Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Frida Dalin"'
Autor:
Casey J. A. Smith-Anttila, Sophie Bensing, Mohammad Alimohammadi, Frida Dalin, Mikael Oscarson, Ming-Dong Zhang, Jaakko Perheentupa, Eystein S. Husebye, Jan Gustafsson, Peyman Björklund, Anette Fransson, Gunnel Nordmark, Lars Rönnblom, Antonella Meloni, Rodney J. Scott, Tomas Hökfelt, Patricia A. Crock, Olle Kämpe
Publikováno v:
Autoimmunity, Vol 50, Iss 4, Pp 223-231 (2017)
Autoimmune polyendocrine syndrome type 1 (APS1) is a rare monogenic autoimmune disorder caused by mutations in the autoimmune regulator (AIRE) gene. High titer autoantibodies are a characteristic feature of APS1 and are often associated with particul
Externí odkaz:
https://doaj.org/article/d12fd0d765a948b6a07150cf43b52896
Autor:
Jaakko Perheentupa, Sophie Bensing, Mikael Oscarson, Lars Rönnblom, Olle Kämpe, Jan Gustafsson, Antonella Meloni, Anette Fransson, Rodney J. Scott, Ming-Dong Zhang, Eystein S. Husebye, Casey J. A. Smith-Anttila, Peyman Björklund, Mohammad Alimohammadi, Patricia Crock, Frida Dalin, Gunnel Nordmark, Tomas Hökfelt
Publikováno v:
Autoimmunity. 50:223-231
Autoimmune polyendocrine syndrome type 1 (APS1) is a rare monogenic autoimmune disorder caused by mutations in the autoimmune regulator (AIRE) gene. High titer autoantibodies are a characteristic feature of APS1 and are often associated with particul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd619b58b57047a44006ab9d344198cd
https://doi.org/10.1080/08916934.2017.1332183
https://doi.org/10.1080/08916934.2017.1332183
Autor:
Jennifer R. S. Meadows, Karolina Tandre, Argyri Mathioudaki, Frida Dalin, Peter Söderkvist, Olle Kämpe, Olov Ekwall, Nils Landegren, Jakob Skov, Daniel Eriksson, Jessika Nordin, Jeanette Wahlberg, Anna-Lena Hulting, Lina Hultin-Rosenberg, Solbritt Rantapää Dahlqvist, Per Dahlqvist, Åsa Hallgren, Kerstin Lindblad-Toh, Lars Rönnblom, Matteo Bianchi, Göran Andersson, Sophie Bensing, Gerli Pielberg
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
Autoimmune Addisons disease (AAD) is the predominating cause of primary adrenal failure. Despite its high heritability, the rarity of disease has long made candidate-gene studies the only feasible methodology for genetic studies. Here we conducted a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10574b41d13fec44b6afec60138e9155
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-357556
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-357556
Autor:
Matteo Bianchi, Kerstin Lindblad-Toh, Mohammad Alimohammadi, Olle Kämpe, Gerli Pielberg, Eystein S. Husebye, Per Dahlqvist, Jeanette Wahlberg, Anna-Lena Hulting, Åsa Hallgren, Olov Ekwall, Per M. Knappskog, Ola Winqvist, Frida Dalin, Sophie Bensing, Gabriel Nordling Eriksson, Daniel Eriksson, Johan Rönnelid, Nils Landegren, Sergiu-Bogdan Catrina
Context: Autoimmune polyendocrine syndrome type 1 (APS1) is a monogenic disorder that features autoimmune Addison disease as a major component. Although APS1 accounts for only a small fraction of all patients with Addison disease, early identificatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1194332ae3ef441a25c697a52f0e767
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-343355
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-343355
Autor:
Jessika Nordin, Fabiana H. G. Farias, Jeanette Wahlberg, Anna-Lena Hulting, Anna Lobell, Daniel Eriksson, Gerli Pielberg, Argyri Mathioudaki, Andreas Karlsson, Olov Ekwall, Peter Söderkvist, Karolina Tandre, Göran Andersson, Kerstin Lindblad-Toh, Jennifer R. S. Meadows, Lina Hultin-Rosenberg, Lars Rönnblom, Anna Hallgren, Solbritt Rantapää Dahlqvist, Sophie Bensing, Frida Dalin, H. Zetterqvist, Eva Murén, Nils Landegren, Johanna Dahlqvist, Olle Kämpe, Gabriel Nordling Eriksson, Per Dahlqvist, Matteo Bianchi, Kerstin M. Ahlgren
BackgroundAutoimmune disease is one of the leading causes of morbidity and mortality worldwide. In Addisons disease, the adrenal glands are targeted by destructive autoimmunity. Despite being the most common cause of primary adrenal failure, little i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b933ca67585f957255165f15f182fe7
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-127426
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-127426
Autor:
Josefine Palle, Sten Andréasson, Therése Hugosson, Olle Kämpe, Mohammad Alimohammadi, Britt-Marie Frost, Eva Landgren, Åsa Hallgren, Frida Dalin
Publikováno v:
Scandinavian Journal of Immunology. 71:474-548
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7164f636bb805079e9851926529b5420
https://doi.org/10.1111/j.1365-3083.2010.02398.x
https://doi.org/10.1111/j.1365-3083.2010.02398.x
Autor:
Maria Elfving, Anna Lena Hulting, Karel Duchén, Emma Lindskog, Sigridur Bjornsdottir, Stefan Söderberg, Ola Winqvist, Gabriel Nordling Eriksson, Per Dahlqvist, Åsa Hallgren, Sergiu-Bogdan Catrina, Sophie Bensing, Jan Åman, Jeanette Wahlberg, Olov Ekwall, Maria Laudius, Magnus Isaksson, Frida Dalin, Jan Gustafsson, Olle Kämpe, Gennet Gebre-Medhin, Anna Karin Åkerman, Maria Halldin Stenlid, Annika Janson, Berit Kriström, Gudmundur Johannsson, Per Olcén, Johan Rönnelid, Mona Landin-Olsson, Erik Waldenström, Ragnhildur Bergthorsdottir
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. :jc.2016-2522
CONTEXT: Studies on clinical and immunological features of Autoimmune Addison's disease (AAD) are needed to understand the disease burden and increased mortality. OBJECTIVE: To provide upgraded data on autoimmune comorbidities, replacement therapy, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74caadeb727a74ebaf2c71e3e7e588d4
https://doi.org/10.1210/jc.2016-2522
https://doi.org/10.1210/jc.2016-2522
Autor:
Mohammad Alimohammadi, Olle Kämpe, Margaret Moriarty-Kelsey, Megan K. Dishop, Jennifer B. Soep, Jonathan Popler, Frida Dalin, Jennifer M. Barker, Robin R. Deterding
Publikováno v:
Pediatric pulmonology. 47(1)
Autoimmune polyendocrine syndrome type 1 (APS-1), also known as Autoimmune Polyendocrinopathy Candidiasis and Ectodermal Dysplasia (APECD) is a disorder caused by mutations in the autoimmune regulator (AIRE) gene. In some APS-1 patients, significant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42df27d5d7aa1170984bfc4bab8742bf
https://pubmed.ncbi.nlm.nih.gov/21901851
https://pubmed.ncbi.nlm.nih.gov/21901851