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A Cassio

Showing results (31-40 of 42) with videos related to

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Clinical Endocrinology|August 10, 2000
CYP21 analysis and phenotype/genotype relationship in the screened population of the Italian Emilia-Romagna regionA Balsamo, E Cacciari, L Baldazzi, et al.
European Journal of Endocrinology|July 1, 1997
Final height of patients treated for isolated GH deficiency: examination of 83 patientsE Cacciari, A Cicognani, P Pirazzoli, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Low growth hormone-binding protein in infants with congenital hypothyroidismA Cassio, E Cacciari, A Balsamo, et al.
Hormone Research|January 1, 1982
Neonatal screening for congenital adrenal hyperplasia using a microfilter paper method for 17-alpha-hydroxyprogesterone radioimmunoassay. Experience gained from the study of 22,233 casesE Cacciari, A Balsamo, A Cassio, et al.
Clinical Endocrinology|January 13, 2006
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative studyA Cassio, A Corrias, S Gualandi, et al.
Journal of Endocrinological Investigation|September 7, 2022
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidismD Gentilini, M Muzza, T de Filippis, et al.
Journal of Endocrinological Investigation|February 14, 2013
The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillanceA Cassio, C Corbetta, I Antonozzi, et al.
Journal of Endocrinological Investigation|December 28, 2022
A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotypeS Palumbo, G Cirillo, G Sanchez, et al.
Italian Journal of Pediatrics|June 2, 2019
X-linked hypophosphatemic rickets: an Italian experts' opinion surveyF Emma, M Cappa, F Antoniazzi, et al.
Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Clinical Endocrinology|August 10, 2000
CYP21 analysis and phenotype/genotype relationship in the screened population of the Italian Emilia-Romagna regionA Balsamo, E Cacciari, L Baldazzi, et al.
European Journal of Endocrinology|July 1, 1997
Final height of patients treated for isolated GH deficiency: examination of 83 patientsE Cacciari, A Cicognani, P Pirazzoli, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Low growth hormone-binding protein in infants with congenital hypothyroidismA Cassio, E Cacciari, A Balsamo, et al.
Hormone Research|January 1, 1982
Neonatal screening for congenital adrenal hyperplasia using a microfilter paper method for 17-alpha-hydroxyprogesterone radioimmunoassay. Experience gained from the study of 22,233 casesE Cacciari, A Balsamo, A Cassio, et al.
Clinical Endocrinology|January 13, 2006
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative studyA Cassio, A Corrias, S Gualandi, et al.
Journal of Endocrinological Investigation|September 7, 2022
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidismD Gentilini, M Muzza, T de Filippis, et al.
Journal of Endocrinological Investigation|February 14, 2013
The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillanceA Cassio, C Corbetta, I Antonozzi, et al.
Journal of Endocrinological Investigation|December 28, 2022
A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotypeS Palumbo, G Cirillo, G Sanchez, et al.
Italian Journal of Pediatrics|June 2, 2019
X-linked hypophosphatemic rickets: an Italian experts' opinion surveyF Emma, M Cappa, F Antoniazzi, et al.
Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.
Pageof 5