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European Journal of Endocrinology, ISSN 0804-4643, 2014, Volume 170, Issue 4, pp. R147 - R157
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 06/2012, Volume 97, Issue 6, pp. 2093 - 2104
Context: Ectopic GHRH secretion is a rare cause of acromegaly, and case reports are mainly isolated. Setting: From the registry of the sole laboratory... 
CELL TUMOR | NEUROENDOCRINE TUMOR | ACTING SOMATOSTATIN ANALOG | IN-VITRO | PANCREATIC-ISLET TUMOR | BRONCHIAL CARCINOID-TUMOR | SOMATOTROPH HYPERPLASIA | OCTREOTIDE TREATMENT | ENDOCRINOLOGY & METABOLISM | MULTIPLE ENDOCRINE NEOPLASIA | BIOCHEMICAL REMISSION | Pituitary Neoplasms - surgery | Carcinoid Tumor - surgery | Prognosis | Follow-Up Studies | Carcinoid Tumor - complications | Humans | Middle Aged | Growth Hormone-Secreting Pituitary Adenoma - complications | Neuroendocrine Tumors - complications | Male | Multiple Endocrine Neoplasia Type 1 - complications | Growth Hormone-Releasing Hormone - blood | Pituitary Neoplasms - complications | Multiple Endocrine Neoplasia Type 1 - secretion | Acromegaly - etiology | Growth Hormone-Secreting Pituitary Adenoma - surgery | Pituitary Neoplasms - secretion | Adult | Bronchial Neoplasms - surgery | Female | Registries | France | Growth Hormone-Releasing Hormone - secretion | Pancreatic Neoplasms - secretion | Bronchial Neoplasms - complications | Pancreatic Neoplasms - surgery | Acromegaly - metabolism | Treatment Outcome | Bronchial Neoplasms - secretion | Acromegaly - surgery | Adolescent | Growth Hormone-Secreting Pituitary Adenoma - secretion | Neuroendocrine Tumors - surgery | Aged | Carcinoid Tumor - secretion | Neuroendocrine Tumors - secretion | Multiple Endocrine Neoplasia Type 1 - surgery | Pancreatic Neoplasms - complications | Neuroendocrine Tumors | Carcinoid Tumor | Multiple Endocrine Neoplasia Type 1 | Acromegaly | Bronchial Neoplasms | Growth Hormone-Releasing Hormone | Growth Hormone-Secreting Pituitary Adenoma | Pituitary Neoplasms | Life Sciences | Pancreatic Neoplasms | Cancer
Journal Article
Cancer, ISSN 0008-543X, 10/2011, Volume 117, Issue 19, pp. 4381 - 4389
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 02/2016, Volume 101, Issue 2, pp. 445 - 452
Journal Article
Endocrine Practice, ISSN 1530-891X, 08/2017, Volume 23, Issue 8, pp. 907 - 914
Objective: Ectopic adrenocorticotropic hormone (ACTH) secretion is a less common cause of Cushing syndrome and is seen in 5 to 10% of cases with endogenous... 
DIAGNOSIS | THYMUS | NEUROENDOCRINE TUMORS | MANAGEMENT | BILATERAL ADRENALECTOMY | NEOPLASMS | ACTH SYNDROME | ENDOCRINOLOGY & METABOLISM | FOLLOW-UP | ADRENOCORTICOTROPIN | SECRETION | Thymus Neoplasms - secretion | Cushing Syndrome - physiopathology | Acne Vulgaris - etiology | Humans | Middle Aged | Thyroid Neoplasms - diagnostic imaging | Hyperpigmentation - etiology | Hydrocortisone - metabolism | Cushing Syndrome - etiology | Male | Positron-Emission Tomography | Cushing Syndrome - metabolism | Organometallic Compounds | Young Adult | Edema - epidemiology | Neuroendocrine Tumors - diagnostic imaging | ACTH Syndrome, Ectopic - diagnostic imaging | ACTH Syndrome, Ectopic - complications | Adult | Female | Retrospective Studies | Radiopharmaceuticals | Pancreatic Neoplasms - secretion | Muscle Weakness - etiology | Neoplasms - secretion | Thymus Neoplasms - diagnostic imaging | Tertiary Care Centers | ACTH Syndrome, Ectopic - physiopathology | Carcinoid Tumor - diagnostic imaging | Neoplasms - diagnostic imaging | ACTH Syndrome, Ectopic - metabolism | Bronchial Neoplasms - secretion | India | Obesity, Abdominal - etiology | Lung Neoplasms - secretion | Carcinoma, Neuroendocrine - diagnostic imaging | Thyroid Neoplasms - secretion | Carcinoma, Neuroendocrine - secretion | Lung Neoplasms - diagnostic imaging | Carcinoid Tumor - secretion | Neuroendocrine Tumors - secretion | Bronchial Neoplasms - diagnostic imaging | Pancreatic Neoplasms - diagnostic imaging
Journal Article
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 05/2015, Volume 19, Issue 5, pp. 948 - 959
Hypersecretion is the major symptom of functional neuroendocrine tumours. The mechanisms that contribute to this excessive secretion of hormones are still... 
neuroendocrine secretion | ADP‐ribosylation factor | carcinoid syndrome | insulin‐like growth factor 1 | Golgi apparatus | ADP-ribosylation factor | Neuroendocrine secretion | Insulin-like growth factor 1 | Carcinoid syndrome | MIGRATION | SYSTEM | MEDICINE, RESEARCH & EXPERIMENTAL | PROTEIN | NEUROTENSIN SECRETION | ADP-RIBOSYLATION FACTOR-1 | FAMILY | CELL BIOLOGY | GROWTH-FACTOR RECEPTOR | BREAST-CANCER CELLS | THERAPY | PATHWAY | insulin-like growth factor 1 | Microscopy, Electron, Transmission | Receptor, IGF Type 1 - metabolism | Insulin-Like Growth Factor I - pharmacology | Autoantigens - metabolism | Humans | Blotting, Western | Carcinoid Tumor - metabolism | Carcinoid Tumor - pathology | Insulin-Like Growth Factor I - secretion | Microscopy, Confocal | Carcinoid Tumor - genetics | MAP Kinase Signaling System - drug effects | RNA Interference | Chromogranin A - secretion | Cell Line, Tumor | Protein Binding | ADP-Ribosylation Factor 1 - metabolism | Golgi Apparatus - metabolism | Cell Proliferation - drug effects | ADP-Ribosylation Factor 1 - genetics | Golgi Apparatus - ultrastructure | Goods and services tax | G proteins | Tumors | Medical research | Insulin-like growth factors | Endocrine system | Rodents | Cells | Phosphorylation | Insulin-like growth factor I | Trafficking | Menopause | Activation | Hormones | Kinases | ADP | ARF protein | Proteins | Signal transduction | Autocrine signalling | Ribosylation | Pancreas | Growth factors | Golgi cells | Deoxyribonucleic acid--DNA | Secretion | Cloning | Extracellular signal-regulated kinase | Tumor cell lines | Insulin | Studies | Budding | Cancer | Neuroendocrine tumors | Original
Journal Article
Journal Article
Seminars in Nuclear Medicine, ISSN 0001-2998, 2006, Volume 36, Issue 3, pp. 228 - 247
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 03/2015, Volume 39, Issue 3, pp. 374 - 382
Adrenocorticotropic hormone (ACTH)-secreting pancreatic neuroendocrine tumors (PanNETs), although rare, are responsible for about 15% of ectopic Cushing... 
ACTH | neuroendocrine tumor | pancreas | acinar cell carcinoma | Cushing syndrome | SURVIVAL | SURGERY | MARKER | ENDOCRINE TUMORS | PATHOLOGY | CARBOXYL ESTER LIPASE | CARCINOMAS | CELL-DIFFERENTIATION | EXPRESSION | ADENOMAS | IMMUNOPHENOTYPE | INSIGHTS | Immunohistochemistry | Biomarkers, Tumor - secretion | Predictive Value of Tests | Neuroendocrine Tumors - blood | Pancreatic Neoplasms - diagnosis | Humans | Middle Aged | Cushing Syndrome - diagnosis | Neuroendocrine Tumors - complications | Cushing Syndrome - etiology | Male | Neuroendocrine Tumors - diagnosis | New York City | Cushing Syndrome - therapy | ACTH Syndrome, Ectopic - etiology | ACTH Syndrome, Ectopic - mortality | Time Factors | Adult | Female | Pancreatic Neoplasms - mortality | Adrenocorticotropic Hormone - blood | Pancreatic Neoplasms - secretion | Cushing Syndrome - mortality | Pancreatic Neoplasms - blood | Diagnosis, Differential | Kaplan-Meier Estimate | ACTH Syndrome, Ectopic - therapy | Treatment Outcome | ACTH Syndrome, Ectopic - diagnosis | Adrenocorticotropic Hormone - secretion | Biomarkers, Tumor - blood | Adolescent | Neuroendocrine Tumors - mortality | Cushing Syndrome - blood | Italy | Neuroendocrine Tumors - secretion | Neuroendocrine Tumors - therapy | ACTH Syndrome, Ectopic - blood | Pancreatic Neoplasms - complications | Pancreatic Neoplasms - therapy
Journal Article