Detalles de la búsqueda
1.
Combined treatment by octreotide and everolimus: Octreotide enhances inhibitory effect of everolimus in aggressive meningiomas.
J Neurooncol
; 124(1): 33-43, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-26015296
2.
Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies.
BMC Med Genet
; 15: 139, 2014 Dec 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-25524009
3.
Unilateral agenesis of internal carotid artery associated with congenital combined pituitary hormone deficiency and pituitary stalk interruption without HESX1, LHX4 or OTX2 mutation: a case report.
Pituitary
; 15 Suppl 1: S81-6, 2012 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-22797803
4.
Detection of genetic hypopituitarism in an adult population of idiopathic pituitary insufficiency patients with growth hormone deficiency.
Pituitary
; 14(3): 208-16, 2011 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-21132537
5.
Should routine analysis of the MEN1 gene be performed in all patients with primary hyperparathyroidism under 40 years of age?
World J Surg
; 34(6): 1294-8, 2010 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-20058152
6.
18F-FDG avidity of pheochromocytomas and paragangliomas: a new molecular imaging signature?
J Nucl Med
; 50(5): 711-7, 2009 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-19372492
7.
Ubiquitination as a priming process of PKC alpha and PKC epsilon degradation in the alphaT3-1 gonadotrope cell line.
Neuroendocrinology
; 89(3): 252-66, 2009.
Artículo
en Inglés
| MEDLINE | ID: mdl-18931473
8.
Mutations in the aryl hydrocarbon receptor interacting protein gene are not highly prevalent among subjects with sporadic pituitary adenomas.
J Clin Endocrinol Metab
; 92(5): 1952-5, 2007 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-17299063
9.
Involvement of the pituitary-specific transcription factor pit-1 in somatolactotrope cell growth and death: an approach using dominant-negative pit-1 mutants.
Mol Endocrinol
; 20(12): 3212-27, 2006 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-16901973
10.
Epidermal growth factor triggers an original, caspase-independent pituitary cell death with heterogeneous phenotype.
Mol Biol Cell
; 15(11): 4938-48, 2004 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-15331766
11.
Lessons from monogenic causes of growth hormone deficiency.
Ann Endocrinol (Paris)
; 78(2): 77-79, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-28483366
12.
Regulation of the RAP1/RAF-1/extracellularly regulated kinase-1/2 cascade and prolactin release by the phosphoinositide 3-kinase/AKT pathway in pituitary cells.
Endocrinology
; 147(12): 6036-45, 2006 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-16935846
13.
Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.
J Clin Endocrinol Metab
; 91(9): 3329-36, 2006 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-16735499
14.
Identification and functional analysis of the novel S179R POU1F1 mutation associated with combined pituitary hormone deficiency.
J Clin Endocrinol Metab
; 91(12): 4981-7, 2006 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-16968807
15.
The analysis of quantitative expression of somatostatin and dopamine receptors in gastro-entero-pancreatic tumours opens new therapeutic strategies.
Eur J Endocrinol
; 155(6): 849-57, 2006 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-17132755
16.
Regulation of Cre recombinase by ligand-induced complementation of inactive fragments.
Nucleic Acids Res
; 31(21): e131, 2003 Nov 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-14576331
17.
MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiency.
Eur J Endocrinol
; 174(6): R239-47, 2016 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-26733480
18.
In vitro impact of pegvisomant on growth hormone-secreting pituitary adenoma cells.
Endocr Relat Cancer
; 23(7): 509-19, 2016 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-27267119
19.
An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domain.
J Clin Endocrinol Metab
; 90(8): 4880-7, 2005 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-15941866
20.
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.
J Clin Endocrinol Metab
; 90(3): 1323-31, 2005 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-15613420