Zobrazeno 1 - 10
of 4 358
pro vyhledávání: '"alpha‐1‐antitrypsin"'
Autor:
Vítězslav Jiřík, Ondřej Machaczka, Petra Riedlová, Dagmar Kramná, Grzegorz Siemiatkowski, Leszek Ośródka, Ewa Krajny, Antonín Ambrož, Jan Topinka, Pavel Rössner
Publikováno v:
Environmental Sciences Europe, Vol 36, Iss 1, Pp 1-17 (2024)
Abstract Background Air pollution is associated with adverse health effects, especially on the respiratory and cardiovascular systems, but according to recent research, even in cognitive health, metabolic, and immune systems. The objective was to ana
Externí odkaz:
https://doaj.org/article/6063d8cd4e7a4cbba01bdaa5087a1f28
Autor:
Jeffrey H. Teckman, Paula Buchanan, Keith Steven Blomenkamp, Nina Heyer-Chauhan, Keith Burling, David A. Lomas
Publikováno v:
Gastro Hep Advances, Vol 3, Iss 6, Pp 842-850 (2024)
Background and Aims: Children with alpha-1-antitrypsin deficiency (AATD) exhibit a wide range of liver disease outcomes from portal hypertension and transplant to asymptomatic without fibrosis. Individual outcomes cannot be predicted. Liver injury in
Externí odkaz:
https://doaj.org/article/260a905276dd4f2daf38a50bb0057f12
Autor:
Daniela Zöller, Christian Haverkamp, Adeline Makoudjou, Ghislain Sofack, Saskia Kiefer, Denis Gebele, Michelle Pfaffenlehner, Martin Boeker, Harald Binder, Kapil Karki, Christian Seidemann, Bernd Schmeck, Timm Greulich, Harald Renz, Stefanie Schild, Susanne A. Seuchter, Dativa Tibyampansha, Roland Buhl, Gernot Rohde, Franziska C. Trudzinski, Robert Bals, Sabina Janciauskiene, Daiana Stolz, Sebastian Fähndrich
Publikováno v:
Respiratory Research, Vol 25, Iss 1, Pp 1-10 (2024)
Abstract Background Chronic obstructive pulmonary disease (COPD) is an inflammatory multisystemic disease caused by environmental exposures and/or genetic factors. Inherited alpha-1-antitrypsin deficiency (AATD) is one of the best recognized genetic
Externí odkaz:
https://doaj.org/article/3f847567425d47e5befc939a121eab8a
Autor:
Amy Dickinson, Sakari Joenväärä, Tiialotta Tohmola, Jutta Renkonen, Petri Mattila, Timo Carpén, Antti Mäkitie, Suvi Silén
Publikováno v:
FASEB BioAdvances, Vol 6, Iss 1, Pp 26-39 (2024)
Abstract Protein glycosylation responds sensitively to disease states. It is implicated in every hallmark of cancer and has recently started to be considered as a hallmark itself. Changes in N‐glycosylation microheterogeneity are more dramatic than
Externí odkaz:
https://doaj.org/article/5535a1baeeaa44a4891f6896541cdc82
Publikováno v:
Children, Vol 11, Iss 6, p 694 (2024)
Objectives: This study aimed to analyse the clinical course of 45 children with severe alpha-1-antitrypsin deficiency (AATD) registered in our clinic to detect possible predictors of poor outcomes. Methods: The clinical and biological data of 45 pati
Externí odkaz:
https://doaj.org/article/31bda375f01d4d91b58063dbf51c4ba6
Autor:
Tobias Meischl, Karin Schmid-Scherzer, Florian Vafai-Tabrizi, Gert Wurzinger, Eva Traunmüller-Wurm, Kristina Kutics, Markus Rauter, Fikreta Grabcanovic-Musija, Simona Müller, Norbert Kaufmann, Judith Löffler-Ragg, Arschang Valipour, Georg-Christian Funk
Publikováno v:
Respiratory Research, Vol 24, Iss 1, Pp 1-12 (2023)
Abstract Background Alpha-1-antitrypsin (AAT) deficiency (AATD) is a genetic disorder that can manifest as lung disease. A delay between onset of symptoms and diagnosis of AATD is common and associated with worse clinical status and more advanced dis
Externí odkaz:
https://doaj.org/article/f62071369b1843859c1a7e78dac7599c
Autor:
Nygren D, Mölstad U, Thulesius H, Hillman M, Broman LM, Tanash H, Landin-Olsson M, Rasmussen M, Thunander M
Publikováno v:
International Journal of General Medicine, Vol Volume 15, Pp 5843-5848 (2022)
David Nygren,1 Ulrica Mölstad,2 Hans Thulesius,2– 4 Magnus Hillman,5,6 Lars Mikael Broman,7,8 Hanan Tanash,9,10 Mona Landin-Olsson,5,6 Magnus Rasmussen,1 Maria Thunander2,6,11 1Division of Infection Medicine, Department of Clinical Sciences, Lund
Externí odkaz:
https://doaj.org/article/fd0a56bd59854680a5ced2ec0d6d9985
Akademický článek
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Autor:
Myriam Calle Rubio, José Luis López-Campos, Marc Miravitlles, Francisco Javier Michel de la Rosa, José María Hernández Pérez, Carmen Montero Martínez, José Bruno Montoro Ronsano, Francisco Casas Maldonado, Juan Luis Rodríguez Hermosa, Eva María Tabernero Huguet, José Manuel Martínez Sesmero, Carlos Martínez Rivera, Francisco Javier Callejas González, María Torres Durán
Publikováno v:
BMC Health Services Research, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background Patients with alpha-1 antitrypsin deficiency (AATD), commonly categorized as a rare disease, have been affected by the changes in healthcare management brought about by COVID-19. This study’s aim was to identify the changes that
Externí odkaz:
https://doaj.org/article/429bc7d19eca4b2496fe4ad37649380f
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.