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Titlebook: Basic Research and Clinical Aspects of Adamantinomatous Craniopharyngioma; Juan Pedro Martinez-Barbera,Cynthia Lilian Andonia Book 2017 Sp

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Transcriptomic and Genomic Analyses of Human Craniopharyngioma,tome, while few, have raised additional therapeutic possibilities, such as potentially targeting matrix metallopeptidases. While a phase II clinical trial for targeted therapy in PCP is forthcoming, additional studies and confirmation of the current preliminary findings are required for advancing novel therapies for ACP.
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Endocrine Deficits in Patients with Human Craniopharyngioma,t familiar in managing patients with multiple endocrinopathies. Post-operatively, virtually all survivors face a lifetime risk of evolving endocrine deficits that may be extremely complex to manage, therefore requiring careful long-term follow-up and monitoring into adulthood with appropriate plans for transition between paediatric and adult care.
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https://doi.org/10.1007/3-540-34582-5illation of intracystic agents. This mode of drug delivery aims to obtain durable cyst shrinkage with minimum consequent morbidity and toxicity for patients. In this chapter we will highlight common agents used to date, paying particular attention to the drug currently gaining interest, interferon-alpha.
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https://doi.org/10.1007/978-3-319-51890-9Stem cell; adult pituitary stem cells; pituitary development; radiology; tumor biology
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978-3-319-84770-2Springer International Publishing AG 2017
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Vladimir Stantchev,Miroslaw Maleka result, controversy than does the craniopharyngioma”. This statement clarifies the situation of medical specialists such as endocrinologists, neurosurgeons, neuropathologists, neurooncologists, paediatric oncologists and neuro-radiologists involved in treatment of craniopharyngioma (CP) patients.
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