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M'Liss A. Hudson

Researcher at Washington University in St. Louis

Publications -  42
Citations -  4394

M'Liss A. Hudson is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Prostate & Prostate-specific antigen. The author has an hindex of 23, co-authored 41 publications receiving 4327 citations. Previous affiliations of M'Liss A. Hudson include University of Texas Health Science Center at San Antonio & United States Department of Veterans Affairs.

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Comparison of digital rectal examination and serum prostate specific antigen in the early detection of prostate cancer: results of a multicenter clinical trial of 6,630 men.

TL;DR: In this paper, a prospective clinical trial at 6 university centers of 6,630 male volunteers 50 years old or older who underwent PSA determination (Hybritech Tandom-E or Tandem-R assays) and digital rectal examination was conducted.
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Clinical use of Prostate Specific Antigen in Patients with Prostate Cancer

TL;DR: It is concluded that the serum prostate specific antigen assay is most useful clinically to monitor the response to therapy of prostate cancer patients.
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Risks and benefits of repeated courses of intravesical bacillus Calmette-Guerin therapy for superficial bladder cancer

TL;DR: The results suggest that patients who have failed 2 courses of bacillus Calmette-Guerin therapy (as given in the treatment protocol) should be considered for alternative treatment.
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Effect of patient age on early detection of prostate cancer with serum prostate-specific antigen and digital rectal examination

TL;DR: The use of both tests in combination provided the highest rate of detection in all age groups, and younger men have the longest projected life expectancy and, therefore, the most to gain from early prostate cancer detection.
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Results of a Multicenter Trial using the BTA Test to Monitor for and Diagnose Recurrent Bladder Cancer

TL;DR: The bladder tumor antigen test is a simple, rapid and inexpensive adjunct to cystoscopy, and the results are equivalent or superior to those of voided cytology as performed in this trial.