His primary scientific interests are in Internal medicine, Cardiology, Cardiomyopathy, Arrhythmogenic right ventricular dysplasia and Marfan syndrome. His Internal medicine study typically links adjacent topics like Endocrinology. His work in Cardiology addresses subjects such as Genetic testing, which are connected to disciplines such as MEDLINE and Intensive care medicine.
His Cardiomyopathy research incorporates themes from Heart disease, Dilated cardiomyopathy, Sudden death and Ventricular fibrillation. Daniel P. Judge has included themes like Penetrance, Sudden cardiac death and Ventricular tachycardia in his Arrhythmogenic right ventricular dysplasia study. The study incorporates disciplines such as Aortic aneurysm and Aorta in addition to Marfan syndrome.
Daniel P. Judge mainly investigates Internal medicine, Cardiology, Cardiomyopathy, Arrhythmogenic right ventricular dysplasia and Heart failure. His Internal medicine study frequently draws parallels with other fields, such as Endocrinology. His Ejection fraction, Right ventricular cardiomyopathy, Dilated cardiomyopathy and Implantable cardioverter-defibrillator study, which is part of a larger body of work in Cardiology, is frequently linked to In patient, bridging the gap between disciplines.
His Cardiomyopathy research is multidisciplinary, incorporating perspectives in Gene mutation, Disease, Pathology, Penetrance and Sudden cardiac death. His studies in Pathology integrate themes in fields like Marfan syndrome and Fibrillin. His work deals with themes such as Proband, Mutation, Ventricular fibrillation, Electrocardiography and Heart disease, which intersect with Arrhythmogenic right ventricular dysplasia.
Daniel P. Judge mostly deals with Cardiomyopathy, Internal medicine, Cardiology, Transthyretin and Amyloidosis. Daniel P. Judge interconnects Phenotype, Dilated cardiomyopathy, Disease and Sudden cardiac death in the investigation of issues within Cardiomyopathy. Internal medicine is a component of his Cardiac amyloidosis, Heart failure and Ventricular assist device studies.
Cardiology connects with themes related to Genetic testing in his study. His Amyloid cardiomyopathy study in the realm of Transthyretin connects with subjects such as Tafamidis and Placebo. His work on Attr amyloidosis as part of general Amyloidosis research is often related to In patient, thus linking different fields of science.
Daniel P. Judge focuses on Cardiomyopathy, Internal medicine, Cardiology, Right ventricular cardiomyopathy and Transthyretin. His Cardiomyopathy study deals with the bigger picture of Heart failure. Specifically, his work in Internal medicine is concerned with the study of Amyloidosis.
He is involved in the study of Cardiology that focuses on Cardiac amyloidosis in particular. His Right ventricular cardiomyopathy research is multidisciplinary, incorporating elements of Genetics, Arrhythmogenic right ventricular dysplasia, Hypertrophic cardiomyopathy, Disease and Penetrance. His Arrhythmogenic right ventricular dysplasia study incorporates themes from Differential diagnosis and Interquartile range.
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Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome.
Jennifer P. Habashi;Daniel P. Judge;Tammy M. Holm;Ronald D. Cohn.
Science (2006)
HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
Michael J. Ackerman;Silvia G. Priori;Stephan Willems;Charles Berul.
Heart Rhythm (2011)
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
Bart L. Loeys;Junji Chen;Enid R. Neptune;Daniel P. Judge.
Nature Genetics (2005)
Marfan’s syndrome
Daniel P Judge;Harry C Dietz.
The Lancet (2005)
Angiotensin II Blockade and Aortic-Root Dilation in Marfan's Syndrome
Benjamin S. Brooke;Jennifer P. Habashi;Daniel P. Judge;Nishant Patel.
The New England Journal of Medicine (2008)
HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies
Michael J. Ackerman;Silvia G. Priori;Stephan Willems;Charles Berul.
Europace (2011)
Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy
Mathew S. Maurer;Jeffrey H. Schwartz;Balarama Gundapaneni;Perry M. Elliott.
The New England Journal of Medicine (2018)
Angiotensin II type 1 receptor blockade attenuates TGF-β–induced failure of muscle regeneration in multiple myopathic states
Ronald D Cohn;Christel van Erp;Jennifer P Habashi;Arshia A Soleimani.
Nature Medicine (2007)
TGF-β–dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome
Connie M. Ng;Alan Cheng;Loretha A. Myers;Francisco Martinez-Murillo.
Journal of Clinical Investigation (2004)
Arrhythmogenic Right Ventricular Dysplasia A United States Experience
Darshan Dalal;Khurram Nasir;Chandra Bomma;Kalpana Prakasa.
Circulation (2005)
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