H
Henry D. Tazelaar
Researcher at Mayo Clinic
Publications - 312
Citations - 18176
Henry D. Tazelaar is an academic researcher from Mayo Clinic. The author has contributed to research in topics: Transplantation & Lung. The author has an hindex of 71, co-authored 304 publications receiving 16815 citations. Previous affiliations of Henry D. Tazelaar include University of Rochester & Max Planck Society.
Papers
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Journal ArticleDOI
Prognostic Significance of Histopathologic Subsets in Idiopathic Pulmonary Fibrosis
Julie A. Bjoraker,Jay H. Ryu,Mark K. Edwin,Jeffrey L. Myers,Henry D. Tazelaar,Darrell R. Schroeder,Kenneth P. Offord +6 more
TL;DR: Retrospective analysis of 104 patients with IPF who had open lung biopsy at Mayo Medical Center from 1976 to 1985 was performed to establish the overall survival rate, the spectrum of histopathological subgroups and their associated prognostic significance.
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The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy
Virginia V. Michels,Patricia P. Moll,Fletcher A. Miller,A. Jamil Tajik,Julia S. Chu,David J. Driscoll,John C. Burnett,Richard J. Rodeheffer,James H. Chesebro,Henry D. Tazelaar +9 more
TL;DR: Dilated cardiomyopathy was found to be familial in at least one in five of the patients in this study, a considerably higher percentage than in previous reports.
Journal ArticleDOI
Polymyositis-dermatomyositis-associated interstitial lung disease.
William W. Douglas,Henry D. Tazelaar,Thomas E. Hartman,Robert P. Hartman,Paul A. Decker,Darrell R. Schroeder,Jay H. Ryu +6 more
TL;DR: Survival was significantly better than that observed for historical control subjects with idiopathic UIP, and was more consistent with survival previously reported in idiopathsic NSIP, while there was no difference in survival between Jo-1 positive and Jo- 1 negative groups.
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Congenitally bicuspid aortic valves: a surgical pathology study of 542 cases (1991 through 1996) and a literature review of 2,715 additional cases.
TL;DR: Functionally, the most common fate of congenitally bicuspid aortic valves was calcific stenosis with or without regurgitation, and because valve replacement is currently the only treatment of symptomatic AS, this disorder will continue to affect health-care costs.
Journal ArticleDOI
Constrictive Pericarditis in 26 Patients With Histologically Normal Pericardial Thickness
Deepak R. Talreja,William D. Edwards,Gordon K. Danielson,Hartzell V. Schaff,A. Jamil Tajik,Henry D. Tazelaar,Jerome F. Breen,Jae K. Oh +7 more
TL;DR: When clinical, echocardiographic, or invasive hemodynamic features indicate constriction in patients with heart failure, pericardiectomy should not be denied on the basis of normal thickness as demonstrated by noninvasive imaging.