cardiomyopathy and hypertrophic cardiomyopathy

Sarcomere Gene Mutations Are Associated With Increased Cardiovascular Events in Left Ventricular Hypertrophy

Mutations in the Genes for Sarcomeric Proteins in Japanese Patients With Onset Sporadic Hypertrophic Cardiomyopathy After Age 40 Years

Cardiac involvement in mitochondrial diseases : a study on 17 patients with documented mitochondrial DNA defects

Intracardiac thrombus, superior vena cava syndrome, and pulmonary embolism in a patient with Behçet's disease: a case report and literature review

Prevalence and time of appearance of Brugada electrocardiographic pattern in young male adolescents from a three-year follow-up study

Disease entity of ischemic cardiomyopathy

Limitation of Angiography to Identify the Culprit Plaque in Acute Myocardial Infarction With Coronary Total Occlusion

Usefulness and Cost Effectiveness of Cardiovascular Screening of Young Adolescents

A novel deletion mutation in the cardiac myosin-binding protein C gene as a cause of Maron’s type IV hypertrophic cardiomyopathy

Usefulness and cost effectiveness of cardiovascular screening of young adolescents

Fabry Disease and/or Hypertrophic Cardiomyopathy

Sarcomere gene mutations are associated with increased cardiovascular events in left ventricular hypertrophy: results from multicenter registration in Japan

Limitation of angiography to identify the culprit plaque in acute myocardial infarction with coronary total occlusion utility of coronary plaque temperature measurement to identify the culprit plaque

Mutations in the Genes for Cardiac Troponin T and α-Tropomyosin in Hypertrophic Cardiomyopathy

Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3

Prognostic implications of novel β cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy

Limitation of Angiography to Identify the Culprit Plaque in Acute Myocardial Infarction With Coronary Total Occlusion : Utility of Coronary Plaque Temperature Measurement to Identify the Culprit Plaque. Commentary

Novel cardiac ?-myosin heavy chain gene missense mutations (R869C and R870C) that cause familial hypertrophic cardiomyopathy

Suchergebnisse filtern