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Clinical Endocrinology
|
November 1, 1992
Thyroid function and thyroid autoimmunity independently modulate serum concentration of soluble interleukin 2 (IL-2) receptor (sIL-2R) in thyroid diseases
S Mariotti, P Caturegli, G Barbesino, et al.
Journal of Endocrinological Investigation
|
March 25, 2010
Patients affected by vitiligo and autoimmune diseases do not show antibodies interfering with the activity of the melanocortin 1 receptor
P Agretti, G De Marco, D Sansone, et al.
Thyroid : Official Journal of the American Thyroid Association
|
November 18, 2000
Sporadic nonautoimmune congenital hyperthyroidism due to a strong activating mutation of the thyrotropin receptor gene
M Tonacchera, P Agretti, V Rosellini, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1996
Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia
M Tonacchera, J Van Sande, F Cetani, et al.
Journal of Endocrinological Investigation
|
June 8, 2024
Thyroid autoimmunity in different phenotypes of polycystic ovary syndrome: a single-center experience
E Benelli, M Marradi, E Sciarroni, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 14, 2000
Activating thyrotropin receptor mutations are present in nonadenomatous hyperfunctioning nodules of toxic or autonomous multinodular goiter
M Tonacchera, P Agretti, L Chiovato, et al.
Acta Medica Austriaca
|
January 1, 1992
Maturation of pituitary-thyroid function in the anencephalic fetus
P Beck-Peccoz, D Cortelazzi, L Persani, et al.
Journal of Endocrinological Investigation
|
April 9, 2013
The W520X mutation in the TSHR gene brings on subclinical hypothyroidism through an haploinsufficiency mechanism
S Moia, M Godi, G E Walker, et al.
Journal of Endocrinological Investigation
|
January 15, 2005
Absence of interference of serum IgGs from patients with breast cancer and thyroid autoimmunity on the function of human iodide symporter gene stably transfected in CHO cells
P Fierabracci, A Pinchera, M Tonacchera, et al.
Journal of Endocrinological Investigation
|
March 24, 2011
Hyperthyroidism and pregnancy. An Italian Thyroid Association (AIT) and Italian Association of Clinical Endocrinologists (AME) joint statement for clinical practice
R Negro, P Beck-Peccoz, L Chiovato, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 82) with videos related to
Sort By:
Page
of 9
Clinical Endocrinology
|
November 1, 1992
Thyroid function and thyroid autoimmunity independently modulate serum concentration of soluble interleukin 2 (IL-2) receptor (sIL-2R) in thyroid diseases
S Mariotti, P Caturegli, G Barbesino, et al.
Journal of Endocrinological Investigation
|
March 25, 2010
Patients affected by vitiligo and autoimmune diseases do not show antibodies interfering with the activity of the melanocortin 1 receptor
P Agretti, G De Marco, D Sansone, et al.
Thyroid : Official Journal of the American Thyroid Association
|
November 18, 2000
Sporadic nonautoimmune congenital hyperthyroidism due to a strong activating mutation of the thyrotropin receptor gene
M Tonacchera, P Agretti, V Rosellini, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1996
Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia
M Tonacchera, J Van Sande, F Cetani, et al.
Journal of Endocrinological Investigation
|
June 8, 2024
Thyroid autoimmunity in different phenotypes of polycystic ovary syndrome: a single-center experience
E Benelli, M Marradi, E Sciarroni, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 14, 2000
Activating thyrotropin receptor mutations are present in nonadenomatous hyperfunctioning nodules of toxic or autonomous multinodular goiter
M Tonacchera, P Agretti, L Chiovato, et al.
Acta Medica Austriaca
|
January 1, 1992
Maturation of pituitary-thyroid function in the anencephalic fetus
P Beck-Peccoz, D Cortelazzi, L Persani, et al.
Journal of Endocrinological Investigation
|
April 9, 2013
The W520X mutation in the TSHR gene brings on subclinical hypothyroidism through an haploinsufficiency mechanism
S Moia, M Godi, G E Walker, et al.
Journal of Endocrinological Investigation
|
January 15, 2005
Absence of interference of serum IgGs from patients with breast cancer and thyroid autoimmunity on the function of human iodide symporter gene stably transfected in CHO cells
P Fierabracci, A Pinchera, M Tonacchera, et al.
Journal of Endocrinological Investigation
|
March 24, 2011
Hyperthyroidism and pregnancy. An Italian Thyroid Association (AIT) and Italian Association of Clinical Endocrinologists (AME) joint statement for clinical practice
R Negro, P Beck-Peccoz, L Chiovato, et al.
Page
of 9