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International Journal of Obesity (2005)
|
July 26, 2012
The soluble form of the receptor of advanced glycation endproducts increases after bariatric surgery in morbid obesity
J M Brix, F Höllerl, H-P Kopp, et al.
Molecular Genetics and Metabolism
|
May 18, 1999
A novel mutation (R97C) in the neurophysin moiety of prepro-vasopressin-neurophysin II associated with autosomal-dominant neurohypophyseal diabetes insipidus
J Rutishauser, P Kopp, M B Gaskill, et al.
Molecular Genetics and Metabolism
|
May 18, 1999
Combined pituitary hormone deficiency in an inbred Brazilian kindred associated with a mutation in the PROP-1 gene
C R Nogueira, L Sabacan, J L Jameson, et al.
European Journal of Endocrinology
|
October 3, 2001
Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II)
C E Flück, J Deladoëy, S Nayak, et al.
Endocrinology
|
June 1, 1996
Sexually dimorphic transcriptional responses to gonadotropin-releasing hormone require chronic in vivo exposure to estradiol
I M Colin, A C Bauer-Dantoin, S Sundaresan, et al.
European Journal of Clinical Investigation
|
May 11, 2006
Soluble CD40L in patients with morbid obesity: significant reduction after bariatric surgery
G-H Schernthaner, H-P Kopp, K Krzyzanowska, et al.
Journal of Neurochemistry
|
February 1, 1994
Age-associated changes of rat brain neuronal and astroglial poly(ADP-ribose) polymerase activity
M Messripour, D Weltin, A Rastegar, et al.
The Journal of Clinical Investigation
|
September 18, 1997
Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor
P Kopp, S Muirhead, N Jourdain, et al.
Molecular Genetics and Metabolism
|
October 27, 1998
A novel aminoterminal mutation in the KAL-1 gene in a large pedigree with X-linked Kallmann syndrome
W X Gu, J S Colquhoun-Kerr, P Kopp, et al.
International Journal of Obesity (2005)
|
May 27, 2005
Effects of marked weight loss on plasma levels of adiponectin, markers of chronic subclinical inflammation and insulin resistance in morbidly obese women
H-P Kopp, K Krzyzanowska, M Möhlig, et al.
Page
of 22
Search research articles
Search
Showing results (131-140 of 214) with videos related to
Sort By:
Page
of 22
International Journal of Obesity (2005)
|
July 26, 2012
The soluble form of the receptor of advanced glycation endproducts increases after bariatric surgery in morbid obesity
J M Brix, F Höllerl, H-P Kopp, et al.
Molecular Genetics and Metabolism
|
May 18, 1999
A novel mutation (R97C) in the neurophysin moiety of prepro-vasopressin-neurophysin II associated with autosomal-dominant neurohypophyseal diabetes insipidus
J Rutishauser, P Kopp, M B Gaskill, et al.
Molecular Genetics and Metabolism
|
May 18, 1999
Combined pituitary hormone deficiency in an inbred Brazilian kindred associated with a mutation in the PROP-1 gene
C R Nogueira, L Sabacan, J L Jameson, et al.
European Journal of Endocrinology
|
October 3, 2001
Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II)
C E Flück, J Deladoëy, S Nayak, et al.
Endocrinology
|
June 1, 1996
Sexually dimorphic transcriptional responses to gonadotropin-releasing hormone require chronic in vivo exposure to estradiol
I M Colin, A C Bauer-Dantoin, S Sundaresan, et al.
European Journal of Clinical Investigation
|
May 11, 2006
Soluble CD40L in patients with morbid obesity: significant reduction after bariatric surgery
G-H Schernthaner, H-P Kopp, K Krzyzanowska, et al.
Journal of Neurochemistry
|
February 1, 1994
Age-associated changes of rat brain neuronal and astroglial poly(ADP-ribose) polymerase activity
M Messripour, D Weltin, A Rastegar, et al.
The Journal of Clinical Investigation
|
September 18, 1997
Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor
P Kopp, S Muirhead, N Jourdain, et al.
Molecular Genetics and Metabolism
|
October 27, 1998
A novel aminoterminal mutation in the KAL-1 gene in a large pedigree with X-linked Kallmann syndrome
W X Gu, J S Colquhoun-Kerr, P Kopp, et al.
International Journal of Obesity (2005)
|
May 27, 2005
Effects of marked weight loss on plasma levels of adiponectin, markers of chronic subclinical inflammation and insulin resistance in morbidly obese women
H-P Kopp, K Krzyzanowska, M Möhlig, et al.
Page
of 22