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1 r 1, typically resulting from a GH-secreting pituitary adenoma.
2 owth hormone, most commonly arising due to a pituitary adenoma.
3 and influence the prognosis and treatment of pituitary adenoma.
4 ely among different histological subtypes of pituitary adenoma.
5 nsus guideline to cover the care of CYP with pituitary adenoma.
6 el mutation of DKC1 (DKC1(S485G)) in a human pituitary adenoma.
7 like growth factor I (IGF1), most often by a pituitary adenoma.
8 repared from a human pituitary nonfunctional pituitary adenoma.
9 eningioma tumors was higher than uptake into pituitary adenoma.
10 on 4 patients after surgical removal of the pituitary adenoma.
11 in the development of a subgroup of sporadic pituitary adenomas.
12 s and TGF-beta-RII in normal pituitaries and pituitary adenomas.
13 s on recent developments in the treatment of pituitary adenomas.
14 ective in the treatment of hormone-secreting pituitary adenomas.
15 eningiomas, 10 vestibular schwannomas and 31 pituitary adenomas.
16 her conditions such as aseptic meningitis or pituitary adenomas.
17 , therapy and outcomes for all patients with pituitary adenomas.
18 emerged as promising new approaches to treat pituitary adenomas.
19 lomo et al. performed a whole-exome study of pituitary adenomas.
20 ormone secreting and nonsecreting (NS) human pituitary adenomas.
21 endoscopic than with microscopic removal of pituitary adenomas.
22 increasingly more popular for the removal of pituitary adenomas.
23 rgeted treatment for corticotropin-secreting pituitary adenomas.
24 or growth in a mouse model of ACTH-secreting pituitary adenomas.
25 an update on the diagnosis and treatment of pituitary adenomas.
26 portant for the progression of nonfunctional pituitary adenomas.
27 annoma, testicular Sertoli-cell tumours, and pituitary adenomas.
28 ction in treating patients with GH-secreting pituitary adenomas.
29 al genes with altered expression patterns in pituitary adenomas.
30 and identified as being under-represented in pituitary adenomas.
31 fashion with pttg in experimental and human pituitary adenomas.
32 nd bFGF expression in experimental and human pituitary adenomas.
33 ses on developments in treatment options for pituitary adenomas.
34 h was used as a positive control, but not in pituitary adenomas.
35 yperplasia, pancreatic endocrine tumors, and pituitary adenomas.
36 e diagnoses were 19 meningiomas (0.52%), six pituitary adenomas (0.16%), five cavernous malformations
37 1), glioblastoma (1.14, 1.01-1.28, p=0.038), pituitary adenoma (1.13, 1.05-1.22, p<0.0001), and vesti
38 ), glioblastoma (1.19, 1.12-1.28, p<0.0001), pituitary adenoma (1.21, 1.16-1.25, p<0.0001), and vesti
39 ecommendation against surgical resection for pituitary adenoma (1.80, 1.41-2.30, p<0.0001) and vestib
40 oma (meningioma [1.18, 1.08-1.28, p<0.0001], pituitary adenoma [1.20, 1.09-1.31, p<0.0001], and vesti
41 irm this initial report that the majority of pituitary adenomas (22 of 33; 67%) do not express GADD45
42 4 genes from the DLK1-MEG3 locus in 44 human pituitary adenomas (25 NFAs, 7 ACTH-secreting, 7 GH-secr
43 cted in four oligodendrogliomas (17.4%), one pituitary adenoma (3.2%), one meningioma (2.4%), one ast
44 22.2%]), trigeminal neuralgia (565 [11.5%]), pituitary adenomas (641 [13.1%]), haemangioblastoma (29
46 A specific MEN1 mutation was detected in a pituitary adenoma and corresponding germ-line DNA in a p
47 ecretion is usually caused by a GH-secreting pituitary adenoma and leads to acromegaly - a disorder o
52 ular basis, we investigated 11 nonfunctional pituitary adenomas and eight normal pituitary glands, us
53 xcessive hormonal production from functional pituitary adenomas and generally classify pituitary aden
54 multiple, clinically relevant parameters on pituitary adenomas and may represent a valuable therapeu
56 l distribution of pancreastatin secretion in pituitary adenomas and that the hypothalamic hormone gon
58 edial wall resection was performed in 47% of pituitary adenomas, and 39/50 walls confirmed pathologic
59 ), and p27 expression in normal pituitaries, pituitary adenomas, and carcinomas to analyze the possib
60 atively constant in nontumorous pituitaries, pituitary adenomas, and carcinomas, indicating that p27
64 nd molecular classification of nonfunctional pituitary adenomas, and suggest that therapeutic targeti
65 , but not in normal anterior pituitary or in pituitary adenomas, and the differential expression of P
75 mours and of Central Nervous System Tumours, pituitary adenomas are reclassified as neuroendocrine tu
77 d in normal pituitaries and in all groups of pituitary adenomas by RT-PCR, whereas PVR-1 and -3 mRNAs
78 al pituitary adenomas and generally classify pituitary adenomas by using statistical and machine lear
81 GF-beta1-induced apoptosis in the HP75 human pituitary adenoma cell line and that PACAP, TGF-beta1, f
85 GH transcription and secretion in senescent pituitary adenoma cells and also in nonpituitary (human
86 AR-gamma is an important molecular target in pituitary adenoma cells and PPAR-gamma ligands inhibit t
93 and, a large anterior mediastinal mass and a pituitary adenoma during a study done to evaluate recurr
98 targeted therapy of clinically nonfunctional pituitary adenomas, for which there is currently no medi
100 ic pituitary adenomas from 38 patients and 1 pituitary adenoma from a familial MEN1 patient were exam
101 secutive patients who underwent 219 EETS for pituitary adenoma from February 2007 and July 2018.
103 gene in pituitary tumorigenesis, 39 sporadic pituitary adenomas from 38 patients and 1 pituitary aden
104 is receptor in normal anterior pituitary and pituitary adenomas, GHRH-R mRNA was analyzed in 2 normal
105 r methods in the diagnosis and treatment for pituitary adenomas greatly expand our ability to care fo
107 le of PACAP in regulating apoptosis in human pituitary adenomas has not previously been examined.
108 status of other genes at this locus in human pituitary adenomas has not previously been reported.
109 primary lesions included craniopharyngioma, pituitary adenoma, Hodgkin's lymphoma, ependymoma, pinea
110 sampling correctly identified ACTH-secreting pituitary adenomas in 80% of patients with proven Cushin
111 Given the link between Hh signaling and pituitary adenomas in humans, our data suggest misregula
113 iterature reveals that endoscopic removal of pituitary adenoma, in the short term, does not seem to c
114 report describes the analysis of inheritable pituitary adenomas induced by expression of the human po
116 that transsphenoidal microscopic removal of pituitary adenomas is a well-established procedure with
118 used by adrenocorticotropin (ACTH)-secreting pituitary adenomas leads to hypercortisolemia predisposi
120 uble null mice, on the other hand, developed pituitary adenomas, multifocal gastric neuroendocrine hy
121 22 673), glioblastoma (n=35 258; n=104 047), pituitary adenoma (n=27 506; n=87 772), vestibular schwa
122 in, in human normal pituitaries (n = 11) and pituitary adenomas (n = 169) revealed that expression pa
123 /secretion, cell viability and apoptosis) in pituitary adenomas (n = 74), and to compare with the res
126 ange, 29-82 y) with clinically nonfunctional pituitary adenomas on MRI underwent preoperative imaging
127 study, we evaluated 107 consecutive primary pituitary adenomas operated on by a single neurosurgeon
128 Pituitary histopathology did not uncover any pituitary adenomas or somatotroph hyperplasia in either
129 and the most common cause in adulthood is a pituitary adenoma, or treatment with pituitary surgery o
132 ne tissues, including parathyroid neoplasia, pituitary adenomas, pancreatic neuroendocrine tumors, an
134 To date, no studies are available in which pituitary adenomas (PAs) have been studied using techniq
136 In most patients with suspected or confirmed pituitary adenomas (PAs), MRI, performed using T1- (with
143 endonasal transsphenoidal surgery (EETS) for pituitary adenoma resection: TachoSil patching versus Du
144 te that overexpression of FRalpha mRNA by NF pituitary adenomas results in production of properly fol
148 ome sequencing of 159 prospectively resected pituitary adenomas showed that somatic copy number alter
149 f-function AIP mutations are associated with pituitary adenomas, suggesting that AIP acts as a tumor
151 erred to as CYP) presenting with a suspected pituitary adenoma to inform specialist care and improve
154 disposition for a wide range of tumors, from pituitary adenomas to pancreatic and liver cancers, comm
155 ould contribute to pathogenesis of different pituitary adenomas types, and suggest that this variant
157 o assay of folate receptors in nonfunctional pituitary adenomas using preoperative (99m)Tc-folate SPE
159 a new diagnosis of meningioma, glioblastoma, pituitary adenoma, vestibular schwannoma, astrocytoma, a
160 S and pseudo-MS/MS methods, and subtyping of pituitary adenomas was performed by using principal comp
162 ry roles of PACAP and its receptors in human pituitary adenomas, we investigated the expression of va
163 atin on pituitary cell function, 17 cultured pituitary adenomas were examined for immunoreactive panc
164 uence and mRNA levels appear normal in human pituitary adenomas while p27 protein levels are decrease
165 we find that Max inactivation alone produces pituitary adenomas, while Max inactivation cooperates wi
166 te adequate neurosurgical decompression of a pituitary adenoma with compression of the optic apparatu
167 tuitary tumors, and in 23 of 26 GH-producing pituitary adenomas with high PTTG levels, senescence was