H R KEISER
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Explore the profile of H R KEISER including associated specialties, affiliations and a list of published articles.
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Articles
231
Citations
2686
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Recent Articles
1.
Eisenhofer G, Walther M, KEISER H, Lenders J, Friberg P, Pacak K
Braz J Med Biol Res
. 2000 Sep;
33(10):1157-69.
PMID: 11004716
Pheochromocytomas are rare chromaffin cell tumors that nevertheless must be excluded in large numbers of patients who develop sustained or episodic hypertension as well as in many others with suggestive...
2.
Rao F, KEISER H, OConnor D
Hypertension
. 2000 Jan;
36(6):1045-52.
PMID: 11116123
Chromaffin granule transmitters such as chromogranin A and catecholamines have been used in the diagnosis of pheochromocytoma, but the diagnostic and prognostic value of chromogranin A have not been explored...
3.
Oriji G, KEISER H
Am J Hypertens
. 1999 Dec;
12(11 Pt 1):1091-7.
PMID: 10604485
Chronic treatment with cyclosporine A (CsA), an immunosuppressive agent, causes hypertension. The effect of CsA on vascular responses was determined in Sprague-Dawley rats and isolated rat aortic rings. Male rats...
4.
Avila N, Doppman J, Walther M, KEISER H
Clin Radiol
. 1999 Dec;
54(11):772-4.
PMID: 10580770
No abstract available.
5.
Walther M, Herring J, Enquist E, KEISER H, Linehan W
J Urol
. 1999 Oct;
162(5):1582-6.
PMID: 10524872
Purpose: We review the literature and characterize the clinical findings of von Recklinghausen's associated pheochromocytoma. Materials And Methods: A Grateful Med search for the years 1966 to 1999 was performed...
6.
Walther M, Reiter R, KEISER H, Choyke P, Venzon D, Hurley K, et al.
J Urol
. 1999 Aug;
162(3 Pt 1):659-64.
PMID: 10458336
Purpose: Families with von Hippel-Lindau disease have variable risk of pheochromocytoma. Patients with von Hippel-Lindau disease and pheochromocytoma identified by screening can have no characteristic signs or symptoms. Families with...
7.
Eisenhofer G, Lenders J, Linehan W, Walther M, Goldstein D, KEISER H
N Engl J Med
. 1999 Jun;
340(24):1872-9.
PMID: 10369850
Background: The detection of pheochromocytomas in patients at risk for these tumors, such as patients with von Hippel-Lindau disease or multiple endocrine neoplasia type 2 (MEN-2), is hindered by the...
8.
Bottner A, Eisenhofer G, Torpy D, Ehrhart-Bornstein M, KEISER H, Chrousos G, et al.
Metabolism
. 1999 May;
48(5):543-5.
PMID: 10337850
Leptin is a major regulator of body weight and energy balance and is subject to a variety of regulatory inputs. From several previous studies, catecholamines have been suggested to exert...
9.
Walther M, KEISER H, Linehan W
World J Urol
. 1999 Mar;
17(1):35-9.
PMID: 10096149
Pheochromocytoma is a catecholamine-producing tumor of the sympathetic nervous system. Signs and symptoms are generally related to catecholamine excess; these include hypertension, sweating, palpitatione, headaches, and anxiety attacks. Abdominal imaging...
10.
Walther M, KEISER H, Choyke P, Rayford W, Lyne J, Linehan W
J Urol
. 1999 Jan;
161(2):395-8.
PMID: 9915410
Purpose: In patients with von Hippel-Lindau disease multiple bilateral adrenal pheochromocytoma can develop, which has traditionally been treated with adrenalectomy. Partial adrenalectomy can preserve normal adrenal function and avoid the...