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Cellular and Molecular Life Sciences : CMLS
|
August 31, 2022
Keratin 8 is a scaffolding and regulatory protein of ERAD complexes
Iwona 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 receptor
Jan 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 registry
Marc 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 registry
Marc 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 registry
Marc 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 cirrhosis
Lorenz 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 deficiency
Christina 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 deficiency
Timm 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 Mutation
Karim 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.
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Showing results (101-110 of 110) with videos related to
Sort By:
Page
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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 complexes
Iwona 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 receptor
Jan 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 registry
Marc 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 registry
Marc 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 registry
Marc 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 cirrhosis
Lorenz 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 deficiency
Christina 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 deficiency
Timm 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 Mutation
Karim 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.
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of 11