Results 201 to 210 of about 176,228 (323)

Expanding the boundaries of EUS: EUS-guided fiducial placement and fine-needle biopsy in oligometastatic disease of the adrenal gland

Ricardo Marrero Torres, Hari Gopakumar, Dushyant Singh Dahiya, Aqsa Khan, Uday Patel, Sahib Singh, Talia F. Malik, Marzena Muller, Mariajose Rojas De Leon, Neil Sharma   +9 more
openalex   +1 more source

Incretion and metabolism. Factors and treatment of the adrenal gland disease drew attention recently.

, 1997
名和田 新
openalex   +2 more sources

Diagnosis of Growth Hormone Deficiency in Children: Comparative Performance of Arginine Versus Glucagon as the First Stimulation Test

Clinical Endocrinology, EarlyView.
ABSTRACT Objective Growth hormone deficiency (GHD) diagnosis typically requires the performance of two sequential stimulation tests. Glucagon stimulation test (GST) and arginine stimulation test (AST) are widely used. This study aimed to determine the most suitable order of tests.
David Shaki, Daria Shvarts, Eli Hershkovitz, Lior Carmon, Hazan Guy, Bachar Yoav, Alon Haim   +6 more
wiley   +1 more source

Operative Experience of U.S. General Surgery Residents with Diseases of the Adrenal Glands, Endocrine Pancreas, and Other Less Common Endocrine Organs [PDF]

, 1996
Jay K. Harness, Claude H. Organ, Norman W. Thompson   +2 more
openalex   +1 more source

Physiological Basis of Sex Differences in Human Performance and Exercise‐Associated Pathology

Clinical Endocrinology, EarlyView.
ABSTRACT The presence of sex differences in human physical performance is well‐established and shaped by distinct endocrine, anatomical and physiological mechanisms. Despite sustained advances, our understanding of how inherent biological factors drive variations in exercise capacity and related pathologies is still developing.
David A. Holdsworth, Thomas J. O'Leary, Craig L. Doig, Natalie Taylor, Jasminder Dosanjh, David R. Woods, Michael J. Stacey, Robert M. Gifford   +7 more
wiley   +1 more source

CYP11B2/CYP11B1 Immunophenotyping of 111 Adrenal Glands Excised from Primary Aldosteronism Patients leads to a Novel Classification of the Disease

, 2016
Francesca Gioco
openalex   +1 more source

Obesity in Classic Congenital Adrenal Hyperplasia: Mechanisms, Complications and Management

Clinical Endocrinology, EarlyView.
ABSTRACT Classic congenital adrenal hyperplasia (CCAH) is an autosomal recessive genetic disorder primarily caused by 21‐hydroxylase deficiency. Although the survival rate of patients has significantly improved with glucocorticoid replacement therapy, long‐term use of supraphysiological doses and multiple factors inherent to the disease itself have led
Jialin Mu, Yue Li, Meng Sun, Yulin Li, Panpan Li, Hui Zou   +5 more
wiley   +1 more source

The Adrenal Gland: Common Disease States and Suspected New Applications [PDF]

, 2013
Linda S. Gorman
openalex   +1 more source

Challenges in Diagnosing Central Adrenal Insufficiency in Children: Cortisol‐Stimulating Tests are Safe and Often Required

Clinical Endocrinology, EarlyView.
ABSTRACT Introduction The accuracy and safety of cortisol‐stimulating tests (CSTs) for assessing hypothalamic–pituitary–adrenal (HPA) axis integrity, including the diagnosis of central adrenal insufficiency (CAI), in children remain uncertain. Although these tests can simultaneously evaluate cortisol and growth hormone secretion, the present study ...
Mariana Peduti Halah, Ana Carolina Maia Teodózio, Davi Casale Aragon, Paula Conde Lamparelli Elias, Margaret de Castro, Ayrton Custodio Moreira, Sonir Rauber Antonini   +6 more
wiley   +1 more source

HISTOLOGICAL STUDIES ON THE RELATION OF THE ADRENAL GLANDS AND OVARIES TO THE NEOPLASTIC DISEASES OF THE BREAST

, 1958
Ko Takuma
openalex   +1 more source