Diagnostics, treatment, and follow-up in craniopharyngioma

HL Müller - Frontiers in Endocrinology, 2011 - frontiersin.org
Craniopharyngiomas are partly cystic embryogenic malformations of the sellar and
parasellar region, with up to half the 0.5–2.0 new cases per million population per year …

Advances in the management of craniopharyngioma in children and adults

M Jensterle, S Jazbinsek, R Bosnjak… - Radiology and …, 2019 - sciendo.com
Background. Childhood and adult-onset craniopharyngioma is a rare embryogenic tumor of
the sellar, suprasellar, and parasellar region. Survival rates are high; however, tumor …

Childhood craniopharyngioma—current concepts in diagnosis, therapy and follow-up

HL Müller - Nature Reviews Endocrinology, 2010 - nature.com
Craniopharyngiomas have an overall incidence of 0.5–2.0 new cases per million of the
population per year, and∼ 30–50% of all cases represent childhood craniopharyngioma …

Risk-adapted treatment and follow-up management in childhood-onset craniopharyngioma

HL Müller - Expert review of neurotherapeutics, 2016 - Taylor & Francis
Craniopharyngiomas are rare embryonic malformations of the sellar/parasellar region with
low histological grade. Here, we review findings on the diagnosis, treatment, clinical course …

Craniopharyngiomas: a life-changing tumor

P Mortini - Endocrine, 2017 - Springer
Craniopharyngioma is the most common lesion of the hypothalamic and suprasellar region
in childhood with a frequent compromised pituitary function. The reported rates for deficits of …

Surgical strategies in childhood craniopharyngioma

J Flitsch, HL Müller, T Burkhardt - Frontiers in endocrinology, 2011 - frontiersin.org
Craniopharyngiomas are biologically benign lesions (WHO Grade 1) of the sellar and
suprasellar region, associated with a serious morbidity. About 50% of these tumors become …

Craniopharyngioma

HL Müller - Endocrine reviews, 2014 - academic.oup.com
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 …

Neuroendocrine disorders in pediatric craniopharyngioma patients

AMM Daubenbüchel, HL Müller - Journal of clinical medicine, 2015 - mdpi.com
Childhood-onset craniopharyngiomas are partly cystic embryonic malformations of the
sellar/parasellar region. The therapy of choice in patients with favorable tumor localization is …

Childhood craniopharyngioma

HL Müller - Pituitary, 2013 - Springer
Craniopharyngiomas (CP) are partly cystic embryogenic malformations of the sellar and
parasellar region. With an overall incidence of 0.5–2.0 new cases/million population/year …

Diagnosis, treatment, clinical course, and prognosis of childhood-onset craniopharyngioma patients.

HL Müller - Minerva endocrinologica, 2017 - europepmc.org
For decades gross-total resection was the preferred treatment option in childhood-onset
craniopharyngioma, assuming that radical strategies at the time of initial diagnosis and …