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[PDF] Top 20 Psychosocial Function During Treatment for Familial Hypercholesterolemia

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Psychosocial Function During Treatment for Familial Hypercholesterolemia

Psychosocial Function During Treatment for Familial Hypercholesterolemia

... It has been suggested that the identification of children who are at risk for cardiovascular disease is unnecessary and may be harmful.9”#{176} Thus, some au- thors disagree with the exp[r] ... See full document

9

Optimal management of familial hypercholesterolemia: treatment and management strategies

Optimal management of familial hypercholesterolemia: treatment and management strategies

... Familial hypercholesterolemia is a serious genetic dis- order affecting patients in the early years of ...Various treatment options are available at the ... See full document

10

Familial Hypercholesterolemia: From Diagnosis to Treatment

Familial Hypercholesterolemia: From Diagnosis to Treatment

... Familial hypercholesterolemia (FH) is an inherited common autosomal Mendelian disorder of lipoprotein metabolism with a population prevalence of 1 in ...and treatment of FH patients will reduce ... See full document

11

Anti-PCSK9 antibodies for the treatment of heterozygous familial hypercholesterolemia: patient selection and perspectives

Anti-PCSK9 antibodies for the treatment of heterozygous familial hypercholesterolemia: patient selection and perspectives

... Heterozygous familial hypercholesterolemia (FH) is a genetic disorder character- ized by high low-density lipoprotein cholesterol levels from birth, which exposes the arteries to high levels of atherogenic ... See full document

9

Combination therapy of statin and ezetimibe for the treatment of familial hypercholesterolemia

Combination therapy of statin and ezetimibe for the treatment of familial hypercholesterolemia

... the treatment of adult patients with heterozygous familial hypercholesterolemia (heFH), as the result of numerous studies in patients with primary hypercholesterolemia or ... See full document

15

Mipomersen and other therapies for the treatment of severe familial hypercholesterolemia

Mipomersen and other therapies for the treatment of severe familial hypercholesterolemia

... Abstract: Familial hypercholesterolemia (FH) is an autosomal dominant condition with a population prevalence of one in 300–500 (heterozygous) that is characterized by high levels of low-density lipoprotein ... See full document

9

THE TREATMENT OF FAMILIAL HYPERCHOLESTEROLEMIA WITH A PLANT STEROL

THE TREATMENT OF FAMILIAL HYPERCHOLESTEROLEMIA WITH A PLANT STEROL

... bow a concentration of chobesterob in the serum as does a low- or cholesterol-free diet with added sitosterol. There was no weight loss in either child during the course[r] ... See full document

5

Long-term Treatment of Severe Familial Hypercholesterolemia in Children: Effect of Sitosterol and Bezafibrate

Long-term Treatment of Severe Familial Hypercholesterolemia in Children: Effect of Sitosterol and Bezafibrate

... Seven prepubertal children (age range 5.3 to 10.8 years) with severe heterozygous familial hyper- cholesterolemla (serum cholesterol concentration 416 ± 85 mg/dL and low-density lipoprot[r] ... See full document

7

Extracorporeal LDL-Cholesterol Elimination in the Treatment of Severe Familial Hypercholesterolemia

Extracorporeal LDL-Cholesterol Elimination in the Treatment of Severe Familial Hypercholesterolemia

... in treatment of homozygous patients – it is practically a case of life- saving ...Homozygous familial hypercholesterolaemia occurs in a frequency 1 : ... See full document

5

<p>Clinical Evaluation Of Evolocumab For The Treatment Of Homozygous Familial Hypercholesterolemia In Chinese Patients</p>

<p>Clinical Evaluation Of Evolocumab For The Treatment Of Homozygous Familial Hypercholesterolemia In Chinese Patients</p>

... In the post-hoc analysis of the FOURIER trial, which included 27,564 participants, the effects of adding evolocu- mab (either 140 mg subcutaneously every 2 weeks or 420 mg subcutaneously monthly) versus matching placebo ... See full document

8

Treatment of Familial Hypercholesterolemia in Children and Adolescents: Effect of Lovastatin

Treatment of Familial Hypercholesterolemia in Children and Adolescents: Effect of Lovastatin

... Lovastatin therapy in receptor-negative homozygous familial hypercholesterolemia: lack of effect on low-density lipoprotein concentrations or turnover. Ducobu J, Brasseur D, Chaudron JM,[r] ... See full document

12

Improving the genetic diagnosis of familial hypercholesterolemia

Improving the genetic diagnosis of familial hypercholesterolemia

... especially in children (Sjouke et al., 2016). Although not considered to be appropriate for prenatal screening, because it is so eminently treatable, some families might appreciate knowing the discrete genetic basis for ... See full document

132

NOVEL THERAPEUTIC OPTIONS FOR FAMILIAL HYPERCHOLESTEROLEMIA

NOVEL THERAPEUTIC OPTIONS FOR FAMILIAL HYPERCHOLESTEROLEMIA

... of treatment, transaminases returned to normal in all ...transaminase during mipomersen treatment is unclear, and it was not seen in preclinical ... See full document

8

Myeloperoxidase modulation by LDL apheresis in Familial Hypercholesterolemia

Myeloperoxidase modulation by LDL apheresis in Familial Hypercholesterolemia

... whether hypercholesterolemia is associated with MPO up-regulation and whether MPO serum levels are affected by cholesterol ...with Familial Hypercholes- terolemia (FH) undergoing LDL (Low Density ... See full document

8

Correlating corneal arcus with atherosclerosis in familial hypercholesterolemia

Correlating corneal arcus with atherosclerosis in familial hypercholesterolemia

... (mean age 13 ± 12) than those with arcus (mean age 31 ± 11). The data on these 17 patients was collected over sev- eral decades and in some cases is ongoing. With the advent of newer therapies such as LDL removal by ... See full document

9

Changes in lipoprotein lipase and endothelial lipase mass in familial hypercholesterolemia during three-drug lipid-lowering combination therapy

Changes in lipoprotein lipase and endothelial lipase mass in familial hypercholesterolemia during three-drug lipid-lowering combination therapy

... showing primary hyper-LDL cholesterolemia (>160 mg/dl). Exclusion criteria of the present study were FH patients with a homozygous gene mutation, patients under LDL apheresis therapy or any immunomodulatory ... See full document

6

The genetics of familial hypercholesterolemia and emerging therapies

The genetics of familial hypercholesterolemia and emerging therapies

... 2-year treatment with pravastatin in 8–18-year-old children with FH induced a significant regression of carotid intima-media thickness without any adverse events; this finding suggests “the younger, the better” ... See full document

10

Genetic screening for homozygous and heterozygous familial hypercholesterolemia

Genetic screening for homozygous and heterozygous familial hypercholesterolemia

... Abstract: Familial hypercholesterolemia (FH) is a common inherited disorder that results in premature ...of treatment can modify disease progression and ...mutations. Familial defective Apo B ... See full document

11

Molecular Diagnosis of Familial Hypercholesterolemia

Molecular Diagnosis of Familial Hypercholesterolemia

... 22-Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection. Evaluation and treatment of high blood cholesterol in adults (Adult treatment Panel III). JAMA 2001 May 16; ... See full document

12

Familial hypercholesterolemia

Familial hypercholesterolemia

... sis begins early in life for individuals with FH (especially in HoFH), childhood screening is intended to facilitate early identification and treatment. Despite the theo- retical benefits of the National Heart ... See full document

6

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