Printer Friendly

Browse Hypercholesterolemia topic

Genetic aspects subtopic

Articles

1-77 out of 77 article(s)
Title Author Type Date Words
Effect of Statin Therapy in Tpe-Interval and Tpe/Qtc Ratio in Patients with Familial Hypercholesterolemia. Kucukosmanoglu, Mehmet; Kilic, Salih; Saracoglu, Erhan; Cekici, Yusuf; Vuruskan, Ertan; Kayikcioglu, Sep 1, 2020 4742
Impact on Longevity of Genetic Cardiovascular Risk and Lifestyle including Red Meat Consumption. da Silva, Alda Pereira; Costa, Maria do Ceu; Aguiar, Laura; Matos, Andreia; Gil, Angela; Gorjao-Clar Jul 31, 2020 9836
Simvastatin Attenuates Abdominal Aortic Aneurysm Formation Favoured by Lack of Nrf2 Transcriptional Activity. Kopacz, Aleksandra; Werner, Ewa; Grochot-Przeczek, Anna; Kloska, Damian; Hajduk, Karolina; Neumayer, Jun 30, 2020 9180
Cutaneous Xanthoma--A Clue to Familial Hypercholesterolemia. Philip, Shilpa Accamma; Sri, Swarna; Jeshtadi, Anunayi Jun 22, 2020 1473
Hypoprolactinemia as a Clue to Diagnosis of Mild Central Hypothyroidism due to IGSF1 Deficiency. Papadimitriou, Anastasios; Papadopoulou, Anna; Kleanthous, Kleanthis; Papadimitriou, Dimitrios T.; P Report Jun 1, 2020 3007
Public Policy Recs Updated for Familial Hypercholesterolemia; Goals include enhancing awareness of familial hypercholesterolemia as a global public health issue. Jan 3, 2020 256
Lipoprotein(a) Should Be Measured in All Individuals Suspected of Having Familial Hypercholesterolemia. Langsted, Anne; Nordestgaard, Borge G. Oct 1, 2019 2240
Effects of common variations of NOS3 and CAV1 genes on hypercholesterolemic profile in coronary heart disease. Ilikay, Serap; Cockunpinar, Ender; Kurnaz-Gomleksiz, Ozlem; Bugra, Zehra; Eronat, Allison P.; Ozturk Aug 1, 2019 7544
Effects of common variations of NOS3 and CAV1 genes on hypercholesterolemic profile in coronary heart disease. Ilikay, Serap; Coskunpinar, Ender; Kurnaz-Gomleksiz, Ozlem; Bugra, Zehra; Eronat, Allison P.; Ozturk Aug 1, 2019 7469
Severe hypercholesterolaemia with a high risk of atherosclerosis may be precipitated by a high-sterol diet. Marais, A.D.; Segal, D. Clinical report Sep 1, 2018 611
Only Half of Adults With Familial Hypercholesterolemia on Statins; And, only 30.3 percent of patients with definite or probable FH on statins take high-intensity statin. Mar 26, 2018 276
Premature Coronary Artery Disease due to Homozygous Familial Hypercholesterolemia in a 12-Year-Old Girl. Ekici, Filiz; Ozcobanoglu, Salih; Kardelen, Firat Case study Mar 1, 2018 2333
Imputation of Baseline LDL Cholesterol Concentration in Patients with Familial Hypercholesterolemia on Statins or Ezetimibe. Ruel, Isabelle; Aljenedil, Sumayah; Sadri, Iman; de Varennes, Emilie; Hegele, Robert A.; Couture, Pa Feb 1, 2018 5024
Recent Advances in the Development of Vaccines for Diabetes, Hypertension, and Atherosclerosis. Lu, Kongye; Su, Benli; Meng, Xiuxiang Report Jan 1, 2018 6815
Thiol/Disulfide Balance in Patients with Familial Hypercholesterolemia. Simsek, Ozgur; Carlioglu, Ayse; Alisik, Murat; Edem, Efe; Bicer, Cemile Koca Jan 1, 2018 4345
Characterization of Atherosclerosis Formation in a Murine Model of Type IIa Human Familial Hypercholesterolemia. Miyajima, Chiharu; Iwaki, Takayuki; Umemura, Kazuo; Ploplis, Victoria A.; Castellino, Francis J. Jan 1, 2018 8988
New Treatments on the Horizon for Familial Hypercholesterolemia. Rasadi, Khalid Al-; Waili, Khalid Al- Editorial Nov 1, 2017 1480
Investigation of LDLR Gene Mutations in Turkish Patients with Familial Hypercholesterolemia. Okur, Ilyas; Ezgu, Fatih Suheyl; Inci, Asli; Olgac, Asburce Bike; Tumer, Leyla Brief article Jun 1, 2017 191
Regeneron passes US FDA breakthrough therapy designation for Evinacumab for Homozygous Familial Hypercholesterolemia (HoFH). Apr 7, 2017 203
Regeneron passes US FDA breakthrough therapy designation for Evinacumab for Homozygous Familial Hypercholesterolemia (HoFH). Apr 7, 2017 199
Association Between Soluble CD40 Ligand and Hypercholesterolemia in Children and Adolescents/Cocuk ve Adolesanlarda Soluble CD40 Ligandi ile Yuksek Kolesterol Duzeylerinin Iliskisi. Yavas, Aynur Kucukcongar; Eminoglu, Tuba Fatma; Okur, Ilyas; Aral, Arzu; Hasanoglu, Alev; Tumer, Ley Report Mar 1, 2017 3789
Esperion begins three pivotal Phase 3 studies of bempedoic acid in heterozygous familial, hypercholesterolemia and statin intolerant patients. Jan 9, 2017 330
Esperion begins three pivotal Phase 3 studies of bempedoic acid in heterozygous familial, hypercholesterolemia and statin intolerant patients. Jan 9, 2017 326
Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia. Fahed, Akl C.; Shibbani, Kamel; Andary, Rabih R.; Arabi, Mariam T.; Habib, Robert H.; Nguyen, Denis Report Jan 1, 2017 5479
Cholesterol Levels in Genetically Determined Familial Hypercholesterolemia in Russian Karelia. Korneva, V.A.; Kuznetsova, T.Yu.; Bogoslovskaya, T.Yu.; Polyakov, D.S.; Vasilyev, V.B.; Orlov, A.V.; Report Jan 1, 2017 3879
Increased Risk of the APOB rs11279109 Polymorphism for CHD among the Kuwaiti Population. Bustan, Suzanne A. Al-; Ismael, Fatma G.; Serri, Ahmad Al-; Rashdan, Ibrahim Al- Report Jan 1, 2017 6492
A Genetic Variant (S4338N) in Apolipoprotein B Gene in Hypercholesterolemic Families from Pakistan. Ali, Akhtar; Babar, Masroor Ellahi; Awan, Ali Raza; Tayyab, Muhammad; Shehzad, Wasim; Imran, Muhamma Report Oct 31, 2016 4555
Familial high cholesterol more common than previously thought. May 1, 2016 119
The Impact of Lipoprotein-Associated Oxidative Stress on Cell-Specific Microvesicle Release in Patients with Familial Hypercholesterolemia. Nielsen, M.H.; Irvine, H.; Vedel, S.; Raungaard, B.; Beck-Nielsen, H.; Handberg, A. Jan 1, 2016 6087
Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries. Futema, Marta; Shah, Sonia; Cooper, Jackie A.; Li, KaWah; Whittall, Ros A.; Sharifi, Mahtab; Goldber Report Jan 1, 2015 5580
Sorting the wheat from the chaff in familial hypercholesterolemia. Hooper, Amanda J.; Watts, Gerald F. Editorial Jan 1, 2015 2436
Two cases of myocardial infarction in children. Ray, Hemant Narayan Oct 27, 2014 1267
Single step PCR for the identification of Low Density Lipoprotein Receptor (LDL-R) gene mutations. Report Aug 31, 2014 2265
SQU Hospital Successfully Treats the 1st Pregnant Patient with Familial Hypercholesterolemia. Medical condition overview Jan 8, 2014 151
Body mass index is associated with hypercholesterolemia following thyroid hormone withdrawal in thyroidectomized patients. Shin, Dong Yeob; Kim, Kwang Joon; Cho, Yongin; Park, Kyeong Hye; Hwang, Sena; Chung, Woong Youn; Lee Report Jan 1, 2014 5462
PCSK9--a new and potent approach to lowering cholesterol. Whayne, Thomas F., Jr. Editorial May 1, 2013 3148
Mipomersen approved for familial hypercholesterolemia. Mechcatie, Elizabeth Feb 15, 2013 524
Mutation in the PCSK9 gene in Omani Arab subjects with autosomal dominant hypercholesterolemia and its effect on PCSK9 protein structure. Waili, Khalid Al-; Zidi, Ward Al-Muna Al-; Abri, Abdul Rahim Al-; Rasadi, Khalid Al-; Sabti, Hilal A Jan 1, 2013 2900
Microfluidic amplification as a tool for massive parallel sequencing of the familial hypercholesterolemia genes. Hollants, Silke; Redeker, Egbert J.W.; Matthijs, Gert Report Apr 1, 2012 4950
Genetic basis for diagnosis of novel mutation of LDL receptor gene. Khan, Samia Perwaiz; Ghani, Rubina; Ahmed, Khwaja Zafar; Yaqub, Zia Report Dec 1, 2011 3099
HSCRP, F2-Isoprostane & homocysteine in primary hypercholesterolaemia. Rahman, T.; Chew, Y.Y.; Chan, S.P.; Muid, S.; Osman, N.S.; Razali, R.; Nawawi, H.; Thevarajah, M. Report Oct 1, 2011 2984
Genzyme seeks EU nod for mipomersen for homozygous and severe heterozygous familial hypercholesterolemia. Jul 28, 2011 170
THE GENETIC CHARACTERIZATION OF FAMILIAL HYPERCHOLESTEROLEMIA IN PAKISTAN. Report Jun 30, 2011 2725
Off-pump coronary bypass in a child with familial hypercholesterolemia: premature atherosclerosis of the ascending aorta/Familyal hiperkolesterolemili cocukta cikan aortanin erken aterosklerozu nedeniyle calisan kalpte baypas. Gulcan, Oner; Yildirim, Selman Vefa; Turkoz, Riza Jun 1, 2011 1021
C-reactive protein 1059G/C gene polymorphism in type 2 diabetic patients/Tip 2 diabetik hastalarda C-reaktif protein 1059G/C gen polimorfizmi. Yazici, Dilek; Yavuz, Dilek Gogas; Yuksel, Meral; Ozben, Beste; Sancak, Seda; Deyneli, Oguzhan; Akal Report Dec 1, 2010 2768
Pfizer Inc. Jul 12, 2010 223
Identification of four novel LDL receptor gene mutations in the north-west Moroccan population. Benyahya, F.; Bennani, M.; Barakat, A.; Blesa, S.; Gonzalez-Albert, V.; Carmena, R.; Chaves, F.J.; G Report Jun 1, 2010 2713
Influence of red clover (Trifolium pratense) isoflavones on gene and protein expression profiles in liver of ovariectomized rats. Pakalapati, Geeta; Li, Li; Gretz, Norbert; Koch, Egon; Wink, Michael Report Sep 1, 2009 6281
Berberine increases expression of GATA-2 and GATA-3 during inhibition of adipocyte differentiation. Hu, Y.; Davies, G.E. Report Sep 1, 2009 5273
The effects of hydroxycinnamic acid derivatives on adiponectin secretion. Ohara, Kazuyuki; Uchida, Asako; Nagasaka, Reiko; Ushio, Hideki; Ohshima, Toshiaki Report Mar 1, 2009 4178
Elin, 16, is safe thanks to the early detection of her high cholesterol; HEALTH WALES Screening of genetic link could help thousands more in Wales says medic. Sep 8, 2008 604
Genzyme and Isis Obtain Apolipoprotein B (apoB) Expression Antisense Modulation Patent. Jul 1, 2008 1108
An unusual case of severe hypertriglyceridemia and splenomegaly. Rahalkar, Amit R.; Wang, Jian; Sirrs, Sandra; Dimmick, James; Holmes, Daniel; Urquhart, Nadine; Hege Mar 1, 2008 3263
Target obesity in kids with genetic syndromes: reserve medications for those with genetic conditions such as familial hypercholesterolemia. Bates, Betsy Jan 15, 2008 699
Serum proprotein convertase subtilisin kexin type 9 is correlated directly with serum LDL cholesterol. Alborn, William E.; Cao, Guoqing; Careskey, Holly E.; Qian, Yue-Wei; Subramaniam, Danise R.; Davies, Oct 1, 2007 3531
Homocysteine, 5, 10-methylenetetrahydrofolate reductase 677C>T polymorphism, nutrient intake, and incident cardiovascular disease in 24 968 initially healthy women. Zee, Robert Y.L.; Mora, Samia; Cheng, Suzanne; Erlich, Henry A.; Lindpaintner, Klaus; Rifai, Nader; Clinical report May 1, 2007 5941
Call for help with cholesterol. Feb 26, 2007 88
Reliable low-density DNA array based on allele-specific probes for detection of 118 mutations causing familial hypercholesterolemia. Tejedor, Diego; Castillo, Sergio; Mozas, Pilar; Jimenez, Elisa; Lopez, Monica; Tejedor, M. Teresa; A Clinical report Jul 1, 2005 5875
Platelet-activating factor acetylhydrolase is not associated with carotid intima-media thickness in hypercholesterolemic Sicilian individuals. Campo, Salvatore; Sardo, Maria A.; Bitto, Alessandra; Bonaiuto, Antonio; Trimarchi, Giuseppe; Bonaiu Nov 1, 2004 4280
Lipid disorders and mutations in the APOB gene. Whitfield, Amanda J.; Barrett, P. Hugh R.; van Bockxmeer, Frank M.; Burnett, John R. Oct 1, 2004 5633
Familial hypercholesterolemia: genetic predisposition to atherosclerosis. Engler, Mary B. Aug 1, 2004 3013
Familial hypercholesterolemia in childhood: therapeutical options. Rodenburg, Jessica Jul 1, 2004 1251
New cholesterol treatment for families at high risk: for patients with an inherited disorder called hypercholesterolemia, an emerging therapy is opening the door to a brighter future. (Heartbeat: the healthy heart report). Perry, Patrick Jul 1, 2003 932
Instability of lipoprotein(a) in plasma stored at -70[degrees]C: effects of concentration, apolipoprotein(a) genotype, and donor cardiovascular disease. Simo, Josep M.; Camps, Jordi; Vilella, Elisabet; Gomez, Federico; Paul, Antonio; Joven, Jorge Sep 1, 2001 4581
Compound heterozygous familial hypercholesterolemia and familial defective apolipoprotein B-100 produce exaggerated hypercholesterolemia. Tai, E. Shyong; Koay, Evelyn S.C.; Chan, Edmund; Seng, Tzer Ding; Loh, Lih Ming; Sethi, Sunil K.; Ta Mar 1, 2001 4071
Identification of two LDL-receptor mutations causing familial hypercholesterolemia in Indian subjects by a simplified rapid PCR-heteroduplex method. Ashavaid, Tester F.; Kondkar, Altaf A.; Nair, Kappiareth G. Aug 1, 2000 1702
High cholesterol families. Brief Article Mar 1, 2000 293
Flow cytometric assessment of LDL ligand function for detection of heterozygous familial defective apolipoprotein B-100. Raungaard, Bent; Heath, Finn; Hansen, Peter Steen; Brorholt-Petersen, Jens Uffe; Jensen, Henrik Kjae Feb 1, 2000 6896
Long-distance PCR-based screening for large rearrangements of the LDL receptor gene in Korean patients with familial hypercholesterolemia. Kim, Sung Han; Bae, Ji Hyun; Chae, Jae Jin; Kim, Un Kyung; Choe, Seong-Joon; Namkoong, Yong; Kim, Hy Sep 1, 1999 4168
Mutations in the apolipoprotein (apo) B-100 receptor-binding region: detection of apo B-100 ([Arg.sup.3500] [right arrow] Trp) associated with two new haplotypes and evidence that apo B-100 ([Glu.sup.3405] [right arrow] Gln) diminishes receptor-mediated uptake of LDL. Fisher, Eva; Scharnagl, Hubert; Hoffmann, Michael M.; Kusterer, Klaus; Wittmann, Daniela; Wieland, H Clinical report Jul 1, 1999 9254
Flow cytometry with a monoclonal antibody to the low density lipoprotein receptor compared with gene mutation detection in diagnosis of heterozygous familial hypercholesterolemia. Raungaard, Bent; Heath, Finn; Brorholt-Petersen, Jens Uffe; Jensen, Henrik Kjaerulf; Faergeman, Ole May 1, 1998 4261
Low plasma vitamin A concentrations in familial combined hyperlipidemia. Ribalta, Josep; LaVille, Agnes E.; Girona, Josefa; Vallve, Joan C.; Masana, Lluis Dec 1, 1997 3382
Detecting familial defective apolipoprotein B-100: three molecular scanning methods compared. Henderson, Bryony G.; Wenham, Philip R.; Ashby, J. Peter; Blundell, Gillian Sep 1, 1997 3760
Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: two cases of [arginine.sub.3500] [right arrow] tryptophan mutation associated with a unique haplotype. Choong, Meng-Ling; Koay, Evelyn S.C.; Khoo, Kah-lin; Khaw, Min-Cheh; Sethi, Sunil K. Jun 1, 1997 6232
Single-strand conformation polymorphism analysis with high throughput modifications, and its use in mutation detection in familial hypercholesterolemia. Humphries, Steve E.; Gudnason, Vilmundur; Whittall, Ros; Day, Ian N.M. Mar 1, 1997 6854
Rabbit trail may lead to human gene therapy. Chen, Ingfei Nov 10, 1990 762
Even skinny pigs lose heart. Jan 10, 1987 193

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters