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

Jan Stolk

Showing results (101-110 of 110) with videos related to

Pageof 11
Sort By:
You have reached the last page of results.This site can display upto 110 results.
Cellular and Molecular Life Sciences : CMLS|August 31, 2022
Keratin 8 is a scaffolding and regulatory protein of ERAD complexesIwona Maria Pranke, Benoit Chevalier, Aiswarya Premchandar, et al.
The European Respiratory Journal|January 28, 2012
Randomised controlled trial for emphysema with a selective agonist of the γ-type retinoic acid receptorJan Stolk, Robert A Stockley, Berend C Stoel, et al.
Respiratory Research|December 16, 2022
Clinical and functional characteristics of individuals with alpha-1 antitrypsin deficiency: EARCO international registryMarc Miravitlles, Alice M Turner, María Torres-Duran, et al.
Respiratory Research|February 21, 2023
Correction: Clinical and functional characteristics of individuals with alpha-1 antitrypsin deficiency: EARCO international registryMarc Miravitlles, Alice M Turner, María Torres-Duran, et al.
The European Respiratory Journal|March 30, 2023
Characteristics of individuals with alpha-1 antitrypsin deficiency from Northern and Southern European countries: EARCO international registryMarc Miravitlles, Alice M Turner, María Torres-Duran, et al.
JHEP Reports : Innovation in Hepatology|June 19, 2025
Severe alpha-1 antitrypsin deficiency is associated with a higher risk of complications after first decompensation than other aetiologies of cirrhosisLorenz Balcar, Malin Fromme, Naomi Kappe, et al.
Hepatology (Baltimore, Md.)|March 11, 2026
Original research: Amplification of genetic and metabolic factors in alpha-1 antitrypsin deficiencyChristina Schrader, Malin Fromme, Paul Ellis, et al.
ERJ Open Research|March 11, 2020
Protocol for the EARCO Registry: a pan-European observational study in patients with α<sub>1</sub>-antitrypsin deficiencyTimm Greulich, Alan Altraja, Miriam Barrecheguren, et al.
Gastroenterology|May 24, 2019
Liver Fibrosis and Metabolic Alterations in Adults With alpha-1-antitrypsin Deficiency Caused by the Pi*ZZ MutationKarim Hamesch, Mattias Mandorfer, Vítor M Pereira, et al.
Gastroenterology|October 16, 2024
Longitudinal Evaluation of Individuals With Severe Alpha-1 Antitrypsin Deficiency (Pi∗ZZ Genotype)Malin Fromme, Audrey Payancé, Mattias Mandorfer, et al.
Pageof 11

Showing results (101-110 of 110) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 110 results.
Cellular and Molecular Life Sciences : CMLS|August 31, 2022
Keratin 8 is a scaffolding and regulatory protein of ERAD complexesIwona Maria Pranke, Benoit Chevalier, Aiswarya Premchandar, et al.
The European Respiratory Journal|January 28, 2012
Randomised controlled trial for emphysema with a selective agonist of the γ-type retinoic acid receptorJan Stolk, Robert A Stockley, Berend C Stoel, et al.
Respiratory Research|December 16, 2022
Clinical and functional characteristics of individuals with alpha-1 antitrypsin deficiency: EARCO international registryMarc Miravitlles, Alice M Turner, María Torres-Duran, et al.
Respiratory Research|February 21, 2023
Correction: Clinical and functional characteristics of individuals with alpha-1 antitrypsin deficiency: EARCO international registryMarc Miravitlles, Alice M Turner, María Torres-Duran, et al.
The European Respiratory Journal|March 30, 2023
Characteristics of individuals with alpha-1 antitrypsin deficiency from Northern and Southern European countries: EARCO international registryMarc Miravitlles, Alice M Turner, María Torres-Duran, et al.
JHEP Reports : Innovation in Hepatology|June 19, 2025
Severe alpha-1 antitrypsin deficiency is associated with a higher risk of complications after first decompensation than other aetiologies of cirrhosisLorenz Balcar, Malin Fromme, Naomi Kappe, et al.
Hepatology (Baltimore, Md.)|March 11, 2026
Original research: Amplification of genetic and metabolic factors in alpha-1 antitrypsin deficiencyChristina Schrader, Malin Fromme, Paul Ellis, et al.
ERJ Open Research|March 11, 2020
Protocol for the EARCO Registry: a pan-European observational study in patients with α<sub>1</sub>-antitrypsin deficiencyTimm Greulich, Alan Altraja, Miriam Barrecheguren, et al.
Gastroenterology|May 24, 2019
Liver Fibrosis and Metabolic Alterations in Adults With alpha-1-antitrypsin Deficiency Caused by the Pi*ZZ MutationKarim Hamesch, Mattias Mandorfer, Vítor M Pereira, et al.
Gastroenterology|October 16, 2024
Longitudinal Evaluation of Individuals With Severe Alpha-1 Antitrypsin Deficiency (Pi∗ZZ Genotype)Malin Fromme, Audrey Payancé, Mattias Mandorfer, et al.
Pageof 11