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The main cause for most pheochromocytoma is not yet known.
President Eisenhower's death may have been caused by a pheochromocytoma.
It has been used in the treatment of pheochromocytoma.
The most common symptoms of pheochromocytoma are hypertension or high blood pressure.
Inherited pheochromocytoma is a 10 to 20 percent chance of causing the disease.
According to some research patients recently diagnosed with hypertension have pheochromocytoma.
In addition, the tests for the pheochromocytoma were negative.
Data to guide management are limited because regional disease is diagnosed in very few patients who present with pheochromocytoma.
It is used in the treatment of hypertension, and specifically that caused by pheochromocytoma.
Phenoxybenzamine is used control blood pressure and reduce sweating in people with pheochromocytoma.
There is no standard staging system for pheochromocytoma and paraganglioma.
Patients experiencing symptoms associated with pheochromocytoma should be aware that it is rare.
Type 2C is at risk for only pheochromocytoma.
Other rare tumors my be dangerous to biopsy, such as pheochromocytoma.
The incidence of pheochromocytoma is 2 to 8 per million persons per year.
It is a marker for catecholamine-secreting tumors such as pheochromocytoma.
Therefore, it is usually advised to "salt load" pheochromocytoma patients before their surgery.
Certain rare tumors (such as a pheochromocytoma) can increase the amount of catecholamines in the blood.
House returns to an old idea, a pheochromocytoma.
Occasionally pheochromocytoma and primary hyperparathyroidism may be the initial diagnosis.
Thus, the clinical presentation may resemble pheochromocytoma or Kawasaki disease.
It can be the source of paraganglioma or pheochromocytoma.
There are many ways to treat the pheochromocytoma.
Cancer that forms in the adrenal medulla is called pheochromocytoma.
This gene has been shown mutated in cases of hereditary pheochromocytoma.