Results 101 to 110 of about 9,658 (273)

The Concise Guide to PHARMACOLOGY 2025/26: Enzymes

British Journal of Pharmacology, Volume 182, Issue S1, Page S307-S403, December 2025.
The Concise Guide to Pharmacology 2025/26 marks the seventh edition in this series of biennial publications in the British Journal of Pharmacology. Presented in landscape format, the guide provides a comparative overview of the pharmacology of drug target families. The concise nature of the Concise Guide refers to the style of presentation, being clear,
Stephen P. H. Alexander, Doriano Fabbro, Alasdair J. Gibb, Eamonn Kelly, Alistair A. Mathie, Chloe J. Peach, Emma L. Veale, Jane F. Armstrong, Elena Faccenda, Simon D. Harding, Christopher Southan, Jamie A. Davies, Stephanie Annett, Detlev Boison, Kathryn Elisa Burns, Carmen Dessauer, Jürg Gertsch, Nuala Ann Helsby, Angelo A. Izzo, Rennolds Ostrom, Ester Pagano, Andreas Papapetropoulos, Nigel J. Pyne, Susan Pyne, Tracy Robson, Roland Seifert, Johannes‐Peter Stasch, Csaba Szabo, Mario van der Stelt, Albert van der Vliet, Val Watts, Szu Shen Wong   +31 more
wiley   +1 more source

Atypical Neuroblastoma With Absent Urinary Catecholamine Excretion and 123ImIBG Avidity Are of Favorable Outcome: A Retrospective French Single‐Center Study

Pediatric Blood &Cancer, Volume 72, Issue 11, November 2025.
Abstract Background In neuroblastoma (NB), urinary catecholamine excretion and 123ImIBG avidity—depending on tumor enzymatic activity and norepinephrine transporter expression, respectively—are diagnostic standards. The prognostic impact of atypical NB, without urinary catecholamine excretion and/or 123ImIBG avidity, remains to be determined. We sought
Anna Borovkov, Juliette Assy, Isabelle Aerts, Franck Bourdeaut, Camille Cordero, Valérie Laurence, Amaury Leruste, Sarah Winter, Jean Michon, Daniel Orbach, Hélène Pacquement, Pascale Philippe‐Chomette, Gaelle Pierron, Julien Masliah‐Planchon, Sylvie Helfre, Isabelle Janoueix‐Lerosey, Anne‐Sophie Defachelles, Claudia Pasqualini, Nina Jehanno, Joanna Cyrta, Arnaud Gauthier, Véronique Mosseri, François Doz, Sabine Sarnacki, Liesbeth Cardoen, Hervé J. Brisse, Marie Luporsi, Gudrun Schleiermacher   +27 more
wiley   +1 more source

Differences in Clinical Presentation Between Pheochromocytomas and Paragangliomas

Clinical Endocrinology, Volume 103, Issue 5, Page 651-658, November 2025.
ABSTRACT Objectives Pheochromocytomas and sympathetic paragangliomas (PPGLs) are similar in most aspects. However, they differ in genetic etiology, hormonal secretion, and associated neoplasms. This study aimed to investigate differences in clinical presentation between PPGLs. Design This study employs a retrospective cohort design. Patients The cohort
Vincent E. D. Pihlblad, Jan Calissendorff, Henrik Falhammar   +2 more
wiley   +1 more source

Untying the Next Genetic Thread in a Family With MEN2A Syndrome: A Case Report

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Multiple endocrine neoplasia type 2A (MEN2A) is a rare autosomal dominant syndrome characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, and primary hyperparathyroidism. Early genetic screening is crucial for timely intervention. We report a familial case of MEN2A involving four affected members across two generations.
Riyaz Shrestha, Mohammad Adnan Adil, Binita Basnet, Himal Karki, Pukar Maskey, Samir Shrestha, Mohammad Nasim Alam   +6 more
wiley   +1 more source

Bilateral Adrenal Mass Secondary to Bilateral Infantile Neuroblastoma in an Infant With Beckwith‐Wiedemann Syndrome

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Infants with Beckwith‐Wiedemann syndrome face a high risk of embryonal tumors, necessitating early and consistent surveillance. This case illustrates how timely imaging and biochemical monitoring enabled successful non‐surgical management of bilateral adrenal neuroblastoma.
Mulualeme Nigusie, Gashaw Arega, Abel Hailu, Abreham Kassahun, Getasew Fikad, Tigest Chalachew, Bargude Balta   +6 more
wiley   +1 more source

Plasma and urinary metanephrine and normetanephrine concentrations using liquid chromatography with tandem mass spectrometry in healthy cats and in a cat with pheochromocytoma [PDF]

, 2023
Maria Teresa Prego, Maria Joana Dias, Rui Lemos Ferreira, Salomé Gonçalves, Tiago Dias Domingues, Greet Junius, Evi Van den Steen, Sara Galac, Rodolfo Oliveira Leal   +8 more
openalex   +1 more source

Pseudo‐Hypoaldosteronism Type 2 due to New Variants of KLHL3 Gene Diagnosed in an Adult Woman With Very High Sensitivity to Hydrochlorothiazide

Clinical Case Reports, Volume 13, Issue 9, September 2025.
ABSTRACT We report a case of pseudo‐hypoaldosteronism type 2 (PHA II) in a hypertensive 55‐year‐old woman who carried new variants of the KLHL3 gene. Hypersensitivity to hydrochlorothiazide was noted. Low dosages of hydrochlorothiazide were needed to restore potassium levels.
Massimo Giusti, Monica Repetto, Carmela Caputo   +2 more
wiley   +1 more source

Late‐Onset Bone Metastasis 46 Years After Initial Surgery for Pheochromocytoma: A Case Report

IJU Case Reports, Volume 8, Issue 5, Page 533-538, September 2025.
ABSTRACT Introduction Pheochromocytoma is a rare catecholamine‐producing tumor with metastatic potential. Recurrence after more than 40 years is exceptionally rare. Case Presentation During evaluation for ischemic colitis, a 71‐year‐old woman was found to have multiple bone metastases, possibly linked to catecholamine excess.
Fumio Ishizaki, Kaede Hiruma, Yusuke Tani, Hideaki Sugino, Tatsuro Sanami, Tsutomu Anraku, Masahiro Ikeda, Masayuki Tasaki, Kazuhide Saito, Yoshihiko Tomita   +9 more
wiley   +1 more source

Trends of surgical treatment and enhanced recovery after surgery (ERAS) application for adrenal tumors: An 11‐year observational study based on electronic medical record

UroPrecision, Volume 3, Issue 3, Page 153-160, September 2025.
Abstract Background Adrenal tumor is a common condition that often requires adrenalectomy. The objective of this study is to compare the safety and implementation of the enhanced recovery after surgery (ERAS) among patients who received open, laparoscopic and robotic‐assisted operation.
Bingfeng Luo, Chi Yao, Yongle Zhan, Yuan Yuan, Sucai Liao, Zhenquan Lu, Rong Na, Richard K. Lo   +7 more
wiley   +1 more source

Paraganglioma: A cause of hypertension in a young patient [PDF]

, 2012
Introduction. Collections of neuroendocrine cells dispersed throughout the body are known as paraganglia and the tumor arising from these paraganglia are known as paragangliomas.
Marković Slobodan, Rakonjac Nataša
core   +1 more source