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...

Comment on: Brentuximab vedotin-related neuropathy in a patient with Gilbert syndrome: Do mutations of UGT1A1 gene affect brentuximab toxicity?

Pediatric blood & cancer, 2023-11, Vol.70 (11), p.e30527-e30527

2023

Volltextzugriff (PDF)

KIF6 gene as a pharmacogenetic marker for lipid-lowering effect in statin treatment

PloS one, 2018-10, Vol.13 (10), p.e0205430-e0205430

2018

Volltextzugriff (PDF)

Precipitated sdLDL: An easy method to estimate LDL particle size

Journal of clinical laboratory analysis, 2020-07, Vol.34 (7), p.e23282-n/a

2020

Volltextzugriff (PDF)

ANRIL as a genetic marker for cardiovascular events in renal transplant patients – an observational follow‐up cohort study

Transplant international, 2018-09, Vol.31 (9), p.1018-1027

2018

Volltextzugriff (PDF)

Influence of 6 genetic variants on the efficacy of statins in patients with dyslipidemia

Journal of clinical laboratory analysis, 2018-10, Vol.32 (8), p.e22566-n/a

2018

Volltextzugriff (PDF)

Genetic contribution to lipid target achievement with statin therapy: a prospective study

The pharmacogenomics journal, 2020-06, Vol.20 (3), p.494-504

2020

Volltextzugriff (PDF)

Asymptomatic Carotid Atherosclerosis Cardiovascular Risk Factors and Common Hypertriglyceridemia Genetic Variants in Patients with Systemic Erythematosus Lupus

Journal of clinical medicine, 2021-05, Vol.10 (10), p.2218

2021

Volltextzugriff (PDF)

Intermediate Repeat Expansion in the ATXN2 Gene as a Risk Factor in the ALS and FTD Spanish Population

Biomedicines, 2024-02, Vol.12 (2), p.356

2024

Volltextzugriff (PDF)

Physicochemical Properties of Lipoproteins Assessed by Nuclear Magnetic Resonance as a Predictor of Premature Cardiovascular Disease. PRESARV-SEA Study

Journal of clinical medicine, 2021-03, Vol.10 (7), p.1379

2021

Volltextzugriff (PDF)

Reference values assessment in a Mediterranean population for small dense low-density lipoprotein concentration isolated by an optimized precipitation method

Vascular health and risk management, 2017-01, Vol.13, p.201-207

2017

Volltextzugriff (PDF)

Polygenic Risk of Hypertriglyceridemia Is Modified by BMI

International journal of molecular sciences, 2022-08, Vol.23 (17), p.9837

2022

Volltextzugriff (PDF)

Deciphering complexity: TULP1 variants linked to an atypical retinal dystrophy phenotype

Frontiers in genetics, 2024-02, Vol.15, p.1352063-1352063

2024

Volltextzugriff (PDF)

Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think?

BMC medical genomics, 2023-12, Vol.16 (1), p.312-312, Article 312

2023

Volltextzugriff (PDF)

Implication between Genetic Variants from APOA5 and ZPR1 and NAFLD Severity in Patients with Hypertriglyceridemia

Nutrients, 2021-02, Vol.13 (2), p.552

2021

Volltextzugriff (PDF)

Study of common hypertriglyceridaemia genetic variants and subclinical atherosclerosis in a group of women with SLE and a control group

Lupus science & medicine, 2022-08, Vol.9 (1), p.e000774

2022

Volltextzugriff (PDF)

APOE Variants E2, E3, and E4 Can Be Miscalled By Classical PCR‐RFLP When The Christchurch Variant Is Also Present

Journal of clinical laboratory analysis, 2017-03, Vol.31 (2), p.e22040-n/a

2017

Volltextzugriff (PDF)

Improving Hereditary Hemorrhagic Telangiectasia Molecular Diagnosis: A Referral Center Experience

Genes, 2023-03, Vol.14 (3), p.772

2023

Volltextzugriff (PDF)

Properties and units in the clinical laboratory sciences part XXIV. Properties and units in clinical molecular genetics (technical report 2017)

Clinica chimica acta, 2018-09, Vol.484, p.122-131

2018

Volltextzugriff (PDF)

HLA-B57: 01 genotyping in the prevention of hypersensitivity to abacavir: 5 years of experience

Pharmacogenetics and genomics, 2016-08, Vol.26 (8), p.390-396

2016

Volltextzugriff (PDF)

Properties and units in the clinical laboratory sciences part XXIV. Properties and units in clinical molecular genetics (IUPAC Technical Report)

Pure and applied chemistry, 2018-07, Vol.90 (7), p.1199-1220

2018

Volltextzugriff (PDF)

Meeting report: present state of molecular genetics in clinical laboratories. Report on the VII European Symposium on Clinical Laboratory and In Vitro Diagnostic Industry in Barcelona

Clinical chemistry and laboratory medicine, 2015-02, Vol.53 (2), p.199

2015

Volltextzugriff (PDF)

Disadvantages of using biological variation data for reference change values

Clinical chemistry and laboratory medicine, 2012-05, Vol.50 (5), p.961-961

2012

Volltextzugriff (PDF)

Pneumomediastinum as an Early Manifestation in Birt–Hogg–Dubé Syndrome

Archivos de bronconeumología (English ed.), 2024-10

2024

Volltextzugriff (PDF)

Genetic basis of hypertriglyceridemies

Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis, 2021-05, Vol.33 Suppl 2, p.14

2021

Volltextzugriff (PDF)

Bases genéticas de las hipertrigliceridemias

Clínica e investigación en arteriosclerosis, 2021-05, Vol.33, p.14-19

2021

Volltextzugriff (PDF)

1 – 25 von 42

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(38)
Mit Volltextzugriff
(35)

Publikationsform

Artikel
(42)

Sprache

Englisch
(37)
Spanisch
(6)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Comment on: Brentuximab vedotin-related neuropathy in a patient with Gilbert syndrome: Do mutations of UGT1A1 gene affect brentuximab toxicity?

KIF6 gene as a pharmacogenetic marker for lipid-lowering effect in statin treatment

Precipitated sdLDL: An easy method to estimate LDL particle size

ANRIL as a genetic marker for cardiovascular events in renal transplant patients – an observational follow‐up cohort study

Influence of 6 genetic variants on the efficacy of statins in patients with dyslipidemia

Genetic contribution to lipid target achievement with statin therapy: a prospective study

Asymptomatic Carotid Atherosclerosis Cardiovascular Risk Factors and Common Hypertriglyceridemia Genetic Variants in Patients with Systemic Erythematosus Lupus

Intermediate Repeat Expansion in the ATXN2 Gene as a Risk Factor in the ALS and FTD Spanish Population

Physicochemical Properties of Lipoproteins Assessed by Nuclear Magnetic Resonance as a Predictor of Premature Cardiovascular Disease. PRESARV-SEA Study

Reference values assessment in a Mediterranean population for small dense low-density lipoprotein concentration isolated by an optimized precipitation method

Polygenic Risk of Hypertriglyceridemia Is Modified by BMI

Deciphering complexity: TULP1 variants linked to an atypical retinal dystrophy phenotype

Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think?

Implication between Genetic Variants from APOA5 and ZPR1 and NAFLD Severity in Patients with Hypertriglyceridemia

Study of common hypertriglyceridaemia genetic variants and subclinical atherosclerosis in a group of women with SLE and a control group

APOE Variants E2, E3, and E4 Can Be Miscalled By Classical PCR‐RFLP When The Christchurch Variant Is Also Present

Improving Hereditary Hemorrhagic Telangiectasia Molecular Diagnosis: A Referral Center Experience

Properties and units in the clinical laboratory sciences part XXIV. Properties and units in clinical molecular genetics (technical report 2017)

HLA-B57: 01 genotyping in the prevention of hypersensitivity to abacavir: 5 years of experience

Properties and units in the clinical laboratory sciences part XXIV. Properties and units in clinical molecular genetics (IUPAC Technical Report)

Meeting report: present state of molecular genetics in clinical laboratories. Report on the VII European Symposium on Clinical Laboratory and In Vitro Diagnostic Industry in Barcelona

Disadvantages of using biological variation data for reference change values

Pneumomediastinum as an Early Manifestation in Birt–Hogg–Dubé Syndrome

Genetic basis of hypertriglyceridemies

Bases genéticas de las hipertrigliceridemias

Suchergebnisse filtern