Search research articles
Contact Us
Filters
Showing results (41-50 of 69) with videos related to
Page
of 7
Sort By:
Journal of Endocrinological Investigation
|
November 23, 2011
Autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy in Calabria: clinical, immunological and genetic patterns
C Betterle, L Ghizzoni, A Cassio, et al.
Journal of Endocrinological Investigation
|
November 1, 1993
Combined treatment with growth hormone and luteinizing hormone releasing hormone-analogue (LHRHa) of pubertal children with familial short stature
C Volta, S Bernasconi, P Tondi, et al.
Metabolism: Clinical and Experimental
|
March 1, 1994
Dynamics of 24-hour pulsatile cortisol, 17-hydroxyprogesterone, and androstenedione release in prepubertal patients with nonclassic 21-hydroxylase deficiency and normal prepubertal children
L Ghizzoni, S Bernasconi, R Virdis, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
March 7, 2000
Ketoacidosis and hyperosmolarity as first symptoms of type 1 diabetes mellitus following ingestion of high-carbohydrate-containing fluids
M Vanelli, G Chiari, L Ghizzoni, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 16, 1998
[Hypopituitarism during the first year of life. A collaborative Italian study]
De Luca Ff2p4, T Arrigo, M Bozzola, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
July 18, 2001
Leptin inhibits steroid biosynthesis by human granulosa-lutein cells
L Ghizzoni, A Barreca, G Mastorakos, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1996
Pituitary-ovarian responses to leuprolide acetate testing in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
L Ghizzoni, R Virdis, A Vottero, et al.
Journal of Endocrinological Investigation
|
March 5, 2021
POR polymorphisms are associated with 21 hydroxylase deficiency
F Pecori Giraldi, S Einaudi, A Sesta, et al.
European Journal of Endocrinology
|
June 1, 1997
Ovarian 17 alpha-hydroxyprogesterone responses to GnRH analog testing in oligomenorrheic insulin-dependent diabetic adolescents
R Virdis, M Zampolli, M E Street, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 13, 2006
Decreased androgen receptor gene methylation in premature pubarche: a novel pathogenetic mechanism?
A Vottero, M Capelletti, S Giuliodori, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 69) with videos related to
Sort By:
Page
of 7
Journal of Endocrinological Investigation
|
November 23, 2011
Autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy in Calabria: clinical, immunological and genetic patterns
C Betterle, L Ghizzoni, A Cassio, et al.
Journal of Endocrinological Investigation
|
November 1, 1993
Combined treatment with growth hormone and luteinizing hormone releasing hormone-analogue (LHRHa) of pubertal children with familial short stature
C Volta, S Bernasconi, P Tondi, et al.
Metabolism: Clinical and Experimental
|
March 1, 1994
Dynamics of 24-hour pulsatile cortisol, 17-hydroxyprogesterone, and androstenedione release in prepubertal patients with nonclassic 21-hydroxylase deficiency and normal prepubertal children
L Ghizzoni, S Bernasconi, R Virdis, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
March 7, 2000
Ketoacidosis and hyperosmolarity as first symptoms of type 1 diabetes mellitus following ingestion of high-carbohydrate-containing fluids
M Vanelli, G Chiari, L Ghizzoni, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 16, 1998
[Hypopituitarism during the first year of life. A collaborative Italian study]
De Luca Ff2p4, T Arrigo, M Bozzola, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
July 18, 2001
Leptin inhibits steroid biosynthesis by human granulosa-lutein cells
L Ghizzoni, A Barreca, G Mastorakos, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1996
Pituitary-ovarian responses to leuprolide acetate testing in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
L Ghizzoni, R Virdis, A Vottero, et al.
Journal of Endocrinological Investigation
|
March 5, 2021
POR polymorphisms are associated with 21 hydroxylase deficiency
F Pecori Giraldi, S Einaudi, A Sesta, et al.
European Journal of Endocrinology
|
June 1, 1997
Ovarian 17 alpha-hydroxyprogesterone responses to GnRH analog testing in oligomenorrheic insulin-dependent diabetic adolescents
R Virdis, M Zampolli, M E Street, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 13, 2006
Decreased androgen receptor gene methylation in premature pubarche: a novel pathogenetic mechanism?
A Vottero, M Capelletti, S Giuliodori, et al.
Page
of 7