Familial Hypercholesterolemia
Homozygous Familial Hypercholesterolemia - March 2, 2015
What is homozygous familial hypercholesterolemia? Information from the FH Foundation
Long-term clinical results of microsomal triglyceride transfer protein inhibitor use in a patient with homozygous familial hypercholesterolemia.
Raper Anna et al. J Clin Lipidol 2015 Jan-Feb;9(1):107-12.
Raper Anna et al. J Clin Lipidol 2015 Jan-Feb;9(1):107-12.
Pharmacological treatment of a Sardinian patient affected by Autosomal Recessive Hypercholesterolemia (ARH).
Muntoni Sandro et al. J Clin Lipidol 2015 Jan-Feb;9(1):103-6.
Muntoni Sandro et al. J Clin Lipidol 2015 Jan-Feb;9(1):103-6.
Impact of LDL apheresis on aortic root atheroma in children with homozygous familial hypercholesterolemia.
Lefort Bruno et al. Atherosclerosis 2015 Mar (1) 158-62
Lefort Bruno et al. Atherosclerosis 2015 Mar (1) 158-62
The doctor's dilemma: challenges in the diagnosis and care of homozygous familial hypercholesterolemia.
Baum Seth J et al. J Clin Lipidol 2014 Nov-Dec;8(6):542-9.
Baum Seth J et al. J Clin Lipidol 2014 Nov-Dec;8(6):542-9.
Seven-year clinical follow-up of a Chinese homozygous familial hypercholesterolemia child with premature xanthomas and coronary artery disease--a need for early diagnosis and aggressive treatment.
Jiang Long et al. Int. J. Cardiol. 2014 Nov 15. (1) 188-91
Jiang Long et al. Int. J. Cardiol. 2014 Nov 15. (1) 188-91
Normalization of low-density lipoprotein receptor expression in receptor defective homozygous familial hypercholesterolemia by inhibition of PCSK9 with alirocumab.
Lambert Gilles et al. J. Am. Coll. Cardiol. 2014 Dec 2. (21) 2299-300
Lambert Gilles et al. J. Am. Coll. Cardiol. 2014 Dec 2. (21) 2299-300
Inhibition of PCSK9 with evolocumab in homozygous familial hypercholesterolaemia (TESLA Part B): a randomised, double-blind, placebo-controlled trial.
Raal Frederick J et al. Lancet 2015 Jan 24. (9965) 341-50
Raal Frederick J et al. Lancet 2015 Jan 24. (9965) 341-50
Management of homozygous familial hypercholesterolaemia--unmet needs, updated recommendations, and clinical experience with the MTP inhibitor, lomitapide. Concluding comments.
Catapano Alberico L et al. Atheroscler Suppl 2014 Sep (2) 52
Catapano Alberico L et al. Atheroscler Suppl 2014 Sep (2) 52
Daily life, experience and needs of persons suffering from homozygous familial hypercholesterolaemia: insights from a patient survey.
Bruckert Eric et al. Atheroscler Suppl 2014 Sep (2) 46-51
Bruckert Eric et al. Atheroscler Suppl 2014 Sep (2) 46-51
What are we able to achieve today for our patients with homozygous familial hypercholesterolaemia, and what are the unmet needs?
Santos Raul D et al. Atheroscler Suppl 2014 Sep (2) 19-25
Santos Raul D et al. Atheroscler Suppl 2014 Sep (2) 19-25
New strategies for the management of patients with homozygous familial hypercholesterolaemia.
Catapano Alberico L et al. Atheroscler Suppl 2014 Sep (2) 17-8
Catapano Alberico L et al. Atheroscler Suppl 2014 Sep (2) 17-8
Homozygous familial hypercholesterolemia: the c.1055G>A mutation in the LDLR gene and clinical heterogeneity.
Magaña Torres María Teresa et al. J Clin Lipidol 2014 Sep-Oct;8(5):525-7.
Magaña Torres María Teresa et al. J Clin Lipidol 2014 Sep-Oct;8(5):525-7.
Homozygous familial hypercholesterolemia.
Alicezah M K et al. Malays J Pathol 2014 Aug (2) 131-7
Alicezah M K et al. Malays J Pathol 2014 Aug (2) 131-7
Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society.
Cuchel Marina et al. Eur. Heart J. 2014 Aug 21. (32) 2146-57
Cuchel Marina et al. Eur. Heart J. 2014 Aug 21. (32) 2146-57
Lomitapide for the management of homozygous familial hypercholesterolemia.
deGoma Emil M et al. Rev Cardiovasc Med 2014 (2) 109-18
deGoma Emil M et al. Rev Cardiovasc Med 2014 (2) 109-18
Genotypic and phenotypic features in homozygous familial hypercholesterolemia caused by proprotein convertase subtilisin/kexin type 9 (PCSK9) gain-of-function mutation.
Mabuchi Hiroshi et al. Atherosclerosis 2014 Sep (1) 54-61
Mabuchi Hiroshi et al. Atherosclerosis 2014 Sep (1) 54-61
Xanthoma tuberosum in homozygous familial hypercholesterolemia.
Moorthy Nagaraja et al. Ann Pediatr Cardiol 2014 May (2) 118-9
Moorthy Nagaraja et al. Ann Pediatr Cardiol 2014 May (2) 118-9
Lomitapide: A novel agent for the treatment of homozygous familial hypercholesterolemia.
Davis Kyle A et al. Am J Health Syst Pharm 2014 Jun 15. (12) 1001-8
Davis Kyle A et al. Am J Health Syst Pharm 2014 Jun 15. (12) 1001-8
Inhibition of hepatic microsomal triglyceride transfer protein - a novel therapeutic option for treatment of homozygous familial hypercholesterolemia.
Vuorio Alpo et al. Vasc Health Risk Manag 2014 263-70
Vuorio Alpo et al. Vasc Health Risk Manag 2014 263-70
Familial Hypercholesterolemia: Call to Action and Recent Insights - February 19, 2015
New CDC feature: Genomics and Heart Disease
Familial hypercholesterolemia: Underdiagnosed, risks underappreciated; new treatments on horizon,
Cardiology Today, February 2015
Cardiology Today, February 2015
Long-term statin treatment in children with familial hypercholesterolemia: More insight into tolerability and adherence
Braamskamp M, et al. Pediatric Drugs, Feb 2015
Braamskamp M, et al. Pediatric Drugs, Feb 2015
Big data used to help identify patients at risk of deadly high-cholesterol disorder,
by Tracie White, Scope, Jan 29
by Tracie White, Scope, Jan 29
Find FH: The FH Foundation, AMGEN and Stanford University launch the Find FH initiative (Flag, Identify, Network, Deliver), Jan 29
Cascade screening for familial hypercholesterolemia,
by Mary Louise Brumit, FH Foundation (2014)
by Mary Louise Brumit, FH Foundation (2014)
CDC paper: Reducing the burden of disease and death from familial hypercholesterolemia: A call to action.
Knowles JW, et al Am Heart J. 2014 Dec;168(6):807-11
Knowles JW, et al Am Heart J. 2014 Dec;168(6):807-11
Proceedings of the FH Foundation's inaugural Familial Hypercholesterolemia Summit: Awareness to Action, the FH Foundation (2014)
Familial hypercholesterolemia-epidemiology, diagnosis, and screening.
Singh S, Bittner V. Curr Atheroscler Rep. 2015 Feb;17(2):482
Singh S, Bittner V. Curr Atheroscler Rep. 2015 Feb;17(2):482
A framework for bridging the gap in the care of familial hypercholesterolaemia in the community: pragmatic and economic perspectives.
Purchase S, et al Int J Evid Based Healthc. 2014 Dec
Purchase S, et al Int J Evid Based Healthc. 2014 Dec
Mortality among patients with familial hypercholesterolemia: a registry-based study in norway, 1992-2010.
Mundal L, et al J Am Heart Assoc. 2014 Dec 2;3(6).
Mundal L, et al J Am Heart Assoc. 2014 Dec 2;3(6).
Familial hypercholesterolemia in Brazil: Cascade screening program, clinical and genetic aspects.
Jannes CE, et al. Atherosclerosis. 2014 Nov 14;238(1):101-107
Jannes CE, et al. Atherosclerosis. 2014 Nov 14;238(1):101-107
Canadian Cardiovascular Society position statement on familial hypercholesterolemia.
Genest J, et al. Can J Cardiol. 2014 Dec;30(12):1471-81
Genest J, et al. Can J Cardiol. 2014 Dec;30(12):1471-81
Recommendations for the management of patients with familial hypercholesterolemia.
Feldman DI, et al. Curr Atheroscler Rep. 2015 Jan;17(1):473
Feldman DI, et al. Curr Atheroscler Rep. 2015 Jan;17(1):473
Systematic detection of familial hypercholesterolaemia in primary health care: A community based prospective study of three methods.
Kirke AB, et al. Heart Lung Circ. 2014 Sep 30
Kirke AB, et al. Heart Lung Circ. 2014 Sep 30
Prevalence and clinical correlates of familial hypercholesterolemia founder mutations in the general population.
Lahtinen AM, et al. Atherosclerosis. 2014 Nov 18;238(1):64-69
Lahtinen AM, et al. Atherosclerosis. 2014 Nov 18;238(1):64-69
Therapy: PCSK9 inhibitors for treating familial hypercholesterolaemia.
Mabuchi H, Nohara A. Nat Rev Endocrinol. 2014 Nov 18
Mabuchi H, Nohara A. Nat Rev Endocrinol. 2014 Nov 18
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Nature. 2014 Dec 10
Nature. 2014 Dec 10
Molecular basis for familial hypercholesterolemia, Brown and Goldstein Video (Sept 2014)
Familial Hypercholesterolemia: Saving Lives Through Early Detection - September 25, 2014
New CDC paper: Reducing the burden of disease and death from familial hypercholesterolemia: A call to action
Joshua W. Knowles, Emily C. O'Brien, Karen Greendale, Katherine Wilemon, Jacques Genest, Laurence S. Sperling, William A. Neal, Daniel J. Rader, Muin J. Khoury. American Heart Journal 2014 Sept 16
Joshua W. Knowles, Emily C. O'Brien, Karen Greendale, Katherine Wilemon, Jacques Genest, Laurence S. Sperling, William A. Neal, Daniel J. Rader, Muin J. Khoury. American Heart Journal 2014 Sept 16
What is familial hypercholesterolemia? Information from the CDC Public Health Genomics toolkit.
History of discovery- The LDL receptor
Joseph L. Goldstein and Michael S. Brown Arteriosclerosis, Thrombosis, and Vascular Biology. 2009; 29: 431-438
Joseph L. Goldstein and Michael S. Brown Arteriosclerosis, Thrombosis, and Vascular Biology. 2009; 29: 431-438
Understanding familial hypercholesterolemia, Preventive Cardiology, July 2014
What are state public health programs doing about reducing burden of familial hypercholesterolemia? Information from CDC clickable state map
Helping patients with familial hypercholesterolemia find healthcare providers, information from the FH Foundation
No hay comentarios:
Publicar un comentario