Results 101 to 110 of about 47,675 (242)

Genetic Testing Referral Rates for Pheochromocytoma and Paraganglioma in an Academic Tertiary Centre

open access: yesClinical Endocrinology, Volume 103, Issue 2, Page 147-156, August 2025.
ABSTRACT Background Clinical guidelines recommend genetic counselling for all patients with pheochromocytoma or paraganglioma (PPGL). Barriers to accessing genetics evaluation are incompletely understood. The objective of this study was to identify individual‐ and provider‐level barriers to genetic testing.
Brian Ruhle   +8 more
wiley   +1 more source

Anaesthetic management of pheochromocytoma [PDF]

open access: bronze, 1966
Evelyn R. Engelbrecht   +2 more
openalex   +1 more source

Pheochromocytoma [PDF]

open access: yesScandinavian Journal of Surgery, 2004
L, Fernández-Cruz   +3 more
openaire   +2 more sources

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

open access: yesClinical Endocrinology, Volume 103, Issue 2, Page 157-166, August 2025.
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   +3 more
wiley   +1 more source

Recurrent Takotsubo Cardiomyopathy With Variable Patterns and Psychiatric Comorbidities: A Case Report and Comprehensive Literature Review

open access: yesClinical Case Reports, Volume 13, Issue 7, July 2025.
ABSTRACT Takotsubo cardiomyopathy (TTC) is a transient stress‐induced cardiac syndrome that can mimic acute coronary syndrome but typically lacks obstructive coronary disease. We report a case of a 50‐year‐old woman with complex psychiatric comorbidities who developed classical apical TTC following acute emotional distress—distinct from a prior reverse
Hamza AlKowatli   +7 more
wiley   +1 more source

Transmission ratio distortion of germline TP53 variants in Li–Fraumeni syndrome families

open access: yesCancer, Volume 131, Issue 13, 1 July 2025.
Abstract Background Li–Fraumeni syndrome (LFS) is a rare autosomal‐dominant cancer‐predisposition syndrome caused by germline pathogenic or likely pathogenic variants (P/LPVs) in the TP53 gene. Classical autosomal‐dominant inheritance predicts a 50% transmission rate of TP53 P/LPV from each carrier parent to their offspring.
Naama Halpern   +10 more
wiley   +1 more source

Actinidia spp. (Kiwifruit): A Comprehensive Review of Its Nutraceutical Potential in Disease Mitigation and Health Enhancement

open access: yesFood Frontiers, Volume 6, Issue 4, Page 1765-1788, July 2025.
Nutraceutical Potential in Disease Mitigation and Health Enhancement of Actinidia spp. (Kiwifruit) ABSTRACT This review offers an in‐depth exploration of the Actinidia species (kiwifruit) nutritional composition, the pivotal role of its primary bioactive compounds, and their potential applications across the aforementioned health concerns. Furthermore,
Allah Rakha   +7 more
wiley   +1 more source

PHEOCHROMOCYTOMA [PDF]

open access: bronze, 1961
R. O. Diefendort   +2 more
openalex   +1 more source

Mid‐Regional Proadrenomedullin Can Be Reliably Measured in Cerebrospinal Fluid to Improve Diagnosis of Central Nervous System Diseases

open access: yesJournal of Clinical Laboratory Analysis, Volume 39, Issue 13, July 2025.
Numerous evidences suggest that Adrenomedullin represents an important regulator of endothelial homeostasis also in the central nervous system and may have a role in infectious, inflammatory, and degenerative neurological diseases. Mid‐regional proadrenomedullin (MR‐proADM) can be reliably measured in cerebrospinal fluid using commercially available ...
Matteo Furlani   +7 more
wiley   +1 more source

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