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Desmin mutation responsible for idiopathic dilated cardiomyopathy

Circulation (New York, N.Y.), 1999-08, Vol.100 (5), p.461-464

1999

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Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23

Circulation (New York, N.Y.), 1998-12, Vol.98 (25), p.2791-2795

1998

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The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14

American journal of human genetics, 2000-01, Vol.66 (1), p.148-156

2000

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Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy

Circulation (New York, N.Y.), 2001-07, Vol.104 (2), p.128-130

2001

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Tissue Doppler imaging predicts the development of hypertrophic cardiomyopathy in subjects with subclinical disease

Circulation (New York, N.Y.), 2003-07, Vol.108 (4), p.395-398

2003

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Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

Circulation (New York, N.Y.), 2001-10, Vol.104 (18), p.2188-2193

2001

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Angiotensin-I converting enzyme genotypes and left ventricular hypertrophy in patients with hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 1995-10, Vol.92 (7), p.1808-1812

1995

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Tissue doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and

Circulation (New York, N.Y.), 2001-07, Vol.104 (2), p.128

2001

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Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32

Circulation (New York, N.Y.), 1995-12, Vol.92 (12), p.3387-3389

1995

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The Value of Electrophysiology Study and Prophylactic Implantation of Cardioverter Defibrillator in Patients with Hypertrophic Cardiomyopathy

Pacing and clinical electrophysiology, 1998-01, Vol.21 (1), p.299-302

1998

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Detection of a new mutation in the β-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy

The Journal of clinical investigation, 1992-12, Vol.90 (6), p.2156-2165

1992

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Concept mapping, graphic organizing and structuring: visual techniques for functional content-centered reading comprehension

Education (Chula Vista), 1994-10, Vol.115 (1), p.26-30

Hill, Rita C

1994

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Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population

Circulation (New York, N.Y.), 1991-05, Vol.83 (5), p.1592-1597

1991

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Expression of a missense mutation in the messenger RNA for β-myosin heavy chain in myocardial tissue in hypertrophic cardiomyopathy

The Journal of clinical investigation, 1992-07, Vol.90 (1), p.271-277

1992

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Hypertrophic cardiomyopathy mutation is expressed in messenger RNA of skeletal as well as cardiac muscle

Circulation (New York, N.Y.), 1993-02, Vol.87 (2), p.406-412

1993

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Localization of the gene for familial idiopathic dilated cardiomyopathy to chromosome 1q32

Journal of the American College of Cardiology, 1996-02, Vol.27 (2), p.2-2

1996

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Prostaglandin E 1 does not accelerate rTPA-induced thrombolysis in acute myocardial infarction

The American heart journal, 1994, Vol.127 (4), p.738-743

1994

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Prostaglandin E1 does not accelerate rTPA-induced thrombolysis in acute myocardial infarction

The American heart journal, 1994-04, Vol.127 (4), p.738-743

1994

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Monotype Printing

Sch Arts, 1969, Vol.68 (7), p.36

Hill, Rita

1969

Volltextzugriff (PDF)

Localization of the gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse American population

Journal of the American College of Cardiology, 1991-02, Vol.17 (2), p.A165-A165

1991

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ALIAS SHAKESPEARE, THE TOWN NOBODY KNEW

New Mexico historical review, 1967-07, Vol.42 (3), p.211

1967

Volltextzugriff (PDF)

Molecular genetics of hypertrophic cardiomyopathy

Journal of molecular and cellular cardiology, 1991-04, Vol.23, p.S1-S1

1991

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AGE DIFFERENCE IN SELF-CONCEPT FROM EARLY ADULTHOOD THROUGH OLD AGE

GRANT, CARMEN RITA HILL

1967

Volltextzugriff (PDF)

Sequence Polymorphism in MSTN Predicts Sprinting Ability and Racing Stamina in Thoroughbred Horses

PloS one, 2010-01, Vol.5 (1), p.e8645-e8645

2010

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Vancomycin and nisin A are effective against biofilms of multi-drug resistant Staphylococcus aureus isolates from human milk

PloS one, 2020-05, Vol.15 (5), p.e0233284-e0233284

2020

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Desmin mutation responsible for idiopathic dilated cardiomyopathy

Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23

The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14

Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy

Tissue Doppler imaging predicts the development of hypertrophic cardiomyopathy in subjects with subclinical disease

Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

Angiotensin-I converting enzyme genotypes and left ventricular hypertrophy in patients with hypertrophic cardiomyopathy

Tissue doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and

Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32

The Value of Electrophysiology Study and Prophylactic Implantation of Cardioverter Defibrillator in Patients with Hypertrophic Cardiomyopathy

Detection of a new mutation in the β-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy

Concept mapping, graphic organizing and structuring: visual techniques for functional content-centered reading comprehension

Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population

Expression of a missense mutation in the messenger RNA for β-myosin heavy chain in myocardial tissue in hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy mutation is expressed in messenger RNA of skeletal as well as cardiac muscle

Localization of the gene for familial idiopathic dilated cardiomyopathy to chromosome 1q32

Prostaglandin E 1 does not accelerate rTPA-induced thrombolysis in acute myocardial infarction

Prostaglandin E1 does not accelerate rTPA-induced thrombolysis in acute myocardial infarction

Monotype Printing

Localization of the gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse American population

ALIAS SHAKESPEARE, THE TOWN NOBODY KNEW

Molecular genetics of hypertrophic cardiomyopathy

AGE DIFFERENCE IN SELF-CONCEPT FROM EARLY ADULTHOOD THROUGH OLD AGE

Sequence Polymorphism in MSTN Predicts Sprinting Ability and Racing Stamina in Thoroughbred Horses

Vancomycin and nisin A are effective against biofilms of multi-drug resistant Staphylococcus aureus isolates from human milk

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