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Diagnosis and management of hypertrophic cardiomyopathy [[electronic resource] /] / edited by Barry J. Maron
Diagnosis and management of hypertrophic cardiomyopathy [[electronic resource] /] / edited by Barry J. Maron
Pubbl/distr/stampa Malden, Mass., : Blackwell Futura, c2004
Descrizione fisica 1 online resource (526 p.)
Disciplina 616.1/24
616.124
Altri autori (Persone) MaronBarry J <1941-> (Barry Joel)
Soggetto topico Heart - Hypertrophy
Soggetto genere / forma Electronic books.
ISBN 1-280-19730-7
9786610197309
0-470-79903-X
0-470-98746-4
1-4051-4615-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Diagnosis and Management of Hypertrophic Cardiomyopathy; Contents; Foreword; Dedication and Acknowledgments; List of Contributors; 1 Phenotypic Expression and Clinical Course of Hypertrophic Cardiomyopathy; 2 Genetic Mutations that Remodel the Heart in Hypertrophic Cardiomyopathy; 3 Genetic Basis and Genotype-Phenotype Relationships in Familial Hypertrophic Cardiomyopathy; 4 Historical Perspective, Mechanism, and Clinical Significance of Left Ventricular Outflow Tract Obstruction in Hypertrophic Cardiomyopathy
5 Hypertrophic Cardiomyopathy with Latent (Provocable) Obstruction: Pathophysiology and Management6 Pathophysiology and Clinical Consequences of Atrial Fibrillation in Hypertrophic Cardiomyopathy; 7 Other Modes of Disability or Death Including Stroke, and Treatment Strategies, in Hypertrophic Cardiomyopathy; 8 Disturbed Vascular Control in Hypertrophic Cardiomyopathy: Mechanisms and Clinical Significance; 9 Clinical Significance of Diastolic Dysfunction and the Effect of Therapeutic Interventions
10 Value of Exercise Testing in Assessing Clinical State and Prognosis in Hypertrophic Cardiomyopathy11 Pathophysiology and Significance of Myocardial Ischemia in Hypertrophic Cardiomyopathy; 12 Hypertrophic Cardiomyopathy in Japan: Clinical, Morphologic and Genetic Expression; 13 Prevalence, Prevention and Treatment of Infective Endocarditis in Hypertrophic Cardiomyopathy; 14 Pharmacologic Treatment of Symptomatic Hypertrophic Cardiomyopathy; 15 Obstructive Hypertrophic Cardiomyopathy: Results of Septal Myectomy
16 United States Perspectives on the Role of Dual-Chamber Pacing in Patients with Hypertrophic Cardiomyopathy17 Dual-Chamber Pacing for Hypertrophic Obstructive Cardiomyopathy; 18 Alcohol Septal Ablation; 19 Alcohol Septal Ablation in the Treatment of Hypertrophic Obstructive Cardiomyopathy: A Seven-Year Experience; 20 Role of Septal Ablation in a Surgical Center; 21 Molecular and Clinical Tools for Sudden Death Risk Assessment in Hypertrophic Cardiomyopathy; 22 Risk Stratification for Sudden Death in Hypertrophic Cardiomyopathy: Extreme Left Ventricular Hypertrophy as a New Indicator of Risk
23 Implantable Defibrillator for Prevention of Sudden Death in Hypertrophic Cardiomyopathy24 Hypertrophic Cardiomyopathy and Other Causes of Sudden Death in the Trained Athlete: An Electrophysiologist Perspective on the Management of Benign and Not So Benign Arrhythmias; 25 The Athlete's Heart, ECG, and Differential Diagnosis with Hypertrophic Cardiomyopathy and Other Cardiomyopathies; 26 Importance of Congenital Coronary Artery Anomalies
27 Arrhythmogenic Right Ventricular Cardiomyopathy and Hypertrophic Cardiomyopathy: Identification with the Italian Preparticipation Athlete Screening Program
Record Nr. UNINA-9910143294503321
Malden, Mass., : Blackwell Futura, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Diagnosis and management of hypertrophic cardiomyopathy [[electronic resource] /] / edited by Barry J. Maron
Diagnosis and management of hypertrophic cardiomyopathy [[electronic resource] /] / edited by Barry J. Maron
Pubbl/distr/stampa Malden, Mass., : Blackwell Futura, c2004
Descrizione fisica 1 online resource (526 p.)
Disciplina 616.1/24
616.124
Altri autori (Persone) MaronBarry J <1941-> (Barry Joel)
Soggetto topico Heart - Hypertrophy
ISBN 1-280-19730-7
9786610197309
0-470-79903-X
0-470-98746-4
1-4051-4615-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Diagnosis and Management of Hypertrophic Cardiomyopathy; Contents; Foreword; Dedication and Acknowledgments; List of Contributors; 1 Phenotypic Expression and Clinical Course of Hypertrophic Cardiomyopathy; 2 Genetic Mutations that Remodel the Heart in Hypertrophic Cardiomyopathy; 3 Genetic Basis and Genotype-Phenotype Relationships in Familial Hypertrophic Cardiomyopathy; 4 Historical Perspective, Mechanism, and Clinical Significance of Left Ventricular Outflow Tract Obstruction in Hypertrophic Cardiomyopathy
5 Hypertrophic Cardiomyopathy with Latent (Provocable) Obstruction: Pathophysiology and Management6 Pathophysiology and Clinical Consequences of Atrial Fibrillation in Hypertrophic Cardiomyopathy; 7 Other Modes of Disability or Death Including Stroke, and Treatment Strategies, in Hypertrophic Cardiomyopathy; 8 Disturbed Vascular Control in Hypertrophic Cardiomyopathy: Mechanisms and Clinical Significance; 9 Clinical Significance of Diastolic Dysfunction and the Effect of Therapeutic Interventions
10 Value of Exercise Testing in Assessing Clinical State and Prognosis in Hypertrophic Cardiomyopathy11 Pathophysiology and Significance of Myocardial Ischemia in Hypertrophic Cardiomyopathy; 12 Hypertrophic Cardiomyopathy in Japan: Clinical, Morphologic and Genetic Expression; 13 Prevalence, Prevention and Treatment of Infective Endocarditis in Hypertrophic Cardiomyopathy; 14 Pharmacologic Treatment of Symptomatic Hypertrophic Cardiomyopathy; 15 Obstructive Hypertrophic Cardiomyopathy: Results of Septal Myectomy
16 United States Perspectives on the Role of Dual-Chamber Pacing in Patients with Hypertrophic Cardiomyopathy17 Dual-Chamber Pacing for Hypertrophic Obstructive Cardiomyopathy; 18 Alcohol Septal Ablation; 19 Alcohol Septal Ablation in the Treatment of Hypertrophic Obstructive Cardiomyopathy: A Seven-Year Experience; 20 Role of Septal Ablation in a Surgical Center; 21 Molecular and Clinical Tools for Sudden Death Risk Assessment in Hypertrophic Cardiomyopathy; 22 Risk Stratification for Sudden Death in Hypertrophic Cardiomyopathy: Extreme Left Ventricular Hypertrophy as a New Indicator of Risk
23 Implantable Defibrillator for Prevention of Sudden Death in Hypertrophic Cardiomyopathy24 Hypertrophic Cardiomyopathy and Other Causes of Sudden Death in the Trained Athlete: An Electrophysiologist Perspective on the Management of Benign and Not So Benign Arrhythmias; 25 The Athlete's Heart, ECG, and Differential Diagnosis with Hypertrophic Cardiomyopathy and Other Cardiomyopathies; 26 Importance of Congenital Coronary Artery Anomalies
27 Arrhythmogenic Right Ventricular Cardiomyopathy and Hypertrophic Cardiomyopathy: Identification with the Italian Preparticipation Athlete Screening Program
Record Nr. UNISA-996214611603316
Malden, Mass., : Blackwell Futura, c2004
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Diagnosis and management of hypertrophic cardiomyopathy [[electronic resource] /] / edited by Barry J. Maron
Diagnosis and management of hypertrophic cardiomyopathy [[electronic resource] /] / edited by Barry J. Maron
Pubbl/distr/stampa Malden, Mass., : Blackwell Futura, c2004
Descrizione fisica 1 online resource (526 p.)
Disciplina 616.1/24
616.124
Altri autori (Persone) MaronBarry J <1941-> (Barry Joel)
Soggetto topico Heart - Hypertrophy
ISBN 1-280-19730-7
9786610197309
0-470-79903-X
0-470-98746-4
1-4051-4615-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Diagnosis and Management of Hypertrophic Cardiomyopathy; Contents; Foreword; Dedication and Acknowledgments; List of Contributors; 1 Phenotypic Expression and Clinical Course of Hypertrophic Cardiomyopathy; 2 Genetic Mutations that Remodel the Heart in Hypertrophic Cardiomyopathy; 3 Genetic Basis and Genotype-Phenotype Relationships in Familial Hypertrophic Cardiomyopathy; 4 Historical Perspective, Mechanism, and Clinical Significance of Left Ventricular Outflow Tract Obstruction in Hypertrophic Cardiomyopathy
5 Hypertrophic Cardiomyopathy with Latent (Provocable) Obstruction: Pathophysiology and Management6 Pathophysiology and Clinical Consequences of Atrial Fibrillation in Hypertrophic Cardiomyopathy; 7 Other Modes of Disability or Death Including Stroke, and Treatment Strategies, in Hypertrophic Cardiomyopathy; 8 Disturbed Vascular Control in Hypertrophic Cardiomyopathy: Mechanisms and Clinical Significance; 9 Clinical Significance of Diastolic Dysfunction and the Effect of Therapeutic Interventions
10 Value of Exercise Testing in Assessing Clinical State and Prognosis in Hypertrophic Cardiomyopathy11 Pathophysiology and Significance of Myocardial Ischemia in Hypertrophic Cardiomyopathy; 12 Hypertrophic Cardiomyopathy in Japan: Clinical, Morphologic and Genetic Expression; 13 Prevalence, Prevention and Treatment of Infective Endocarditis in Hypertrophic Cardiomyopathy; 14 Pharmacologic Treatment of Symptomatic Hypertrophic Cardiomyopathy; 15 Obstructive Hypertrophic Cardiomyopathy: Results of Septal Myectomy
16 United States Perspectives on the Role of Dual-Chamber Pacing in Patients with Hypertrophic Cardiomyopathy17 Dual-Chamber Pacing for Hypertrophic Obstructive Cardiomyopathy; 18 Alcohol Septal Ablation; 19 Alcohol Septal Ablation in the Treatment of Hypertrophic Obstructive Cardiomyopathy: A Seven-Year Experience; 20 Role of Septal Ablation in a Surgical Center; 21 Molecular and Clinical Tools for Sudden Death Risk Assessment in Hypertrophic Cardiomyopathy; 22 Risk Stratification for Sudden Death in Hypertrophic Cardiomyopathy: Extreme Left Ventricular Hypertrophy as a New Indicator of Risk
23 Implantable Defibrillator for Prevention of Sudden Death in Hypertrophic Cardiomyopathy24 Hypertrophic Cardiomyopathy and Other Causes of Sudden Death in the Trained Athlete: An Electrophysiologist Perspective on the Management of Benign and Not So Benign Arrhythmias; 25 The Athlete's Heart, ECG, and Differential Diagnosis with Hypertrophic Cardiomyopathy and Other Cardiomyopathies; 26 Importance of Congenital Coronary Artery Anomalies
27 Arrhythmogenic Right Ventricular Cardiomyopathy and Hypertrophic Cardiomyopathy: Identification with the Italian Preparticipation Athlete Screening Program
Record Nr. UNINA-9910830565003321
Malden, Mass., : Blackwell Futura, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Diagnosis and management of hypertrophic cardiomyopathy / / edited by Barry J. Maron
Diagnosis and management of hypertrophic cardiomyopathy / / edited by Barry J. Maron
Pubbl/distr/stampa Malden, Mass., : Blackwell Futura, c2004
Descrizione fisica 1 online resource (526 p.)
Disciplina 616.1/24
616.124
Altri autori (Persone) MaronBarry J <1941-> (Barry Joel)
Soggetto topico Heart - Hypertrophy
ISBN 1-280-19730-7
9786610197309
0-470-79903-X
0-470-98746-4
1-4051-4615-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Diagnosis and Management of Hypertrophic Cardiomyopathy; Contents; Foreword; Dedication and Acknowledgments; List of Contributors; 1 Phenotypic Expression and Clinical Course of Hypertrophic Cardiomyopathy; 2 Genetic Mutations that Remodel the Heart in Hypertrophic Cardiomyopathy; 3 Genetic Basis and Genotype-Phenotype Relationships in Familial Hypertrophic Cardiomyopathy; 4 Historical Perspective, Mechanism, and Clinical Significance of Left Ventricular Outflow Tract Obstruction in Hypertrophic Cardiomyopathy
5 Hypertrophic Cardiomyopathy with Latent (Provocable) Obstruction: Pathophysiology and Management6 Pathophysiology and Clinical Consequences of Atrial Fibrillation in Hypertrophic Cardiomyopathy; 7 Other Modes of Disability or Death Including Stroke, and Treatment Strategies, in Hypertrophic Cardiomyopathy; 8 Disturbed Vascular Control in Hypertrophic Cardiomyopathy: Mechanisms and Clinical Significance; 9 Clinical Significance of Diastolic Dysfunction and the Effect of Therapeutic Interventions
10 Value of Exercise Testing in Assessing Clinical State and Prognosis in Hypertrophic Cardiomyopathy11 Pathophysiology and Significance of Myocardial Ischemia in Hypertrophic Cardiomyopathy; 12 Hypertrophic Cardiomyopathy in Japan: Clinical, Morphologic and Genetic Expression; 13 Prevalence, Prevention and Treatment of Infective Endocarditis in Hypertrophic Cardiomyopathy; 14 Pharmacologic Treatment of Symptomatic Hypertrophic Cardiomyopathy; 15 Obstructive Hypertrophic Cardiomyopathy: Results of Septal Myectomy
16 United States Perspectives on the Role of Dual-Chamber Pacing in Patients with Hypertrophic Cardiomyopathy17 Dual-Chamber Pacing for Hypertrophic Obstructive Cardiomyopathy; 18 Alcohol Septal Ablation; 19 Alcohol Septal Ablation in the Treatment of Hypertrophic Obstructive Cardiomyopathy: A Seven-Year Experience; 20 Role of Septal Ablation in a Surgical Center; 21 Molecular and Clinical Tools for Sudden Death Risk Assessment in Hypertrophic Cardiomyopathy; 22 Risk Stratification for Sudden Death in Hypertrophic Cardiomyopathy: Extreme Left Ventricular Hypertrophy as a New Indicator of Risk
23 Implantable Defibrillator for Prevention of Sudden Death in Hypertrophic Cardiomyopathy24 Hypertrophic Cardiomyopathy and Other Causes of Sudden Death in the Trained Athlete: An Electrophysiologist Perspective on the Management of Benign and Not So Benign Arrhythmias; 25 The Athlete's Heart, ECG, and Differential Diagnosis with Hypertrophic Cardiomyopathy and Other Cardiomyopathies; 26 Importance of Congenital Coronary Artery Anomalies
27 Arrhythmogenic Right Ventricular Cardiomyopathy and Hypertrophic Cardiomyopathy: Identification with the Italian Preparticipation Athlete Screening Program
Record Nr. UNINA-9910877204703321
Malden, Mass., : Blackwell Futura, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
A guide to hypertrophic cardiomyopathy : for patients, families, and interested physicians / / Barry J. Maron, Lisa Salberg
A guide to hypertrophic cardiomyopathy : for patients, families, and interested physicians / / Barry J. Maron, Lisa Salberg
Autore Maron Barry J (Barry Joel), <1941->
Edizione [Third edition.]
Pubbl/distr/stampa Chichester, England ; : , : John Wiley & Sons, , 2014
Descrizione fisica 1 online resource (152 pages) : illustrations (some color), map, tables
Disciplina 616.12
Altri autori (Persone) SalbergLisa
Soggetto topico Heart - Hypertrophy
ISBN 1-118-72549-2
1-118-72552-2
1-118-72553-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto What is hypertrophic cardiomyopathy (HCM)? -- Historical perspective and names -- How common is HCM? -- What is the cause of HCM? -- Structure of the heart -- Heart function in HCM -- Left ventricular outflow obstruction -- When does HCM develop? -- Gender and race -- What are the symptoms of HCM? -- How is HCM diagnosed and what tests are used? -- Other tests that may be useful in assessing HCM in selected patients -- Inaccurate diagnosis -- General outlook for patients with HCM -- Complications of HCM -- Special considerations : athletes and sports activities -- Treatments for HCM -- Special considerations for implantable defibrillators -- Obstructive sleep apnea and HCM -- Gene therapy and stem cells -- Automated external defibrillators (AEDs) -- HCM as a chronic disease : is a cure available? -- Are you newly diagnosed? -- Adapting psychologically to HCM -- Family screening -- What about having children? Pregnancy and delivery -- Routine medical care -- Community screening for HCM -- Community outreach -- Driving -- Traveling -- Military service -- Social security benefits -- Family and medical leave act -- Health insurance -- Life insurance -- Students -- HCM centers -- Support and advocacy groups (HCMA) -- What research is being conducted? -- The 36 most frequently asked questions about HCM that are addressed to the HCMA by patients, caregivers, and family members.
Record Nr. UNINA-9910208817403321
Maron Barry J (Barry Joel), <1941->  
Chichester, England ; : , : John Wiley & Sons, , 2014
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
A guide to hypertrophic cardiomyopathy : for patients, families, and interested physicians / / Barry J. Maron, Lisa Salberg
A guide to hypertrophic cardiomyopathy : for patients, families, and interested physicians / / Barry J. Maron, Lisa Salberg
Autore Maron Barry J (Barry Joel), <1941->
Edizione [Third edition.]
Pubbl/distr/stampa Chichester, England ; : , : John Wiley & Sons, , 2014
Descrizione fisica 1 online resource (152 pages) : illustrations (some color), map, tables
Disciplina 616.12
Altri autori (Persone) SalbergLisa
Soggetto topico Heart - Hypertrophy
ISBN 1-118-72549-2
1-118-72552-2
1-118-72553-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto What is hypertrophic cardiomyopathy (HCM)? -- Historical perspective and names -- How common is HCM? -- What is the cause of HCM? -- Structure of the heart -- Heart function in HCM -- Left ventricular outflow obstruction -- When does HCM develop? -- Gender and race -- What are the symptoms of HCM? -- How is HCM diagnosed and what tests are used? -- Other tests that may be useful in assessing HCM in selected patients -- Inaccurate diagnosis -- General outlook for patients with HCM -- Complications of HCM -- Special considerations : athletes and sports activities -- Treatments for HCM -- Special considerations for implantable defibrillators -- Obstructive sleep apnea and HCM -- Gene therapy and stem cells -- Automated external defibrillators (AEDs) -- HCM as a chronic disease : is a cure available? -- Are you newly diagnosed? -- Adapting psychologically to HCM -- Family screening -- What about having children? Pregnancy and delivery -- Routine medical care -- Community screening for HCM -- Community outreach -- Driving -- Traveling -- Military service -- Social security benefits -- Family and medical leave act -- Health insurance -- Life insurance -- Students -- HCM centers -- Support and advocacy groups (HCMA) -- What research is being conducted? -- The 36 most frequently asked questions about HCM that are addressed to the HCMA by patients, caregivers, and family members.
Record Nr. UNINA-9910813583603321
Maron Barry J (Barry Joel), <1941->  
Chichester, England ; : , : John Wiley & Sons, , 2014
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Heart failure reviews
Heart failure reviews
Pubbl/distr/stampa [Norwell, Ma], : Kluwer Academic Publishers
Disciplina 616.129
Soggetto topico Heart failure
Heart - Hypertrophy
Heart Failure
Insuffisance cardiaque
Cœur - Hypertrophie
Soggetto genere / forma Periodical
Periodicals.
ISSN 1573-7322
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNINA-9910142804903321
[Norwell, Ma], : Kluwer Academic Publishers
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Heart failure reviews
Heart failure reviews
Pubbl/distr/stampa [Norwell, Ma], : Kluwer Academic Publishers
Disciplina 616.129
Soggetto topico Heart failure
Heart - Hypertrophy
Heart Failure
Insuffisance cardiaque
Cœur - Hypertrophie
Soggetto genere / forma Periodical
Periodicals.
ISSN 1573-7322
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNISA-996208165803316
[Norwell, Ma], : Kluwer Academic Publishers
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Hypertrophic cardiomyopathy [[electronic resource] ] : for patients, their families and interested physicians / / Barry J. Maron & Lisa Salberg
Hypertrophic cardiomyopathy [[electronic resource] ] : for patients, their families and interested physicians / / Barry J. Maron & Lisa Salberg
Autore Maron Barry J (Barry Joel), <1941->
Edizione [2nd ed.]
Pubbl/distr/stampa Oxford, : Blackwell, 2006
Descrizione fisica 1 online resource (127 p.)
Disciplina 616.124
Altri autori (Persone) SalbergLisa
Soggetto topico Heart - Hypertrophy
Cardiology
Soggetto genere / forma Electronic books.
ISBN 1-280-74888-5
9786610748884
0-470-76454-6
0-470-75089-8
1-4051-7256-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Hypertrophic Cardiomyopathy: for patients, their families and interested physicians; Contents; Acknowledgments; Dedication; Foreword; Introduction; What is hypertrophic cardiomyopathy (HCM)?; Historical perspective and names; How common is HCM?; What is the cause of HCM?; Heart structure in HCM; When does HCM develop?: HCM in infants and children; Gender and race; What are the symptoms of HCM?; How is HCM diagnosed and what tests are used?; Other investigations that may be useful; General outlook for patients with HCM; Complications of HCM
Special considerations: Athletes and sports activitiesTreatments for HCM; Is a cure available?; Family screening; What about having children?: Pregnancy and delivery; Routine medical care; General lifestyle advice; Support and advocacy groups; What research is being conducted?; The 34 most frequently asked questions by patients about HCM, as addressed to the HCMA; Glossary; Key HCM references; Appendix; HCMA membership application; Index
Record Nr. UNINA-9910143297103321
Maron Barry J (Barry Joel), <1941->  
Oxford, : Blackwell, 2006
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Hypertrophic cardiomyopathy [[electronic resource] ] : for patients, their families and interested physicians / / Barry J. Maron & Lisa Salberg
Hypertrophic cardiomyopathy [[electronic resource] ] : for patients, their families and interested physicians / / Barry J. Maron & Lisa Salberg
Autore Maron Barry J (Barry Joel), <1941->
Edizione [2nd ed.]
Pubbl/distr/stampa Oxford, : Blackwell, 2006
Descrizione fisica 1 online resource (127 p.)
Disciplina 616.124
Altri autori (Persone) SalbergLisa
Soggetto topico Heart - Hypertrophy
Cardiology
ISBN 1-280-74888-5
9786610748884
0-470-76454-6
0-470-75089-8
1-4051-7256-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Hypertrophic Cardiomyopathy: for patients, their families and interested physicians; Contents; Acknowledgments; Dedication; Foreword; Introduction; What is hypertrophic cardiomyopathy (HCM)?; Historical perspective and names; How common is HCM?; What is the cause of HCM?; Heart structure in HCM; When does HCM develop?: HCM in infants and children; Gender and race; What are the symptoms of HCM?; How is HCM diagnosed and what tests are used?; Other investigations that may be useful; General outlook for patients with HCM; Complications of HCM
Special considerations: Athletes and sports activitiesTreatments for HCM; Is a cure available?; Family screening; What about having children?: Pregnancy and delivery; Routine medical care; General lifestyle advice; Support and advocacy groups; What research is being conducted?; The 34 most frequently asked questions by patients about HCM, as addressed to the HCMA; Glossary; Key HCM references; Appendix; HCMA membership application; Index
Record Nr. UNISA-996213070503316
Maron Barry J (Barry Joel), <1941->  
Oxford, : Blackwell, 2006
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui