Results 291 to 300 of about 241,535 (385)

Endocrinology of the hypothalamus and the pituitary gland [PDF]

, 1973
Kuhlendahl, Hans, Scriba, Peter Christian   +1 more
core   +1 more source

Diverse clinical manifestations and management strategies in autoimmune polyglandular syndrome: a review of cases. [PDF]

Ann Med Surg (Lond)
Lalrehman U, Hamza HM, Malik MM, Ali M, Nayab U, Ahmed S, Awan AA.   +6 more
europepmc   +1 more source

Cytological Assessment of Adrenal Tumours: Insights From 22‐Years Single Centre Experience

Clinical Endocrinology, EarlyView.
ABSTRACT Objective The incidence of adrenal tumours has increased in the last decades, mainly due to increased use of imaging. The diagnostic evaluation of adrenal masses can be complex and, in some cases, necessitates cytological evaluation. However, concerns remain regarding the potential complications associated with adrenal gland biopsy.
Ana Carasel, Jan Calissendorff, C. Christofer Juhlin, Henrik Falhammar   +3 more
wiley   +1 more source

Adrenal Tumors in Children and Adolescents in Sweden: A Register-Based Study Covering 15 Years. [PDF]

J Endocr Soc
Terezaki E, Calissendorff J, Mannheimer B, Lindh JD, Falhammar H.   +4 more
europepmc   +1 more source

Predictors of Mortality in Patients With Multiple Endocrine Neoplasia Type 1

Clinical Endocrinology, EarlyView.
SUMMARY Objective Multiple Endocrine Neoplasia Type 1 (MEN 1) is an autosomal dominant disease predisposing to hyperplasia and neoplasia in diverse endocrine tissues. Patients typically present with endocrine abnormalities before the age of 30 years and have reduced life expectancy.
Jasmine J. Zhu, John R Burgess
wiley   +1 more source

Cytologic Evaluation as a Diagnostic Tool to Differentiate Adrenocortical Tumors and Pheochromocytomas. [PDF]

J Vet Intern Med
Piegols HJ, Williams RW, Pathak N, Selmic LE, Tremolada G, Sakacs R, Millward L, Lapsley J.   +7 more
europepmc   +1 more source

Salivary Testosterone, Androstenedione and 11‐Oxygenated 19‐Carbon Concentrations Differ by Age and Sex in Children

Clinical Endocrinology, EarlyView.
ABSTRACT Background The diagnosis and management of childhood adrenal disorders is challenging. Clinical markers of hormone excess or deficiency may take months to manifest, and traditional biomarkers correlate only partially with clinical outcomes.
Julie Park, Andrew Titman, Orla Bright, Silothabo Dliso, Alena Shantsila, Gregory Y. H. Lip, Jo Adaway, Brian Keevil, Daniel B. Hawcutt, Joanne Blair   +9 more
wiley   +1 more source

Oncocytic Adrenal Tumors: A Tri-Focal Review with Integrated Cytopathological, Pathological, and Molecular Perspectives.

Acta Cytol
Condello V, Bongiovanni M, Juhlin CC.
europepmc   +1 more source

The ACTH test fails to diagnose adrenal insufficiency and augments cytokine production in sepsis. [PDF]

JCI Insight
Hao D, Wang Q, Ito M, Xue J, Guo L, Huang B, Mineo C, Shaul PW, Li XA.   +8 more
europepmc   +1 more source

Delayed Bone Maturation and Extended Growth Phase as Distinctive Features of 17α‐Hydroxylase/17,20‐Lyase Deficiency: A Retro‐Prospective Study of a Large Patient Cohort

Clinical Endocrinology, EarlyView.
ABSTRACT Introduction Worldwide, combined 17‐hydroxylase/17,20‐lyase deficiency (CYP17D) is a rare form of congenital adrenal hyperplasia, but it is the second most prevalent type in Brazil. An absence of sexual differentiation and hypergonadotropic hypogonadism arise from a reduction in the usual pattern of sex steroid formation in the adrenals and ...
Rafaela Fontenele, Flávia A. Costa‐Barbosa, Marivânia Costa‐Santos, Rafael L. Batista, Lívia M. Mermejo, Berenice B. Mendonça, Margaret de Castro, Gil Guerra‐Júnior, Claudio E. Kater, Brazilian Congenital Adrenal Hyperplasia Multicenter Study Group (BCAHMSG)   +9 more
wiley   +1 more source