نتائج البحث - "Familial Combined"

71

Haplotype analyses of the APOA5 gene in patients with familial combined hyperlipidemia

المؤلفون: Wu-Wei Zeng, Geesje M. Dallinga-Thie, Aaron Isaacs, Anton F. H. Stalenhoef, Cornelia M. van Duijn, Gerly M. van der Vleuten, Ewoud ter Avest, Philippa J. Talmud, Jacqueline de Graaf

المساهمون: Faculteit Medische Wetenschappen/UMCG, Epidemiology, Internal Medicine, Vascular Medicine, Experimental Vascular Medicine

المصدر: Biochimica et biophysica acta, 1772(1), 81-88
Biochimica et Biophysica Acta-Molecular Basis of Disease, 1772(1), 81-88. Elsevier
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1772(1), 81-88. Elsevier
Biochimica et Biophysica Acta. Molecular Basis of Disease, 1772, 1, pp. 81-8
Biochimica et Biophysica Acta. Molecular Basis of Disease, 1772, 81-8

مصطلحات موضوعية: Lipoproteins, LDL/blood, Male, Apolipoprotein B, Triglyceride level, Intima-media thickness, Hyperlipidemia, Familial Combined, Cardiovascular Diseases/blood, Vascular medicine and diabetes [UMCN 2.2], Hyperlipidemia, Familial Combined/blood, chemistry.chemical_compound, Polymorphism (computer science), Hyperlipidemia, Haplotype, Netherlands, Ultrasonography, Genetics, Cholesterol, HDL/blood, Cardiovascular diseases [NCEBP 14], biology, medicine.diagnostic_test, Homozygote, Remnant-like particle, Middle Aged, LDL/blood, Lipoproteins, LDL, APOA5 gene, Triglycerides/blood, Cholesterol, Carotid Arteries, Cardiovascular Diseases, HDL/blood, Population study, Molecular Medicine, Female, lipids (amino acids, peptides, and proteins), Adult, medicine.medical_specialty, Health aging / healthy living [IGMD 5], Familial combined hyperlipidemia, Lipoproteins, Risk Assessment, Genetic, Apolipoproteins A/genetics, Internal medicine, medicine, Humans, Familial Combined/blood, Genetic Predisposition to Disease, Polymorphism, Allele, Carotid Arteries/diagnostic imaging, Molecular Biology, Apolipoproteins A, Triglycerides, Polymorphism, Genetic, Cholesterol, HDL, medicine.disease, Endocrinology, chemistry, Haplotypes, Apolipoprotein A-V, biology.protein, Lipid profile

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c4238cda9dc6c7736e695ae11b4ee6eTest
https://doi.org/10.1016/j.bbadis.2006.10.012Test

72

Metabolic syndrome prevalence and characteristics in Greek adults with familial combined hyperlipidemia

المؤلفون: Christodoulos Stefanadis, Christina Chrysohoou, Demosthenes B. Panagiotakos, Christos Pitsavos, John Skoumas, Constantina Masoura, N. Giotsas, Marina Toutouza, L. Papadimitriou

المصدر: Metabolism. 56:135-141

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ee93ec17118947cfbafc26bfd757ea4Test
https://doi.org/10.1016/j.metabol.2006.09.007Test

73

Lipoprotein apheresis as a treatment modality for familial combined hyperlipidemia (FCH) with non-alcoholic fatty liver disease (NAFLD) and coronary heart disease: a casuistic approach

المؤلفون: Asgeir Græsdal, Ane Stensønes Dybvig

المصدر: Atherosclerosis. 263:e243-e244

مصطلحات موضوعية: medicine.medical_specialty, business.industry, Fatty liver, Non alcoholic, Disease, medicine.disease, Coronary heart disease, Familial combined hyperlipidemia, Treatment modality, Internal medicine, medicine, Cardiology, Cardiology and Cardiovascular Medicine, business, Lipoprotein apheresis

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::37ad370dcf984af13f5362380ad7ce1eTest
https://doi.org/10.1016/j.atherosclerosis.2017.06.788Test

74

Contribution of mutations in low density lipoprotein receptor (LDLR) and lipoprotein lipase (LPL) genes to familial combined hyperlipidemia (FCHL): a reappraisal by using a resequencing approach

المؤلفون: Anna Montali, Giovanni Pigna, Marcello Arca, Cristina Prisco, Ilenia Minicocci, Alessia Di Costanzo, Fabrizio Ceci

المصدر: Atherosclerosis. 242(2)

مصطلحات موضوعية: Adult, Male, Heterozygote, Genotype, DNA Mutational Analysis, Hyperlipidemia, Familial Combined, Mutation, Missense, Biology, medicine, Missense mutation, Humans, Allele, Gene, Alleles, Genetic testing, Aged, Genetics, Family Health, Lipoprotein lipase, medicine.diagnostic_test, nutritional and metabolic diseases, Genetic Variation, Middle Aged, medicine.disease, Alternative Splicing, Lipoprotein Lipase, Phenotype, Italy, Receptors, LDL, Case-Control Studies, LDL receptor, Association study, Familial combined hyperlipidemia, LDLR gene, LPL gene, Polymorphisms, Rare mutations, Resequencing, Cardiology and Cardiovascular Medicine, Mutation, lipids (amino acids, peptides, and proteins), Female, Dyslipidemia, Lipoprotein

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f702fbdf9533aec5fb833b82a010b98Test
https://pubmed.ncbi.nlm.nih.gov/26342331Test

75

Association of USF1 and APOA5 polymorphisms with Familial Combined Hyperlipidemia in an Italian population

المؤلفون: Marco Gentile, Maria Nicoletta D'Agostino, Antonietta D'Angelo, Maria Donata Di Taranto, Gennaro Marotta, Paolo Rubba, Antonino Staiano, Elena Bloise, Giuliana Fortunato, Alberto Morgante

المساهمون: DI TARANTO, MARIA DONATA, Staiano, A, D'Agostino, MARIA NICOLETTA, D'Angelo, A, Bloise, E, Morgante, A, Marotta, Gennaro, Gentile, M, Rubba, PAOLO OSVALDO FEDERICO, Fortunato, Giuliana

مصطلحات موضوعية: Apolipoprotein E, Adult, Male, medicine.medical_specialty, Apolipoprotein B, Familial combined hyperlipidemia, Upstream stimulatory factor 1 (USF1), European Continental Ancestry Group, Upstream Stimulatory Factor, USF1, Hyperlipidemia, Familial Combined, Single-nucleotide polymorphism, Genetic Association Studie, Polymorphism, Single Nucleotide, Triglyceride, White People, Body Mass Index, Single nucleotide polymorphism (SNP), Internal medicine, medicine, SNP, Humans, Genetic Predisposition to Disease, Molecular Biology, Genetic Association Studies, Triglycerides, Apolipoproteins A, Genetics, Apolipoprotein A-V (APOA5), biology, PCSK9, Case-control study, Cell Biology, Middle Aged, Endocrinology, Italy, Apolipoprotein A-V, Case-Control Studies, biology.protein, KIF6, Upstream Stimulatory Factors, lipids (amino acids, peptides, and proteins), Female, Case-Control Studie, Human