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M Tonacchera

Showing results (51-60 of 82) with videos related to

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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 diseasesS 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 receptorP 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 geneM 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 hyperplasiaM 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 experienceE 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 goiterM Tonacchera, P Agretti, L Chiovato, et al.
Acta Medica Austriaca|January 1, 1992
Maturation of pituitary-thyroid function in the anencephalic fetusP 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 mechanismS 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 cellsP 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 practiceR Negro, P Beck-Peccoz, L Chiovato, et al.
Pageof 9

Showing results (51-60 of 82) with videos related to

Sort By:
Pageof 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 diseasesS 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 receptorP 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 geneM 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 hyperplasiaM 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 experienceE 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 goiterM Tonacchera, P Agretti, L Chiovato, et al.
Acta Medica Austriaca|January 1, 1992
Maturation of pituitary-thyroid function in the anencephalic fetusP 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 mechanismS 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 cellsP 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 practiceR Negro, P Beck-Peccoz, L Chiovato, et al.
Pageof 9