Results 281 to 290 of about 166,918 (340)

Dermatologic Features of Endocrine Tumor Syndromes—Systematic Review and Meta‐Analysis

open access: yesInternational Journal of Dermatology, EarlyView.
ABSTRACT Endocrine tumor syndromes, including multiple endocrine neoplasia types 1, 2A, and 2B (MEN1, MEN2A, MEN2B), Carney complex (CNC), and PTEN hamartoma tumor syndrome (PHTS), are hereditary conditions characterized by multisystem tumor development.
Sára Pálla   +8 more
wiley   +1 more source

The Saline‐Immersion/Irrigation TEchnique for Endoscopic Submucosal Dissection of Colorectal Lesions: Outcomes From a Large Western Cohort

open access: yesJournal of Gastroenterology and Hepatology, EarlyView.
ABSTRACT Background and Study Aims Endoscopic submucosal dissection (ESD) is increasingly used for the resection of complex lesions of the gastrointestinal tract. However, its adoption in the management of colonic lesions in Western practice remains challenging, mainly due to the anatomical complexities of the colon.
Elisabet Maristany Bosch   +5 more
wiley   +1 more source

High incidence and poor prognosis of bone metastases in functioning small intestinal neuroendocrine tumors. [PDF]

open access: yesFront Endocrinol (Lausanne)
Mathew A   +5 more
europepmc   +1 more source

Systematic review and meta‐analysis of the efficacy and safety of [177Lu]Lu‐edotreotide ([177Lu]Lu‐DOTATOC) for the treatment of neuroendocrine tumors

open access: yesJournal of Neuroendocrinology, EarlyView.
Abstract [177Lu]Lu‐edotreotide is a radiopharmaceutical therapy (RPT) targeting somatostatin receptors, which are commonly overexpressed on neuroendocrine tumors (NETs). This systematic literature review and meta‐analysis describes the efficacy and safety of [177Lu]Lu‐edotreotide in patients with NETs.
Richard P. Baum   +11 more
wiley   +1 more source

Diagnosis and treatment of paragangliomas and pheochromocytomas: a survey from the Italian Association for Neuroendocrine Tumors. [PDF]

open access: yesFront Endocrinol (Lausanne)
Pietroluongo E   +10 more
europepmc   +1 more source

Cystic masses of the pancreas : how useful is cyst fluid analysis in the diagnosis? [PDF]

open access: yes, 2011
Cesmeli, Ercan   +5 more
core   +1 more source

Epidemiology of acquired hypothalamic obesity following traumatic brain injury and nonspecific hypothalamic microinjury: A nationwide German claims data analysis

open access: yesJournal of Neuroendocrinology, EarlyView.
Abstract Acquired hypothalamic obesity (aHO) is characterized by rapid and persistent weight gain resulting from structural or functional damage to the hypothalamus, typically accompanied by neuroendocrine dysfunction. While aHO is well described in the context of hypothalamic or suprasellar tumors, particularly craniopharyngioma, little is known about
Julian Witte   +5 more
wiley   +1 more source

Somatostatin analogs in neuroendocrine tumors with Ki‐67 index of ≥10%

open access: yesJournal of Neuroendocrinology, EarlyView.
Abstract Somatostatin analogs (SSAs) are an established first‐line therapy in intestinal and pancreatic neuroendocrine tumors (NETs). Based on Phase III studies, their use is recommended in NET with a Ki‐67 index of up to 10%. The effect of first‐line SSA therapy on differentiated NET with a Ki‐67 index ≥10% is poorly understood.
Johanna Braegelmann   +6 more
wiley   +1 more source

Development of gastric mucosa-associated microbiota in autoimmune gastritis with neuroendocrine tumors. [PDF]

open access: yesJ Gastroenterol
Otani K   +15 more
europepmc   +1 more source

Bone metastases from neuroendocrine neoplasms: Results of an Italian nationwide survey of natural history and management

open access: yesJournal of Neuroendocrinology, EarlyView.
Abstract Bone metastases (BMs) were reported in <15% of cases of neuroendocrine neoplasms (NENs). Their clinical behavior is various and clinical management is still undefined. This study aimed to describe the clinical practical management and survival outcome of neuroendocrine neoplasm patients with BMs.
Nicola Fazio   +28 more
wiley   +1 more source

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