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P E Macchia

Showing results (21-30 of 31) with videos related to

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Thyroid : Official Journal of the American Thyroid Association|June 1, 1997
Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesisP Lapi, P E Macchia, L Chiovato, et al.
Journal of Endocrinological Investigation|November 22, 2017
High-resolution melting analysis (HRM) for mutational screening of Dnajc17 gene in patients affected by thyroid dysgenesisI C Nettore, S Desiderio, E De Nisco, et al.
Biosensors & Bioelectronics|April 26, 2023
SERS assisted sandwich immunoassay platforms for ultrasensitive and selective detection of human ThyroglobulinS Spaziani, G Quero, S Managò, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alphaP E Macchia, Y Takeuchi, T Kawai, et al.
Journal of Endocrinological Investigation|June 23, 2009
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesisA M Ferrara, L De Sanctis, G Rossi, et al.
Nature Genetics|August 11, 1998
A mouse model for hereditary thyroid dysgenesis and cleft palateM De Felice, C Ovitt, E Biffali, et al.
The Journal of Clinical Endocrinology and Metabolism|September 29, 2012
Thyroid nodules treated with percutaneous radiofrequency thermal ablation: a comparative studyA Faggiano, V Ramundo, A P Assanti, et al.
Journal of Endocrinological Investigation|November 10, 2010
Screening for mutations in the ISL1 gene in patients with thyroid dysgenesisA M Ferrara, G Rossi, E Zampella, et al.
Development (Cambridge, England)|May 9, 1998
Transient dwarfism and hypogonadism in mice lacking Otx1 reveal prepubescent stage-specific control of pituitary levels of GH, FSH and LHD Acampora, S Mazan, F Tuorto, et al.
Nature Genetics|May 20, 1998
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesisP E Macchia, P Lapi, H Krude, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Thyroid : Official Journal of the American Thyroid Association|June 1, 1997
Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesisP Lapi, P E Macchia, L Chiovato, et al.
Journal of Endocrinological Investigation|November 22, 2017
High-resolution melting analysis (HRM) for mutational screening of Dnajc17 gene in patients affected by thyroid dysgenesisI C Nettore, S Desiderio, E De Nisco, et al.
Biosensors & Bioelectronics|April 26, 2023
SERS assisted sandwich immunoassay platforms for ultrasensitive and selective detection of human ThyroglobulinS Spaziani, G Quero, S Managò, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alphaP E Macchia, Y Takeuchi, T Kawai, et al.
Journal of Endocrinological Investigation|June 23, 2009
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesisA M Ferrara, L De Sanctis, G Rossi, et al.
Nature Genetics|August 11, 1998
A mouse model for hereditary thyroid dysgenesis and cleft palateM De Felice, C Ovitt, E Biffali, et al.
The Journal of Clinical Endocrinology and Metabolism|September 29, 2012
Thyroid nodules treated with percutaneous radiofrequency thermal ablation: a comparative studyA Faggiano, V Ramundo, A P Assanti, et al.
Journal of Endocrinological Investigation|November 10, 2010
Screening for mutations in the ISL1 gene in patients with thyroid dysgenesisA M Ferrara, G Rossi, E Zampella, et al.
Development (Cambridge, England)|May 9, 1998
Transient dwarfism and hypogonadism in mice lacking Otx1 reveal prepubescent stage-specific control of pituitary levels of GH, FSH and LHD Acampora, S Mazan, F Tuorto, et al.
Nature Genetics|May 20, 1998
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesisP E Macchia, P Lapi, H Krude, et al.
Pageof 4