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🐜
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Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry.
13 auth.
Martina M Erichsen,
K. Løvås,
Beate Skinningsrud,
A. Wolff,
D. Undlien,
J. Svartberg,
K. Fougner,
T. J. Berg,
J. Bollerslev,
B. Mella,
...
J. Carlson,
H. Erlich,
E. Husebye
|
8 |
2009 |
8
🐜
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|
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Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases.
33 auth.
B. Oftedal,
Alexander Hellesen,
Alexander Hellesen,
Martina M Erichsen,
E. Bratland,
Ayelet Vardi,
J. Perheentupa,
E. Kemp,
Torunn Fiskerstrand,
Torunn Fiskerstrand,
M. K. Viken,
A. Weetman,
S. Fleishman,
Siddharth Banka,
Siddharth Banka,
...
William G. Newman,
William G. Newman,
W.A.C. Sewell,
L. Sozaeva,
T. Zayats,
K. Haugarvoll,
E. Orlova,
J. Haavik,
Stefan Johansson,
Stefan Johansson,
P. Knappskog,
P. Knappskog,
K. Løvås,
K. Løvås,
A. Wolff,
J. Abramson,
E. Husebye,
E. Husebye
|
7 |
2015 |
7
🐜
|
|
🦁
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Autoimmune polyendocrine syndrome type 1 in Norway: phenotypic variation, autoantibodies, and novel mutations in the autoimmune regulator gene.
10 auth.
A. Wolff,
Martina M Erichsen,
A. Meager,
N. F. Magitta,
A. Myhre,
J. Bollerslev,
...
K. Fougner,
K. Lima,
P. Knappskog,
E. Husebye
|
7 |
2007 |
7
🦁
|
|
🐜
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A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes
21 auth.
N. F. Magitta,
N. F. Magitta,
N. F. Magitta,
A. Wolff,
A. Wolff,
S. Johansson,
S. Johansson,
Beate Skinningsrud,
B. Lie,
K. Myhr,
...
K. Myhr,
D. Undlien,
G. Joner,
P. Njølstad,
P. Njølstad,
T. Kvien,
Ø. Førre,
P. Knappskog,
P. Knappskog,
E. Husebye,
E. Husebye
|
7 |
2009 |
7
🐜
|
|
🐜
|
A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes
21 auth.
N. F. Magitta,
N. F. Magitta,
N. F. Magitta,
A. Wolff,
A. Wolff,
S. Johansson,
S. Johansson,
Beate Skinningsrud,
B. Lie,
K. Myhr,
...
K. Myhr,
D. Undlien,
G. Joner,
P. Njølstad,
P. Njølstad,
T. Kvien,
Ø. Førre,
P. Knappskog,
P. Knappskog,
E. Husebye,
E. Husebye
|
7 |
2009 |
7
🐜
|
|
🐜
|
Glucocorticoid replacement therapy and pharmacogenetics in Addison's disease: effects on bone.
13 auth.
K. Løvås,
C. G. Gjesdal,
M. Christensen,
A. Wolff,
B. Almås,
J. Svartberg,
K. Fougner,
U. Syversen,
J. Bollerslev,
J. Falch,
...
P. Hunt,
V. Chatterjee,
E. Husebye
|
7 |
2009 |
7
🐜
|
|
🐜
|
Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility.
10 auth.
Anna L. Mitchell,
Heather J. Cordell,
Rachel Soemedi,
Kate Owen,
Beate Skinningsrud,
A. Wolff,
...
Martina Ericksen,
Dag E. Undlien,
E. Husebye,
Simon H. S. Pearce
|
7 |
2009 |
7
🐜
|
|
🐜
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Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency.
9 auth.
Beate Skinningsrud,
E. Husebye,
S. Pearce,
D. McDonald,
K. Brandal,
A. Wolff,
...
K. Løvås,
T. Egeland,
D. Undlien
|
6 |
2008 |
6
🐜
|
|
🐜
|
Interferon autoantibodies associated with AIRE deficiency decrease the expression of IFN-stimulated genes
22 auth.
K. Kisand,
Maire Link,
A. Wolff,
A. Meager,
L. Tserel,
Tõnis Org,
A. Murumägi,
R. Uibo,
N. Willcox,
K. Trebušak Podkrajšek,
...
T. Battelino,
A. Lobell,
O. Kämpe,
K. Lima,
A. Meloni,
Berrin Ergun-Longmire,
N. Maclaren,
J. Perheentupa,
K. Krohn,
H. Scott,
E. Husebye,
P. Peterson
|
6 |
2008 |
6
🐜
|
|
🐬
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AIRE-mutations and autoimmune disease.
Øyvind Bruserud,
B. Oftedal,
A. Wolff,
E. Husebye
|
6 |
2016 |
6
🐬
|
