Results 181 to 190 of about 48,572 (243)
Radiologically Probable Late-Onset Von Hippel-Lindau Syndrome: A Case Report. [PDF]
Y V +4 more
europepmc +1 more source
Non-Traumatic Unilateral Spontaneous Adrenal Mass Rupture: A Retrospective Case Series Study. [PDF]
Al-Thani H +5 more
europepmc +1 more source
Case Report: Feline adrenal pheochromocytoma with a synaptophysin-positive, chromogranin A-negative immunophenotype. [PDF]
Kim J, Yoon S, Lee S.
europepmc +1 more source
Metanephrine-secreting adrenocortical carcinoma in a dog with clinical and biochemical features suggestive of pheochromocytoma. [PDF]
Kim D, Park SG, Moon J, O IS, Kim MS.
europepmc +1 more source
Recurrent Primary Hyperparathyroidism Due to Adenoma Formation in Autotransplanted Parathyroid Tissue 28 Years After Parathyroidectomy in a Patient With Multiple Endocrine Neoplasia Type 2A. [PDF]
Farnin R +9 more
europepmc +1 more source
The book is divided into six sections. The first three sections focus on the pathophysiology of the disease, showing anatomo- and histopathological aspects, experimental models and signaling pathways and programmed cell death related to pheochromocytoma.
Sadiqa, Edmonds +2 more
core +4 more sources
Some of the next articles are maybe not open access.
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Current Treatment Options in Oncology, 2001
The only definitive therapy for patients with pheochromocytoma is surgical resection [1,2**]. Advances in preoperative medical management of hypertension/hypovolemia and improved intraoperative anesthetic care have reduced the operative mortality rate for pheochromocytoma to less than 5% in most series.
M S, Eigelberger, Q Y, Duh
openaire +4 more sources
The only definitive therapy for patients with pheochromocytoma is surgical resection [1,2**]. Advances in preoperative medical management of hypertension/hypovolemia and improved intraoperative anesthetic care have reduced the operative mortality rate for pheochromocytoma to less than 5% in most series.
M S, Eigelberger, Q Y, Duh
openaire +4 more sources

