UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Comparison of Genetic Versus Clinical Diagnosis in Familial Hypercholesterolemia

The American journal of cardiology, 2008-11, Vol.102 (9), p.1187-1193.e1

2008

Volltextzugriff (PDF)

PCSK9 continues surprising us

Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis, 2016-03, Vol.28 (2), p.79

Pocoví, Miguel

2016

Volltextzugriff (PDF)

The influence of genetic variability and proinflammatory status on the development of bone disease in patients with Gaucher disease

PloS one, 2015-05, Vol.10 (5), p.e0126153-e0126153

2015

Volltextzugriff (PDF)

Diagnosis features of pediatric Gaucher disease patients in the era of enzymatic therapy, a national-base study from the Spanish Registry of Gaucher Disease

Orphanet journal of rare diseases, 2017-05, Vol.12 (1), p.84-84, Article 84

2017

Volltextzugriff (PDF)

Glycated Hemoglobin, Fasting Insulin and the Metabolic Syndrome in Males. Cross-Sectional Analyses of the Aragon Workers' Health Study Baseline

PloS one, 2015-08, Vol.10 (8), p.e0132244-e0132244

2015

Volltextzugriff (PDF)

Mutation analysis and genotype/phenotype relationships of Gaucher disease patients in Spain

Journal of human genetics, 2007-05, Vol.52 (5), p.391-396

2007

Volltextzugriff (PDF)

Real-world clinical experience with long-term miglustat maintenance therapy in type 1 Gaucher disease: the ZAGAL project

Haematologica (Roma), 2009-12, Vol.94 (12), p.1771-1775

2009

Volltextzugriff (PDF)

Removing Lipemia in Serum/Plasma Samples: A Multicenter Study

Annals of Laboratory Medicine, 2018, 38(6), , pp.518-523

2018

Volltextzugriff (PDF)

The island of Gran Canaria: A genetic isolate for familial hypercholesterolemia

Journal of clinical lipidology, 2019-07, Vol.13 (4), p.618-626

2019

Volltextzugriff (PDF)

Mapping the genetic and clinical characteristics of Gaucher disease in the Iberian Peninsula

Orphanet journal of rare diseases, 2012-03, Vol.7 (1), p.17-17

2012

Volltextzugriff (PDF)

Aragon workers' health study--design and cohort description

BMC cardiovascular disorders, 2012-06, Vol.12 (1), p.45-45, Article 45

2012

Volltextzugriff (PDF)

Femoral and Carotid Subclinical Atherosclerosis Association With Risk Factors and Coronary Calcium

Journal of the American College of Cardiology, 2016-03, Vol.67 (11), p.1263-1274

2016

Volltextzugriff (PDF)

Mechanism of Low Density Lipoprotein (LDL) Release in the Endosome: IMPLICATIONS OF THE STABILITY AND Ca²⁺ AFFINITY OF THE FIFTH BINDING MODULE OF THE LDL RECEPTOR

The Journal of biological chemistry, 2008-08, Vol.283 (33), p.22670-22679

2008

Volltextzugriff (PDF)

Evaluation of Spanish Gaucher disease patients after a 6-month imiglucerase shortage

Blood cells, molecules, & diseases, 2011-01, Vol.46 (1), p.115-118

2011

Volltextzugriff (PDF)

Higher Incidence of Mild Cognitive Impairment in Familial Hypercholesterolemia

The American journal of medicine, 2010-03, Vol.123 (3), p.267-274

2010

Volltextzugriff (PDF)

Recommendations for the detection and diagnosis of Niemann-Pick disease type C: An update

Neurology. Clinical practice, 2017-12, Vol.7 (6), p.499-511

2017

Volltextzugriff (PDF)

Genetic Variants of LDLR and PCSK9 Associated with Variations in Response to Antihypercholesterolemic Effects of Armolipid Plus with Berberine

PloS one, 2016-03, Vol.11 (3), p.e0150785-e0150785

2016

Volltextzugriff (PDF)

Relation between Gastrointestinal Adverse Effects in Gaucher Disease Patients and Intestinal Disaccharidases Activity Evaluated by Methane Hydrogen Breath Test

Journal of pharmacy and pharmacology (El Monte), 2017-02, Vol.5 (2), p.85-97

Blanca Medrano-Engay Marcio Andrade-Campos Maria Pilar Irun Miguel Pocovi Pilaf Giraldo

2017

Volltextzugriff (PDF)

Femoral and Carotid Subclinical Atherosclerosis Association With Risk Factors and Coronary Calcium: The AWHS Study

Journal of the American College of Cardiology, 2016-03, Vol.67 (11), p.1263-1274

2016

Volltextzugriff (PDF)

A Third Major Locus for Autosomal Dominant Hypercholesterolemia Maps to 1p34.1-p32

American journal of human genetics, 1999-05, Vol.64 (5), p.1378-1387

1999

Volltextzugriff (PDF)

Expression and purification of recombinant apolipoprotein A-I Zaragoza (L144R) and formation of reconstituted HDL particles

Protein expression and purification, 2011-11, Vol.80 (1), p.110-116

2011

Volltextzugriff (PDF)

Usefulness of Triglycerides-to–High-Density Lipoprotein Cholesterol Ratio for Predicting the First Coronary Event in Men

The American journal of cardiology, 2009-11, Vol.104 (10), p.1393-1397

2009

Volltextzugriff (PDF)

Common genetic variants contribute to primary hypertriglyceridemia without differences between familial combined hyperlipidemia and isolated hypertriglyceridemia

Circulation. Cardiovascular genetics, 2014-12, Vol.7 (6), p.814-821

2014

Volltextzugriff (PDF)

The fine line between familial and polygenic hypercholesterolemia

Clinical lipidology, 2013-06, Vol.8 (3), p.303-306

2013

Volltextzugriff (PDF)

Frequency of Low-Density Lipoprotein Receptor Gene Mutations in Patients With a Clinical Diagnosis of Familial Combined Hyperlipidemia in a Clinical Setting

Journal of the American College of Cardiology, 2008-11, Vol.52 (19), p.1546-1553

2008

Volltextzugriff (PDF)

1 – 25 von 214

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(202)
Mit Volltextzugriff
(187)

Publikationsform

Sprache

Englisch
(183)
Spanisch
(32)
Japanisch
(20)

Erscheinungsjahr

n.n

Thema

Science & Technology
(113)
Humans
(112)
Life Sciences & Biomedicine
(107)
Male
(68)
Adult
(62)
Middle Aged
(62)
Female
(60)
Biological And Medical Sciences
(42)
Mutation
(36)
Aged
(35)
Cardiovascular System & Cardiology
(35)
Medical Sciences
(35)
Cardiac & Cardiovascular Systems
(25)
Adolescent
(24)
Familial Hypercholesterolemia
(24)
Hyperlipoproteinemia Type Ii - Genetics
(24)
Peripheral Vascular Disease
(21)
Receptors, Ldl - Genetics
(21)
Cardiovascular
(20)
Spain - Epidemiology
(20)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Comparison of Genetic Versus Clinical Diagnosis in Familial Hypercholesterolemia

PCSK9 continues surprising us

The influence of genetic variability and proinflammatory status on the development of bone disease in patients with Gaucher disease

Diagnosis features of pediatric Gaucher disease patients in the era of enzymatic therapy, a national-base study from the Spanish Registry of Gaucher Disease

Glycated Hemoglobin, Fasting Insulin and the Metabolic Syndrome in Males. Cross-Sectional Analyses of the Aragon Workers' Health Study Baseline

Mutation analysis and genotype/phenotype relationships of Gaucher disease patients in Spain

Real-world clinical experience with long-term miglustat maintenance therapy in type 1 Gaucher disease: the ZAGAL project

Removing Lipemia in Serum/Plasma Samples: A Multicenter Study

The island of Gran Canaria: A genetic isolate for familial hypercholesterolemia

Mapping the genetic and clinical characteristics of Gaucher disease in the Iberian Peninsula

Aragon workers' health study--design and cohort description

Femoral and Carotid Subclinical Atherosclerosis Association With Risk Factors and Coronary Calcium

Mechanism of Low Density Lipoprotein (LDL) Release in the Endosome: IMPLICATIONS OF THE STABILITY AND Ca²⁺ AFFINITY OF THE FIFTH BINDING MODULE OF THE LDL RECEPTOR

Evaluation of Spanish Gaucher disease patients after a 6-month imiglucerase shortage

Higher Incidence of Mild Cognitive Impairment in Familial Hypercholesterolemia

Recommendations for the detection and diagnosis of Niemann-Pick disease type C: An update

Genetic Variants of LDLR and PCSK9 Associated with Variations in Response to Antihypercholesterolemic Effects of Armolipid Plus with Berberine

Relation between Gastrointestinal Adverse Effects in Gaucher Disease Patients and Intestinal Disaccharidases Activity Evaluated by Methane Hydrogen Breath Test

Femoral and Carotid Subclinical Atherosclerosis Association With Risk Factors and Coronary Calcium: The AWHS Study

A Third Major Locus for Autosomal Dominant Hypercholesterolemia Maps to 1p34.1-p32

Expression and purification of recombinant apolipoprotein A-I Zaragoza (L144R) and formation of reconstituted HDL particles

Usefulness of Triglycerides-to–High-Density Lipoprotein Cholesterol Ratio for Predicting the First Coronary Event in Men

Common genetic variants contribute to primary hypertriglyceridemia without differences between familial combined hyperlipidemia and isolated hypertriglyceridemia

The fine line between familial and polygenic hypercholesterolemia

Frequency of Low-Density Lipoprotein Receptor Gene Mutations in Patients With a Clinical Diagnosis of Familial Combined Hyperlipidemia in a Clinical Setting

Suchergebnisse filtern