Rationale and design of the familial hypercholesterolemia foundation CAscade SCreening for Awareness and DEtection of Familial Hypercholesterolemia registry.
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Emily C. O'Brien | J. Knowles | D. Rader | K. Watson | E. Peterson | C. Ballantyne | S. Gidding | E. O'Brien | M. Roe | L. Hemphill | L. Hudgins | J. Genest | James A. Underberg | Katherine A. Wilemon | Elizabeth S. Fraulo | P. Moriarty | J. Ross | I. Kindt | E. Hammond | D. Pickhardt | K. Wilemon
[1] Catherine Boileau,et al. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease , 2013, European heart journal.
[2] D. Rader,et al. Familial hypercholesterolemias: prevalence, genetics, diagnosis and screening recommendations from the National Lipid Association Expert Panel on Familial Hypercholesterolemia. , 2011, Journal of clinical lipidology.
[3] Jennifer G. Robinson,et al. Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia. , 2011, Journal of clinical lipidology.
[4] Muin J Khoury,et al. Evidence-based classification of recommendations on use of genomic tests in clinical practice: Dealing with insufficient evidence , 2010, Genetics in Medicine.
[5] J. Witteman,et al. Efficacy of statins in familial hypercholesterolaemia: a long term cohort study , 2008, BMJ : British Medical Journal.
[6] S. Humphries,et al. Reductions in all-cause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: a prospective registry study , 2008, European heart journal.
[7] Michael Higgins,et al. An Electronic Health Record - Public Health (EHR-PH) System Prototype for Interoperability in 21st Century Healthcare Systems , 2005, AMIA.
[8] Carolyn M Hutter,et al. Genetic causes of monogenic heterozygous familial hypercholesterolemia: a HuGE prevalence review. , 2004, American journal of epidemiology.
[9] F. Civeira,et al. Familial hypercholesterolemia in Spain: case-finding program, clinical and genetic aspects. , 2004, Seminars in vascular medicine.
[10] J. Kastelein,et al. Cost-effectiveness analysis of the genetic screening program for familial hypercholesterolemia in The Netherlands. , 2004, Seminars in vascular medicine.
[11] T. Leren,et al. Application of molecular genetics for diagnosing familial hypercholesterolemia in Norway: results from a family-based screening program. , 2004, Seminars in vascular medicine.
[12] J. Kastelein,et al. Long-term compliance with lipid-lowering medication after genetic screening for familial hypercholesterolemia. , 2003, Archives of internal medicine.
[13] E. Sijbrands,et al. Review of first 5 years of screening for familial hypercholesterolaemia in the Netherlands , 2001, The Lancet.
[14] D. Bhatnagar,et al. Outcome of case finding among relatives of patients with known heterozygous familial hypercholesterolaemia , 2000, BMJ : British Medical Journal.
[15] S. Humphries,et al. Extent of underdiagnosis of familial hypercholesterolaemia in routine practice: prospective registry study , 2000, BMJ : British Medical Journal.
[16] N. Calonge,et al. Validation of self-reported chronic conditions and health services in a managed care population. , 2000, American journal of preventive medicine.
[17] S. Humphries,et al. MED-PED: An Integrated Genetic Strategy for Preventing Early Deaths , 1996 .
[18] Y. Christen,et al. Genetic Approaches to Noncommunicable Diseases , 1996, Springer Berlin Heidelberg.
[19] M. C. Leske,et al. Comparing self-reported and physician-reported medical history. , 1994, American journal of epidemiology.
[20] M. Leppert,et al. Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics. , 1993, The American journal of cardiology.
[21] Charles R.scriver,et al. The Metabolic basis of inherited disease , 1989 .
[22] S. Rose. HUMAN PERFECTIBILITY , 1984, The Lancet.
[23] L. Solomon,et al. The Metabolic Basis of Inherited Disease , 1979 .
[24] J. Slack. RISKS OF ISCHÆMIC HEART-DISEASE IN FAMILIAL HYPERLIPOPROTEINÆMIC STATES , 1969 .
[25] J. Slack. Risks of ischaemic heart-disease in familial hyperlipoproteinaemic states. , 1969, Lancet.