Anji T Yetman

Summary

Affiliation: LDS Hospital
Country: USA

Publications

  1. pmc Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplification
    Larissa V Furtado
    Department of Pathology, University of Utah Health Science Center, Salt Lake City, UT 84108, USA
    BMC Med Genet 12:119. 2011
  2. ncbi request reprint Cardiovascular pharmacotherapy in patients with Marfan syndrome
    Anji 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
  3. pmc Importance of the clinical recognition of Loeys-Dietz syndrome in the neonatal period
    Anji 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
  4. doi request reprint Living at altitude adversely affects survival among patients with a Fontan procedure
    Joy T Johnson
    Division of Cardiology, Department of Pediatrics, Primary Children s Medical Center, University of Utah, Salt Lake City, Utah 84113, USA
    J Am Coll Cardiol 61:1283-9. 2013
  5. doi request reprint The dilated aorta in patients with congenital cardiac defects
    Anji 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
  6. doi request reprint Cardiovascular surgery in children with Marfan syndrome or Loeys-Dietz syndrome
    Melanie 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
  7. doi request reprint Management of cardiovascular disease in Turner syndrome
    Joshua Thomas
    University of Utah, Salt Lake City, UT 84105, USA
    Expert Rev Cardiovasc Ther 7:1631-41. 2009
  8. ncbi request reprint Absence of TGFBR1 and TGFBR2 mutations in patients with bicuspid aortic valve and aortic dilation
    Cammon 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
  9. doi request reprint The immediate and long-term impact of pregnancy on aortic growth rate and mortality in women with Marfan syndrome
    Ryan 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
  10. pmc The prevalence and clinical impact of obesity in adults with Marfan syndrome
    Anji T Yetman
    University of Utah, Primary Children s Medical Center, Salt Lake City, 84108, USA
    Can J Cardiol 26:137-9. 2010

Collaborators

Detail Information

Publications24

  1. pmc Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplification
    Larissa V Furtado
    Department of Pathology, University of Utah Health Science Center, Salt Lake City, UT 84108, USA
    BMC Med Genet 12:119. 2011
    ....
  2. ncbi request reprint Cardiovascular pharmacotherapy in patients with Marfan syndrome
    Anji 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
    ....
  3. pmc Importance of the clinical recognition of Loeys-Dietz syndrome in the neonatal period
    Anji 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...
  4. doi request reprint Living at altitude adversely affects survival among patients with a Fontan procedure
    Joy T Johnson
    Division of Cardiology, Department of Pediatrics, Primary Children s Medical Center, University of Utah, Salt Lake City, Utah 84113, USA
    J Am Coll Cardiol 61:1283-9. 2013
    ..This study sought to determine whether survival in this cohort of patients was adversely affected by increased residential altitude...
  5. doi request reprint The dilated aorta in patients with congenital cardiac defects
    Anji 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...
  6. doi request reprint Cardiovascular surgery in children with Marfan syndrome or Loeys-Dietz syndrome
    Melanie 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...
  7. doi request reprint Management of cardiovascular disease in Turner syndrome
    Joshua 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...
  8. ncbi request reprint Absence of TGFBR1 and TGFBR2 mutations in patients with bicuspid aortic valve and aortic dilation
    Cammon 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...
  9. doi request reprint The immediate and long-term impact of pregnancy on aortic growth rate and mortality in women with Marfan syndrome
    Ryan 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...
  10. pmc The prevalence and clinical impact of obesity in adults with Marfan syndrome
    Anji 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...
  11. doi request reprint Moving on up: is it safe for patients to relocate to higher altitude following the fontan procedure?
    James L Gottlieb
    Department of Pediatrics, Division of Pediatric Cardiology, University of Utah, Salt Lake City, UT, 84113, USA
    Pediatr Cardiol 33:1411-4. 2012
    ..Clinical deterioration at higher altitude is common in patients who have undergone Fontan surgery. Physicians at lower altitudes should caution these patients about the potential risks of relocation to moderate altitude...
  12. doi request reprint Comparison of clinical characteristics and frequency of adverse outcomes in patients with Marfan syndrome diagnosed in adulthood versus childhood
    Lisa 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...
  13. ncbi request reprint Usefulness of enalapril versus propranolol or atenolol for prevention of aortic dilation in patients with the Marfan syndrome
    Anji 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...
  14. doi request reprint The role of iron deficiency in protein-losing enteropathy following the Fontan procedure
    Anji 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...
  15. doi request reprint Relation of maternal anti-Ro/La antibodies to aortic dilation in patients with congenital complete heart block
    Debra 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...
  16. doi request reprint 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...
  17. ncbi request reprint Mitral valve avulsion after a four-wheel all-terrain vehicle crash
    Sherry 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
  18. ncbi request reprint Comparison of outcome of the Marfan Syndrome in patients diagnosed at age < or =6 years versus those diagnosed at >6 years of age
    Anji 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
  19. ncbi request reprint Radiofrequency ablation of a left-sided atrioventricular pathway in a patient with Marfan syndrome
    Anji T Yetman
    Department of Cardiology, Arkansas Children s Hospital, Little Rock, AR 72202, USA
    Cardiol Young 12:494-5. 2002
    ....
  20. ncbi request reprint Progression of aortic dilation in children with a functionally normal bicuspid aortic valve
    Rebecca 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...
  21. ncbi request reprint 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...
  22. ncbi request reprint Ventricular septal rupture in an amateur rodeo rider
    Anji T Yetman
    Department of Cardiology, Arkansas Children s Hospital, 800 Marshall Street, Little Rock, AR 72202, USA
    J Trauma 56:697-9. 2004
  23. ncbi request reprint 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...
  24. ncbi request reprint Comparison of the pattern of aortic dilation in children with the Marfan's syndrome versus children with a bicuspid aortic valve
    Rebecca 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...