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Surgical management of craniopharyngiomas. A review of 74 cases
David S. Baskin
, C. B. Wilson
Department of Neurosurgery
Academic Institute
Kenneth R. Peak Brain & Pituitary Treatment Center
Neurological Institute
Houston Methodist Hospital
Houston Methodist
Weill Cornell Medical College
Research output
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Contribution to journal
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Article
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peer-review
255
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Scopus citations
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Keyphrases
Surgical Management
100%
Remission
100%
Craniopharyngioma
100%
Tumor Size
66%
Surgical Intervention
66%
Pediatric Population
33%
Radiotherapy
33%
Neurological Deficit
33%
Presenting Symptoms
33%
Symptomatology
33%
Complete Removal
33%
Clinical Improvement
33%
Hypothyroidism
33%
No Recurrence
33%
Ophthalmological
33%
Radiological Assessment
33%
Craniotomy
33%
Impotence
33%
Hydrocephalus
33%
Adult Population
33%
Transcallosal Approach
33%
Multiple Procedures
33%
Primary Amenorrhea
33%
Direct Results
33%
Transsphenoidal Approach
33%
Tumor Removal
33%
Subtemporal Approach
33%
Visual Field Defect
33%
Sex Drive
33%
Hypoadrenalism
33%
Growth Failure
33%
Galactorrhea
33%
Neurological Status
33%
Subfrontal
33%
Secondary Amenorrhea
33%
Being Present
33%
Diabetes Insipidus
33%
Uncontrolled Disease
33%
Suboccipital Craniectomy
33%
Visual Dysfunction
33%
Severe Headache
33%
Medicine and Dentistry
Neoplasm
100%
Craniopharyngioma
100%
Diseases
33%
Pediatrics
33%
Headache
33%
Radiation Therapy
33%
Recurrent Disease
33%
Symptomatology
33%
Hypothyroidism
33%
Growth Disorder
33%
Craniotomy
33%
Hydrocephalus
33%
Craniectomy
33%
Visual Dysfunction
33%
Visual Field Defect
33%
Diabetes Insipidus
33%
Libido
33%
Galactorrhea
33%
Secondary Amenorrhea
33%
Primary Amenorrhea
33%
Neuroscience
Craniopharyngioma
100%
Radiation Therapy
33%
Craniotomy
33%
Headache
33%
Hydrocephalus
33%
Diabetes Insipidus
33%
Visual Field Defect
33%
Growth Disorder
33%
Visual Dysfunction
33%
Hypothyroidism
33%