Research Topics
Species | Anji T YetmanSummaryAffiliation: LDS Hospital Country: USA Publications
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Detail Information
Publications
Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplificationLarissa V Furtado
Department of Pathology, University of Utah Health Science Center, Salt Lake City, UT 84108, USA
BMC Med Genet 12:119. 2011....
Cardiovascular pharmacotherapy in patients with Marfan syndromeAnji T Yetman
Department of Pediatric Cardiology, Primary Children s Medical Center, 100 N Medical Drive, Salt Lake City, UT 84113, USA
Am J Cardiovasc Drugs 7:117-26. 2007....
Importance of the clinical recognition of Loeys-Dietz syndrome in the neonatal periodAnji T Yetman
Department of Pediatrics, Division of Cardiology, Primary Children s Medical Center, University of Utah, Salt Lake City, Utah 84113, USA
Pediatrics 119:e1199-202. 2007..Patients had progressive aortic enlargement, which necessitated surgical intervention for 3 patients and resulted in the death of 1 patient. Delay in diagnosis of Loeys-Dietz syndrome may be associated with adverse prognosis...
Cardiovascular surgery in children with Marfan syndrome or Loeys-Dietz syndromeMelanie D Everitt
Division of Cardiology, Intermountain West Marfan Cardiology Center, Primary Children s Medical Center, University of Utah, Salt Lake City, Utah 84113, USA
J Thorac Cardiovasc Surg 137:1327-32; discussion 1332-3. 2009..This study was undertaken to assess the frequency and outcome of cardiovascular surgery in children with Marfan or Loeys-Dietz syndrome...
The dilated aorta in patients with congenital cardiac defectsAnji T Yetman
Adult Congenital Cardiology Program, Department of Pediatrics and Medicine, Division of Cardiology, Primary Children s Medical Center, The University of Utah, Salt Lake City, UT 84108, USA
J Am Coll Cardiol 53:461-7. 2009..The mechanisms underlying aortic dilation in this patient cohort are described, and the similarities to the pathophysiologic alterations seen in Marfan syndrome are highlighted. Indications for treatment are discussed...
Absence of TGFBR1 and TGFBR2 mutations in patients with bicuspid aortic valve and aortic dilationCammon B Arrington
Department of Pediatrics, Division of Cardiology, University of Utah School of Medicine, Salt Lake City, Utah, USA
Am J Cardiol 102:629-31. 2008..Analysis of these genes in 35 patients with BAVs identified only known single-nucleotide polymorphisms or novel synonymous or intronic substitutions. In conclusion, mutations in TGFBR1 and TGFBR2 rarely cause sporadic BAV...
Management of cardiovascular disease in Turner syndromeJoshua Thomas
University of Utah, Salt Lake City, UT 84105, USA
Expert Rev Cardiovasc Ther 7:1631-41. 2009..This review summarizes the current state of knowledge of the cardiovascular pathology present in patients with Turner syndrome and outlines recommendations for cardiac care from birth through to adulthood...
The immediate and long-term impact of pregnancy on aortic growth rate and mortality in women with Marfan syndromeRyan T Donnelly
Division of Cardiology, Department of Pediatrics, Primary Children s Medical Center, University of Utah, Salt Lake City, Utah 84113, USA
J Am Coll Cardiol 60:224-9. 2012..The study sought to assess the impact of pregnancy on the rate of aortic growth as well as on short- and long-term clinical outcomes in women with Marfan syndrome...
The prevalence and clinical impact of obesity in adults with Marfan syndromeAnji T Yetman
University of Utah, Primary Children s Medical Center, Salt Lake City, 84108, USA
Can J Cardiol 26:137-9. 2010..Patients with Marfan syndrome characteristically have an asthenic body habitus and are considered to be exempt from the obesity epidemic...
Usefulness of enalapril versus propranolol or atenolol for prevention of aortic dilation in patients with the Marfan syndromeAnji T Yetman
Division of Cardiology, Department of Pediatrics, The Children s Hospital, University of Colorado Health Sciences Center, Denver, Colorado 80220, USA
Am J Cardiol 95:1125-7. 2005..These favorable hemodynamic changes were associated with a smaller increase in aortic root diameter (0.1 +/- 1.0 vs 5.8 +/- 5.2 mm) and fewer clinical end points during follow-up...
Comparison of clinical characteristics and frequency of adverse outcomes in patients with Marfan syndrome diagnosed in adulthood versus childhoodLisa Willis
Department of Pediatrics, Section of Pediatric Cardiology, The Children s Hospital, Aurora, CO 80045, USA
Pediatr Cardiol 30:289-92. 2009..Our research demonstrates the importance of educating pediatric clinicians in early MFS diagnosis in hopes of improving the long-term outcome of all MFS patients...
Relation of maternal anti-Ro/La antibodies to aortic dilation in patients with congenital complete heart blockDebra L Davey
Division of Critical Care, Department of Pediatrics, Primary Children s Medical Center, University of Utah, Salt Lake City, Utah, USA
Am J Cardiol 108:561-4. 2011..001 and p <0.001, respectively). In conclusion, patients with autoimmune-mediated cCAVB merit periodic echocardiographic monitoring into adulthood to assess persistent or progressive aortic dilation and its attendant complications...
The role of iron deficiency in protein-losing enteropathy following the Fontan procedureAnji T Yetman
Adult Congenital Cardiac Program, Primary Children s Medical Center, University of Utah, Salt Lake City, Utah, USA
Congenit Heart Dis 6:370-3. 2011..Investigations revealed iron deficiency anemia which was treated with intravenous iron sucrose leading to resolution of both the anemia as well as symptoms of protein-losing enteropathy...
Would access to device therapies improve transplant outcomes for adults with congenital heart disease? Analysis of the United Network for Organ Sharing (UNOS)Melanie D Everitt
University of Utah, and Division of Pediatric Cardiology, Primary Children s Medical Center, 100 Mario Capecchi Drive, Salt Lake City, UT 84113, USA
J Heart Lung Transplant 30:395-401. 2011..HF management and approach to orthotopic heart transplant (OHT) may differ from adults without CHD. We sought to compare OHT waitlist characteristics and outcomes for these 2 groups...
Mitral valve avulsion after a four-wheel all-terrain vehicle crashSherry Pye
Department of Pediatric Cardiology, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72202, USA
J Trauma 57:175-6. 2004
Comparison of outcome of the Marfan Syndrome in patients diagnosed at age < or =6 years versus those diagnosed at >6 years of ageAnji T Yetman
Department of Cardiology, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA
Am J Cardiol 91:102-3. 2003
Long-term outcome in patients with Marfan syndrome: is aortic dissection the only cause of sudden death?Anji T Yetman
University of Arkansas for Medical Sciences, Arkansas Children s Hospital, Little Rock, USA
J Am Coll Cardiol 41:329-32. 2003..We sought to assess outcomes in a series of young patients with Marfan syndrome and to define the prevalence of ventricular arrhythmias in this patient population...
Ventricular septal rupture in an amateur rodeo riderAnji T Yetman
Department of Cardiology, Arkansas Children's Hospital, 800 Marshall Street, Little Rock, AR 72202, USA
J Trauma 56:697-9. 2004
Radiofrequency ablation of a left-sided atrioventricular pathway in a patient with Marfan syndromeAnji T Yetman
Department of Cardiology, Arkansas Children s Hospital, Little Rock, AR 72202, USA
Cardiol Young 12:494-5. 2002....
Progression of aortic dilation in children with a functionally normal bicuspid aortic valveRebecca S Beroukhim
The Children's Hospital Heart Institute, The Children's Hospital, Denver, Colorado, USA
Am J Cardiol 98:828-30. 2006..2 +/- 0.08 vs 0.6 +/- 0.08 mm/year, p <0.0001). In conclusion, BAV is complicated by progressive aortic dilation beginning in childhood...
Surgical correction of mitral valve prolapse : a cure for recurrent ventricular tachycardia in Marfan syndrome?Rebecca S Beroukhim
Children s Hospital Heart Institute, University of Colorado Health Sciences Center and The Children s Hospital, 1056 E 19th Avenue, B 100, Denver, CO 80218, USA
Pediatr Cardiol 27:755-8. 2006..The patient had resolution of ventricular tachycardia following surgical intervention consisting of a valve-sparing aortic root replacement and mitral valve annuloplasty...
Comparison of the pattern of aortic dilation in children with the Marfan's syndrome versus children with a bicuspid aortic valveRebecca S Beroukhim
The Children's Hospital Heart Institute, University of Colorado Health Sciences Center, Denver, Colorado, USA
Am J Cardiol 98:1094-5. 2006..In conclusion, despite similar histologic abnormalities, the anatomic pattern of aortic dilation differs in children with MS and BAVs...
