Citations
Mayo Clinic
22 citation(s) found for "Judge, Daniel P".
HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies
Ackerman, Michael J. , Willems, Stephan , Berul, Charles I. , Calkins, Hugh , Camm, A. John , Ellinor, Patrick T. , Gollob, Michael H. , Hamilton, Robert M. , Hershberger, Ray E. , Judge, Daniel P. , Marec, Hervé Le , McKenna, William J. , Schulze‐Bahr, Eric , Semsarian, Christopher , Towbin, Jeffrey A. , Watkins, Hugh , Wilde, Arthur A.M. , Wolpert, Christian, Zipes, Douglas P. , Schwartz, Peter J. , Priori, Silvia G. , Brugada, Ramón , McKenna, William J. , Schwartz, Peter J. , Ellinor, Patrick T , Hamilton, Robert , Watkins, Hugh , Gollob, Michael H , Zipes, Douglas P , Judge, Daniel P
Europace | August 2, 2011 | Volume: 13 | Issue: 8 | Pages: 1077-1109
Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome
Loeys, Bart , Gerber, Elizabeth E. , Riegert‐Johnson, Douglas L. , Iqbal, Sarah , Whiteman, Pat, McConnell, Vivienne, Chillakuri, Chandramouli , Macaya, Daniela , Coucke, Paul , Paepe, Anne De , Judge, Daniel P. , Wigley, Fredrick M. , Mardon, Helen J., Handford, Penny A. , Keene, Douglas R. , Sakai, Lynn Y. , Dietz, Harry C. , Davis, Elise C. , Judge, Daniel P
Science Translational Medicine | March 17, 2010 | Volume: 2 | Issue: 23 | Pages: No page available
10.1126/scitranslmed.3000488
| PMID 20375004
Stiff skin syndrome, an autosomal dominant congenital form of scleroderma, is caused by mutations in the domain of fibrillin-1 that mediates integrin binding.