Results 121 to 130 of about 8,269 (177)

Effectiveness and safety of GLP-1 receptor agonists in craniopharyngioma patients with obesity: A multicentre real-world study. [PDF]

open access: yesDiabetes Obes Metab
Lambert F   +6 more
europepmc   +1 more source

Editorial: Advances and challenges in adult-onset craniopharyngioma. [PDF]

open access: yesFront Endocrinol (Lausanne)
Cooper O, Glezer A, Cuny T.
europepmc   +1 more source

Nordic survey on practice of neurosurgical management of craniopharyngioma in children. [PDF]

open access: yesChilds Nerv Syst
Frič R   +5 more
europepmc   +1 more source

Craniopharyngioma [PDF]

open access: yesEndocrine Reviews, 2014
Abstract This report is a review of findings on the diagnosis, treatment, clinical course, and prognosis of craniopharyngioma patients. Craniopharyngiomas are rare, partly cystic and calcified embryonic malformations of the sellar/parasellar region with low histological grade (WHO I°). A bimodal age distribution has been shown, with peak
Hermann L Müller
exaly   +4 more sources
Some of the next articles are maybe not open access.

Related searches:

Craniopharyngiomas

La Presse Médicale, 2021
Craniopharyngiomas are rare epithelial tumours situated primarily in the sellar/parasellar region, occurring along the path of the craniopharyngeal duct. Whilst classed as histologically benign tumours, their unpredictable growth pattern and proximity to vital structures including the optic chiasm, hypothalamus, and pituitary gland renders them a ...
Ross Hamblin   +2 more
openaire   +2 more sources

Craniopharyngioma

Pituitary, 2006
Craniopharyngiomas are benign tumors of the parasellar region. These tumors may be cystic, solid, or combinations of the two. They have a bimodal age distribution and no apparent gender predilection. Patients may present with endocrinopathy or symptoms related to mass effect from the growing tumor.
John A, Jane, Edward R, Laws
openaire   +4 more sources

Giant Craniopharyngioma

World Neurosurgery, 2023
A 6-year-old girl presented with moderate-intensity headache, frequent vomiting, visual disturbance, and left-sided decreased hearing for 7 months. The neurologic examination revealed a right upper motor neuron facial nerve palsy, left-sided 4-mm sluggish pupil (right: 3-mm reactive), and unsteady gait. Fundoscopy was notable for bilateral papilledema.
Ali Alkhaibary   +2 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy