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Cardiology -- Programmed instruction. : Commonsense approach to coronary care : a program / Marielle Ortiz Vinsant, Martha I. Spence  1989 1
Cardiology -- Psychological aspects   3
Cardiology -- Research.   4
Cardiology -- Research -- Asia -- Periodicals : Heart Asia    1
Cardiology -- Research -- Pacific Area -- Periodicals : Heart Asia    1
Cardiology -- Research -- Periodicals   4
Cardiology -- Reviews -- Periodicals   2
 

Cardiology Service, Hospital -- See Also Coronary Care Units


The hospital unit in which patients with acute cardiac disorders receive intensive care
  1
Cardiology Service, Hospital   2
 

Cardiology Services, Hospital -- See Cardiology Service, Hospital


The hospital department responsible for the administration and provision of diagnostic and therapeutic services for the cardiac patient
  1
Cardiology -- standards : Textbook of interventional cardiology / [edited by] Eric J. Topol, Paul S. Teirstein  2020 1
Cardiology -- Terminology.   2
Cardiology -- Terminology -- Periodicals : Cardiology coding alert    1
Cardiology -- Textbooks : Braunwald's heart disease : a textbook of cardiovascular medicine / edited by Douglas P. Zipes, Peter Libby, Robert O. Bonow, Douglas L. Mann, Gordon F. Tomaselli ; founding editor and online editor Eugene Braunwald  2019 1
Cardiology -- United States -- Biography : Eugene Braunwald and the rise of modern medicine / Thomas H. Lee  2013 1
Cardiology -- United States -- History   2
 

Cardiomegaly -- See Heart Hypertrophy


  1
Cardiomegaly   3
Cardiomegaly -- physiopathology : Molecular mechanisms of cardiac hypertrophy and failure / edited by Richard Walsh  2005 1
 

Cardiomyocyte -- See Myocytes, Cardiac


Striated muscle cells found in the heart. They are derived from cardiac myoblasts (MYOBLASTS, CARDIAC)
  1
  Cardiomyocytes -- 2 Related Subjects   2
 

Cardiomyopathies -- See Myocardium Diseases


  1
Cardiomyopathies   15
Cardiomyopathies -- epidemiology. : Founder mutations in inherited cardiac diseases in the Netherlands / edited by Arthur A.M. Wilde, J. Peter Tintelen ; with a preface of H.J. Wellens  2014 1
Cardiomyopathies -- etiology. : Cardiomyopathies and heart failure : biomolecular, infectious and immune mechanisms / edited by Akira Matsumori  2003 1
Cardiomyopathies -- genetics.   2
 

Cardiomyopathies, Hypertrophic -- See Cardiomyopathy, Hypertrophic


A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY)
  1
 

Cardiomyopathies, Hypertrophic Obstructive -- See Cardiomyopathy, Hypertrophic


A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY)
  1
Cardiomyopathies -- immunology. : Cardiomyopathies and heart failure : biomolecular, infectious and immune mechanisms / edited by Akira Matsumori  2003 1
Cardiomyopathies -- physiopathology : Cardioskeletal myopathies in children and young adults / edited by John Lynn Jefferies, Burns C. Blaxall, Jeffrey Robbins, Jeffrey A. Towbin  2017 1
 

Cardiomyopathies, Primary -- See Cardiomyopathies


A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS)
  1
 

Cardiomyopathies, Secondary -- See Cardiomyopathies


A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS)
  1
Cardiomyopathies -- therapy.   3
  Cardiomyopathy -- 2 Related Subjects   2
 

Cardiomyopathy, Dilated, 3B -- See Muscular Dystrophy, Duchenne


An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)
  1
Cardiomyopathy, Dilated -- genetics : Dilated cardiomyopathy (Sinagra)  2019 1
Cardiomyopathy, Dilated -- therapy : Dilated cardiomyopathy (Sinagra)  2019 1
 

Cardiomyopathy, Dilated, X-Linked -- See Muscular Dystrophy, Duchenne


An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)
  1
Cardiomyopathy, Hypertrophic   2
 

Cardiomyopathy, Hypertrophic, Familial -- See Also Tropomyosin


A protein found in the thin filaments of muscle fibers. It inhibits contraction of the muscle unless its position is modified by TROPONIN
  1
 

Cardiomyopathy, Hypertrophic Obstructive -- See Cardiomyopathy, Hypertrophic


A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY)
  1
 

Cardiomyopathy, Primary -- See Cardiomyopathies


A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS)
  1
 

Cardiomyopathy, Secondary -- See Cardiomyopathies


A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS)
  1
 

Cardiomyopathy, Stress -- See Takotsubo Cardiomyopathy


A transient left ventricular apical dysfunction or ballooning accompanied by electrocardiographic (ECG) T wave inversions. This abnormality is associated with high levels of CATECHOLAMINES, either administered or endogenously secreted from a tumor or during extreme stress
  1
 

Cardiomyopathy, Tako-tsubo -- See Takotsubo Cardiomyopathy


A transient left ventricular apical dysfunction or ballooning accompanied by electrocardiographic (ECG) T wave inversions. This abnormality is associated with high levels of CATECHOLAMINES, either administered or endogenously secreted from a tumor or during extreme stress
  1
 

Cardiomyopathy, Takotsubo -- See Takotsubo Cardiomyopathy


A transient left ventricular apical dysfunction or ballooning accompanied by electrocardiographic (ECG) T wave inversions. This abnormality is associated with high levels of CATECHOLAMINES, either administered or endogenously secreted from a tumor or during extreme stress
  1
 

Cardionatrin -- See Atrial natriuretic peptides


  1
Cardiopathies. : Heart disease diagnosis and therapy : a practical approach / M. Gabriel Khan ; foreword by Henry J.L. Marriott  2005 1
Cardiopathies -- √©tiologie. : Diabetes and cardiovascular disease / edited by Michael T. Johnstone, Aristidis Veves  2005 1
Cardiopathies -- physiopathologie. : Cardiac gap junctions : physiology, regulation, pathophysiology, and pharmacology / S. Dhein  1998 1
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