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...

Efficacy of a novel antimicrobial solution (Prontoderm) in decolonising MRSA nasal carriage

The Journal of hospital infection, 2010-03, Vol.74 (3), p.290-291

Madeo, M

2010

Volltextzugriff (PDF)

Product evaluation of a new chlorhexidine gluconate transparent intravenous line dressing

The Journal of hospital infection, 2010-06, Vol.75 (2), p.143-144

2010

Volltextzugriff (PDF)

Infection thesis as explanation of the higher incidence of myocardial infarction in males

Deutsche medizinische Wochenschrift, 2000-09, Vol.125 (37), p.1095-1097

2000

Volltextzugriff (PDF)

Understanding the MRSA experience

Nursing times (1987), 2001-07, Vol.97 (30), p.36-37

Madeo, M

2001

Volltextzugriff (PDF)

A randomized trial comparing Arglaes (a transparent dressing containing silver ions) to Tegaderm (a transparent polyurethane dressing) for dressing peripheral arterial catheters and central vascular catheters

Intensive & critical care nursing, 1998-08, Vol.14 (4), p.187-191

1998

Volltextzugriff (PDF)

A randomized study comparing IV 3000 (transparent polyurethane dressing) to a dry gauze dressing for peripheral intravenous catheter sites

Journal of intravenous nursing, 1997-09, Vol.20 (5), p.253-256

1997

Volltextzugriff (PDF)

Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes

Journal of medical genetics, 2011-11, Vol.48 (11), p.767-775

2011

Volltextzugriff (PDF)

Cancer exosomes induce tumor innervation

Nature communications, 2018-10, Vol.9 (1), p.4284-15, Article 4284

2018

Volltextzugriff (PDF)

Metabolic effects of fasting on human and mouse blood in vivo

Autophagy, 2017-03, Vol.13 (3), p.567-578

2017

Volltextzugriff (PDF)

Modification of Human Hearing Loss by Plasma-Membrane Calcium Pump PMCA2

The New England journal of medicine, 2005-04, Vol.352 (15), p.1557-1564

2005

Volltextzugriff (PDF)

Cardioprotection and lifespan extension by the natural polyamine spermidine

Nature Medicine, 2016-12, Vol.22 (12), p.1428-1438

2016

Volltextzugriff (PDF)

Isolated erythrocytosis: study of 67 patients and identification of three novel germ-line mutations in the prolyl hydroxylase domain protein 2 (PHD2) gene

Haematologica (Roma), 2012-01, Vol.97 (1), p.123-127

2012

Volltextzugriff (PDF)

Prevalence of mental disorders and psychological trauma among conflict- affected population in Somalia: a cross-sectional study

Frontiers in public health, 2023-09, Vol.11, p.1219992-1219992

2023

Volltextzugriff (PDF)

The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases

Genetics in medicine, 2012, Vol.14 (1), p.51-59

2012

Volltextzugriff (PDF)

Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28

Human molecular genetics, 2002-11, Vol.11 (23), p.2877-2885

2002

Volltextzugriff (PDF)

Effects of Undergoing Multiplex Genetic Susceptibility Testing on Parent Attitudes towards Testing Their Children

Annals of behavioral medicine, 2014-06, Vol.47 (3), p.388-394

2014

Volltextzugriff (PDF)

Very high prevalence of ultrasound thyroid scan abnormalities in healthy volunteers in Modena, Italy

Journal of endocrinological investigation, 2013-10, Vol.36 (9), p.722-728

2013

Volltextzugriff (PDF)

The diagnostic value of calcitonin measurement in wash-out fluid from fine-needle aspiration of thyroid nodules in the diagnosis of medullary thyroid cancer

Endocrine practice, 2013-09, Vol.19 (5), p.769-779

2013

Volltextzugriff (PDF)

A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1

Clinical genetics, 2008-04, Vol.73 (4), p.367-372

2008

Volltextzugriff (PDF)

Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain

American journal of medical genetics. Part A, 2007-07, Vol.143A (14), p.1592-1598

2007

Volltextzugriff (PDF)

Intraindividual consistency of the activated protein C resistance phenotype

British journal of haematology, 2004-08, Vol.126 (3), p.405-409

2004

Volltextzugriff (PDF)

Phenotypic APC resistance in carriers of the A20210 prothrombin mutation is associated with an increased risk of venous thrombosis

Thrombosis and haemostasis, 2001-09, Vol.86 (3), p.804-808

2001

Volltextzugriff (PDF)

The Effects of Citalopram and Fluoxetine on Sexual Behavior in Healthy Men: Evidence of Delayed Ejaculation and Unaffected Sexual Desire. A Randomized, Placebo‐Controlled, Double‐Blind, Double‐Dummy, Parallel Group Study

Journal of sexual medicine, 2008-10, Vol.5 (10), p.2431-2441

2008

Volltextzugriff (PDF)

1 – 25 von 31

Suche als RSS-Feed

Aktive Filter

ThemaAdult

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(28)
Mit Volltextzugriff
(26)

Publikationsform

Artikel
(30)
magazinearticle
(1)

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(31)
Male
(30)
Female
(25)
Middle Aged
(24)
Science & Technology
(22)
Life Sciences & Biomedicine
(21)
Aged
(16)
Adolescent
(9)
Aged, 80 And Over
(9)
Biological And Medical Sciences
(9)
Medical Sciences
(9)
Phenotype
(6)
Prospective Studies
(6)
Animals
(5)
Child
(5)
Endocrinology & Metabolism
(5)
Pedigree
(5)
Fundamental And Applied Biological Sciences. Psychology
(4)
Genetics & Heredity
(4)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Efficacy of a novel antimicrobial solution (Prontoderm) in decolonising MRSA nasal carriage

Product evaluation of a new chlorhexidine gluconate transparent intravenous line dressing

Infection thesis as explanation of the higher incidence of myocardial infarction in males

Understanding the MRSA experience

A randomized trial comparing Arglaes (a transparent dressing containing silver ions) to Tegaderm (a transparent polyurethane dressing) for dressing peripheral arterial catheters and central vascular catheters

A randomized study comparing IV 3000 (transparent polyurethane dressing) to a dry gauze dressing for peripheral intravenous catheter sites

Alternate Day Fasting Improves Physiological and Molecular Markers of Aging in Healthy, Non-obese Humans

Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes

Cancer exosomes induce tumor innervation

Metabolic effects of fasting on human and mouse blood in vivo

Modification of Human Hearing Loss by Plasma-Membrane Calcium Pump PMCA2

Cardioprotection and lifespan extension by the natural polyamine spermidine

Isolated erythrocytosis: study of 67 patients and identification of three novel germ-line mutations in the prolyl hydroxylase domain protein 2 (PHD2) gene

Glucose Metabolism and Metabolomic Changes in Response to Prolonged Fasting in Individuals with Obesity, Type 2 Diabetes and Non-Obese People-A Cohort Trial

Prevalence of mental disorders and psychological trauma among conflict- affected population in Somalia: a cross-sectional study

The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases

Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28

Effects of Undergoing Multiplex Genetic Susceptibility Testing on Parent Attitudes towards Testing Their Children

Very high prevalence of ultrasound thyroid scan abnormalities in healthy volunteers in Modena, Italy

The diagnostic value of calcitonin measurement in wash-out fluid from fine-needle aspiration of thyroid nodules in the diagnosis of medullary thyroid cancer

A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1

Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain

Intraindividual consistency of the activated protein C resistance phenotype

Phenotypic APC resistance in carriers of the A20210 prothrombin mutation is associated with an increased risk of venous thrombosis

The Effects of Citalopram and Fluoxetine on Sexual Behavior in Healthy Men: Evidence of Delayed Ejaculation and Unaffected Sexual Desire. A Randomized, Placebo‐Controlled, Double‐Blind, Double‐Dummy, Parallel Group Study

Aktive Filter

Suchergebnisse filtern