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P E Macchia

Showing results (1-10 of 31) with videos related to

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Molecular Medicine Today|January 19, 2000
Recent advances in understanding the molecular basis of primary congenital hypothyroidismP E Macchia
Journal of Endocrinological Investigation|February 24, 2007
FOXE1 polymorphisms: a new piece in the puzzle of thyroid dysgenesisP E Macchia
Annali Dell'Istituto Superiore Di Sanita|March 3, 1999
[Endemic goiter: clinical picture and evolution]P E Macchia, G Fenzi
Current Opinion in Genetics & Development|June 23, 1999
Molecular genetics of congenital hypothyroidismP E Macchia, M De Felice, R Di Lauro
Journal of Endocrinological Investigation|February 28, 2015
Effects of treatment modalities for Graves' hyperthyroidism on Graves' orbitopathy: a 2015 Italian Society of Endocrinology Consensus StatementL Bartalena, P E Macchia, C Marcocci, et al.
Biochimie|July 14, 1999
Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2)P E Macchia, M G Mattei, P Lapi, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1993
Integrin expression in thyroid cells from normal glands and nodular goitersM Vitale, V Bassi, G Fenzi, et al.
Journal of Endocrinological Investigation|April 21, 2001
High-dose intravenous corticosteroid therapy for Graves' ophthalmopathyP E Macchia, M Bagattini, G Lupoli, et al.
Journal of Endocrinological Investigation|May 24, 2013
The molecular causes of thyroid dysgenesis: a systematic reviewI C Nettore, V Cacace, C De Fusco, et al.
Journal of Endocrinological Investigation|February 1, 1993
Epidermal growth factor receptor and lipid membrane components in human lung cancersA Di Carlo, A Mariano, P E Macchia, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Molecular Medicine Today|January 19, 2000
Recent advances in understanding the molecular basis of primary congenital hypothyroidismP E Macchia
Journal of Endocrinological Investigation|February 24, 2007
FOXE1 polymorphisms: a new piece in the puzzle of thyroid dysgenesisP E Macchia
Annali Dell'Istituto Superiore Di Sanita|March 3, 1999
[Endemic goiter: clinical picture and evolution]P E Macchia, G Fenzi
Current Opinion in Genetics & Development|June 23, 1999
Molecular genetics of congenital hypothyroidismP E Macchia, M De Felice, R Di Lauro
Journal of Endocrinological Investigation|February 28, 2015
Effects of treatment modalities for Graves' hyperthyroidism on Graves' orbitopathy: a 2015 Italian Society of Endocrinology Consensus StatementL Bartalena, P E Macchia, C Marcocci, et al.
Biochimie|July 14, 1999
Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2)P E Macchia, M G Mattei, P Lapi, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1993
Integrin expression in thyroid cells from normal glands and nodular goitersM Vitale, V Bassi, G Fenzi, et al.
Journal of Endocrinological Investigation|April 21, 2001
High-dose intravenous corticosteroid therapy for Graves' ophthalmopathyP E Macchia, M Bagattini, G Lupoli, et al.
Journal of Endocrinological Investigation|May 24, 2013
The molecular causes of thyroid dysgenesis: a systematic reviewI C Nettore, V Cacace, C De Fusco, et al.
Journal of Endocrinological Investigation|February 1, 1993
Epidermal growth factor receptor and lipid membrane components in human lung cancersA Di Carlo, A Mariano, P E Macchia, et al.
Pageof 4