Results 51 to 60 of about 47,675 (242)

A case of pheochromocytoma presenting with cardiac manifestation: case report

open access: yesBMC Pediatrics, 2020
Background Pheochromocytomas are rare tumors originating in chromaffin cells which predominantly are located in adrenal glands. Sustained or paroxysmal hypertension (HT) is the most frequent sign of pheochromocytoma.
Akbar Molaei   +2 more
doaj   +1 more source

Cordycepin mediates neuroprotection against apoptosis via ERK/CREB signaling activation in Aβ1–42‐induced neuronal cell models

open access: yesIbrain, Volume 11, Issue 1, Page 84-97, Spring 2025.
This study demonstrates cordycepin's neuroprotective effects against Aβ1–42‐induced apoptosis in neuronal cells, mediated through the activation of the extracellular signal‐regulated kinase/cyclic AMP‐responsive element‐binding protein (ERK/CREB) signaling pathway.
Wenshu Zhou   +6 more
wiley   +1 more source

Recurrent malignant pheochromocytoma with lymph nodal metastasis in a child: A rare case

open access: yesJournal of Indian Association of Pediatric Surgeons, 2017
Malignant pheochromocytoma in children manifesting as local recurrence with multiple lymph nodal metastasis is a rare entity. We report a case of a 14-year-old child with recurrent sporadic malignant pheochromocytoma presenting 8 years after primary ...
Jayesh Mittal   +3 more
doaj   +1 more source

Ocular muscle metastasis as the initial presentation of a malignant pheochromocytoma: A unique case

open access: yesClinical Case Reports, 2020
In this paper, we discuss a unique manifestation of malignant pheochromocytoma, which presented with ocular pain. The histopathological study pointed to a possible pheochromocytoma origin.
Gholamreza Khataminia   +6 more
doaj   +1 more source

Giant cystic pheochromocytoma: A silent entity

open access: yesUrology Annals, 2016
Pheochromocytoma is a catecholamine secreting tumor that originate from chromaffin cells. Usually, it is solid neoplasm of the adrenal medulla, however cystic pheochromocytoma is a rare neuro-endocrine tumour that is frequently asymptomatic and often ...
Amit Gupta   +3 more
doaj   +1 more source

A comparative analysis of surgically excised hereditary and sporadic pheochromocytomas: Insights from a single‐center experience

open access: yesKaohsiung Journal of Medical Sciences
Pheochromocytoma is a tumor that usually originating from adrenal medullary chromaffin cells and producing one or more catecholamines, can manifest as hereditary or sporadic.
Narin Nasiroglu Imga   +5 more
doaj   +1 more source

Investigating the Optical and Thermodynamic Properties of 2D MoGe2P4: Potential Material for Photothermal Therapy

open access: yesNano Select, EarlyView.
• 2D MoGe2P4 demonstrates excellent optical absorption in the NIR‐I window (750–1000 nm). • High thermal conductivity (63 W/m/K) and photothermal stability over multiple laser cycles. • Efficient photothermal conversion under low laser power (0.5 W/cm2, operating λ = 808 nm), achieving therapeutic temperature thresholds within 2 min.
Sudipta Saha   +3 more
wiley   +1 more source

Epidemiologic Profile and Clinical Outcomes of Patients with Pheochromocytoma at the University of the Philippines - Philippine General Hospital (UP-PGH)

open access: yesJournal of the ASEAN Federation of Endocrine Societies
Objective. This study aims to describe the epidemiologic profile and determine the clinical outcomes of patients with pheochromocytoma at the University of the Philippines Philippine General Hospital (UP-PGH). Methodology.
Edrome Hernandez   +2 more
doaj   +1 more source

A comprehensive review on adaptive plasticity and recovery mechanisms post‐acquired brain injury

open access: yesNeuroprotection, EarlyView.
This figure illustrates the dynamic process of neurogenesis following brain injury, focusing on the roles of neural stem and progenitor cells at the injury site. Key mechanisms include axonal sprouting, synaptogenesis, dendritic remodeling, and brain‐derived neurotrophic factor signaling via TrkB receptors.
Ravi Kumar Rajan
wiley   +1 more source

Laparoscopic management of recurrent pheochromocytoma: A case report

open access: yesJournal of Minimal Access Surgery, 2016
Recurrence of pheochromocytoma after a total adrenalectomy is uncommon. Such recurrent tumours are mostly managed by the open technique, with very few studies reporting laparoscopic management.
Harshit Garg   +3 more
doaj   +1 more source

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