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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
45                          Clinically manifest pituitary adenomas affect approximately 1 in 1100 people
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
48              The most common etiologies were pituitary adenoma and meningioma.
49 nfirmed in a validation group of 37 surgical pituitary adenomas and 11 normal pituitary glands.
50 87.5%) ACTH carcinomas, but not in 112 other pituitary adenomas and carcinomas.
51 rgical resection is indicated for incidental pituitary adenomas and cystic sellar lesions.
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
55                                              Pituitary adenomas and NETs exhibit some morphological a
56 l distribution of pancreastatin secretion in pituitary adenomas and that the hypothalamic hormone gon
57 ndocrine cancers including pheochromocytoma, pituitary adenoma, and small cell lung cancer.
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
61 the gene product in nontumorous pituitaries, pituitary adenomas, and carcinomas.
62 benign schwannomas, WHO grade 1 meningiomas, pituitary adenomas, and haemangioblastoma.
63                            Normal pituitary, pituitary adenomas, and pituitary carcinomas all express
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
66                                              Pituitary adenomas are classified as either macroadenoma
67                                              Pituitary adenomas are frequently encountered in practic
68                        However, unlike NETs, pituitary adenomas are highly prevalent, yet indolent an
69                     As commonly encountered, pituitary adenomas are invariably benign.
70                                     Although pituitary adenomas are monoclonal proliferations, somati
71                                              Pituitary adenomas are neoplasms of the pituitary adenoh
72                            Thirty percent of pituitary adenomas are nonfunctioning adenomas, which do
73                         Approximately 53% of pituitary adenomas are prolactinomas, which can cause hy
74                                              Pituitary adenomas are rare in children and young people
75 mours and of Central Nervous System Tumours, pituitary adenomas are reclassified as neuroendocrine tu
76 eric for Rb deficiency, invariably died from pituitary adenomas by 3 months.
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
79                                              Pituitary adenomas can develop sporadically or as a part
80                                              Pituitary adenomas cause significant morbidity caused by
81 GF-beta1-induced apoptosis in the HP75 human pituitary adenoma cell line and that PACAP, TGF-beta1, f
82               Analysis of the cultured human pituitary adenoma cell line HP75, which expresses all th
83                        An immortalized human pituitary adenoma cell line, HP75, developed in our labo
84 ted cell cycle protein p27 in the HP75 human pituitary adenoma cell line.
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
87                   Interestingly, in cultured pituitary adenoma cells In1-ghrelin treatment (acylated
88                                              Pituitary adenomas cells cultured for 7 days in defined
89                                              Pituitary adenomas comprise 10% of intracranial tumors a
90                                              Pituitary adenomas comprise a heterogeneous subset of pa
91 ogues in primary human GH- and PRL-secreting pituitary adenoma cultures.
92 s to accelerate medullary thyroid C cell and pituitary adenoma development.
93 and, a large anterior mediastinal mass and a pituitary adenoma during a study done to evaluate recurr
94 ounts of immunoreactive pancreastatin in all pituitary adenomas except prolactin adenomas.
95 and -3 mRNAs were expressed in all groups of pituitary adenomas, except for most prolactinomas.
96 ypes I and II binding sites in all groups of pituitary adenomas, except prolactinomas.
97                                              Pituitary adenomas expressing and secreting GH are invar
98 targeted therapy of clinically nonfunctional pituitary adenomas, for which there is currently no medi
99                                   Functional pituitary adenomas (FPAs) are associated with hormonal h
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.
102 3-mediated senescence, likely protecting the pituitary adenoma from progression to malignancy.
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
106                   Drivers of sporadic benign pituitary adenoma growth are largely unknown.
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
112              We describe cells isolated from pituitary adenomas in two patients with multiple endocri
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
115                                For all other pituitary adenomas, initial therapy is generally transsp
116  that transsphenoidal microscopic removal of pituitary adenomas is a well-established procedure with
117                               ACTH-secreting pituitary adenomas lead to hypercortisolemia and cause s
118 used by adrenocorticotropin (ACTH)-secreting pituitary adenomas leads to hypercortisolemia predisposi
119                                              Pituitary adenomas may hypersecrete hormones or cause ma
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
124                              Non-functioning pituitary adenomas (NFPAs) are the most frequent pituita
125                           Clinically evident pituitary adenomas occur in approximately 1 in 1100 pers
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
130                                              Pituitary adenoma (PA) is one of the most common intracr
131       However, the potential role of LDHA in pituitary adenoma (PA) remains unknown.
132 ne tissues, including parathyroid neoplasia, pituitary adenomas, pancreatic neuroendocrine tumors, an
133                                              Pituitary adenomas (PAs) are benign growths arising from
134   To date, no studies are available in which pituitary adenomas (PAs) have been studied using techniq
135                    The complete resection of pituitary adenomas (PAs) is unlikely when there is an ex
136 In most patients with suspected or confirmed pituitary adenomas (PAs), MRI, performed using T1- (with
137                  Tissue analysis confirmed a pituitary adenoma/pituitary neuroendocrine tumor of the
138                  Observations: Prevalence of pituitary adenomas ranges from 1 in 865 adults to 1 in 2
139                           CYP with suspected pituitary adenomas require careful clinical examination,
140 tary surgery is first-line therapy for other pituitary adenomas requiring treatment.
141 ebrospinal fluid (CSF) leaks during EETS for pituitary adenoma resection.
142 neal shunts for presumed IIH and had a prior pituitary adenoma resection.
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
145        In humans, excess GH secretion due to pituitary adenoma, seen in patients with acromegaly, res
146                                Patients with pituitary adenomas should be identified at an early stag
147                          Four of 39 sporadic pituitary adenomas showed a deletion of one copy of the
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
150 t-term results of endoscopic and microscopic pituitary adenoma surgery.
151 erred to as CYP) presenting with a suspected pituitary adenoma to inform specialist care and improve
152 implications of the classification change of pituitary adenoma to NET.
153  markers to predict the ultimate response of pituitary adenomas to BIM-23A760.
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
156 2 normal human pituitary glands and 16 human pituitary adenomas using in situ hybridization.
157 o assay of folate receptors in nonfunctional pituitary adenomas using preoperative (99m)Tc-folate SPE
158 tracer may have promise for the detection of pituitary adenomas, using PET.
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
161            Compared with adult patients with pituitary adenomas, we highlight that, in the CYP group,
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

 
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