Results 51 to 60 of about 36,515 (205)

The effects of royal jelly on human health: A narrative review of clinical studies

JSFA reports, EarlyView.
Abstract Royal jelly (RJ) is a natural bioactive substance with documented effects on human health. This narrative review synthesizes evidence from clinical and clinically relevant experimental studies evaluating the therapeutic potential of RJ.
Georgios Goras, Andreas Thrasyvoulou, Evanthia Tsilimpokou   +2 more
wiley   +1 more source

Bidirectional Ventricular Tachycardia due to Pheochromocytoma: A Case Report

Annals of Noninvasive Electrocardiology
Pheochromocytoma, a type of neuroendocrine tumor, can cause numerous symptoms and signs similar to those of other clinical conditions, with the classic triad being palpitations, headache, and diaphoresis.
Gui‐yang Li, Man‐Xin Lin, Fa‐Guang Zhou, Qiang Li   +3 more
doaj   +1 more source

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

Journal 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, Cecilia Jimeno, Elizabeth Paz-Pacheco   +2 more
doaj   +1 more source

Update on the Pathophysiology, Aetiology and Management of Central Sleep Apnoea

Respirology, EarlyView.
ABSTRACT Central sleep apnoea (CSA) of the periodic breathing type occurs during the transition between wakefulness and stage 1 and 2 non‐REM sleep. In adults at sea level, it occurs most commonly due to advanced heart failure (HF) or chronic opioid use and in ~5% of obstructive sleep apnoea patients initiating CPAP.
Sahan D. Chandrasekara, Matthew T. Naughton   +1 more
wiley   +1 more source

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

Kaohsiung 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, Muzaffer Serdar Deniz, Belma Ozlem Tural Balsak, Yilmaz Aslan, Altug Tuncel, Dilek Berker   +5 more
doaj   +1 more source

Management of bladder pheochromocytoma by transurethral resection

Asian Journal of Urology, 2019
Bladder pheochromocytoma is the most common extra-adrenal genitourinary tumor. Endoscopic management is feared due to the risk of intra-operative hypertensive crisis.
Aditya P. Sharma, Girdhar S. Bora, Ravimohan S. Mavuduru, Vikas K. Panwar, Bhagwant R. Mittal, Shrawan K. Singh   +5 more
doaj   +1 more source

Effects of Tributyltin Chloride on Human Neuronal Differentiation and Mice Brain Development

Environmental Toxicology, EarlyView.
ABSTRACT According to the developmental origins of health and disease hypothesis, perinatal exposure to an environmental toxicant during the development of the nervous system could cause a permanent cellular modification that may promote the appearance of neurodegenerative diseases at an older age.
Ester López‐Gallardo, Patricia Meade, Irene Jiménez‐Salvador, Carmen Hernández‐Ainsa, Eldris Iglesias, Alba Pesini, Nuria Garrido‐Pérez, Sonia Emperador, David Pacheu‐Grau, Pilar Bayona‐Bafaluy, Eduardo Ruiz‐Pesini   +10 more
wiley   +1 more source

Functional urinary bladder paraganglioma in a child presenting with obstructive uropathy: A rare case report

UroPrecision, EarlyView.
Abstract Background Pediatric urinary bladder paraganglioma is an exceptionally rare neuroendocrine tumor arising from chromaffin cells within the detrusor muscle. Due to its rarity and variable presentation, early diagnosis can be challenging, often requiring a high index of clinical suspicion and multimodal evaluation.
Shameer Tahir, Eisha Sattar, Javeria Khan   +2 more
wiley   +1 more source

A case of pheochromocytoma presenting with cardiac manifestation: case report

BMC 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, Vahideh Abarzadeh-Bairami, Seyyed-Reza Sadat-Ebrahimi   +2 more
doaj   +1 more source

Laparoscopic management of recurrent pheochromocytoma: A case report

Journal 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, Manpreet Uppal, Sreesanth Kelu Sreedharan, Sandeep Aggarwal   +3 more
doaj   +1 more source