DR. DAVID E MARTIN, MD
Radiology at Shaffer St, Kalamazoo, MI

License number
Michigan 4301044228
Category
Radiology
Type
Thoracic Surgery (Cardiothoracic Vascular Surgery)
Address
Address
1722 Shaffer St SUITE 2, Kalamazoo, MI 49048
Phone
(269) 343-1555
(269) 343-3209 (Fax)

Professional information

David E Martin Photo 1

Dr. David E Martin, Kalamazoo MI - MD (Doctor of Medicine)

Specialties:
Cardiac Surgery
Address:
Borgess Cardiothoracic Surgery
1722 Shaffer St SUITE 2, Kalamazoo 49048
(269) 343-1555 (Phone), (269) 343-3207 (Fax)
Procedures:
Cardiac Surgical Procedures, Coronary Angioplasty, Atherectomy and Stent, Heart Surgery
Conditions:
Cardiovascular Disorders, Congestive Heart Failure, Heart Attack (Acute Myocardial Infarction)
Certifications:
General Surgery, 1986, Thoracic Cardiovascular Surgery, 1989
Awards:
Healthgrades Honor Roll
Languages:
English
Hospitals:
Borgess Cardiothoracic Surgery
1722 Shaffer St SUITE 2, Kalamazoo 49048
Borgess Medical Center
1521 Gull Rd, Kalamazoo 49048
Philosophy:
Patients by physician referral only. Borgess Cardiothoracic Surgery is a part of Borgess Heart Institute, offering outstanding contributions toward improving cardiac patient outcomes throughout southwest Michigan. We strive to provide high-quality care with personal attention to your questions and concerns.
Education:
Medical School
Wayne State University School Of Medicine
Wayne State University Affiliated Hospitals


David Martin Photo 2

Leed Ap Bd+C, Project Director, Senior Associate At Kingscott

Position:
Project Director, Senior Associate at Kingscott
Location:
Kalamazoo, Michigan Area
Industry:
Architecture & Planning
Work:
Kingscott - Kalamazoo, Michigan since Sep 2000 - Project Director, Senior Associate
Education:
Ferris State University 1980 - 1983
Kellogg Community College
Skills:
LEED, Sustainable Design, Construction Documents, Interior Design, Healthcare, Architectural Design, Engineering, Contract Negotiation, Renovation, K-12, Revit, LEED AP, Architecture, Submittals
Interests:
Musician and Guitar Player, Loves music, hunting and fishing. Skilled with all aspects of technology equipment and software.


David E Martin Photo 3

David E Martin, Kalamazoo MI

Specialties:
Thoracic Surgery, Cardiothoracic Vascular Surgery, Surgery, Vascular Surgery
Work:
Borgess Cardiothoracic Surgery
1722 Shaffer St, Kalamazoo, MI 49048 Cardiac Surgery Institute
1030 Harrington St, Mount Clemens, MI 48043 Cardiac Surgery Institute
22151 Moross Rd, Grosse Pointe, MI 48236 Cardiac Surgery Institute
22250 Providence Dr, Southfield, MI 48075 Cardiac Surgery Institute
18181 Oakwood Blvd, Dearborn, MI 48124 Sinai-Grace Hospital
6767 W Outer Dr, Detroit, MI 48235
Education:
Wayne State University (1980)


David E Martin Photo 4

David E Martin, Kalamazoo MI

Specialties:
Cardiothoracic Surgeon
Address:
1722 Shaffer St, Kalamazoo, MI 49048
Education:
Wayne State University, School of Medicine - Doctor of Medicine
Detroit Receiving Hospital-University Health Center - Fellowship - Thoracic Surgery
Detroit Receiving Hospital-University Health Center - Residency - Thoracic Surgery
Detroit Receiving Hospital-University Health Center - Residency - Surgery
Board certifications:
American Board of Thoracic Surgery Certification in Thoracic and Cardiac Surgery (Thoracic Surgery)


David Martin Photo 5

Composition Of Matter And Process

US Patent:
4169888, Oct 2, 1979
Filed:
Oct 17, 1977
Appl. No.:
5/842914
Inventors:
Ladislav J. Hanka - Kalamazoo MI
David G. Martin - Kalamazoo MI
Assignee:
The Upjohn Company - Kalamazoo MI
International Classification:
C12D 914, C07G 1100
US Classification:
424121
Abstract:
Novel antibiotic CC-1065 producible in a fermentation under controlled conditions using the new microorganism Streptomyces zelensis, NRRL 11,183. This antibiotic is active against Gram-positive bacteria, for example, Staphylococcus aureus, Bacillus subtilis, Streptococcus pyogenes, Sarcina lutea, and Streptococcus faecalis. It is also active against Gram-negative bacteria, for example, Escherichia coli, Proteus vulgaris, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Salmonella pullorum. Thus, antibiotic CC-1065 can be used in various environments to eradicate or control such bacteria.


David Martin Photo 6

.Alpha.s, 4S, 5R .Alpha.-Amino-3-Chloro-4-Hydroxy-2-Isoxazoline-5-Acetic Acid

US Patent:
3944562, Mar 16, 1976
Filed:
Apr 17, 1974
Appl. No.:
5/461635
Inventors:
David G. Martin - Kalamazoo MI
Ladislav J. Hanka - Kalamazoo MI
Assignee:
The Upjohn Company - Kalamazoo MI
International Classification:
c07D26104
US Classification:
260307F
Abstract:
Antibiotic U-43,795, producible by culturing Streptomyces sviceus in an aqueous nutrient medium has the following structure ##EQU1## The absolute configuration of U-43,795 was determined to be. alpha. S, 4S, 5R. alpha. -amino-3-chloro-4-hydroxy-2-isoxazoline-5-acetic acid. It is an amphoteric compound and can exist in different ionic forms according to the pH of the environment. At low pH, U-43,795 exists in the acid-addition salt form, at a higher pH in a zwitterion form, and at still higher pH in a metal salt form. U-43,795 inhibits the growth of Bacillus subtilis and Sarcina lutea, and can be used to inhibit such microorganisms in various environments.


David Martin Photo 7

Antibiotic Pentalenolactone Derivative

US Patent:
4150036, Apr 17, 1979
Filed:
Jun 15, 1978
Appl. No.:
5/915615
Inventors:
David G. Martin - Kalamazoo MI
Assignee:
The Upjohn Company - Kalamazoo MI
International Classification:
C07D31194
US Classification:
26034321
Abstract:
Novel antibiotic U-36,699 which has been identified as the. alpha. -methylene derivative of pentalenolactone. Antibiotic U-36,699 has the following structural formula ##STR1## This antibiotic is produced in a chemical process using pentalenolactone (also known as antibiotic P. A. 132), as the starting material. Antibiotic U-36,699 is active against Staphylococus aureua, Sarcina lutea, Mycobacterium phlei, Mycobacterium avium, Saccharomyces cerevisiae, and Penicillium oxalicum. Thus, antibiotic U-36,699 can be used in various environments to eradicate or control such fungi and bacteria. Further, antibiotic U-36,699 inhibits P 388 leukemia cells in laboratory mice. Thus, this antibiotic can be used to treat laboratory mice harboring P 388 leukemia cells.


David Martin Photo 8

Purification Of At-125

US Patent:
4188324, Feb 12, 1980
Filed:
Nov 13, 1978
Appl. No.:
5/960217
Inventors:
David G. Martin - Kalamazoo MI
Assignee:
The Upjohn Company - Kalamazoo MI
International Classification:
C07D26104
US Classification:
548240
Abstract:
Process for the purification of L-(. alpha. s,5s)-. alpha. -amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid (AT-125). Also provided are AT-125 analogs prepared in the process.


David Martin Photo 9

Purification Of At-125

US Patent:
4232164, Nov 4, 1980
Filed:
Jun 23, 1978
Appl. No.:
5/918569
Inventors:
David G. Martin - Kalamazoo MI
Assignee:
The Upjohn Company - Kalamazoo MI
International Classification:
C07D26104
US Classification:
548240
Abstract:
Process for the purification of L-(. alpha. S,5S)-. alpha. -amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid (AT-125). Also provided are AT-125 analogs prepared in the process.


David Martin Photo 10

Cc-1065 Analogs

US Patent:
5332837, Jul 26, 1994
Filed:
Jan 22, 1993
Appl. No.:
8/010526
Inventors:
Robert C. Kelly - Augusta MI
David G. Martin - Kalamazoo MI
Paul A. Aristoff - Portage MI
Assignee:
The Upjohn Company - Kalamazoo MI
International Classification:
C07D48704, C07D48708, A61K 3140
US Classification:
548433
Abstract:
This invention concerns 2-acyl-4,5,8,8a-tetrahydro-4-oxycyclopropan[c]pyrrol(3,2-e) indole derivatives of Formula I': ##STR1## the compounds of Formula I' are useful as uv light absorber substances, as chemical intermediates and as prodrugs of known spirocyclopropylpyrroloindole CC-1065 analogs. Representative Formula I' compounds have been shown to possess useful ranges of antitumor activity in standard laboratory animal tests.