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...

Therapeutic management and adjustment of long-term treatment

Revue des maladies respiratoires, 2024-09, Vol.41 Suppl 1, p.e35

2024

Volltextzugriff (PDF)

Genetic analysis of osteogenesis imperfecta in a large Brazilian cohort

Bone (New York, N.Y.), 2023-04, Vol.169, p.116683-116683, Article 116683

2023

Volltextzugriff (PDF)

Changes in forced vital capacity over ≤ 13 years among patients with late-onset Pompe disease treated with alglucosidase alfa: new modeling of real-world data from the Pompe Registry

Journal of neurology, 2024-08, Vol.271 (8), p.5433-5446

2024

Volltextzugriff (PDF)

Microdeletion and Microduplication Syndromes

The journal of histochemistry and cytochemistry, 2012-05, Vol.60 (5), p.346-358

2012

Volltextzugriff (PDF)

L’asthme de la femme au fil du temps : l’adolescence

Revue française d'allergologie (2009), 2013-04, Vol.53 (3), p.201-204

2013

Volltextzugriff (PDF)

Recommandations nationales pour la prise en charge du nourrisson dépisté atteint de mucoviscidose. Consensus de la fédération des centres de ressources et de compétences de la mucoviscidose

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2014-06, Vol.21 (6), p.654-662

2014

Volltextzugriff (PDF)

A conceptual framework to develop a patient-reported experience questionnaire on the cystic fibrosis journey in France: the ExPaParM collaborative study

Orphanet journal of rare diseases, 2023-02, Vol.18 (1), p.31-31, Article 31

2023

Volltextzugriff (PDF)

Collaborative research protocol to define patient-reported experience measures of the cystic fibrosis care pathway in France: the ExPaParM study

Orphanet journal of rare diseases, 2022-02, Vol.17 (1), p.73-73, Article 73

2022

Volltextzugriff (PDF)

Ventilator-associated pneumonia due to colistin susceptible-only microorganisms

The European respiratory journal, 2007-08, Vol.30 (2), p.307-313

2007

Volltextzugriff (PDF)

Personal exposure to PM2.5 oxidative potential and its association to birth outcomes

Journal of exposure science & environmental epidemiology, 2023-05, Vol.33 (3), p.416-426

2023

Volltextzugriff (PDF)

Association between household cleaning product profiles evaluated by the Ménag’Score® index and asthma symptoms among women from the SEPAGES cohort

International archives of occupational and environmental health, 2022-10, Vol.95 (8), p.1719-1729

2022

Volltextzugriff (PDF)

Differences in topographic and soil habitat specialization between trees and two understorey plant groups in a Costa Rican lowland rain forest

Journal of tropical ecology, 2016-11, Vol.32 (6), p.482-497

2016

Volltextzugriff (PDF)

Clinical and Molecular Characterization of Osteogenesis Imperfecta Type V

Molecular syndromology, 2015-10, Vol.6 (4), p.164-172

2015

Volltextzugriff (PDF)

Morphology of alpaca (Vicugna pacos) embryos in the first third of pregnancy

Reproduction in domestic animals, 2018-06, Vol.53 (3), p.655-666

2018

Volltextzugriff (PDF)

Prise en charge thérapeutique et adaptation du traitement de fond

Revue des maladies respiratoires, 2024-09, Vol.41, p.e35-e54

2024

Volltextzugriff (PDF)

Dépistage et prise en charge des troubles du métabolisme glucidique chez les patients atteints de mucoviscidose. Étude de pratiques au sein du réseau EMERA

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2009-11, Vol.16 (11), p.1435-1442

2009

Volltextzugriff (PDF)

A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability

Scientific reports, 2018-09, Vol.8 (1), p.13382-8, Article 13382

2018

Volltextzugriff (PDF)

Comment améliorer la transition au sein des CRCM : analyse des besoins des patients et de leurs parents lors de l’arrivée en service adulte

Revue des maladies respiratoires, 2022-02, Vol.39 (2), p.132-139

2022

Volltextzugriff (PDF)

423 Quality improvement program and respiratory function of children

Journal of cystic fibrosis, 2017-06, Vol.16, p.S170-S171

2017

Volltextzugriff (PDF)

Smoothing the transition of adolescents with CF from pediatric to adult care: Pre-transfer needs

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2021-05, Vol.28 (4), p.257-263

2021

Volltextzugriff (PDF)

How can the transition of adolescents from a children's to an adult CF center be improved? Analysis of adolescents' and parents' needs during the post-transfer period

Revue des maladies respiratoires, 2022-02, Vol.39 (2), p.132

2022

Volltextzugriff (PDF)

Novel and Recurrent Mutations in the FGFR3 Gene and Double Heterozygosity Cases in a Cohort of Brazilian Patients with Skeletal Dysplasia

Molecular syndromology, 2018-02, Vol.9 (2), p.92-99

2018

Volltextzugriff (PDF)

High-Resolution Melting Analysis for Rapid Detection of Mutations in Patients with FGFR3 -Related Skeletal Dysplasias

Genetic testing and molecular biomarkers, 2021-10, Vol.25 (10), p.674-682

2021

Volltextzugriff (PDF)

Pneumopathies récidivantes révélant une tumeur carcinoïde bronchique : à propos de deux observations

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2007-08, Vol.14 (8), p.1036-1040

2007

Volltextzugriff (PDF)

Early hematopoietic stem cell transplantation in a patient with severe mucopolysaccharidosis II: A 7 years follow-up

Molecular genetics and metabolism reports, 2017-09, Vol.12 (C), p.62-68

2017

Volltextzugriff (PDF)

1 – 25 von 616

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(521)
Mit Volltextzugriff
(489)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Therapeutic management and adjustment of long-term treatment

Genetic analysis of osteogenesis imperfecta in a large Brazilian cohort

Changes in forced vital capacity over ≤ 13 years among patients with late-onset Pompe disease treated with alglucosidase alfa: new modeling of real-world data from the Pompe Registry

Microdeletion and Microduplication Syndromes

L’asthme de la femme au fil du temps : l’adolescence

Recommandations nationales pour la prise en charge du nourrisson dépisté atteint de mucoviscidose. Consensus de la fédération des centres de ressources et de compétences de la mucoviscidose

A conceptual framework to develop a patient-reported experience questionnaire on the cystic fibrosis journey in France: the ExPaParM collaborative study

Collaborative research protocol to define patient-reported experience measures of the cystic fibrosis care pathway in France: the ExPaParM study

Ventilator-associated pneumonia due to colistin susceptible-only microorganisms

Personal exposure to PM2.5 oxidative potential and its association to birth outcomes

Association between household cleaning product profiles evaluated by the Ménag’Score® index and asthma symptoms among women from the SEPAGES cohort

Differences in topographic and soil habitat specialization between trees and two understorey plant groups in a Costa Rican lowland rain forest

Clinical and Molecular Characterization of Osteogenesis Imperfecta Type V

Morphology of alpaca (Vicugna pacos) embryos in the first third of pregnancy

Prise en charge thérapeutique et adaptation du traitement de fond

Dépistage et prise en charge des troubles du métabolisme glucidique chez les patients atteints de mucoviscidose. Étude de pratiques au sein du réseau EMERA

A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability

Comment améliorer la transition au sein des CRCM : analyse des besoins des patients et de leurs parents lors de l’arrivée en service adulte

423 Quality improvement program and respiratory function of children

Smoothing the transition of adolescents with CF from pediatric to adult care: Pre-transfer needs

How can the transition of adolescents from a children's to an adult CF center be improved? Analysis of adolescents' and parents' needs during the post-transfer period

Novel and Recurrent Mutations in the FGFR3 Gene and Double Heterozygosity Cases in a Cohort of Brazilian Patients with Skeletal Dysplasia

High-Resolution Melting Analysis for Rapid Detection of Mutations in Patients with FGFR3 -Related Skeletal Dysplasias

Pneumopathies récidivantes révélant une tumeur carcinoïde bronchique : à propos de deux observations

Early hematopoietic stem cell transplantation in a patient with severe mucopolysaccharidosis II: A 7 years follow-up

Suchergebnisse filtern