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010   $a1-281-06935-3
010   $a9786611069353
010   $a0-470-69219-7
010   $a0-470-76638-7
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100   $a20070108d2007      uy             0
101 0 $aeng
135   $aur|n|---|||||
181   $ctxt
182   $cc
183   $acr
200 10$aPheochromocytoma$b[electronic resource] $ediagnosis, localization, and treatment /$fKarel Pacak, Jacques W.M. Lenders, Graeme Eisenhofer
210   $aMalden, MA ;$aOxford $cBlackwell Pub.$d2007
215   $a1 online resource (184 p.)
300   $aDescription based upon print version of record.
311   $a1-4051-4950-7 
320   $aIncludes bibliographical references and index.
327   $aHistorical comments -- Pathology -- Clinical presentation of pheochromocytoma -- Current trends in genetics of pheochromocytoma -- Catecholamines and adrenergic receptors -- Current trends in biochemical diagnosis of pheochromocytoma -- Current trends in localization of pheochromocytoma -- Treatment of pheochromocytoma -- Future trends and perspectives.
330   $aPheochromocytomas are rare but treacherous catecholamine-producing tumors, which if missed or not properly treated, will almost invariably prove fatal. Prompt diagnosis is, therefore, essential for effective treatment, usually by surgical resection. The manifestations are diverse and the tumor can mimic a variety of conditions, often resulting in either erroneous diagnoses or a delayed diagnosis. Reflecting the recent leaps in understanding this condition, Pheochromocytoma: Diagnosis, Localization, and Treatment provides a comprehensive update on the improvements in the diagnosis, loc
606   $aPheochromocytoma
615  0$aPheochromocytoma.
676   $a616.99
676   $a616.99445
700   $aPacak$b Karel$0881323
701   $aLenders$b Jacques W. M$0881324
701   $aEisenhofer$b Graeme$0881325
801  0$bMiAaPQ
801  1$bMiAaPQ
801  2$bMiAaPQ
906   $aBOOK
912   $a996202111303316
996   $aPheochromocytoma$91968252
997   $aUNISA