41. Steiner Robert[au] - PubMed Result 1 Haney EM, Huffman LH, Bougatsos C, Freeman M, Fu R, Steiner RD, Helfand M, Nelson HD. Screening for Lipid Disorders in Children and Adolescents Internet. http://www.ncbi.nlm.nih.gov/pubmed?term=Steiner Robert[au]

42. Steiner Robert Inc In Los Angeles, CA - YellowBot Steiner Robert Inc at 6415 Moore Dr, Los Angeles, CA 90048 http://www.yellowbot.com/steiner-robert-inc-los-angeles-ca.html

43. Steiner, Robert, MD - Pediatric Cardiology In Portland, OR - YellowBot Steiner, Robert, MD Pediatric Cardiology at 3181 SW Sam Jackson Park Rd, Portland, OR 97239 http://www.yellowbot.com/steiner-robert-md-pediatric-cardiology-portland-or.html

44. Articles By Author: Steiner, Robert - Free Online Library Free Online Library Articles by Steiner, Robert 18,188,529 articles and books http://www.thefreelibrary.com/Steiner, Robert-a1228

CacheBuster('') Printer Friendly 18,341,598 articles and books Periodicals Literature Keyword Title Author Topic Member login User name Password Remember me Join us Forgot password? Submit articles free The Free Library Browse Steiner, Robert out of article(s) Title Type Date Words When I say 'preposition,' what do you think of? Sep 22, 1997 Publications by Name Publications by Date Authors Literature A-D E-O P-T U-Z ... Submit articles

45. Robert D. Steiner, MD Bob Steiner bio Rare disorders studied. SmithLemli-Opitz syndrome Mevalonate kinase deficiency/HIDS http://www.ohsu.edu/xd/research/clinical-research/hgi/consortium/investigators/r

Skip to Content Skip to Main Navigation Search OHSU Contact OHSU ... Accessibility Statement and OHSU Access Keys Where Healing, Teaching and Discovery Come Together OHSU Home Jobs Directions Contact Search OHSU Enter your search term: Search About OHSU Healthcare Education Research ... Contact Us Search HGI Enter your search term: Search Quick Links Administration Funding Research Expertise Research Calendar Robert D. Steiner, MD Rare disorders studied Smith-Lemli-Opitz syndrome Mevalonate kinase deficiency/HIDS Cerebrotendinous xanthomatosis Osteogenesis imperfecta ... Phenylketonuria Biographical information Research interests Rare disorders activities Co-Chair, NIH CTSA CC-CHOS Rare Disease Workgroup 2006-2009 Standing committee member, HRSA/ACMG Newborn Screening Translational Research Network 2009-present Member, organizing committee for the NIH/ORD "Conference on Clinical Research for Rare Diseases" 2010. Charge: draft the R13 NIH Grant Application (renewal) and provide oversight for the conference (2009) Member, Institute of Medicine (IOM) Committee on Accelerating Rare Diseases Research and Orphan Product Development 2009-2011 Member, medical advisory board, Smith-Lemli-Opitz/RSH Foundation

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