BenjaminB.PeelerMD

PubMed

• 73 citations
  Model for end-stage liver disease predicts mortality for tricuspid valve surgery.
  Gorav Ailawadi, Damien J. LaPar, Brian R. Swenson, Suzanne A. Siefert, Christine L. Lau
  The Annals of Thoracic Surgery. 2009-05-01
• 12 citations
  Traumatic ascending aortopulmonary window following pulmonary artery stent dilatation: therapy with aortic endovascular stent graft.
  Gorav Ailawadi, D. S. Lim, Benjamin B. Peeler, Alan H. Matsumoto, Michael D. Dake
  Pediatric Cardiology. 2007-05-25
• 72 citations
  Central cannulation is safe in acute aortic dissection repair.
  T. Brett Reece, Curtis G. Tribble, Robert L. Smith, Ramesh Singh, Brendon M. Stiles
  The Journal of Thoracic and Cardiovascular Surgery. 2007-02-01

Journal Articles

• Decreased Cumulative Access Survival in Arteriovenous Fistulas Requiring Interventions to Promote Maturation  
  Lee T, Ullah A, Allon M, Succop P, El-Khatib M, and Roy-Chaudhury P, Clin J Am Soc Nephrol, 1/1/2011
• BBS genotype-phenotype assessment of a multi-ethnic patient cohort calls for a revision of the disease definition  
  Deveault, C., Billingsley, G., Duncan, J.L., Bin, J., Theal, R., Vincent, A., Fieggen, K.J., Gerth, C., Noordeh, N., Travoulsi, E.I., Fishman, G.A., Chitayat, D., Knue..., Hum Mutat, 1/1/2011
• Cardiac disease in mucopolysaccharidosis type I attributed to catecholaminergic and hemodynamic deficiencies  
  Palpant NJ, Bedada FB, Peacock B, Blazar BR, Metzger JM, Tolar J, Am J Physiol Heart Circ Physiol, 1/1/2011
• Long-term metabolic, endocrine, and neuropsychological outcome of hematopoietic cell transplantation for Wolman disease  
  Tolar J, Petryk A, Khan K, Bjoraker KJ, Jessurun J, Dolan M, Kivisto T, Charnas L, Shapiro EG, Orchard PJ, Bone Marrow Transplant, 1/1/2009
• Amelioration of epidermolysis bullosa by transfer of wild-type bone marrow cells  
  Tolar J, Ishida-Yamamoto A, Riddle M, McElmurry RT, Osborn M, Xia L, Lund T, Slattery C, Uitto J, Christiano AM, Wagner JE, Blazar BR, Blood, 1/1/2009
• Short-term growth hormone treatment in children with Hurler syndrome after hematopoietic cell transplantation  
  Polgreen LE, Plog M, Schwender JD, Tolar J, Thomas W, Orchard PJ, Miller BS, Petryk A, Bone Marrow Transplant, 1/1/2009
• Lactic acidosis and hypoglycemia with ALL relapse following hematopoietic cell transplant: a case report and brief review of literature  
  Luscri N, Mauer M, Sarafoglou K, Moran A, Tolar J, Pediatr Blood Cancer, 1/1/2009
• Osteopetrosis with micro-lacunar resorption because of defective integrin organization  
  Blair HC, Yaroslavskiy BB, Robinson LJ, Mapara MY, Pangrazio A, Guo L, Chen K, Vezzoni P, Tolar J, Orchard PJ, Lab Invest, 1/1/2009
• Model for End Stage Liver Disease Predicts Mortality for Tricuspid Valve Surgery  
  Ailawadi G, LaPar DJ, Swenson BR, Siefert SA, Lau C, Kern JA, Peeler BB ,Littlewood KE, Kron IL, Ann Thorac Surg, 1/1/2009
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  Osborn MJ, McElmurry RT, Peacock B, Tolar J, Blazar BR, Mol Ther, 1/1/2008
• Case 4-2008: A pregnant woman with a swollen left breast and dyspnea  
  Tolar J, Neglia JP, N Engl J Med, 1/1/2008
• Subfascial Endoscopic Perforating Vein Surgery (SEPS for Treatment of Venous Ulcers  
  Chong TW, Bott MJ, Kern JA, Peeler BB, Tribble CG, Harthun NL, Ostomy/Wound Management, 1/1/2005
• Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia  
  Wagner JE, Tolar J, Levran O, Scholl T, Deffenbaugh A, Satagopan J, Ben-Porat L, Mah K, Batish SD, Kutler DI, MacMillan ML, Hanenberg H, Auerbach AD, Blood, 1/1/2004
• Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)  
  Mykytyn, K., Nishimura, D.Y., Searby, C.C., Beck, G., Bugge, K., Haines, H.L., Cornier, A.S., Cox, G.F., Fulton, A.B., Carmi, R., Iannaccone, A., Jacobson, S.G., Weleb..., Am J Hum Genet, 1/1/2003
• Macular pigment and lutein supplementation in retinitis pigmentosa and Usher syndrome  
  Aleman, T.S., Duncan, J.L., Bieber, M.L., de Castro, E., Marks, D.A., Gardner, L.M., Steinberg, J.D., Cideciyan, A.V., Maguire, M.G. and Jacobson, S.G., Invest Ophthalmol Vis Sci, 1/1/2001
• Amish Nemaline Myopathy: Description of a novel phenotype with a mutation in Troponin T1  
  Johnston JJ, Kelly RI, Crawford TO, Morton DH, Agarwala R, Koch T, Schaffer AA, Francomano CA, and Biesecker LG, Am J Hum Genet, 1/1/2000
• Preliminary experience with Gamma Knife radiosurgery in the treatment of ocular melanoma  
  Robert Woodburn, Ronald Danis, Robert Timmerman, Tom Witt, Robert Cuilla, Morris Bank, Journal of Neurosurgery, 1/1/2000
• De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis  
  Freund, C.L., Wang, Q-L., Chen, S., Muskat, B.L., Sheffield, V.C., Jacobson, S.G., McInnes, R.R., Zack, D.J. and Stone, E.M., Nature Genet, 1/1/1998
• Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man  
  Cideciyan, A.V., Zhao, X., Nielsen, L., Khani, S.C., Jacobson, S.G. and Palczewski, K., Proc Natl Acad Sci USA, 1/1/1998
• The Human Genome Project: Implications for Medical Practice  
  Francomano CA and Collins FS, Today's Internist, 1/1/1997
• Comparison of Soft Tissue Response in Rabbits Following Laryngeal Implantation with Hydroxylapatite, Silicone Rubber, and Teflon  
  Cummings CW, Flint P, Corio RL, Annals of Otology, Rhinology & Laryngology, 1/1/1997
• Achondroplasia is defined by recurrent G380R mutations of FGFR3  
  Bellus GA, Hefferon TW, Ortiz DeLuna RI, Hecht JT, Horton WA, Machado M, Kaitila I, McIntosh I, and Francomano CA, Am J Hum Genet, 1/1/1995
• Report from the Maryland epidemiology schizophrenia linkage study--no evidence for link between schizophrenia and a number of candidate and other genomic regions using...  
  Karayiorgou M, Kasch L, Lasseter VK, Hwang J, Elango R, Bernardini DJ, Kimberland M, Barb R, Francomano CA, Wolyniec PS, Lamacz M, Nestadt G, Meyers D, Ott J, Childs B..., Am J Med Genet, 1/1/1994
• Retinal morphology and visual pigment levels in 6- and 12-month-old rhesus monkeys fed a taurine-free human infant formula  
  Imaki, H., Jacobson, S.G., Kemp, C.M., Knighton, R.W., Neuringer, M. and Sturman, J., J Neurosci Res, 1/1/1994
• Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin  
  Macke, J.P., Davenport, C.M., Jacobson, S.G., Hennessey, J.C., Gonzalez-Fernandez, F., Conway, B.P., Heckenlively, J., Palmer, R., Maumanee, I.H., Sieving, P., Gouras,..., Am J Hum Genet, 1/1/1993
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Books/Book Chapters

• Mesenchymal Stromal Cells: Biology and Clinical Applications. 
  Chapter: MSCs for Graft-Versus-Host Disease. 
  Tolar J, Le Blanc K, Blazar BREditors: Hematti P, Keating A.Humana Press, Springer2013
• JIMD Reports Vol. 10. 
  Chapter: Cardiac Ultrasound Findings in Infants with Severe (Hurler Phenotype) Untreated Mucopolysaccharidosis (MPS) Type I. 
  Schroeder L, Orchard P, Whitley CB, Berry JM, Tolar J, Miller W, Braunlin EEditors: Zschocke J, Gibson KM, Brown G, Morava E, Peters V.SSIEM and Springer Verlag2013
• Fitzpatrick's Dermatology in General Medicine 
  Chapter: Bone marrow transplantation for recessive dystrophic epidermolysis bullosa. 
  Tolar J, Blazar BR, Wagner JEEditors: Wolff K, Goldsmith LA, Katz SI, Gilchrest BA, Paller AS, Leffell DJ.AccessMedicine, McGraw-Hill2011
• Human Gene Mapping 1993: A Compendium. 
  Chapter: Report of the committee for clinical disorders and chromosome aberrations. 
  Page 735 - 772Schinzel A, McKusick VA, Francomano CA, and Pearson PLEditors: Cuticchia AJ and Pearson PL.The Johns Hopkins University Press, Baltimore, MD1993
• The Management of Pain 
  Chapter: Pain in the ear, midface and upper aerodigestive tract. 
  Page 769 - 783Kaplan J, and Cummings CWEditors: Bonica, John J.Lea & Febiger, Philadelphia, PA1990
• Atlas of Laryngeal Surgery 
  Cummings CW, Sessions D, Weymuller EA, Jr, and Wood PC.V. Mosby, St. Louis, MO1984
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Abstracts/Posters

• Cardiac findings in untreated infants <1 year of age with severe mucopolysaccharidosis (MPS) I.
  Braunlin E, Miller WP, Tolar J, Whitley CB, Orchard P, Mol Genet Metabol; Lysosomal Disease Network's WORLD Symposium, Orlando, FL, 1/1/2013
• Genotyping analysis available for patients after hematopoietic cell transplantation for multiple types of lysosomal diseases.
  Cooksley RD, Ahmed A, Shapiro E, Orchard P, Tolar J, Whitley CB, Mol Genet Metabol; Lysosomal Disease Network's WORLD Symposium, Orlando, FL, 1/1/2013
• Hematopoietic stem cell gene therapy with lentiviral vector in 4 patients with cerebral x-linked adrenoleukodystrophy: Long-term outcome and comparison of efficacy wit...
  Orchard P, Cartier N, Hacein-Bey-Abin S, Kurtzberg J, Escolar M, Tolar J, Baruchel A, Dalle JH, Michel G, Blanche S, Bartholoma C, Schmidt M, Bougneres P, van Kalle C,..., Mol Ther; American Society of Cell and Gene Therapy, Salt Lake City, UT, 1/1/2013
• Pheochromocytoma Presenting As Acute Decompensated Heart Failure.
  Mulla C, Marik, P, American Association of Clinical Endocrinologists (AACE) Annual Scientific and Clinical Congress, Philadelphia, PA, 1/1/2012
• Intravenous and intrathecal enzyme replacement before and after hematopoietic cell transplantation for Hurler syndrome.
  Tolar J, Dickson P, Orchard PJ, Biol Blood Marrow Transplant; Tandem Meeting on Biology of Blood and Marrow Transplantation, Tampa, FL, 1/1/2009
• Dual system of RNA trans-splicing element and Sleeping Beauty transposon corrects DNA protein kinase mutation in severe combined immune deficiency.
  Tolar J, Zayed H, Xia L, Yerich A, Yant SR, Kay MA, Puttaraju M, Mansfield SG, Wiest D, McIvor RS, Blazar BR, Haematologica; Congress of the European Hematology Association, Vienna, Austria, 1/1/2007
• The spine and the craniocervical junction in Ehlers-Danlos Syndrome.
  Francomano CA, Razza R, Griswold B, Bolognesse B, Milhorat T, McDonnell NB, Annual Meeting of The American Society of Human Genetics, New Orleans, LA, 1/1/2006
• Sleep disturbance in Ehlers-Danlos Syndromes: Related to chronic pain or an independent entity?
  Griswold B, McDonnell N, Francomano CA, Annual Meeting of The American Society of Human Genetics, New Orleans, LA, 1/1/2006
• Living with Marfan Syndrome: Perceptions of the condition and its management.
  Biesecker BB, Peters KT, Francomano CA, Am J Hum Genet, 1/1/2000
• Biochemical characterization of three fibroblast growth factor receptor 3 mutations at lysine 650 causing three distinct phenotypes.
  Iwata T, Nuckolls G, Shum L, Slavkin HC, and Francomano CA, Am J Hum Genet, 1/1/1998
• Concentration of mutations causing Schmid metaphyseal chondrodysplasia in the NC1 domain of type X collagen.
  McIntosh I, Abbott MH, and Francomano CA, Am J Hum Genet, 1/1/1994
• Mutation of Type X collagen (COL10A1) resulting in Schmid metaphyseal chondrodysplasia.
  McIntosh I, Hefferon TW, Warman ML, Olsen BR, and Francomano CA, Am J Hum Genet, 1/1/1993
• A frameshift mutation in the fibrillin gene: reduced transcript, stable truncated protein, and mild Marfan phenotype.
  Dietz HC, Sakai LY, Cutting GR, Pyeritz RE, and Francomano CA, Clinical Research, 1/1/1992
• Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasia.
  Francomano CA, Finkelstein JE, Yamada Y, Pyeritz RE, Graham JM, Moeschler JB, and Doege K, Am J Hum Genet, 1/1/1989
• Collagen gene linkage analysis in the Marfan and Stickler syndromes.
  Francomano CA, Le P-L, Liberfarb R, Streeten E, and Pyeritz RE, Am J Hum Genet, 1/1/1986
• Respiratory problems in achondroplasia.
  Reid C, Metz S, Meny R, Phillips J III, Francomano CA, and Pyeritz R, Ped Res, 1/1/1984
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Lectures

• Maintaining Access: Novel Therapies and Devices to Treat Vascular Access Dysfunction 
  Orlando, FL - 1/5/2013
• International Gene Therapy Trial for FA 
  Versailles, France - 1/25/2012
• Leber Congenital Amaurosis and Other Eye Disorders 
  Rockville, MD - 1/1/2012
• Epidermolysis Bullosa: Terminal Desperation or Terminal Optimism? 
  University of Minnesota, Minneapolis, MN - 1/8/2011
• Epidermolysis Bullosa: Terminal Desperation and Terminal Optimism 
  University of Minnesota, Minneapolis, MN - 1/8/2011
• Hematopoietic Cell Transplantation for Correction of Extracellular Matrix Disorder, Recessive Dystrophic Epidermolysis Bullosa 
  University of Minnesota, Minneapolis, MN - 1/17/2010
• Stem Cell Transplantation for Epidermolysis Bullosa 
  University of Minnesota, Minneapolis, MN - 1/21/2007
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