Results 31 to 40 of about 148,544 (297)
TRH: Pathophysiologic and clinical implications [PDF]
, 1985 Thyrotropin releasing hormone is thought to be a tonic stimulator of the pituitary TSH secretion regulating the setpoint of the thyrotrophs to the suppressive effect of thyroid hormones. The peptide stimulates the release of normal and elevated prolactin.
Pickardt, C. R., Scriba, Peter Christian
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, 2021 Purpose: Few nationally representative studies have evaluated the epidemiology of PA (pituitary adenoma). This South Korean study evaluated the incidence of different PA subtypes, cardiovascular disease (CVD), and related mortality.
한후재
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INFANTILISM IN PITUITARY DISEASE [PDF]
Archives of Internal Medicine, 1912 Since the appearance of Frohlich's paper1in 1901, it has become generally recognized that tumors in or near the pituitary gland may cause disturbances of body growth and general metabolism which are quite distinct from acromegaly and gigantism. Frankl-Hochwart2has recently collected and analyzed the findings in 155 pituitary affections of this ...
openaire +2 more sources
International Archives of Otorhinolaryngology, 2015 Introduction Hypophysitis is a chronic inflammation of the pituitary gland of complex and still incompletely defined pathogenesis. It belongs to the group of non-hormone-secreting sellar masses, sharing with them comparable clinical presentation and ...
Rafael Loch Batista +7 more
doaj +1 more source
The Autoimmune pituitary inflammation
Journal of Education, Health and Sport, 2022 Autoimmune Hypophysitis (AH) is often refereed in the literature as lymphocytic pituitary inflammation. It is the most common form of rare, chronic inflammation states affecting this gland. In most cases it has autoimmune character. Symptoms of pituitary
Szymon Krzewski +2 more
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Sex-Specific Cardiovascular Risks and Mortality in Patients with Panhypopituitarism: A Nationwide Cohort Study [PDF]
Endocrinology and MetabolismBackground Panhypopituitarism is a condition of combined deficiency of multiple pituitary hormones, which requires lifelong hormone replacement therapy. Hormone deficiency or inadequate hormone replacement may contribute to cardiovascular disease.
Seung Shin Park +6 more
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Pituitary Neuroendocrine Tumors in Multiple Endocrine Neoplasia [PDF]
Endocrinology and MetabolismMultiple endocrine neoplasia type 1 (MEN1) is an autosomal-dominant disorder characterized by tumors of the pituitary, parathyroid, and endocrine-gastrointestinal tract. Pituitary neuroendocrine tumors (PitNETs) occur in about 40% of MEN1 cases, with 10%
Sang Ouk Chin +2 more
doaj +1 more source
Brazilian Journal of Otorhinolaryngology, 2009 Transsphenoidal surgery is the most commonly used surgical procedure to handle the hypophyseal region, sometimes associated with oronasal complications.
Carolina Petry +5 more
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Clinical and genetic features of childhood-onset congenital combined pituitary hormone deficiency: a retrospective, single-center cohort study [PDF]
Annals of Pediatric Endocrinology & MetabolismPurpose To investigate the clinical characteristics and genetic features of childhood-onset congenital combined pituitary hormone deficiency (cCPHD) in Korean patients.
Yoonha Lee +4 more
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Pituitary Tumors: Advances in Neuroimaging.
, 2010 Pediatric pituitary tumors, albeit relatively infrequent, can significantly alter the quality of life of affected children. Accurate diagnostic differentiation is essential for both safe and effective disease management.
ROSSI A. PITUITARY +2 more
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