Results 121 to 130 of about 364,574 (324)
Familial isolated pituitary adenoma (FIPA) occurs in families and is unrelated to multiple endocrine neoplasia type 1 and Carney complex. Mutations in AIP account only for 15-25% of FIPA families.
M. Tichomirowa+33 more
semanticscholar +1 more source
ABSTRACT Objective Patients require additional treatment when pituitary surgery for Cushing's disease is unsuccessful. Exciting innovations in pituitary surgery bring hope for achieving better outcomes. Quantifying the potential value of these innovations using early health economic modelling can provide guidance throughout their development.
Femke J. C. Jacobs+4 more
wiley +1 more source
The study identified sortilin as a promising LTR, enabling targeted degradation of oncogenic proteins through an mRNA‐encoded MedTAC strategy. In a mouse model, MedTACPTK7 reduced PTK7 by up to 80%, extended survival, and showed excellent pharmacokinetics without toxicity, providing a scalable platform for targeted therapies.
Xin Chang+8 more
wiley +1 more source
Human pituitary adenoma is one of the most common intracranial tumors with an incidence as high as 16.7%. Recent evidence has hinted a relationship between growth factors of pituitary or hypothalamic origin and proliferation of human pituitary adenoma ...
Kai Zhou+6 more
doaj +1 more source
EXTRASELLAR EXTENSION OF PITUITARY ADENOMAS [PDF]
Erich G. Krueger, Sol M. Unger
openalex +1 more source
Diagnostic pathology of equine intracranial neoplasms
Equine Veterinary Education, EarlyView.
H. G. Miller, A. Suarez‐Bonnet
wiley +1 more source
Abstract Aims Paltusotine is a novel, nonpeptide, selective somatostatin receptor 2 agonist in development for the treatment of acromegaly and carcinoid syndrome. This study investigated the mass balance, routes of excretion, absolute bioavailability and metabolite profile of orally administered paltusotine.
Rosa Luo+6 more
wiley +1 more source
Acromegaly with no pituitary adenoma and no evidence of ectopic source
More than 99% of patients with acromegaly harbor a growth hormone (GH) secreting pituitary adenoma. As the time from onset of signs/symptoms to diagnosis of acromegaly is long (symptom onset to diagnosis is often 4-10 years), pituitary adenomas that ...
Deepak Khandelwal+3 more
doaj +1 more source
Whole-Exome Sequencing Study of Thyrotropin-Secreting Pituitary Adenomas [PDF]
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Santosh, Sapkota+2 more
core
Computed tomographic features of pituitary apoplexy in a cat
Journal of Small Animal Practice, EarlyView.
W. Swan+3 more
wiley +1 more source