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...

Cystic Fibrosis Mortality in Childhood. Data from European Cystic Fibrosis Society Patient Registry

International journal of environmental research and public health, 2018-09, Vol.15 (9), p.2020

2018

Volltextzugriff (PDF)

Perinatal outcomes in women with cystic fibrosis: Data from the Italian Cystic Fibrosis Registry

Acta obstetricia et gynecologica Scandinavica, 2021-08, Vol.100 (8), p.1439-1444

2021

Volltextzugriff (PDF)

Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review

Frontiers in pediatrics, 2022-08, Vol.10, p.958658-958658

2022

Volltextzugriff (PDF)

Virtual Drug Repositioning as a Tool to Identify Natural Small Molecules That Synergize with Lumacaftor in F508del-CFTR Binding and Rescuing

International journal of molecular sciences, 2022-10, Vol.23 (20), p.12274

2022

Volltextzugriff (PDF)

Trans-heterozygosity for mutations enhances the risk of recurrent/chronic pancreatitis in patients with Cystic Fibrosis

Molecular medicine (Cambridge, Mass.), 2018-07, Vol.24 (1), p.38-38, Article 38

2018

Volltextzugriff (PDF)

A Multicentre Italian Study on the Psychological Impact of an Inconclusive Cystic Fibrosis Diagnosis after Positive Neonatal Screening

Children (Basel), 2023-01, Vol.10 (2), p.177

2023

Volltextzugriff (PDF)

Clinical expression of cystic fibrosis in a large cohort of Italian siblings

BMC pulmonary medicine, 2018-12, Vol.18 (1), p.196-196, Article 196

2018

Volltextzugriff (PDF)

Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease

Clinical immunology (Orlando, Fla.), 2016-03, Vol.164, p.1-9

2016

Volltextzugriff (PDF)

The Diagnosis of Cystic Fibrosis in Adult Age. Data from the Italian Registry

Diagnostics (Basel), 2021-02, Vol.11 (2), p.321

2021

Volltextzugriff (PDF)

The Italian external quality assessment program for Cystic Fibrosis sweat chloride test: CFTR modulators and the impact of a new sweat test report form

Practical laboratory medicine, 2024-05, Vol.40, p.e00403, Article e00403

2024

Volltextzugriff (PDF)

CRMS/CFSPID Subjects Carrying D1152H CFTR Variant: Can the Second Variant Be a Predictor of Disease Development?

Diagnostics (Basel), 2020-12, Vol.10 (12), p.1080

2020

Volltextzugriff (PDF)

Infants with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis and acute recurrent pancreatitis: what definition?

Journal of medical screening, 2022-03, Vol.29 (1), p.64-65

2022

Volltextzugriff (PDF)

Macro- and microvascular functions in cystic fibrosis adults without cardiovascular risk factors: A case-control study

Monaldi archives for chest disease, 2019-05, Vol.89 (2)

2019

Volltextzugriff (PDF)

Case Report: Analysis of Inflammatory Cytokines IL-6, CCL2/MCP1, CCL5/RANTES, CXCL9/MIG, and CXCL10/IP10 in a Cystic Fibrosis Patient Cohort During the First Wave of the COVID-19 Pandemic

Frontiers in pediatrics, 2021-07, Vol.9

2021

Volltextzugriff (PDF)

A conservative treatment for plastic bronchitis in pediatric age

American journal of otolaryngology, 2014-03, Vol.35 (2), p.204-206

2014

Volltextzugriff (PDF)

Asymptomatic case of Covid-19 in an infant with cystic fibrosis

Journal of cystic fibrosis, 2020-05, Vol.19 (3), p.e18-e18

2020

Volltextzugriff (PDF)

Risk factors for adverse outcome in infancy in meconium ileus cystic fibrosis infants: A multicentre Italian study

Journal of cystic fibrosis, 2019-11, Vol.18 (6), p.863-868

2019

Volltextzugriff (PDF)

Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease

Data in brief, 2016-06, Vol.7, p.311-315

2016

Volltextzugriff (PDF)

Biochemical and genetic tools to predict the progression to Cystic Fibrosis in CRMS/CFSPID subjects: A systematic review

Paediatric respiratory reviews, 2024-09, Vol.51, p.46-55

2024

Volltextzugriff (PDF)

No gender differences in growth patterns in a cohort of children with cystic fibrosis born between 1986 and 1995

Clinical nutrition (Edinburgh, Scotland), 2019-08, Vol.38 (4), p.1782-1787

2019

Volltextzugriff (PDF)

Should isolated Pseudo‐Bartter syndrome be considered a CFTR‐related disorder of infancy?

Pediatric pulmonology, 2019-10, Vol.54 (10), p.1578-1583

2019

Volltextzugriff (PDF)

Outcomes of early repeat sweat testing in infants with cystic fibrosis transmembrane conductance regulator‐related metabolic syndrome/CF screen‐positive, inconclusive diagnosis

Pediatric pulmonology, 2021-12, Vol.56 (12), p.3785-3791

2021

Volltextzugriff (PDF)

Patients with cystic fibrosis having a residual function mutation: Data from the Italian registry

Pediatric pulmonology, 2019-02, Vol.54 (2), p.150-157

2019

Volltextzugriff (PDF)

Changing epidemiology of the respiratory bacteriology of patients with cystic fibrosis–data from the European cystic fibrosis society patient registry

Journal of cystic fibrosis, 2020-05, Vol.19 (3), p.376-383

2020

Volltextzugriff (PDF)

Transitory pancreatic insufficiency in cystic fibrosis children

Journal of cystic fibrosis, 2020-01, Vol.19 (1), p.e5-e6

2020

Volltextzugriff (PDF)

1 – 25 von 112

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(105)
Mit Volltextzugriff
(100)

Publikationsform

Artikel
(108)
Berichte
(4)

Sprache

Englisch
(108)
Italienisch
(4)

Erscheinungsjahr

n.n

Thema

Science & Technology
(91)
Life Sciences & Biomedicine
(90)
Humans
(69)
Cystic Fibrosis
(66)
Male
(49)
Female
(40)
Respiratory System
(38)
Child
(36)
Adolescent
(26)
Child, Preschool
(26)
Cystic Fibrosis - Genetics
(26)
Adult
(25)
Infant
(25)
Pediatrics
(25)
Cystic Fibrosis Transmembrane Conductance Regulator - Genetics
(24)
Mutation
(19)
Cystic Fibrosis - Complications
(15)
Infant, Newborn
(15)
Cystic Fibrosis - Epidemiology
(13)
Cystic Fibrosis - Diagnosis
(12)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Cystic Fibrosis Mortality in Childhood. Data from European Cystic Fibrosis Society Patient Registry

Perinatal outcomes in women with cystic fibrosis: Data from the Italian Cystic Fibrosis Registry

Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review

Virtual Drug Repositioning as a Tool to Identify Natural Small Molecules That Synergize with Lumacaftor in F508del-CFTR Binding and Rescuing

Trans-heterozygosity for mutations enhances the risk of recurrent/chronic pancreatitis in patients with Cystic Fibrosis

A Multicentre Italian Study on the Psychological Impact of an Inconclusive Cystic Fibrosis Diagnosis after Positive Neonatal Screening

Clinical expression of cystic fibrosis in a large cohort of Italian siblings

Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease

The Diagnosis of Cystic Fibrosis in Adult Age. Data from the Italian Registry

The Italian external quality assessment program for Cystic Fibrosis sweat chloride test: CFTR modulators and the impact of a new sweat test report form

CRMS/CFSPID Subjects Carrying D1152H CFTR Variant: Can the Second Variant Be a Predictor of Disease Development?

Infants with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis and acute recurrent pancreatitis: what definition?

Macro- and microvascular functions in cystic fibrosis adults without cardiovascular risk factors: A case-control study

Case Report: Analysis of Inflammatory Cytokines IL-6, CCL2/MCP1, CCL5/RANTES, CXCL9/MIG, and CXCL10/IP10 in a Cystic Fibrosis Patient Cohort During the First Wave of the COVID-19 Pandemic

A conservative treatment for plastic bronchitis in pediatric age

Asymptomatic case of Covid-19 in an infant with cystic fibrosis

Risk factors for adverse outcome in infancy in meconium ileus cystic fibrosis infants: A multicentre Italian study

Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease

Biochemical and genetic tools to predict the progression to Cystic Fibrosis in CRMS/CFSPID subjects: A systematic review

No gender differences in growth patterns in a cohort of children with cystic fibrosis born between 1986 and 1995

Should isolated Pseudo‐Bartter syndrome be considered a CFTR‐related disorder of infancy?

Outcomes of early repeat sweat testing in infants with cystic fibrosis transmembrane conductance regulator‐related metabolic syndrome/CF screen‐positive, inconclusive diagnosis

Patients with cystic fibrosis having a residual function mutation: Data from the Italian registry

Changing epidemiology of the respiratory bacteriology of patients with cystic fibrosis–data from the European cystic fibrosis society patient registry

Transitory pancreatic insufficiency in cystic fibrosis children

Suchergebnisse filtern