Results 101 to 110 of about 4,368 (233)

Diagnosis and Management of Aggressive/Refractory Growth Hormone‐Secreting Pituitary Neuroendocrine Tumors

open access: yesInternational Journal of Endocrinology, Volume 2024, Issue 1, 2024.
The majority of acromegaly and gigantism are caused by growth hormone‐secreting pituitary neuroendocrine tumors (PitNETs). Most cases can be cured or controlled by surgery, medical therapy, and/or radiotherapy. However, a few of these tumors are resistant to traditional therapy and always have a poor prognosis.
Xiaojuan Zhang   +4 more
wiley   +1 more source

Patient-reported outcomes of parenteral somatostatin analogue injections in 195 patients with acromegaly. [PDF]

open access: yes, 2016
This work is licensed under a Creative Commons Attribution 3.0 Unported LicenseBACKGROUND: Long-acting somatostatin analogues delivered parenterally are the most widely used medical treatment in acromegaly.
Adelman   +20 more
core   +2 more sources

Serum N-Terminal Type III Procollagen Propeptide: An Indicator of Growth Hormone Excess and Response to Treatment in Feline Hypersomatotropism [PDF]

open access: yes, 2016
BACKGROUND: N‐terminal type III procollagen propeptide (PIIINP) is a biomarker of soft tissue proliferation. Hypersomatotropism (HS) is associated with soft tissue proliferation.
Church, D B   +4 more
core   +2 more sources

AIP and MEN1 mutations and AIP immunohistochemistry in pituitary adenomas in a tertiary referral center. [PDF]

open access: yes, 2019
Background: Pituitary adenomas have a high disease burden due to tumor growth/ invasion and disordered hormonal secretion. Germline mutations in genes such as MEN1 and AIP are associated with early onset of aggressive pituitary adenomas that can be ...
Cano González, David A.   +2 more
core  

Pegvisomant in Acromegaly and Gigantism [PDF]

open access: hybrid, 2020
Claire Briet   +2 more
openalex   +1 more source

ALL-CAUSE MORTALITY IN PATIENTS WITH ACROMEGALY TREATED WITH PEGVISOMANT AN ACROSTUDY ANALYSIS.

open access: yesEuropean Journal of Endocrinology, 2020
OBJECTIVE To examine all-cause mortality rates in patients with acromegaly on pegvisomant and identify pertinent risk factors, including insulin-like growth factor I (IGF-I).
N. Tritos   +8 more
semanticscholar   +1 more source

Tratamiento médico de tumores hipofisarios

open access: yesRevista Médica Clínica Las Condes, 2013
Se presentan los diferentes tipos de tumores hipofisiarios y para cada uno las opciones de tratamiento médico disponibles actualmente. Se detallan sus indicaciones, los resultados que se estima posibles, sus efectos secundarios y contraindicaciones.
Dr. C. Pedro Becker
doaj   +1 more source

Expression of a glycosylphosphatidylinositol-anchored ligand, growth hormone, blocks receptor signalling [PDF]

open access: yes, 2012
We have investigated the interaction between GH (growth hormone) and GHR (GH receptor). We previously demonstrated that a truncated GHR that possesses a transmembrane domain but no cytoplasmic domain blocks receptor signalling.
Aiden H. Riley   +29 more
core   +3 more sources

Pegvisomant in combination or pegvisomant alone after failure of somatostatin analogs in acromegaly patients: an observational French ACROSTUDY cohort study [PDF]

open access: hybrid, 2020
Emmanuelle Kuhn   +12 more
openalex   +1 more source

Pegvisomant and not somatostatin receptor ligands (SRLs) is first line medical therapy for acromegaly.

open access: yesEuropean Journal of Endocrinology, 2020
Current guidelines recommend the use of somatostatin receptor ligands (LA-SRLs) first when surgery fails to correct GH/IGF-I hypersecretion. In this article, a pro- and contra debate outlines which arguments are in favour and which are against ...
A. J. Lely   +5 more
semanticscholar   +1 more source

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