Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Lutz Naehrlich

Showing results (41-50 of 81) with videos related to

Pageof 9
Sort By:
Pediatric Radiology|November 30, 2012
A pilot study of the characterization of hepatic tissue strain in children with cystic-fibrosis-associated liver disease (CFLD) by acoustic radiation force impulse imagingChristopher B Behrens, Juliane H Langholz, Jessika Eiler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2015
Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) geneAnnie Dupuis, Katherine Keenan, Chee Y Ooi, et al.
Respiration; International Review of Thoracic Diseases|April 16, 2023
Survival-Adjusted FEV1 and BMI Percentiles for Patients with Cystic Fibrosis before the Era of Triple CFTR Modulator Therapy in GermanyA Susanne Dittrich, Markus Dumke, Ferdinand Kapl, et al.
Plos One|December 11, 2013
Diabetes in cystic fibrosis: multicenter screening results based on current guidelinesNicole Scheuing, Reinhard W Holl, Gerd Dockter, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 13, 2025
The novel CFAbd-Score.kid<sup>Ⓒ</sup> reveals a significant decline of abdominal symptoms in children with Cystic fibrosis aged 6 through 11 years on Elexacaftor/Tezacaftor/Ivacaftor - first resultsJochen G Mainz, Pauline Sadrieh, Lilith Bechinger, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 14, 2024
Assessment of risk factors for adverse events in analgosedation for pediatric endoscopy: A 10-year retrospective analysisEmmanuel Schneck, Fabienne Knittel, Melanie Markmann, et al.
The European Respiratory Journal|March 8, 2021
Survival estimates in European cystic fibrosis patients and the impact of socioeconomic factors: a retrospective registry cohort studyEdward F McKone, Cono Ariti, Abaigeal Jackson, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 12, 2013
Nasal potential difference measurements in diagnosis of cystic fibrosis: an international surveyLutz Naehrlich, Manfred Ballmann, Jane Davies, et al.
Plos One|November 14, 2014
High variability in oral glucose tolerance among 1,128 patients with cystic fibrosis: a multicenter screening studyNicole Scheuing, Reinhard W Holl, Gerd Dockter, et al.
Orphanet Journal of Rare Diseases|March 28, 2018
Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhoodMeike Hengst, Lutz Naehrlich, Poornima Mahavadi, et al.
Pageof 9

Showing results (41-50 of 81) with videos related to

Sort By:
Pageof 9
Pediatric Radiology|November 30, 2012
A pilot study of the characterization of hepatic tissue strain in children with cystic-fibrosis-associated liver disease (CFLD) by acoustic radiation force impulse imagingChristopher B Behrens, Juliane H Langholz, Jessika Eiler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2015
Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) geneAnnie Dupuis, Katherine Keenan, Chee Y Ooi, et al.
Respiration; International Review of Thoracic Diseases|April 16, 2023
Survival-Adjusted FEV1 and BMI Percentiles for Patients with Cystic Fibrosis before the Era of Triple CFTR Modulator Therapy in GermanyA Susanne Dittrich, Markus Dumke, Ferdinand Kapl, et al.
Plos One|December 11, 2013
Diabetes in cystic fibrosis: multicenter screening results based on current guidelinesNicole Scheuing, Reinhard W Holl, Gerd Dockter, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 13, 2025
The novel CFAbd-Score.kid<sup>Ⓒ</sup> reveals a significant decline of abdominal symptoms in children with Cystic fibrosis aged 6 through 11 years on Elexacaftor/Tezacaftor/Ivacaftor - first resultsJochen G Mainz, Pauline Sadrieh, Lilith Bechinger, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 14, 2024
Assessment of risk factors for adverse events in analgosedation for pediatric endoscopy: A 10-year retrospective analysisEmmanuel Schneck, Fabienne Knittel, Melanie Markmann, et al.
The European Respiratory Journal|March 8, 2021
Survival estimates in European cystic fibrosis patients and the impact of socioeconomic factors: a retrospective registry cohort studyEdward F McKone, Cono Ariti, Abaigeal Jackson, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 12, 2013
Nasal potential difference measurements in diagnosis of cystic fibrosis: an international surveyLutz Naehrlich, Manfred Ballmann, Jane Davies, et al.
Plos One|November 14, 2014
High variability in oral glucose tolerance among 1,128 patients with cystic fibrosis: a multicenter screening studyNicole Scheuing, Reinhard W Holl, Gerd Dockter, et al.
Orphanet Journal of Rare Diseases|March 28, 2018
Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhoodMeike Hengst, Lutz Naehrlich, Poornima Mahavadi, et al.
Pageof 9