Results 51 to 60 of about 40,494 (191)

Optical excitation and detection of neuronal activity [PDF]

, 2017
Optogenetics has emerged as an exciting tool for manipulating neural activity, which in turn, can modulate behavior in live organisms. However, detecting the response to the optical stimulation requires electrophysiology with physical contact or ...
Gillette, Martha, Hu, Chenfei, Kim, Taewoo, Nastasa, Viorel, Popescu, Gabriel, Sam, Richard, Sengupta, Parijat, Shan, Mingguang, Wang, Minqi   +8 more
core   +2 more sources

Clinical comparison and genetic analysis in pheochromocytoma with primary aldosteronism

Endocrine Journal
Pheochromocytoma is a rare form of adrenal hypertension. This study aimed to investigate the clinical characteristics and associated genetic mutations in patients with pheochromocytoma and primary aldosteronism.
Xurong Mai, Mitsuhiro Kometani, Toshiaki Kato, Ko Aiga, Shigehiro Karashima, Daisuke Aono, Seigo Konishi, Koshiro Nishimoto, Kazuyoshi Hosomichi, Atsushi Watanabe, Yuko Noda, Yoshiyu Takeda, Takashi Yoneda   +12 more
doaj   +1 more source

‘Adrenal rush’ in a patient with Neurofibromatosis-1

Journal of Community Hospital Internal Medicine Perspectives, 2020
Neurofibromatosis-1 (NF-1) is a genetic neuro-cutaneous disorder that is associated with an increased prevalence of pheochromocytoma (PHEO). However, this association may not be commonly anticipated by physicians, as patients may be normotensive.
Samiha Khan, Beenish Fayyaz, Janki Patel
doaj   +1 more source

Pheochromocytoma of the urinary bladder: a case report [PDF]

, 2009
Urinary bladder pheochromocytoma is rare. From a case report of unsuspected pheochromocytoma and literature review, the authors develop a diagnostic and therapeutic algorithm for the management of this ectopic pheochromocytoma ...
Ahallal, Youness, Amarti, Afaf, Benlemlih, Amal, Chbani, Leila, EL Fassi, Mohammed Jamal, Farih, Moulay Hassan, Tazi, Elmehdi, Tazi, Mohammed Fadl   +7 more
core   +2 more sources

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

Journal 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, Ramanitharan Manikandan, Lalgudi Narayanan Dorairajan, Pampa Ch Toi   +3 more
doaj   +1 more source

Case Report: Pheochromocytoma and Synchronous Neuroblastoma in a Family With Hereditary Pheochromocytoma Associated With a MAX Deleterious Variant

Frontiers in Endocrinology, 2021
IntroductionPheochromocytomas are rare catecholamine-producing neuroendocrine tumours arising from chromaffin cells of the adrenal medulla or extra-adrenal sympathetic paraganglia.
Diana Borges Duarte, Lia Ferreira, Ana P. Santos, Cláudia Costa, Jorge Lima, Jorge Lima, Jorge Lima, Catarina Santos, Mariana Afonso, Manuel R. Teixeira, Manuel R. Teixeira, Rui Carvalho, Maria Helena Cardoso   +12 more
doaj   +1 more source

Detection of severe hypertension in a patient with neurofibromatosis type 1 during anesthesia induction: a case report

Journal of Medical Case Reports, 2019
Background Neurofibromatosis type 1 has a higher prevalence of pheochromocytoma and paraganglioma than the general population: 1.0–5.7% versus 0.2–0.6%.
Juan Wang, Guohua Wei, Zhongyun Wang, He Huang   +3 more
doaj   +1 more source

Giant cystic pheochromocytoma: A silent entity

Urology 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, Lovenish Bains, Manish Kumar Agarwal, Renu Gupta   +3 more
doaj   +1 more source

Chirurgie der Hyperthyreose [PDF]

, 1978
Pathophysiologie, Diagnostik, Operationsindikation und Vorbehandlung, chirurgisches Krankengut, Operationsverfahren und Nachbehandlung mit funktionellen Spätergebnissen wurden gezeigt.
Günther, B., Heberer, G., Kiffner, E., Pickardt, C. R., Scriba, Peter Christian, Spelsberg, F.   +5 more
core   +1 more source

Pediatric malignant pheochromocytoma with atypical presentation as vision changes, lung metastasis, and recurrence: a case report

Journal of Medical Case Reports
Background This case report documents a case of malignant pheochromocytoma manifested as vision changes with lung metastasis and recurrence. Case presentation A 10-year-old Han Chinese girl presented with vision changes and was eventually diagnosed with ...
Kaijun Zhang, Penghui Yang, Mi Li, Ping Xiang, Zhenli Cheng, Xue Zhou   +5 more
doaj   +1 more source