DIANNA M MILEWICZ, M.D.
Medical Practice at Fannin St, Houston, TX

License number
Texas H1899
Category
Osteopathic Medicine
Type
Internal Medicine
License number
Texas H1899
Category
Medical Practice
Type
Clinical Genetics (M.D.)
Address
Address 2
6410 Fannin St, Houston, TX 77030
PO Box 301173, Dallas, TX 75303
Phone
(713) 500-6727
(713) 500-6556 (Fax)
(713) 500-3500

Personal information

See more information about DIANNA M MILEWICZ at radaris.com
Name
Address
Phone
Dianna Milewicz, age 67
3715 Farber St, Houston, TX 77005
(713) 248-7507
Dianna J Milewicz, age 67
3715 Farber St, Houston, TX 77005
(713) 666-4889
Dianna M Milewicz
6410 Fannin St, Houston, TX 77030
(713) 500-6727
Dianna M Milewicz, age 68
6624 Fannin St, Houston, TX 77030
(713) 796-1600

Professional information

Dianna M Milewicz Photo 1

Dr. Dianna M Milewicz - MD (Doctor of Medicine)

Hospitals:
UT Physicians-Medical Genetics
6410 Fannin St SUITE 500, Houston 77030
Memorial Hermann - Texas Medical Center
6411 Fannin St, Houston 77030
UT Physicians-Medical Genetics
6410 Fannin St SUITE 500, Houston 77030
Memorial Hermann - Texas Medical Center
6411 Fannin St, Houston 77030
Education:
Medical Schools
University Of Texas Southwestern Medical Center At Dallas
Graduated: 1984


Dianna M Milewicz Photo 2

Dianna M Milewicz, Houston TX

Specialties:
Internal Medicine, General Practice, Medical Genetics, Clinical Genetics, M.D.
Work:
Ut Physicians
6410 Fannin St, Houston, TX 77030 Ut
6431 Fannin Pathology, Houston, TX 77030
Education:
The University of Texas Southwestern (1984)


Dianna M Milewicz Photo 3

Dianna M Milewicz, Houston TX

Specialties:
Internist
Address:
6410 Fannin St, Houston, TX 77030
Education:
University of Texas, Southwestern Medical School (Dallas) - Doctor of Medicine
Parkland Memorial Hospital - Residency - Family Medicine
Board certifications:
American Board of Internal Medicine Certification in Internal Medicine, American Board of Medical Genetics Certification in Clinical Genetics (MD) (Medical Genetics)


Dianna Milewicz Photo 4

Detection Of Mutations In Acta2 And Myh11 For Assessing Risk Of Vascular Disease

US Patent:
2011002, Feb 3, 2011
Filed:
Sep 24, 2008
Appl. No.:
12/679770
Inventors:
Dianna M. Milewicz - Houston TX, US
Dongchuan Guo - Pearland TX, US
Hariyadarshi Pannu - Houston TX, US
Van Tran Fadulu - Manvel TX, US
Assignee:
BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM - Austin TX
International Classification:
C40B 30/00
US Classification:
506 7
Abstract:
A method of detecting in an individual an increased risk of hyperplastic vasculomyopathy, or a vascular disease resulting therefrom is disclosed. The method comprises obtaining a DNA genome sample from the individual and detecting in the sample a missense mutation in a gene which is a component of a smooth muscle cell contractile unit. In some embodiments the gene is ACTA2 and in some embodiments the gene is MYH11. In some embodiments, the gene is sequenced and then compared to a panel of control gene sequences which are representative of the same gene in individuals without vascular disease or who are at low risk of developing hyperplastic vasculomyopathy, to detect any missense mutations in the gene. The presence of a missense mutation in the gene indicates an increased risk of hyperplastic vasculomyopathy.


Dianna Milewicz Photo 5

Biomarkers For Use In Vessel Disorders

US Patent:
2008030, Dec 11, 2008
Filed:
Oct 14, 2005
Appl. No.:
11/577287
Inventors:
Dianna M. Milewicz - Houston TX, US
William P. Dubinsky - Houston TX, US
Assignee:
BOARD OF REGENTS, THE UNIVERSITY OF TEXAS - AUSTIN TX
International Classification:
G01N 33/554, C12Q 1/02
US Classification:
435 721, 435 29
Abstract:
The present invention relate to a method of diagnosing a subject having a vessel disorder. More particularly, a biological sample is obtained from a subject suspected of having a vessel disorder. A protein profile is determined or measured in the sample using procedures described herein, for example, mass spectrometry or immunodetection. The protein profile from the subject is compared to a protein profile in a healthy control, wherein an alteration in the levels of a protein of the profile in the subject compared to the healthy control is indicative of a vessel disorder.