Selected Publications by the PresenterSelected Publications by the Presenter
(from a total of 50 publications)
Andersson HC, Kratz L, Kelley R. Desmosterolosis Presenting with Multiple Congenital Anomalies and Profound Developmental Delay. Am J Med Genet 113:315-319, 2002.
Andersson HC, MA Krousel-Wood, KE Jackson, J Rice, IM Lubin.Medical Genetic Test Reporting in Molecular Cystic Fibrosis and Factor V Leiden Tests Based On Reports Solicited From North American Laboratories. Gen in Med 4(5):324-7 2002.
Andersson HC, Charrow J, Kaplan P, Mistry P, Pastores G, Prakesh-Cheng A, Rosenbloom BE, Scott R, Wappner RS, Weinreb NJ. Individualization of Long-term Enzyme Replacement Therapy for Gaucher Disease. Genet in Med Feb 7:105-110, 2005.
Andersson HC, Narumanchi TC, Cunningham A, Bowdish B, Thoene J. Genetic/Metabolic Health Care Delivery During and After Katrina and Rita, Molecular Genetics and Metabolism, 88:3-6, 2006.
Andersson HC, Kaplan P, Kacena K, J Yee. Eight-year clinical outcomes of long-term enzyme replacement therapy in 884 children with type 1 Gaucher disease, Pediatrics 2008; 122;1182-1190.
Andersson HC, Kaplan P, Kacena K, J Yee. Eight-year clinical outcomes of long-term enzyme replacement therapy in 884 children with type 1 Gaucher disease, Pediatr,122:1182, 2008
Andersson, Perry W, Bowdish B, P Floyd-Browning. Emergency preparedness for genetics centers, laboratories and patients: the SouthEast Region Genetics Collaborative strategic plan. Genet Med, ePub: June, 2011, October, 2011.