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...

Percutaneous treatment of chronic MRSA osteomyelitis with a novel plant-derived antiseptic

BMC surgery, 2001-05, Vol.1 (1), p.1-1, Article 1

2001

Volltextzugriff (PDF)

Topical application of a new formulation of eucalyptus oil phytochemical clears methicillin-resistant Staphylococcus aureus infection

American journal of infection control, 2001-10, Vol.29 (5), p.346-346

2001

Volltextzugriff (PDF)

Lumacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR

The New England journal of medicine, 2015-07, Vol.373 (3), p.220-231

2015

Volltextzugriff (PDF)

The Effect of Synonymous Single-Nucleotide Polymorphisms on an Atypical Cystic Fibrosis Clinical Presentation

Life (Basel, Switzerland), 2020-12, Vol.11 (1), p.14

2020

Volltextzugriff (PDF)

MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia

Nature communications, 2014-07, Vol.5 (1), p.4418-4418, Article 4418

2014

Volltextzugriff (PDF)

Ethnicity impacts the cystic fibrosis diagnosis: A note of caution

Journal of cystic fibrosis, 2017-07, Vol.16 (4), p.488-491

2017

Volltextzugriff (PDF)

Treatment of lung infection in patients with cystic fibrosis: Current and future strategies

Journal of cystic fibrosis, 2012-12, Vol.11 (6), p.461-479

2012

Volltextzugriff (PDF)

Practical and conceptual limitations of tissue Doppler imaging to predict reverse remodelling in cardiac resynchronisation therapy

European journal of heart failure, 2008-03, Vol.10 (3), p.281-290

2008

Volltextzugriff (PDF)

Primary ciliary dyskinesia: critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure

Orphanet journal of rare diseases, 2014-01, Vol.9 (1), p.11-11

2014

Volltextzugriff (PDF)

Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: A European consensus

Journal of cystic fibrosis, 2009-09, Vol.8 (5), p.295-315

2009

Volltextzugriff (PDF)

A randomized double blind, placebo controlled phase 2 trial of BIIL 284 BS (an LTB4 receptor antagonist) for the treatment of lung disease in children and adults with cystic fibrosis

Journal of cystic fibrosis, 2014-03, Vol.13 (2), p.148-155

2014

Volltextzugriff (PDF)

Severity of the S1251N allele in cystic fibrosis is affected by the presence of the F508C variant in cis

Journal of cystic fibrosis, 2022-07, Vol.21 (4), p.644-651

2022

Volltextzugriff (PDF)

Is the sensitivity of primary ciliary dyskinesia detection by ciliary function analysis 100%?

The European respiratory journal, 2013-10, Vol.42 (4), p.1159-1161

2013

Volltextzugriff (PDF)

Standards of care for patients with cystic fibrosis: a European consensus

Journal of cystic fibrosis, 2005-03, Vol.4 (1), p.7-26

2005

Volltextzugriff (PDF)

Is there evidence for correct diagnosis in cystic fibrosis registries?

Journal of cystic fibrosis, 2014-05, Vol.13 (3), p.275-280

2014

Volltextzugriff (PDF)

Mutations of the Cystic Fibrosis Gene and Intermediate Sweat Chloride Levels in Children

American journal of respiratory and critical care medicine, 2002-03, Vol.165 (6), p.757-761

2002

Volltextzugriff (PDF)

Ion channel regulators for the treatment of cystic fibrosis

Therapy, 2011-11, Vol.8 (6), p.661-670

2011

Volltextzugriff (PDF)

Genotype-Phenotype Correlations for the Paranasal Sinuses in Cystic Fibrosis

American journal of respiratory and critical care medicine, 1999-05, Vol.159 (5), p.1412-1416

1999

Volltextzugriff (PDF)

Distribution of human β-defensin polymorphisms in various control and cystic fibrosis populations

Genomics (San Diego, Calif.), 2005-05, Vol.85 (5), p.574-581

2005

Volltextzugriff (PDF)

Berufsbildung und "Green Economy": Ein kooperativer Ansatz für die Weiterbildung von internationalen Berufsbildungsfachkräften im Bereich zukunftsorientierter Wirtschaftsbereiche

Berufsbildung, 2013, Vol.67 (141), p.47-49

2013

Volltextzugriff (PDF)

Role of baseline nodule density and changes in density and nodule features in the discrimination between benign and malignant solid indeterminate pulmonary nodules

European journal of radiology, 2009-06, Vol.70 (3), p.492-498

2009

Volltextzugriff (PDF)

Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes: a large European study

Journal of medical genetics, 2001-11, Vol.38 (11), p.777-783

2001

Volltextzugriff (PDF)

CFTR haplotype backgrounds on normal and mutant CFTR genes

Human molecular genetics, 1994-04, Vol.3 (4), p.607-614

1994

Volltextzugriff (PDF)

1 – 25 von 35

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(31)
Mit Volltextzugriff
(32)

Publikationsform

Artikel
(32)
Reviews
(2)
Bücher
(1)

Sprache

Englisch
(29)
Deutsch
(6)

Erscheinungsjahr

n.n

Thema

Humans
(23)
Science & Technology
(21)
Life Sciences & Biomedicine
(20)
Male
(15)
Cystic Fibrosis - Genetics
(12)
Female
(12)
Cystic Fibrosis
(11)
Mutation
(10)
Adolescent
(9)
Respiratory System
(9)
Adult
(8)
Biological And Medical Sciences
(8)
Cystic Fibrosis Transmembrane Conductance Regulator - Genetics
(7)
Medical Sciences
(7)
Child
(6)
Genetics & Heredity
(6)
Gastroenterology. Liver. Pancreas. Abdomen
(5)
Middle Aged
(5)
Other Diseases. Semiology
(5)
Pulmonary/respiratory
(5)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Percutaneous treatment of chronic MRSA osteomyelitis with a novel plant-derived antiseptic

Topical application of a new formulation of eucalyptus oil phytochemical clears methicillin-resistant Staphylococcus aureus infection

Lumacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR

The Effect of Synonymous Single-Nucleotide Polymorphisms on an Atypical Cystic Fibrosis Clinical Presentation

MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia

Ethnicity impacts the cystic fibrosis diagnosis: A note of caution

Treatment of lung infection in patients with cystic fibrosis: Current and future strategies

Practical and conceptual limitations of tissue Doppler imaging to predict reverse remodelling in cardiac resynchronisation therapy

Primary ciliary dyskinesia: critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure

Inhaled medication and inhalation devices for lung disease in patients with cystic fibrosis: A European consensus

A randomized double blind, placebo controlled phase 2 trial of BIIL 284 BS (an LTB4 receptor antagonist) for the treatment of lung disease in children and adults with cystic fibrosis

Severity of the S1251N allele in cystic fibrosis is affected by the presence of the F508C variant in cis

Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease

Is the sensitivity of primary ciliary dyskinesia detection by ciliary function analysis 100%?

Standards of care for patients with cystic fibrosis: a European consensus

Is there evidence for correct diagnosis in cystic fibrosis registries?

Mutations of the Cystic Fibrosis Gene and Intermediate Sweat Chloride Levels in Children

Ion channel regulators for the treatment of cystic fibrosis

Genotype-Phenotype Correlations for the Paranasal Sinuses in Cystic Fibrosis

Distribution of human β-defensin polymorphisms in various control and cystic fibrosis populations

Berufsbildung und "Green Economy": Ein kooperativer Ansatz für die Weiterbildung von internationalen Berufsbildungsfachkräften im Bereich zukunftsorientierter Wirtschaftsbereiche

Role of baseline nodule density and changes in density and nodule features in the discrimination between benign and malignant solid indeterminate pulmonary nodules

Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes: a large European study

Struktur der schmerzmedizinischen Versorgung in Deutschland: Klassifikation schmerzmedizinischer Einrichtungen: Structure of pain management facilities in Germany: Classification of medical and psychological pain treatment services

CFTR haplotype backgrounds on normal and mutant CFTR genes

Suchergebnisse filtern