Results 91 to 100 of about 108,225 (340)

An unusual presentation of pheochromocytoma accompanied by catecholamine-induced cardiomyopathy. [PDF]

ESC Heart Fail
ESC Heart Failure, Volume 12, Issue 5, Page 3776-3779, October 2025.
Roberts HOJ, Munteanu A, Mertens JE.
europepmc   +2 more sources

Mutations of the ret protooncogene in German multiple endocrine neoplasia families: Relation between genotype and phenotype. [PDF]

, 1996
It has been suggested that not only the position but also the nature of the mutations of the ret protooncogene strongly correlate with the clinical manifestation of the multiple endocrine neoplasm type 2 (MEN 2) syndrome.
Deckart, H. F., Dralle, H., Frank-Raue, K., Frilling, A., Haase, R., Hampel, R., Höppner, W., Kirchner, R., Klempa, J., Kotzerke, J., Mann, K., Raue, F., Rendl, J., Ritter, M. M., Scholz, G. H., Seif, F.   +15 more
core   +1 more source

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

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

65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma.

Endocrine-Related Cancer, 2018
Although the authors of the present review have contributed to genetic discoveries in the field of pheochromocytoma research, we can legitimately ask whether these advances have led to improvements in the diagnosis and management of patients with ...
H. Neumann, W. Young, T. Krauss, J. Bayley, F. Schiavi, G. Opocher, C. Boedeker, Amit Tirosh, F. Castinetti, J. Ruf, D. Beltsevich, M. Walz, H. Groeben, E. von Dobschuetz, O. Gimm, N. Wohllk, M. Pfeifer, D. Lourenço, M. Peczkowska, A. Patócs, J. Ngeow, Ö. Makay, N. Shah, A. Tischler, Helena Leijon, G. Pennelli, K. Villar Gómez de las Heras, T. Links, B. Bausch, C. Eng   +29 more
semanticscholar   +1 more source

Somatic symptom disorder in dermatology [PDF]

, 2017
Somatic symptom disorder (SSD) is defined by the prominence of somatic symptoms associated with abnormal thoughts, feelings, and behaviors related to the symptoms, resulting in significant distress and impairment.
Levenson, James L., Ortega-Loayza, Alex G., Sharma, Aditi A.   +2 more
core   +2 more sources

Onion extract and grape seed powder as antioxidants to improve growth: Evidence from studies with oxidative stressed intestinal and liver cells as well as growing broilers

JSFA reports, EarlyView.
Abstract Background Oxidative stress negatively impacts the growth, health, and overall welfare of animals. Plant extracts have great potential in mitigating oxidative stress. This study aims to evaluate the antioxidant capacities of onion extract and grape seed powder in vitro, and the potential benefits of a polyphenol product (obtained from onion ...
Siqiao Wu, Zejian Liu, Poulad Pourazad, Xiaodan Zhou, Wendeline Wouters, Thierry Aubert, Maria Helena Lino Bento, Rachida Benamri, Karin Schwarzbauer, Amrutha Stallinger, Petra Preinfalk, Thomas Pecqueur, Chunqi Gao   +12 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

Synergistic Highly Potent Targeted Drug Combinations in different Pheochromocytoma Models including Human Tumor Cultures.

Endocrinology, 2019
There are no officially approved therapies for metastatic pheochromocytomas apart from ultratrace 131I-MIBG therapy approved only in the United States.
M. Fankhauser, Nicole Bechmann, M. Lauseker, Judith Goncalves, J. Favier, B. Klink, D. William, L. Gieldon, J. Maurer, G. Spöttl, P. Rank, T. Knösel, M. Orth, C. Ziegler, E. T. Aristizabal Prada, G. Rubinstein, M. Fassnacht, C. Spitzweg, A. Grossman, K. Pacak, F. Beuschlein, S. Bornstein, G. Eisenhofer, C. Auernhammer, M. Reincke, S. Nölting   +25 more
semanticscholar   +1 more source

Molecular Aspects of Secretory Granule Exocytosis by Neurons and Endocrine Cells [PDF]

, 1994
Neuronal communication and endocrine signaling are fundamental for integrating the function of tissues and cells in the body. Hormones released by endocrine cells are transported to the target cells through the circulation.
Ahnert-Hilger G., Ahnert-Hilger G., Bader M. F., Baumert M., Bittner M. A., Bittner M. A., Bittner M. A., Blasi J., Elferink L. A., Fischer G., Geppert M., Halpern J. L., Hess S. D., Jahn R., MANFRED GRATZL, Marqueze-Pouey B., McMahon H. T., Schiavo G., Schiavo G., Schiavo G., Schmidle T., Shirataki H., Shoji-Kasai Y., Stecher B., Thomas L., Trimble W. S., Walch-Solimena C., Wright J. F., Yoshida A.   +28 more
core   +1 more source