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Pheochromocytoma arising from an ectopic adrenal tissue in multiple endocrine neoplasia type 2A.

Ohsugi H, Takizawa N, Kinoshita H, Matsuda T.

Endocrinol Diabetes Metab Case Rep. 2019 Oct 12;2019. pii: EDM190073. doi: 10.1530/EDM-19-0073. [Epub ahead of print]


Weight-loss with activation of brown fat: Suspect pheochromocytoma.

Geslot A, Bennet A, Hitzel A, Thoulouzan M, Mouly C, Savagner F, Quintyn-Ranty ML, Caron P, Vezzosi D.

Ann Endocrinol (Paris). 2019 Jul 26. pii: S0003-4266(19)30089-7. doi: 10.1016/j.ando.2019.06.004. [Epub ahead of print]


Pheochromocytoma as a Clinical Model of Peripheral Sympathetic Overdrive: Old and New Findings.

Grassi G, Trevano FQ, Dell'Oro R, Seravalle G, Mancia G.

Curr Hypertens Rep. 2019 Oct 10;21(11):90. doi: 10.1007/s11906-019-0989-9. Review.


Current Management of Pheochromocytoma/Paraganglioma: A Guide for the Practicing Clinician in the Era of Precision Medicine.

Nölting S, Ullrich M, Pietzsch J, Ziegler CG, Eisenhofer G, Grossman A, Pacak K.

Cancers (Basel). 2019 Oct 8;11(10). pii: E1505. doi: 10.3390/cancers11101505. Review.


Hereditary Diseases Predisposing to Pheochromocytoma (VHL, NF-1, Paraganglioma Syndromes, and Novel Genes).

Sarkadi B, Patócs A.

Exp Suppl. 2019;111:129-147. doi: 10.1007/978-3-030-25905-1_8. Review.


Composite Pheochromocytoma: A Rare Form of Tumor.

Lakshminarayana GR.

Indian J Nephrol. 2019 Sep-Oct;29(5):307-308. doi: 10.4103/ijn.IJN_210_18.


Simple adrenal cyst masquerading clinically silent giant cystic pheochromocytoma.

Kumar S, Parmar KM, Aggarwal D, Jhangra K.

BMJ Case Rep. 2019 Sep 30;12(9). pii: e230730. doi: 10.1136/bcr-2019-230730.


Concurrent heterozygous Von-Hippel-Lindau and transmembrane-protein-127 gene mutation causing an erythropoietin-secreting pheochromocytoma in a normotensive patient with severe erythrocytosis.

Negro A, Graiani G, Nicoli D, Farnetti E, Casali B, Verzicco I, Tedeschi S, Ghirarduzzi A, Cannone V, Marco LDE, Filice A, Gemelli G, Giunta A, Cabassi A.

J Hypertens. 2019 Sep 19. doi: 10.1097/HJH.0000000000002253. [Epub ahead of print]


Two cases of pheochromocytoma in pregnancy: a multidisciplinary challenge.

Chmielewski G, Walczyk A, Kowalska A.

Endokrynol Pol. 2019 Sep 30. doi: 10.5603/EP.a2019.0039. [Epub ahead of print]


Therapies targeting the signal pathways of pheochromocytoma and paraganglioma.

Liu Y, Liu L, Zhu F.

Onco Targets Ther. 2019 Sep 4;12:7227-7241. doi: 10.2147/OTT.S219056. eCollection 2019.



Farrugia FA, Charalampopoulos A.

Endocr Regul. 2019 Jul 1;53(3):191-212. doi: 10.2478/enr-2019-0020.


Diagnostic Accuracy of Computed Tomography to Exclude Pheochromocytoma: A Systematic Review, Meta-analysis, and Cost Analysis.

Buitenwerf E, Berends AMA, van Asselt ADI, Korteweg T, Greuter MJW, Veeger NJM, Links TP, Dullaart RPF, Kerstens MN.

Mayo Clin Proc. 2019 Oct;94(10):2040-2052. doi: 10.1016/j.mayocp.2019.03.030. Epub 2019 Sep 9.


Severe arterial hypertension and hyperandrogenism in a boy: a rare case of catecholamine- and β-HCG-secreting pheochromocytoma.

Chiale F, Abrigo E, Lonati L, Di Rosa G, Morra I, Peruzzi L, Einaudi S.

J Pediatr Endocrinol Metab. 2019 Oct 25;32(10):1193-1197. doi: 10.1515/jpem-2019-0216.


Pheochromocytoma: Positive predictive values of mildly elevated urinary fractionated metanephrines in a large cohort of community-dwelling patients.

Hirsch D, Grossman A, Nadler V, Alboim S, Tsvetov G.

J Clin Hypertens (Greenwich). 2019 Oct;21(10):1527-1533. doi: 10.1111/jch.13657. Epub 2019 Sep 5.


Adrenalectomy for huge solid pheochromocytoma: a challenging surgery or piece of cake?

Labib M, Ismail A, Elmansy H, Shahrour W, Prowse O, Kotb A.

J Surg Case Rep. 2019 Aug 22;2019(8):rjz255. doi: 10.1093/jscr/rjz255. eCollection 2019 Aug.


Catecholamine-induced cardiomyopathy in a patient with pheochromocytoma and polycystic kidney and liver disease: a case report.

Sedaia E, Esanu A, Ivanov V, Dumanschi C, Moiseeva A, Abraș M, Eugen C, Tatiana G.

Eur Heart J Case Rep. 2019 Jun 1;3(2). pii: ytz062. doi: 10.1093/ehjcr/ytz062.


Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy.

Neumann HPH, Tsoy U, Bancos I, Amodru V, Walz MK, Tirosh A, Kaur RJ, McKenzie T, Qi X, Bandgar T, Petrov R, Yukina MY, Roslyakova A, van der Horst-Schrivers ANA, Berends AMA, Hoff AO, Castroneves LA, Ferrara AM, Rizzati S, Mian C, Dvorakova S, Hasse-Lazar K, Kvachenyuk A, Peczkowska M, Loli P, Erenler F, Krauss T, Almeida MQ, Liu L, Zhu F, Recasens M, Wohllk N, Corssmit EPM, Shafigullina Z, Calissendorff J, Grozinsky-Glasberg S, Kunavisarut T, Schalin-Jäntti C, Castinetti F, Vlcek P, Beltsevich D, Egorov VI, Schiavi F, Links TP, Lechan RM, Bausch B, Young WF Jr, Eng C; International Bilateral-Pheochromocytoma-Registry Group.

JAMA Netw Open. 2019 Aug 2;2(8):e198898. doi: 10.1001/jamanetworkopen.2019.8898.


Intricacies of the Molecular Machinery of Catecholamine Biosynthesis and Secretion by Chromaffin Cells of the Normal Adrenal Medulla and in Pheochromocytoma and Paraganglioma.

Berends AMA, Eisenhofer G, Fishbein L, Horst-Schrivers ANAVD, Kema IP, Links TP, Lenders JWM, Kerstens MN.

Cancers (Basel). 2019 Aug 6;11(8). pii: E1121. doi: 10.3390/cancers11081121. Review.


Pheochromocytoma and Paraganglioma.

Neumann HPH, Young WF Jr, Eng C.

N Engl J Med. 2019 Aug 8;381(6):552-565. doi: 10.1056/NEJMra1806651. Review. No abstract available.


Presentation, Treatment, Histology, and Outcomes in Adrenal Medullary Hyperplasia Compared With Pheochromocytoma.

Falhammar H, Stenman A, Calissendorff J, Juhlin CC.

J Endocr Soc. 2019 Jun 11;3(8):1518-1530. doi: 10.1210/js.2019-00200. eCollection 2019 Aug 1.

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