Results 91 to 100 of about 82,056 (278)

Pathologic Fracture as Primary Presentation of Malignant Pheochromocytoma: A Case Report

Acta Medica Iranica, 2019
Pheochromocytoma is a relatively rare tumor with no age preference. This tumor is usually diagnosed accidentally.  Pathologic fracture as the primary presentation of malignant pheochromocytoma is an uncommon presentation.
Azar Fanipakdel, Yasamin Davoudi, Seyed Alireza Javadinia, Mahdi Silanian Toosi   +3 more
doaj  

Co‐localization of tau and TDP‐43 after extracellular vesicle delivery to cells

The FEBS Journal, EarlyView.
Extracellular vesicles (EVs) derived from donor cells transfected with EGFP–2N4R‐tau or mCherry‐wtTDP‐43 were taken up by recipient cells, leading to cytosolic co‐localization of tau and TDP‐43. Molecular modeling revealed that tau and TDP‐43 directly interact through hydrogen bonding, suggesting a mechanistic link underlying their co‐pathology ...
Farhang Aliakbari, Kathryn Volkening, Zahra Nayeri, Aysegul Yucel Polat, Neil Donison, Jacqueline Palik, Michael J. Strong   +6 more
wiley   +1 more source

Diagnosis and surgical treatment of multiple endocrine neoplasia type 2A [PDF]

, 2014
BACKGROUND: This study aims to introduce the diagnosis and surgical treatment of the rare disease multiple endocrine neoplasia type 2A (MEN 2A). METHODS: Thirteen cases of MEN 2A were diagnosed as medullary thyroid carcinoma (MTC) and pheochromocytoma by
Kun-Long Tang, Li-Ming Li, Yi Lin
core   +1 more source

FEOCROMOCITOMA PHEOCHROMOCYTOMA

Revista Clínica Escuela de Medicina UCR-HSJD, 2019
El feocromocitoma es un tumor neuroendocrino, derivado de la cresta neural y que se caracteriza por ser productor de catecolaminas. En su mayoría se presentan entre la cuarta y quinta década, sin diferenciación alguna entre los sexos. Un 20 a 40% de los pacientes presenta la triada clásica de los feocromocitomas, compuesta por: cefalea ...
González León, Danny, Arguedas Ortíz, María José, Rockbrand Campos, Leyla Priscilla   +2 more
openaire   +4 more sources

Patients with pheochromocytoma exhibit low aldosterone renin ratio-preliminary reports [PDF]

, 2020
Tomoko Yamada, Hidenori Fukuoka, Yusei Hosokawa, Yukiko Odake, Ken‐ichi Yoshida, Ryusaku Matsumoto, Hironori Bando, Yuko Okada, Yushi Hirota, Genzo Iguchi, Wataru Ogawa, Yutaka Takahashi   +11 more
openalex   +1 more source

Dermatologic Features of Endocrine Tumor Syndromes—Systematic Review and Meta‐Analysis

International Journal of Dermatology, EarlyView.
ABSTRACT Endocrine tumor syndromes, including multiple endocrine neoplasia types 1, 2A, and 2B (MEN1, MEN2A, MEN2B), Carney complex (CNC), and PTEN hamartoma tumor syndrome (PHTS), are hereditary conditions characterized by multisystem tumor development.
Sára Pálla, Zseraldin Metyovinyi, Fanni Adél Meznerics, Arash Mirzahosseini, Judit Tőke, Miklós Tóth, Henriett Butz, Attila Patócs, Márta Medvecz   +8 more
wiley   +1 more source

Succinate dehydrogenase (SDH)-deficient renal carcinoma:a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients [PDF]

, 2014
Succinate dehydrogenase (SDH)-deficient renal carcinoma has been accepted as a provisional entity in the 2013 International Society of Urological Pathology Vancouver Classification.
Belinsky, Cascon, Cascon, Chou, Dwight, Dwight, Eng, Fairchild, Fishbein, Fleming, Gaal, Gill, Gill, Gill, Gill, Gill, Gill, Gill, Gill, Gimm, Henderson, Housley, Janeway, Jasperson, Korpershoek, Malinoc, Miettinen, Miettinen, Miettinen, Neumann, Ni, Oudijk, Paik, Papathomas, Ricketts, Ricketts, Said-Al-Naief, Schimke, Solis, Srigley, Srirangalingam, Srirangalingam, van Nederveen, van Nederveen, Vanharanta, Wagner, Xekouki   +46 more
core   +4 more sources

Recommendations for bone‐directed therapy in patients with neuroendocrine tumour skeletal metastases at the New Zealand National Neuroendocrine Tumour Multidisciplinary Meeting

Internal Medicine Journal, EarlyView.
Abstract The role of anti‐resorptive agents in patients with bone metastases from neuroendocrine neoplasms is unclear. Our aim was to review bone‐specific treatment recommendations by the New Zealand National Neuroendocrine Tumour Multidisciplinary Meeting (MDM).
Gayle Radley, Marianne S Elston, Ben Lawrence, Veronica Boyle   +3 more
wiley   +1 more source

Purification of alpha-toxin from Staphylococcus aureus and application to cell permeabilization [PDF]

, 1987
Crude alpha-toxin was produced by Staphylococcus aureus, strain Wood 46. The amount of exotoxin was monitored during growth and all subsequent purification steps by determination of its hemolytic activity against rabbit erythrocytes.
Ahnert-Hilger, Ahnert-Hilger, Bader, Bhakdi, Bhakdi, Bhakdi, Cassidy, Dunn, Füssle, Laemmli, Lowry, McEwen, Möllby, Reynolds, Thelestam, Wadström, Wilson   +16 more
core   +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