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Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

Journal of the American College of Cardiology, 2009-09, Vol.54 (10), p.930-941

2009

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Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

Science (American Association for the Advancement of Science), 1998-05, Vol.280 (5364), p.750-752

1998

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Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

JAMA : the journal of the American Medical Association, 2005-01, Vol.293 (4), p.447

2005

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Sexually dimorphic effects of prenatal alcohol exposure on the murine skeleton

Biology of sex differences, 2024-06, Vol.15 (1), p.51-19

2024

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TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy

Human molecular genetics, 2014-11, Vol.23 (21), p.5793-5804

2014

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Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

American journal of human genetics, 2003-11, Vol.73 (5), p.1027-1040

2003

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Neurovascular manifestations of heritable connective tissue disorders : a review

Stroke (1970), 1994-04, Vol.25 (4), p.889-903

1994

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Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology

Clinical genetics, 2008-11, Vol.74 (5), p.445-454

2008

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Microsatellite instability in colorectal cancer : Different mutator phenotypes and the principal involvement of hMLH1

Cancer research (Chicago, Ill.), 1998-04, Vol.58 (8), p.1713-1718

1998

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The Frequency of Hereditary Defective Mismatch Repair in a Prospective Series of Unselected Colorectal Carcinomas

American journal of human genetics, 2001-10, Vol.69 (4), p.780-790

2001

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Mutations that Alter the Surface Charge of Alpha-tropomyosin are Associated with Dilated Cardiomyopathy

Journal of molecular and cellular cardiology, 2001-04, Vol.33 (4), p.723-732

2001

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Sexing Bones: Improving Transparency of Sex Reporting to Address Bias Within Preclinical Studies

Journal of bone and mineral research, 2023-01, Vol.38 (1), p.5-13

2023

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Progression of familial and non-familial dilated cardiomyopathy: long term follow up

British heart journal, 2003-07, Vol.89 (7), p.757-761

2003

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Familial aneurysmal subarachnoid hemorrhage: a community-based study

Journal of neurosurgery, 1995-09, Vol.83 (3), p.426-429

1995

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Phase II trial of pirfenidone in adults with neurofibromatosis type 1

Neurology, 2006-11, Vol.67 (10), p.1860-1862

2006

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Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies

Journal of the American College of Cardiology, 2005-02, Vol.45 (4), p.595-598

2005

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Genetic testing: Practical, ethical, and counseling considerations

Mayo Clinic proceedings, 2005, Vol.80 (1), p.63-73

2005

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The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

The New England journal of medicine, 1992-01, Vol.326 (2), p.77-82

1992

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von Hippel-Lindau disease

Mayo Clinic proceedings, 2000-03, Vol.75 (3), p.265-272

2000

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On the inheritance of intracranial aneurysms

Stroke (1970), 1994-10, Vol.25 (10), p.2028-2037

1994

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Heritable connective tissue disorders in cervical artery dissections: a prospective study

Neurology, 1998-04, Vol.50 (4), p.1166-1169

1998

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Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome

The Journal of pediatrics, 1999-12, Vol.135 (6), p.775-781

1999

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Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute Workshop)

The American journal of cardiology, 1992-06, Vol.69 (17), p.1458-1466

1992

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Usual interstitial pneumonia complicating dyskeratosis congenita

Mayo Clinic proceedings, 2005-06, Vol.80 (6), p.817-821

2005

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Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

Sexually dimorphic effects of prenatal alcohol exposure on the murine skeleton

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy

Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

Neurovascular manifestations of heritable connective tissue disorders : a review

Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology

Microsatellite instability in colorectal cancer : Different mutator phenotypes and the principal involvement of hMLH1

The Frequency of Hereditary Defective Mismatch Repair in a Prospective Series of Unselected Colorectal Carcinomas

Mutations that Alter the Surface Charge of Alpha-tropomyosin are Associated with Dilated Cardiomyopathy

Sexing Bones: Improving Transparency of Sex Reporting to Address Bias Within Preclinical Studies

Progression of familial and non-familial dilated cardiomyopathy: long term follow up

Familial aneurysmal subarachnoid hemorrhage: a community-based study

Phase II trial of pirfenidone in adults with neurofibromatosis type 1

Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies

Genetic testing: Practical, ethical, and counseling considerations

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

von Hippel-Lindau disease

On the inheritance of intracranial aneurysms

Heritable connective tissue disorders in cervical artery dissections: a prospective study

Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome

Medical management with or without interventional therapy for unruptured brain arteriovenous malformations (ARUBA): a multicentre, non-blinded, randomised trial

Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute Workshop)

Usual interstitial pneumonia complicating dyskeratosis congenita

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