StephanieBurnsWechslerMD

PubMed

• Frequency of Ventricular Arrhythmias and Other Rhythm Abnormalities in Children and Young Adults With the Marfan Syndrome
  Douglas Y. Mah, Lynn A. Sleeper, Jane E. Crosson, Richard J. Czosek, Barry A. Love, Brian W. McCrindle, Laura Muiño-Mosquera, Aaron K Olson, Thomas A. Pilcher, Elif Se...> ;American Journal of Cardiology. 2018 Oct 15
• Predictors of Rapid Aortic Root Dilation and Referral for Aortic Surgery in Marfan Syndrome.
  Arvind Hoskoppal, Shaji C. Menon, Felicia Trachtenberg, Kristin M. Burns, Julie De Backer, Bruce D. Gelb, Marie L. Gleason, Jeanne James, Wyman W. Lai, Aimee Liou, Lyn...> ;Pediatric Cardiology. 2018 Jun 11
• 1 citations
  PRKAG2 mutations presenting in infancy.
  Rachel D. Torok, Stephanie Austin, Chanika Phornphutkul, Kathleen M. Rotondo, Deeksha Bali, Gregory H. Tatum, Stephanie Burns Wechsler, Anne F. Buckley, Priya S. Kishnani> ;Journal of Inherited Metabolic Disease. 2017 Aug 11
• 2 citations
  Adrenergic receptor genotypes influence postoperative outcomes in infants in the Single-Ventricle Reconstruction Trial.
  Ramroop, R., Manase, G., Lu, D., Manase, D., Chen, S., Kim, R., Lee, T. M., Mahle, W. T., McHugh, K. E., Mitchell, M., Tristani-Firouzi, M., Wechsler, S. B., Wilder, N...> ;The Journal of thoracic and cardiovascular surgery. 2017 Jul 25
• Novel pathogenic variants in FOXP3 in fetuses with echogenic bowel and skin desquamation identified by ultrasound.
  Raymond J. Louie, Queenie K.-G. Tan, Jennifer Gilner, R. Curtis Rogers, Noelle Younge, Stephanie Burns Wechsler, Marie McDonald, Barbara C. Gordon, Christopher A. Sask...> ;American Journal of Medical Genetics Part A. 2017 May 1
• 3 citations
  Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic features
  Hallie Steinfeld, Megan T. Cho, Kyle Retterer, Rick Person, G. Bradley Schaefer, Noelle R. Danylchuk, Saleem Malik, Stephanie Burns Wechsler, Patricia G. Wheeler, Koen...> ;Neurogenetics. 2016 Mar 22
• 6 citations
  Adult surgical experience with Loeys-Dietz syndrome.
  Jason A. Williams, Jennifer M. Hanna, Asad A. Shah, Nicholas D. Andersen, Marie McDonald, Yong-hui Jiang, Stephanie Burns Wechsler, Ali R. Zomorodi, Richard L. McCann,...> ;The Annals of Thoracic Surgery. 2015 Apr 1
• 101 citations
  Atenolol versus Losartan in Children and Young Adults with Marfan's Syndrome
  Ronald V. Lacro, Harry C. Dietz, Lynn A. Sleeper, Anji T. Yetman, Timothy J. Bradley, Steven D. Colan, Gail D. Pearson, E. Seda Selamet Tierney, Jami C. Levine, Andrew...> ;The New England Journal of Medicine. 2014 Nov 26
• 19 citations
  Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics
  Priya S. Kishnani, Stephanie Austin, Jose E. Abdenur, Pamela Arn, Deeksha Bali, Anne Boney, Wendy K. Chung, Aditi I Dagli, David C. Dale, Dwight D. Koeberl, Michael J....> ;Genetics in Medicine. 2014 Nov 1
• 14 citations
  Factors Associated with Neurodevelopment for Children with Single Ventricle Lesions
  Caren S. Goldberg, Minmin Lu, Lynn A. Sleeper, William T. Mahle, J. William Gaynor, Ismee A. Williams, Kathleen A. Mussatto, Richard G. Ohye, Eric M. Graham, Deborah U...> ;The Journal of Pediatrics. 2014 Sep 1
• 19 citations
  Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy
  Ronald V. Lacro, Lin T. Guey, Harry C. Dietz, Gail D. Pearson, Anji T. Yetman, Bruce D. Gelb, Bart Loeys, D. Woodrow Benson, Timothy J. Bradley, Julie De Backer, Geoff...> ;American Heart Journal. 2013 May 1
• Cardiac Pathology in Glycogen Storage Disease Type III
  Stephanie Austin, Alan D. Proia, Michele Spencer-Manzon, J. Butany, Stephanie Burns Wechsler, Priya S. Kishnani> ;JIMD reports. 2012 Jan 1
• 40 citations
  Glycogen Storage Disease Type III diagnosis and management guidelines
  Priya S. Kishnani, Stephanie Austin, Pamela Arn, Deeksha Bali, Anne Boney, Laura E. Case, Wendy K. Chung, Dev M. Desai, Areeg El-Gharbawy, Ronald G. Haller, G. Peter A...> ;Genetics in Medicine. 2010 Jul 1
• 6 citations
  Echocardiographic manifestations of Glycogen Storage Disease III: increase in wall thickness and left ventricular mass over time.
  Vertilus, S. M., Austin, S. L., Foster, K. S., Boyette, K. E., Bali, D. S., Li, J. S., Kishnani, P. S., Wechsler, S. B.> ;Genetics in medicine : official journal of the American College of Medical Genetics. 2010 Jun 8
• 4 citations
  Two-stage total aortic replacement for Loeys-Dietz syndrome.
  Matthew L Williams, Stephanie Burns Wechsler, G Chad Hughes> ;Journal of cardiac surgery. 2010 Mar 1
• 6 citations
  Thoracic endografting in a patient with hereditary hemorrhagic telangiectasia presenting with a descending thoracic aneurysm.
  Andersen, N. D., Dubose, J., Shah, A., Lee, T., Wechsler, S. B., Hughes, G. C.> ;Journal of vascular surgery. 2010 Feb 10
• Two-Stage Total Aortic Replacement for Loeys-Dietz Syndrome.
  Williams, M.L., Wechsler, S.B., Hughes, G.C.> ;J Card Surg. 2010 Jan 7
• Hemolytic anemia secondary to modified blalock-taussig shunt.
  Ryerson, L. M., Wechsler, S. B., Ohye, R. G.> ;Pediatric cardiology. 2007 Apr 18
• 1 citations
  Ventricular Arrhythmia in the X-linked Cardiomyopathy Barth Syndrome
  Carolyn T. Spencer, Barry J. Byrne, Michael H. Gewitz, Stephanie Burns Wechsler, A.C. Kao, Edward P. Gerstenfeld, A.D. Merliss, Michael P. Carboni, Randall M. Bryant> ;Pediatric Cardiology. 2005 Oct 18
• 3 citations
  Tibial aplasia, lower extremity mirror image polydactyly, brachyphalangy, craniofacial dysmorphism and genital hypoplasia: further delineation and mutational analysis.
  Wechsler, S. B., Lehoczky, J. A., Hall, J. G., Innis, J. W.> ;Clinical dysmorphology. 2004 Apr 2
• 3 citations
  Myocardial immediate early gene activation after cardiopulmonary bypass with cardiac ischemia-reperfusion
  David P. Nelson, Stephanie Burns Wechsler, Takuya Miura, Amy Stagg, Jane W. Newburger, John E. Mayer, Ellis J. Neufeld> ;The Annals of Thoracic Surgery. 2002 Jan 1
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