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Minerva Endocrinologica
|
September 1, 1994
[Serum levels of the carboxyterminal telopeptide of type I collagen in patients with thyroid disorders]
A Conti, M Monzani, L Persani, et al.
Endocrinology, Diabetes & Metabolism Case Reports
|
July 20, 2017
Switch to restoration therapy in a testosterone treated central hypogonadism with erythrocytosis
B Cangiano, C Cacciatore, L Persani, et al.
Thyroid : Official Journal of the American Thyroid Association
|
March 24, 1998
Unusual association between a thyrotropin-secreting pituitary adenoma and a papillary thyroid carcinoma
P Gasparoni, D Rubello, L Persani, et al.
Journal of Endocrinological Investigation
|
January 5, 2002
Loss of heterozygosity of the MEN1 gene in a large series of TSH-secreting pituitary adenomas
C Asteria, M Anagni, L Persani, et al.
European Journal of Endocrinology
|
January 23, 1998
Unique binding pattern to concanavalin A lectin of glycoprotein hormones alpha-subunit hypersecreted by non-functioning pituitary adenomas
C Asteria, L Persani, M Ferrari, et al.
Molecular and Cellular Endocrinology
|
June 2, 2009
Thyroid gland development and function in the zebrafish model
P Porazzi, D Calebiro, F Benato, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 12, 2001
Investigating the paradox of hypothyroidism and increased serum thyrotropin (TSH) levels in Sheehan's syndrome: characterization of TSH carbohydrate content and bioactivity
J H Oliveira, L Persani, P Beck-Peccoz, et al.
Neuroendocrinology
|
April 1, 1991
Thyrotropin alpha- and beta-subunit responses to thyrotropin-releasing hormone and domperidone in normal subjects and in patients with microprolactinomas
L Persani, P Beck-Peccoz, G Medri, et al.
Annales D'Endocrinologie
|
April 23, 2011
DUOXS defects: Genotype-phenotype correlations
L Fugazzola, M Muzza, G Weber, et al.
American Journal of Medical Genetics
|
July 16, 1999
Thyroid hemiagenesis and elevated thyrotropin levels in a child with Williams syndrome
V Cammareri, G Vignati, G Nocera, et al.
Page
of 10
Search research articles
Search
Showing results (11-20 of 99) with videos related to
Sort By:
Page
of 10
Minerva Endocrinologica
|
September 1, 1994
[Serum levels of the carboxyterminal telopeptide of type I collagen in patients with thyroid disorders]
A Conti, M Monzani, L Persani, et al.
Endocrinology, Diabetes & Metabolism Case Reports
|
July 20, 2017
Switch to restoration therapy in a testosterone treated central hypogonadism with erythrocytosis
B Cangiano, C Cacciatore, L Persani, et al.
Thyroid : Official Journal of the American Thyroid Association
|
March 24, 1998
Unusual association between a thyrotropin-secreting pituitary adenoma and a papillary thyroid carcinoma
P Gasparoni, D Rubello, L Persani, et al.
Journal of Endocrinological Investigation
|
January 5, 2002
Loss of heterozygosity of the MEN1 gene in a large series of TSH-secreting pituitary adenomas
C Asteria, M Anagni, L Persani, et al.
European Journal of Endocrinology
|
January 23, 1998
Unique binding pattern to concanavalin A lectin of glycoprotein hormones alpha-subunit hypersecreted by non-functioning pituitary adenomas
C Asteria, L Persani, M Ferrari, et al.
Molecular and Cellular Endocrinology
|
June 2, 2009
Thyroid gland development and function in the zebrafish model
P Porazzi, D Calebiro, F Benato, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 12, 2001
Investigating the paradox of hypothyroidism and increased serum thyrotropin (TSH) levels in Sheehan's syndrome: characterization of TSH carbohydrate content and bioactivity
J H Oliveira, L Persani, P Beck-Peccoz, et al.
Neuroendocrinology
|
April 1, 1991
Thyrotropin alpha- and beta-subunit responses to thyrotropin-releasing hormone and domperidone in normal subjects and in patients with microprolactinomas
L Persani, P Beck-Peccoz, G Medri, et al.
Annales D'Endocrinologie
|
April 23, 2011
DUOXS defects: Genotype-phenotype correlations
L Fugazzola, M Muzza, G Weber, et al.
American Journal of Medical Genetics
|
July 16, 1999
Thyroid hemiagenesis and elevated thyrotropin levels in a child with Williams syndrome
V Cammareri, G Vignati, G Nocera, et al.
Page
of 10