A. Johansen
发表
T. Hansen,
O. Pedersen,
S. Ellard,
2005,
Diabetologia.
S. Kreiborg,
T. Darvann,
N. V. Hermann,
2019,
Clinical dysmorphology.
T. Hansen,
O. Pedersen,
A. Astrup,
2010,
PloS one.
T. Hansen,
O. Pedersen,
T. Jørgensen,
2006,
Diabetes.
T. Hansen,
O. Pedersen,
J. Holst,
2003,
The Journal of clinical endocrinology and metabolism.
T. Hansen,
O. Pedersen,
P. Froguel,
2007,
Human mutation.
T. Hansen,
O. Pedersen,
H. Mortensen,
2005,
The Journal of clinical endocrinology and metabolism.
T. Hansen,
O. Pedersen,
K. Borch-Johnsen,
2004,
Diabetes.
T. Hansen,
O. Pedersen,
K. Borch-Johnsen,
2004
.
T. Hansen,
O. Pedersen,
H. Eiberg,
2002,
The Journal of clinical investigation.
B. Olsen,
H. Mortensen,
N. Birkebaek,
2013,
Diabetologia.
O. Pedersen,
O. Søvik,
T. Hansen,
2005,
Diabetic medicine : a journal of the British Diabetic Association.
D. Maahs,
T. Skrivarhaug,
K. Dahl-Jørgensen,
2018,
Diabetes Care.
D. Maahs,
T. Skrivarhaug,
J. Warner,
2018
.
T. Hansen,
O. Pedersen,
T. Jørgensen,
2004,
Diabetologia.
A. Johansen,
N. Birkebaek,
J. Solvig,
1998,
Diabetic medicine : a journal of the British Diabetic Association.
T. Skrivarhaug,
K. Dahl-Jørgensen,
J. Warner,
2019,
Diabetes Care.
T. Hansen,
O. Pedersen,
F. Pociot,
2006,
Diabetes, obesity & metabolism.
T. Skrivarhaug,
A. Pundziute-Lyckå,
J. Svensson,
2018,
Pediatric diabetes.
T. Skrivarhaug,
N. Birkebaek,
L. Hanberger,
2014,
Journal of diabetes science and technology.
T. Hansen,
O. Pedersen,
H. Eiberg,
2002
.
T. Skrivarhaug,
N. Birkebaek,
J. Svensson,
2017,
BMJ Open Diabetes Research & Care.
Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes
T. Hansen,
O. Pedersen,
A. Hattersley,
2009,
Human Genetics.
C. Pipper,
B. Olsen,
H. Mortensen,
2015,
Acta Diabetologica.
S. Gammeltoft,
S. O’Rahilly,
K. Siddle,
2003,
Endocrinology.