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G I Baroncelli

Showing results (71-80 of 84) with videos related to

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Clinical and Experimental Immunology|March 10, 2020
Vitamin D status and the immune assessment in 22q11.2 deletion syndromeA Legitimo, V Bertini, G Costagliola, et al.
Journal of Endocrinological Investigation|April 17, 2020
17β-hydroxysteroid dehydrogenase type 3 deficiency: female sex assignment and follow-upM F Faienza, F Baldinotti, G Marrocco, et al.
Hormone Research|January 1, 1997
Long-term outcome of male-limited gonadotropin-independent precocious pubertyS Bertelloni, G I Baroncelli, R Lala, et al.
Pediatric Research|February 1, 1997
Biochemical selection of prepubertal patients with androgen insensitivity syndrome by sex hormone-binding globulin response to the human chorionic gonadotropin testS Bertelloni, G Federico, G I Baroncelli, et al.
Pediatric Research|March 1, 1997
Bone demineralization in cystic fibrosis: evidence of imbalance between bone formation and degradationG I Baroncelli, F De Luca, G Magazzú, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1995
Effect of combined treatment with gonadotropin releasing hormone analogue and growth hormone in patients with central precocious puberty who had subnormal growth velocity and impaired height prognosisG Saggese, A M Pasquino, S Bertelloni, et al.
Journal of Endocrinological Investigation|September 26, 2023
The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinionG I Baroncelli, G Carlucci, E Freri, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 16, 2009
Body composition and metabolic profile in women with complete androgen insensitivity syndromeE Dati, G I Baroncelli, S Mora, et al.
Journal of Endocrinological Investigation|November 22, 2023
Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic ricketsG I Baroncelli, M R Sessa, C Pelosini, et al.
Hormone Research|February 14, 2004
From bone biology to bone analysisE Schoenau, G Saggese, F Peter, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
Clinical and Experimental Immunology|March 10, 2020
Vitamin D status and the immune assessment in 22q11.2 deletion syndromeA Legitimo, V Bertini, G Costagliola, et al.
Journal of Endocrinological Investigation|April 17, 2020
17β-hydroxysteroid dehydrogenase type 3 deficiency: female sex assignment and follow-upM F Faienza, F Baldinotti, G Marrocco, et al.
Hormone Research|January 1, 1997
Long-term outcome of male-limited gonadotropin-independent precocious pubertyS Bertelloni, G I Baroncelli, R Lala, et al.
Pediatric Research|February 1, 1997
Biochemical selection of prepubertal patients with androgen insensitivity syndrome by sex hormone-binding globulin response to the human chorionic gonadotropin testS Bertelloni, G Federico, G I Baroncelli, et al.
Pediatric Research|March 1, 1997
Bone demineralization in cystic fibrosis: evidence of imbalance between bone formation and degradationG I Baroncelli, F De Luca, G Magazzú, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1995
Effect of combined treatment with gonadotropin releasing hormone analogue and growth hormone in patients with central precocious puberty who had subnormal growth velocity and impaired height prognosisG Saggese, A M Pasquino, S Bertelloni, et al.
Journal of Endocrinological Investigation|September 26, 2023
The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinionG I Baroncelli, G Carlucci, E Freri, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 16, 2009
Body composition and metabolic profile in women with complete androgen insensitivity syndromeE Dati, G I Baroncelli, S Mora, et al.
Journal of Endocrinological Investigation|November 22, 2023
Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic ricketsG I Baroncelli, M R Sessa, C Pelosini, et al.
Hormone Research|February 14, 2004
From bone biology to bone analysisE Schoenau, G Saggese, F Peter, et al.
Pageof 9