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Opioids and Endocrinopathies

Annales d'endocrinologie, 2021-10, Vol.82 (5), p.230

Karavitaki, N.

2021

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Management of craniopharyngiomas

Journal of endocrinological investigation, 2014-03, Vol.37 (3), p.219-228

Karavitaki, N.

2014

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Dopamine agonist resistant prolactinomas: any alternative medical treatment?

Pituitary, 2020-02, Vol.23 (1), p.27-37

2020

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From pituitary adenoma to pituitary neuroendocrine tumor (PitNET): an International Pituitary Pathology Club proposal

Endocrine-related cancer, 2017-04, Vol.24 (4), p.C5-C8

2017

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Pituitary metastases: presentation and outcomes from a pituitary center over the last decade

Pituitary, 2020-06, Vol.23 (3), p.258-265

2020

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Mortality in Cushing's syndrome: systematic analysis of a large series with prolonged follow-up

European journal of endocrinology, 2013-11, Vol.169 (5), p.715-723

2013

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Surgery for Cushing's disease in pregnancy: our experience and a literature review

Annals of the Royal College of Surgeons of England, 2019-01, Vol.101 (1), p.e26-e31

2019

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A thyroxine absorption test followed by weekly thyroxine administration: a method to assess non-adherence to treatment

European journal of endocrinology, 2013-06, Vol.168 (6), p.913-917

2013

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Nelson's syndrome

European journal of endocrinology, 2010-10, Vol.163 (4), p.495-507

2010

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Opioids and Endocrinopathies

Annales d'endocrinologie, 2021-10, Vol.82 (5), p.230-230

Karavitaki, N.

2021

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Craniopharyngiomas in children and adults: systematic analysis of 121 cases with long-term follow-up

Clinical endocrinology (Oxford), 2005-04, Vol.62 (4), p.397-409

2005

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Neurofibromatosis Type 1 and pancreatic islet cell tumours: an association which should be recognized

QJM : An International Journal of Medicine, 2015-07, Vol.108 (7), p.573-576

2015

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Outcome in surgically treated Rathke's cleft cysts: long-term monitoring needed

European journal of endocrinology, 2011-07, Vol.165 (1), p.33-37

2011

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What is the natural history of nonoperated nonfunctioning pituitary adenomas?

Clinical endocrinology (Oxford), 2007-12, Vol.67 (6), p.938-943

2007

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Bilateral adrenal haemorrhage

QJM : An International Journal of Medicine, 2017-03, Vol.110 (3), p.169

2017

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Pituitary apoplexy in non-functioning pituitary adenomas: long term follow up is important because of significant numbers of tumour recurrences

Clinical endocrinology (Oxford), 2011-10, Vol.75 (4), p.501-504

2011

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Surgical debulking of pituitary macroadenomas causing acromegaly improves control by lanreotide

Clinical endocrinology (Oxford), 2008-06, Vol.68 (6), p.970-975

2008

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IGF2-induced hypoglycemia unresponsive to everolimus

QJM : An International Journal of Medicine, 2014-04, Vol.107 (4), p.297-300

2014

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Radiotherapy of other sellar lesions

Pituitary, 2009, Vol.12 (1), p.23-29

Karavitaki, N

2009

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Disconnection hyperprolactinaemia in nonadenomatous sellar/parasellar lesions practically never exceeds 2000 mU/l

Clinical endocrinology (Oxford), 2012-04, Vol.76 (4), p.602-603

2012

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GH replacement in patients with non-functioning pituitary adenoma (NFA) treated solely by surgery is not associated with increased risk of tumour recurrence

Clinical endocrinology (Oxford), 2009-03, Vol.70 (3), p.435-438

2009

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Collision lesions of the sella: co-existence of craniopharyngioma with gonadotroph adenoma and of Rathke’s cleft cyst with corticotroph adenoma

Pituitary, 2008-09, Vol.11 (3), p.317-323

2008

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The value of the oral glucose tolerance test, random serum growth hormone and mean growth hormone levels in assessing the postoperative outcome of patients with acromegaly

Clinical endocrinology (Oxford), 2009-12, Vol.71 (6), p.840-845

2009

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Histopathology of Parasellar Neoplasms

NEUROENDOCRINOLOGY, 2020, Vol.110 (9-10), p.740-752

2020

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P-698 Pituitary functioning gonadotroph adenomas (FGA)-induced ovarian hyperstimulation syndrome (OHSS): results from tertiary neuroendocrine centres in the UK

Human reproduction (Oxford), 2022-06, Vol.37 (Supplement_1)

2022

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Opioids and Endocrinopathies

Management of craniopharyngiomas

Dopamine agonist resistant prolactinomas: any alternative medical treatment?

From pituitary adenoma to pituitary neuroendocrine tumor (PitNET): an International Pituitary Pathology Club proposal

Pituitary metastases: presentation and outcomes from a pituitary center over the last decade

Mortality in Cushing's syndrome: systematic analysis of a large series with prolonged follow-up

Surgery for Cushing's disease in pregnancy: our experience and a literature review

A thyroxine absorption test followed by weekly thyroxine administration: a method to assess non-adherence to treatment

Nelson's syndrome

Opioids and Endocrinopathies

Craniopharyngiomas in children and adults: systematic analysis of 121 cases with long-term follow-up

Neurofibromatosis Type 1 and pancreatic islet cell tumours: an association which should be recognized

Outcome in surgically treated Rathke's cleft cysts: long-term monitoring needed

What is the natural history of nonoperated nonfunctioning pituitary adenomas?

Bilateral adrenal haemorrhage

Pituitary apoplexy in non-functioning pituitary adenomas: long term follow up is important because of significant numbers of tumour recurrences

Surgical debulking of pituitary macroadenomas causing acromegaly improves control by lanreotide

IGF2-induced hypoglycemia unresponsive to everolimus

Radiotherapy of other sellar lesions

Disconnection hyperprolactinaemia in nonadenomatous sellar/parasellar lesions practically never exceeds 2000 mU/l

GH replacement in patients with non-functioning pituitary adenoma (NFA) treated solely by surgery is not associated with increased risk of tumour recurrence

Collision lesions of the sella: co-existence of craniopharyngioma with gonadotroph adenoma and of Rathke’s cleft cyst with corticotroph adenoma

The value of the oral glucose tolerance test, random serum growth hormone and mean growth hormone levels in assessing the postoperative outcome of patients with acromegaly

Histopathology of Parasellar Neoplasms

P-698 Pituitary functioning gonadotroph adenomas (FGA)-induced ovarian hyperstimulation syndrome (OHSS): results from tertiary neuroendocrine centres in the UK

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