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The Journal of Clinical Endocrinology and Metabolism
|
July 15, 1999
Altered bone mass and turnover in female patients with adrenal incidentaloma: the effect of subclinical hypercortisolism
M Torlontano, I Chiodini, M Pileri, et al.
Diabetologia
|
March 1, 1997
Increased adipose tissue PC-1 protein content, but not tumour necrosis factor-alpha gene expression, is associated with a reduction of both whole body insulin sensitivity and insulin receptor tyrosine-kinase activity
L Frittitta, J F Youngren, P Sbraccia, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
March 31, 2001
A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTC
E Chiefari, R Chiarella, U Crocetti, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
October 24, 2003
Evidence for genetic epistasis in human insulin resistance: the combined effect of PC-1 (K121Q) and PPARgamma2 (P12A) polymorphisms
R Baratta, R Di Paola, D Spampinato, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
November 21, 2002
Insulin modulates PC-1 processing and recruitment in cultured human cells
C Menzaghi, R Di Paola, G Baj, et al.
Metabolism: Clinical and Experimental
|
September 25, 2003
Rats that are made insulin resistant by glucosamine treatment have impaired skeletal muscle insulin receptor phosphorylation
D Spampinato, A Giaccari, V Trischitta, et al.
Clinical Genetics
|
February 17, 2012
MODY type 2 P59S GCK mutant: founder effect in South of Italy
M Delvecchio, O Ludovico, E Bellacchio, et al.
Journal of Endocrinological Investigation
|
February 11, 1999
Efficacy of combined treatments in NIDDM patients with secondary failure to sulphonylureas. Is it predictable?
V Trischitta, S Italia, M Raimondo, et al.
Journal of Internal Medicine
|
September 19, 2009
Circulating high molecular weight adiponectin isoform is heritable and shares a common genetic background with insulin resistance in nondiabetic White Caucasians from Italy: evidence from a family-based study
C Menzaghi, L Salvemini, G Paroni, et al.
American Journal of Human Genetics
|
September 14, 2000
Mapping a dominant form of multinodular goiter to chromosome Xp22
F Capon, A Tacconelli, E Giardina, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 85) with videos related to
Sort By:
Page
of 9
The Journal of Clinical Endocrinology and Metabolism
|
July 15, 1999
Altered bone mass and turnover in female patients with adrenal incidentaloma: the effect of subclinical hypercortisolism
M Torlontano, I Chiodini, M Pileri, et al.
Diabetologia
|
March 1, 1997
Increased adipose tissue PC-1 protein content, but not tumour necrosis factor-alpha gene expression, is associated with a reduction of both whole body insulin sensitivity and insulin receptor tyrosine-kinase activity
L Frittitta, J F Youngren, P Sbraccia, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
March 31, 2001
A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTC
E Chiefari, R Chiarella, U Crocetti, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
October 24, 2003
Evidence for genetic epistasis in human insulin resistance: the combined effect of PC-1 (K121Q) and PPARgamma2 (P12A) polymorphisms
R Baratta, R Di Paola, D Spampinato, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
November 21, 2002
Insulin modulates PC-1 processing and recruitment in cultured human cells
C Menzaghi, R Di Paola, G Baj, et al.
Metabolism: Clinical and Experimental
|
September 25, 2003
Rats that are made insulin resistant by glucosamine treatment have impaired skeletal muscle insulin receptor phosphorylation
D Spampinato, A Giaccari, V Trischitta, et al.
Clinical Genetics
|
February 17, 2012
MODY type 2 P59S GCK mutant: founder effect in South of Italy
M Delvecchio, O Ludovico, E Bellacchio, et al.
Journal of Endocrinological Investigation
|
February 11, 1999
Efficacy of combined treatments in NIDDM patients with secondary failure to sulphonylureas. Is it predictable?
V Trischitta, S Italia, M Raimondo, et al.
Journal of Internal Medicine
|
September 19, 2009
Circulating high molecular weight adiponectin isoform is heritable and shares a common genetic background with insulin resistance in nondiabetic White Caucasians from Italy: evidence from a family-based study
C Menzaghi, L Salvemini, G Paroni, et al.
American Journal of Human Genetics
|
September 14, 2000
Mapping a dominant form of multinodular goiter to chromosome Xp22
F Capon, A Tacconelli, E Giardina, et al.
Page
of 9