Results 171 to 180 of about 66,729 (223)

From the perspective of prolactin: a view on obesity. [PDF]

Front Endocrinol (Lausanne)
Wang Y, Luo D, Fang G, Ge M, Huang Y, Deng H.   +5 more
europepmc   +1 more source

Clinical evaluation of determinations of free and serum protein bound triiodthyronine (dextran gel filtration) [PDF]

, 1965
Heinze, H. G., Landgraf, R., Schwarz, K., Scriba, Peter Christian   +3 more
core  

Pituitary Apoplexy Following Gonadotropin-Releasing Hormone Agonist Administration for Prostate Cancer. [PDF]

IJU Case Rep
Fujimura M, Shimizu T, Sakamoto S, Sato H, Suzuki H, Mikami K.   +5 more
europepmc   +1 more source

Lymphocytic panhypophysitis with clival extension and positive anti-rabphilin-3A antibodies: illustrative case. [PDF]

J Neurosurg Case Lessons
Kato T, Ochiai H, Hasegawa M, Iwata N, Fujisawa H, Suzuki A, Sugimura Y, Hasegawa T.   +7 more
europepmc   +1 more source

Hyperprolactinemia in Older Adults: A Narrative Review of Distinct Clinical Challenges and Management Strategies. [PDF]

Cureus
Quimbayo-Cifuentes AF.
europepmc   +1 more source

Giant Sellar Meningocele: Intact Pituitary Function and New-onset Arginine Vasopressin Deficiency After Surgery. [PDF]

JCEM Case Rep
Gómez-Romero OJ, González-Virla B, Vargas-Ortega G, García-Sáenz M, Guinto-Nishimura G, Ichikawa-Escamilla E.   +5 more
europepmc   +1 more source

Differential role of anterior and posterior pituitary lobes in healthy aging and perceived stress. [PDF]

Sci Rep
Doucet GE, Davis M, Mertens AT, Picci G.
europepmc   +1 more source

"Multifocal, intra-axial Langerhans cell histiocytosis presenting with central diabetes insipidus in teenage pregnancy: A case report". [PDF]

Radiol Case Rep
Spirnak J, Mahmoud S.
europepmc   +1 more source

Clival Infiltrative Lesions: A Review of Differential Diagnosis Illustrated by a Rare Case of Coexisting Invasive Pituitary Adenoma and Clival Intravascular Lymphoma. [PDF]

J Belg Soc Radiol
Van Pée E, Daoud L, Tatar IG.
europepmc   +1 more source

A case report of Culler-Jones syndrome with deafness carrying a novel mutation in GLI2 gene. [PDF]

BMC Pediatr
Yuan X, Chu S, Gu W.
europepmc   +1 more source