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Octreotide and pasireotide (dis)similarly inhibit pituitary tumor cells in vitro

Journal of endocrinology, 2016-11, Vol.231 (2), p.135-145

2016

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Marked Response of a Hypermutated ACTH-Secreting Pituitary Carcinoma to Ipilimumab and Nivolumab

The journal of clinical endocrinology and metabolism, 2018-10, Vol.103 (10), p.3925-3930

2018

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Immunohistochemical, genetic and clinical characterization of sporadic aldosterone-producing adenomas

Molecular and cellular endocrinology, 2015-08, Vol.411, p.146-154

2015

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Decreasing mortality and changes in treatment patterns in patients with acromegaly from a nationwide study

European journal of endocrinology, 2018-05, Vol.178 (5), p.459

2018

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Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease

The journal of clinical endocrinology and metabolism, 2017-08, Vol.102 (8), p.2836-2843

2017

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Predictors for Remission after Transsphenoidal Surgery in Acromegaly: A Dutch Multicenter Study

The journal of clinical endocrinology and metabolism, 2021-06, Vol.106 (6), p.1783-1792

2021

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DNA damage and growth hormone hypersecretion in pituitary somatotroph adenomas

The Journal of clinical investigation, 2020-11, Vol.130 (11), p.5738-5755

2020

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Long-term outcomes of patients with acromegaly: a report from the Swedish Pituitary Register

European journal of endocrinology, 2022, Vol.186 (3), p.329

2022

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The improvement of postoperative blood pressure and associated factors in patients with hormone‐negative adrenal adenoma and hypertension

Journal of surgical oncology, 2024-05, Vol.129 (6), p.1073-1081

2024

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Safety and Efficacy of Oral Octreotide in Acromegaly: Results of a Multicenter Phase III Trial

The journal of clinical endocrinology and metabolism, 2015-04, Vol.100 (4), p.1699-1708

2015

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Molecular Biology of Pituitary Adenomas

Neurosurgery clinics of North America, 2019-10, Vol.30 (4), p.391-400

2019

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Histopathology of growth hormone-secreting pituitary tumors: State of the art and new perspectives

Best Practice & Research Clinical Endocrinology & Metabolism, 2024-05, Vol.38 (3), p.101894, Article 101894

2024

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Oncogene-Induced Senescence Relayed by an Interleukin-Dependent Inflammatory Network

Cell, 2008-06, Vol.133 (6), p.1019-1031

2008

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Expression of SSTR2a, but not of SSTRs 1, 3, or 5 in Somatotroph Adenomas Assessed by Monoclonal Antibodies Was Reduced by Octreotide and Correlated With the Acute and Long-Term Effects of Octreotide

The journal of clinical endocrinology and metabolism, 2013-11, Vol.98 (11), p.E1730-E1739

2013

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Genetics of Primary Aldosteronism

Hypertension (Dallas, Tex. 1979), 2022-05, Vol.79 (5), p.887-897

Scholl, Ute I

2022

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Germline AIP Mutations in Apparently Sporadic Pituitary Adenomas: Prevalence in a Prospective Single-Center Cohort of 443 Patients

The journal of clinical endocrinology and metabolism, 2012-04, Vol.97 (4), p.E663-E670

2012

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Subclinical adenomas in postmortem pituitaries: classification and correlations to clinical data

European journal of endocrinology, 2006-05, Vol.154 (5), p.753

2006

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In Vitro Head-to-Head Comparison Between Octreotide and Pasireotide in GH-Secreting Pituitary Adenomas

The journal of clinical endocrinology and metabolism, 2017-06, Vol.102 (6), p.2009-2018

2017

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Pegvisomant and Pasireotide LAR as second line therapy in acromegaly: clinical effectiveness and predictors of response

European journal of endocrinology, 2021-02, Vol.184 (2), p.217

2021

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Adipose Tissue Redistribution and Ectopic Lipid Deposition in Active Acromegaly and Effects of Surgical Treatment

The journal of clinical endocrinology and metabolism, 2015-08, Vol.100 (8), p.2946-2955

2015

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Functional characterization of DLK1/MEG3 locus on chromosome 14q32.2 reveals the differentiation of pituitary neuroendocrine tumors

Aging (Albany, NY.), 2021-01, Vol.13 (1), p.1422-1439

2021

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Immunoreactivity Score Using an Anti-sst2A Receptor Monoclonal Antibody Strongly Predicts the Biochemical Response to Adjuvant Treatment with Somatostatin Analogs in Acromegaly

The journal of clinical endocrinology and metabolism, 2013-01, Vol.98 (1), p.E66-E71

2013

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Targeting Corticotroph HDAC and PI3-Kinase in Cushing Disease

The journal of clinical endocrinology and metabolism, 2021-01, Vol.106 (1), p.e232-e246

2021

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A critical reappraisal of bilateral adrenalectomy for ACTH-dependent Cushing's syndrome

European journal of endocrinology, 2015-10, Vol.173 (4), p.M23

2015

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O-GlcNAcylation Is Essential for Rapid Pomc Expression and Cell Proliferation in Corticotropic Tumor Cells

Endocrinology (Philadelphia), 2021-12, Vol.162 (12)

2021

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Octreotide and pasireotide (dis)similarly inhibit pituitary tumor cells in vitro

Marked Response of a Hypermutated ACTH-Secreting Pituitary Carcinoma to Ipilimumab and Nivolumab

Immunohistochemical, genetic and clinical characterization of sporadic aldosterone-producing adenomas

Decreasing mortality and changes in treatment patterns in patients with acromegaly from a nationwide study

Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease

Predictors for Remission after Transsphenoidal Surgery in Acromegaly: A Dutch Multicenter Study

DNA damage and growth hormone hypersecretion in pituitary somatotroph adenomas

Long-term outcomes of patients with acromegaly: a report from the Swedish Pituitary Register

The improvement of postoperative blood pressure and associated factors in patients with hormone‐negative adrenal adenoma and hypertension

Safety and Efficacy of Oral Octreotide in Acromegaly: Results of a Multicenter Phase III Trial

Molecular Biology of Pituitary Adenomas

Histopathology of growth hormone-secreting pituitary tumors: State of the art and new perspectives

Oncogene-Induced Senescence Relayed by an Interleukin-Dependent Inflammatory Network

Expression of SSTR2a, but not of SSTRs 1, 3, or 5 in Somatotroph Adenomas Assessed by Monoclonal Antibodies Was Reduced by Octreotide and Correlated With the Acute and Long-Term Effects of Octreotide

Genetics of Primary Aldosteronism

Germline AIP Mutations in Apparently Sporadic Pituitary Adenomas: Prevalence in a Prospective Single-Center Cohort of 443 Patients

Subclinical adenomas in postmortem pituitaries: classification and correlations to clinical data

In Vitro Head-to-Head Comparison Between Octreotide and Pasireotide in GH-Secreting Pituitary Adenomas

Pegvisomant and Pasireotide LAR as second line therapy in acromegaly: clinical effectiveness and predictors of response

Adipose Tissue Redistribution and Ectopic Lipid Deposition in Active Acromegaly and Effects of Surgical Treatment

Functional characterization of DLK1/MEG3 locus on chromosome 14q32.2 reveals the differentiation of pituitary neuroendocrine tumors

Immunoreactivity Score Using an Anti-sst2A Receptor Monoclonal Antibody Strongly Predicts the Biochemical Response to Adjuvant Treatment with Somatostatin Analogs in Acromegaly

Targeting Corticotroph HDAC and PI3-Kinase in Cushing Disease

A critical reappraisal of bilateral adrenalectomy for ACTH-dependent Cushing's syndrome

O-GlcNAcylation Is Essential for Rapid Pomc Expression and Cell Proliferation in Corticotropic Tumor Cells

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