Results 91 to 100 of about 597 (108)

Primary pigmented nodular adrenocortical disease associated with Carney complex: case report and literature review. [PDF]

Sao Paulo Med J, 2006
Gonçalves FT, Feibelmann TC, Mendes CM, Fernandes ML, Miranda GH, Gouvêa AP, Jorge PT.   +6 more
europepmc   +1 more source

Giant cystic malignant pheochromocytoma invading right hepatic lobe: report on two cases. [PDF]

Sao Paulo Med J, 2008
Costa SR, Cabral NM, Abhrão AT, Costa RB, Silva LM, Lupinacci RA.   +5 more
europepmc   +1 more source

Retroperitoneoscopic adrenalectomy in an infant with adrenocortical virilizing tumor. [PDF]

Sao Paulo Med J, 2002
Tobias-Machado M, Cartum J, Santos-Machado TM, Gaspar HA, Simoes AS, Cruz R, Rodrigues R, Juliano RV, Wroclawski ER.   +8 more
europepmc   +1 more source

Laparoscopic and open surgery for pheochromocytoma. [PDF]

BMC Surg, 2001
Edwin B, Kazaryan AM, Mala T, Pfeffer PF, Tønnessen TI, Fosse E.   +5 more
europepmc   +1 more source

Reporte de carcinoma adrenal izquierdo con telangiectasia en canino con Cushing Primario [PDF]

El Cushing es una enfermedad endocrina asociada a la exposición crónica al cortisol. Se clasifica principalmente como: Dependiente de pituitaria, Dependiente de Adrenal o Iatrogénico.
Kianman Maceda, Marissa Alexandra
core  

[Adrenal incidentaloma with hyperprocalcitoninemia]. [PDF]

Aten Primaria
Zambudio-Munuera A, Millán-Ramos I, Gutiérrez-Tejero F, Arrabal-Polo MÁ.   +3 more
europepmc   +1 more source

The immediate source of noradrenaline released in the heart by acetyl choline. [PDF]

Br J Pharmacol Chemother, 1966
Cabrera R, Cohen A, Middleton S, Utano L, Viveros H.   +4 more
europepmc   +1 more source

[Pseudocyst of adrenal gland. Case report]. [PDF]

Rev Med Inst Mex Seguro Soc
Rafael-Pérez CI, Paz-López AJ, Ruvalcaba-Contreras N.   +2 more
europepmc   +1 more source

Addison's disease due to adrenal insufficiency in an immunocompetent patient with disseminated cryptococcosis. Case report. [PDF]

Rev Peru Med Exp Salud Publica
Paz-Ibarra J, Concepción-Zavaleta M, Tipiani Mallma M, Delgado Nicolás H, Herrera-Silvestre H, Marcilla-Truyenque L, Arzapalo-Benavides J, Concepción-Urteaga L.   +7 more
europepmc   +1 more source

Manejo clínico y quirúrgico de los feocromocitomas y paragangliomas

Revista del Hospital Italiano de Buenos Aires
Los feocromocitomas y paragangliomas (Feo/PGL) son tumores neurendocrinos raros con diferentes presentaciones clínicas, asociados a alta morbimortalidad. Reconocer los signos y síntomas es el paso diagnóstico inicial.
Valeria de Miguel, Paula Cuffaro, Juan Medici , Demetrio Cavadas   +3 more
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