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Craniopharyngiomas
Kirstie Lithgow
, Ross Hamblin
, Ute Pohl
,
Niki Karavitaki
Metabolism and Systems Science
Research output
:
Chapter in Book/Report/Conference proceeding
›
Chapter
Overview
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Keyphrases
Craniopharyngioma
100%
Adamantinomatous
100%
Papillary Subtype
100%
Endocrine Disorders
50%
Tumor
50%
Management Options
50%
Clinical Manifestations
50%
Gene mutation
50%
Systemic Chemotherapy
50%
Bleomycin
50%
Mortality Rate
50%
Irradiation
50%
Hypothalamo
50%
Pituitary Function
50%
Papillary
50%
Long-term Mortality
50%
Stereotactic Radiosurgery
50%
Large-scale Clinical Trial
50%
Activating mutation
50%
Benign Tumor
50%
High Burden
50%
Morbidity Burden
50%
Intracranial Tumor
50%
Sellar
50%
BRAF V600E
50%
Parasellar Region
50%
Intracystic
50%
Suprasellar Region
50%
BRAF Inhibitor (BRAFi)
50%
Visual Dysfunction
50%
Hypothalamic Dysfunction
50%
External Irradiation
50%
Classification Management
50%
β-catenin Gene
50%
Neuropsychological Dysfunction
50%
Medicine and Dentistry
Craniopharyngioma
100%
Clinical Trial
50%
Neoplasm
50%
Beta-Catenin
50%
Mortality Rate
50%
Gene Mutation
50%
Intracranial Tumor
50%
Benign Tumor
50%
Hypothalamus Hypophysis System
50%
Bleomycin
50%
Stereotactic Radiosurgery
50%
Neuroscience
Craniopharyngioma
100%
Beta-Catenin
50%
Gene Mutation
50%
Face
50%
Intracranial Tumor
50%
Bleomycin
50%