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The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2000
Human somatostatin receptor subtypes in acromegaly: distinct patterns of messenger ribonucleic acid expression and hormone suppression identify different tumoral phenotypes
P Jaquet, A Saveanu, G Gunz, et al.
Journal of Endocrinological Investigation
|
September 10, 2014
Combined pituitary hormone deficiency: current and future status
F Castinetti, R Reynaud, M-H Quentien, et al.
Journal of Neuroendocrinology
|
August 12, 1999
Expression of functional growth hormone secretagogue receptors in human pituitary adenomas: polymerase chain reaction, triple in-situ hybridization and cell culture studies
A Barlier, A J Zamora, M Grino, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 15, 1998
The hormonal response to stress is not modified by the dramatic decrease in prolactin plasma concentration during surgery for microprolactinoma
R Guieu, H Dufour, C Devaux, et al.
Journal of Neurosurgery
|
June 1, 1999
An ultrarapid prognostic index in microprolactinoma surgery
R Guieu, H Dufour, F Grisoli, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 19, 2011
[Genetic aspects of growth hormone deficiency]
R Reynaud, F Castinetti, N Galon-Faure, et al.
European Journal of Endocrinology
|
January 29, 2011
Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms
R Reynaud, F Albarel, A Saveanu, et al.
International Journal of Andrology
|
March 6, 2010
RET gene mutations are not involved in the origin of human testicular seminoma
N Chevalier, A Barlier, C Roche, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 16, 2011
Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutations
C Couture, A Saveanu, A Barlier, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 11, 2001
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency
S Vallette-Kasic, A Barlier, C Teinturier, et al.
Page
of 20
Search research articles
Search
Showing results (181-190 of 193) with videos related to
Sort By:
Page
of 20
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2000
Human somatostatin receptor subtypes in acromegaly: distinct patterns of messenger ribonucleic acid expression and hormone suppression identify different tumoral phenotypes
P Jaquet, A Saveanu, G Gunz, et al.
Journal of Endocrinological Investigation
|
September 10, 2014
Combined pituitary hormone deficiency: current and future status
F Castinetti, R Reynaud, M-H Quentien, et al.
Journal of Neuroendocrinology
|
August 12, 1999
Expression of functional growth hormone secretagogue receptors in human pituitary adenomas: polymerase chain reaction, triple in-situ hybridization and cell culture studies
A Barlier, A J Zamora, M Grino, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 15, 1998
The hormonal response to stress is not modified by the dramatic decrease in prolactin plasma concentration during surgery for microprolactinoma
R Guieu, H Dufour, C Devaux, et al.
Journal of Neurosurgery
|
June 1, 1999
An ultrarapid prognostic index in microprolactinoma surgery
R Guieu, H Dufour, F Grisoli, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 19, 2011
[Genetic aspects of growth hormone deficiency]
R Reynaud, F Castinetti, N Galon-Faure, et al.
European Journal of Endocrinology
|
January 29, 2011
Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms
R Reynaud, F Albarel, A Saveanu, et al.
International Journal of Andrology
|
March 6, 2010
RET gene mutations are not involved in the origin of human testicular seminoma
N Chevalier, A Barlier, C Roche, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 16, 2011
Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutations
C Couture, A Saveanu, A Barlier, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 11, 2001
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency
S Vallette-Kasic, A Barlier, C Teinturier, et al.
Page
of 20