Results 41 to 50 of about 9,522,905 (293)

A multi-disciplinary team model based on CBL in clinical teaching of hypothalamus-pituitary diseases [PDF]

open access: yesJichu yixue yu linchuang, 2020
Objective To explore the effect of case-based learning (CBL) combined with hypothalamus-pituitary MDT clinic in clinical teaching of hypothalamus pituitary diseases. Methods The trainees who participated in the hypothalamus-pituitary MDT discussion and
DUAN Lian, ZHENG Guang-yao, LU Lin, ZHU Hui-juan, YAO Yong, PAN Hui
doaj  

The Autoimmune pituitary inflammation

open access: yesJournal 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
doaj   +1 more source

INFANTILISM IN PITUITARY DISEASE [PDF]

open access: yesArchives 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

Thickened Pituitary Stalk Associated with a Mass in the Sphenoidal Sinus: An Alarm to Suspect Hypophysitis by Immunoglobulin G4?

open access: yesInternational 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

Pituitary Neuroendocrine Tumors in Multiple Endocrine Neoplasia [PDF]

open access: yesEndocrinology and Metabolism
Multiple 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

Oronasal complications in patients after transsphenoidal hypophyseal surgery Complicações oronasais em pacientes pós-abordagem hipofisária via transesfenoidal

open access: yesBrazilian 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
doaj   +1 more source

The hidden hedgehog of the pituitary: hedgehog signaling in development, adulthood and disease of the hypothalamic-pituitary axis

open access: yesFrontiers in Endocrinology, 2023
Hedgehog signaling plays pivotal roles in embryonic development, adult homeostasis and tumorigenesis. However, its engagement in the pituitary gland has been long underestimated although Hedgehog signaling and pituitary embryogenic development are ...
Yehan Bian, Heidi Hahn, Anja Uhmann
doaj   +1 more source

Diagnosis and treatment of canine hypoadrenocorticism [PDF]

open access: yes, 2018
Canine hypoadrenocorticism (Addison’s disease), the ‘great pretender’ of internal medicine, is a disease that should be frequently considered as a differential diagnosis of several clinical presentations, albeit it is less commonly the actual cause of ...
Gunn, Eilidh   +2 more
core   +1 more source

Sex-Specific Cardiovascular Risks and Mortality in Patients with Panhypopituitarism: A Nationwide Cohort Study [PDF]

open access: yesEndocrinology and Metabolism
Background 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
doaj   +1 more source

A rare cause of recurrent spontaneous pneumothorax: Birt-hogg-dube syndrome [PDF]

open access: yes, 2018
Birt-Hogg-Dube (BHD) syndrome is an unusual disorder characterized by the triad of cutaneous lesions, renal tumors and lung cysts. In cases with BHD syndrome, the frequency of recurrent pneumothorax is increased due to presence of multiple lung cysts. It
Demirci, M.   +3 more
core   +1 more source

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