• Mashup Score: 0

    This series of live educational events is designed for regional experts in pituitary care to present live, in-person using interactive case-based discussion which will benefit clinicians to better manage and monitor response to treatment of Cushing’s Disease. During this educational event, attendees will learn about recent advances in managing Cushing’s Syndrome and its complications and enable…

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    • Register for one of our dinner events designed for regional experts in #pituitary care to present live to local care providers. Our first two events will take place next Tuesday, April 11 in Houston and New York City. Join us: https://t.co/22NZy1rcKv #Cushings #CushingsSyndrome https://t.co/O0Qw9jpL2v

  • Mashup Score: 23

    Growth hormone-secreting pituitary adenomas that cause acromegaly arise as monoclonal expansions of differentiated somatotroph cells and are usually sporadic. They are almost invariably benign, yet they can be locally invasive and show progressive growth despite treatment. Persistent excess of both growth hormone and its target hormone insulin-like growth factor 1 (IGF-1) results in a wide array…

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    • RT @TheLancetEndo: #Acromegaly: pathogenesis, diagnosis, and management https://t.co/2fbnM4jFe8 #pituitary #neuroendocrine https://t.co/l4…

  • Mashup Score: 17

    Growth hormone-secreting pituitary adenomas that cause acromegaly arise as monoclonal expansions of differentiated somatotroph cells and are usually sporadic. They are almost invariably benign, yet they can be locally invasive and show progressive growth despite treatment. Persistent excess of both growth hormone and its target hormone insulin-like growth factor 1 (IGF-1) results in a wide array…

    Tweet Tweets with this article
    • RT @TheLancetEndo: #Acromegaly: pathogenesis, diagnosis, and management https://t.co/2fbnM4jFe8 #pituitary #neuroendocrine https://t.co/l4…

  • Mashup Score: 1

    Growth hormone-secreting pituitary adenomas that cause acromegaly arise as monoclonal expansions of differentiated somatotroph cells and are usually sporadic. They are almost invariably benign, yet they can be locally invasive and show progressive growth despite treatment. Persistent excess of both growth hormone and its target hormone insulin-like growth factor 1 (IGF-1) results in a wide array…

    Tweet Tweets with this article
    • #Acromegaly: pathogenesis, diagnosis, and management https://t.co/2fbnM4jFe8 #pituitary #neuroendocrine https://t.co/l4tJA4Hq9A

  • Mashup Score: 7

    Cushing’s disease requires accurate diagnosis, careful treatment selection, and long-term management to optimise patient outcomes. The Pituitary Society convened a consensus workshop comprising more than 50 academic researchers and clinical experts to discuss the application of recent evidence to clinical practice. In advance of the virtual meeting, data from 2015 to present about screening and…

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    • Consensus on diagnosis and management of #Cushing's disease: a guideline update https://t.co/E777qkmu4T #pituitary #neuroendocrine #FREE to read with registration (also FREE)

  • Mashup Score: 6

    Growth hormone-secreting pituitary adenomas that cause acromegaly arise as monoclonal expansions of differentiated somatotroph cells and are usually sporadic. They are almost invariably benign, yet they can be locally invasive and show progressive growth despite treatment. Persistent excess of both growth hormone and its target hormone insulin-like growth factor 1 (IGF-1) results in a wide array…

    Tweet Tweets with this article
    • Acromegaly: pathogenesis, diagnosis, and management https://t.co/2fbnM4jFe8 #acromegaly #neuroendocrine #pituitary https://t.co/iNET248l3a

  • Mashup Score: 2

    Growth hormone-secreting pituitary adenomas that cause acromegaly arise as monoclonal expansions of differentiated somatotroph cells and are usually sporadic. They are almost invariably benign, yet they can be locally invasive and show progressive growth despite treatment. Persistent excess of both growth hormone and its target hormone insulin-like growth factor 1 (IGF-1) results in a wide array…

    Tweet Tweets with this article
    • #Acromegaly: pathogenesis, diagnosis, and management https://t.co/2fbnM4j7oA #pituitary #neuroendocrine #RareDiseaseDay #ShareYourColours #RareDiseases #LightUpForRare

  • Mashup Score: 0

    Oct 7, 2019, marks the 80th anniversary of the death of Harvey Cushing, the father of modern neurosurgery. Here we give a historical perspective from Cushing’s original description of the clinical syndrome that now bears his name through to the modern day. We highlight some of the key milestones that allowed improved understanding and management of this extraordinarily challenging condition, and…

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    • #Cushing's disease—from Minnie G to key issues in the early 21st century https://t.co/ykGYOcKGE7 #neuroendocrine #pituitary #FREE to read with registration (also FREE) #RareDiseaseDay #ShareYourColours #RareDiseases #LightUpForRare

  • Mashup Score: 0

    Cushing’s disease requires accurate diagnosis, careful treatment selection, and long-term management to optimise patient outcomes. The Pituitary Society convened a consensus workshop comprising more than 50 academic researchers and clinical experts to discuss the application of recent evidence to clinical practice. In advance of the virtual meeting, data from 2015 to present about screening and…

    Tweet Tweets with this article
    • Consensus on diagnosis and management of #Cushing's disease: a guideline update https://t.co/E777qkmu4T #neuroendocrine #pituitary #FREE to read with registration (also FREE) #RareDiseaseDay #ShareYourColours #RareDiseases #LightUpForRare