1495 Morehead Dr, Ann Arbor, MI 48103 • 734 668-6728
3201 Asher Rd, Ann Arbor, MI 48104
1000 Wall St, Ann Arbor, MI 48105 • 734 763-9142
Dexter, MI
Boston, MA
1495 Morehead Dr, Ann Arbor, MI 48103 • 734 717-5754
Work
Company:
Ann Arbor Office
Address:
1000 Wall St, Ann Arbor, MI 48105
Phones:
734 763-8122 734 763-1415
Education
School / High School:
University Of Chicago/The Pritzker School Of Medicine
1979
Languages
English
Awards
Healthgrades Honor Roll
Ranks
Certificate:
Anatomic Pathology, 1988
Specialities
Ophthalmology • Anatomic Pathology
Name / Title
Company / Classification
Phones & Addresses
Victor Elner Co-founder, Chief Medical Officer
Ocusciences, Inc Whol Medical/Hospital Equipment
3201 Asher Rd, Ann Arbor, MI 48104
Victor Elner Medical Doctor
Ophthalmology Dept Hospital & Health Care · Medical Doctor's Office College/University · Specialty Hospital College/University · College/University · Child Day Care Services College/University · Trailer Park/Campsites · Allergist · Pediatric Allergist
1000 Wall St, Ann Arbor, MI 48105 900 Wall St, Ann Arbor, MI 48105 1000 Mcintyre St, Ann Arbor, MI 48105 1010 Wall St, Ann Arbor, MI 48105 734 764-2108, 734 763-8122, 734 763-5906, 734 764-0210
Medicine Doctors
Dr. Victor M Elner, Ann Arbor MI - MD (Doctor of Medicine)
Ann Arbor Office 1000 Wall St, Ann Arbor, MI 48105 734 763-8122 (Phone), 734 763-1415 (Fax)
Kellogg Eye Center 1000 Wall St Suite 2051, Ann Arbor, MI 48105 734 763-8122 (Phone)
Certifications:
Anatomic Pathology, 1988 Ophthalmology, 1983
Awards:
Healthgrades Honor Roll
Languages:
English
Hospitals:
Ann Arbor Office 1000 Wall St, Ann Arbor, MI 48105
Kellogg Eye Center 1000 Wall St Suite 2051, Ann Arbor, MI 48105
ProMedica Herrick Hospital 500 East Pottawatamie Street, Tecumseh, MI 49286
Education:
Medical School University Of Chicago/The Pritzker School Of Medicine Graduated: 1979 Medical School University Of Chicago Graduated: 1982 Medical School Armed Forces Institute Graduated: 1985 Medical School University Wisconsin Graduated: 1987
Kellogg Eye CenterUniversity Of Michigan Kellogg Eye Center 1000 Wall St STE 2051, Ann Arbor, MI 48105 734 763-8122 (phone), 734 936-8571 (fax)
Education:
Medical School University of Chicago Pritzker School of Medicine Graduated: 1979
Conditions:
Keratitis Acute Conjunctivitis Glaucoma
Languages:
English Spanish
Description:
Dr. Elner graduated from the University of Chicago Pritzker School of Medicine in 1979. He works in Ann Arbor, MI and specializes in Ophthalmology. Dr. Elner is affiliated with University Of Michigan Hospitals & Health Center.
3621 S State St, Ann Arbor, MI 48108 1000 Wall St, Ann Arbor, MI 48105
Education:
Doctor of Philosophy University of Chicago, Pritzker School of Medicine - Doctor of Medicine University of Wisconsin Hospital & Clinics - Fellowship - Ophthalmic Plastic and Reconstructive Surgery Walter Reed Army Medical Center - Fellowship - Pathology Bernard Mitchell Hospital-University of Chicago Hospitals - Residency - Pathology Bernard Mitchell Hospital-University of Chicago Hospitals - Residency - Ophthalmology
Board certifications:
American Board of Ophthalmology Certification in Ophthalmology American Board of Pathology Certification in Anatomic Pathology (Pathology)
Us Patents
Method For Controlling Configuration Of Laser Induced Breakdown And Ablation
Detao Du - Fremont CA Subrata K. Dutta - Ann Arbor MI Victor Elner - Ann Arbor MI Ron Kurtz - Ann Arbor MI Paul R. Lichter - Ann Arbor MI Xinbing Liu - Acton MA Peter P. Pronko - Dexter MI Jeffrey A. Squier - San Diego CA
Assignee:
The Regents of the University of Michigan - Ann Arbor MI
International Classification:
B23K 2602
US Classification:
21912169
Abstract:
In one aspect the invention provides a method for laser induced breakdown of a material with a pulsed laser beam where the material is characterized by a relationship of fluence breakdown threshold (F ) versus laser beam pulse width (T) that exhibits an abrupt, rapid, and distinct change or at least a clearly detectable and distinct change in slope at a predetermined laser pulse width value. The method comprises generating a beam of laser pulses in which each pulse has a pulse width equal to or less than the predetermined laser pulse width value. The beam is focused to a point at or beneath the surface of a material where laser induced breakdown is desired. The beam may be used in combination with a mask in the beam path. The beam or mask may be moved in the x, y, and Z directions to produce desired features. The technique can produce features smaller than the spot size and Rayleigh range due to enhanced damage threshold accuracy in the short pulse regime.
A method and apparatus for measuring the retinal auto-fluorescence of a subject retina includes an excitation light source for providing an excitation light at a wavelength of at least 450 nm and an image capture device for recording an ocular auto-fluorescence signal generated in response to the excitation light. The image capture device includes a filter for reducing background non-signal wavelengths from the ocular auto-fluorescence signal and an image intensifier for increasing the ocular auto-fluorescence signal strength. The method and apparatus may further include a processor that analyzes the ocular auto-fluorescence signal to determine a contrast change or pattern to thereby detect retinal disease or damage. The processor may compare the images with control images, past images of the same eye or other diagnostic modalities such as fundus photography, angiography, or visual field testing to detect the retinal disease or damage.
Method And Apparatus For Detecting Diseases Associated With The Eye
Victor M. Elner - Ann Arbor MI, US Howard R. Petty - Livonia MI, US Matthew G. Field - Ann arbor MI, US
Assignee:
THE REGENTS OF THE UNIVERSITY OF MICHIGAN - Ann Arbor MI
International Classification:
A61B 6/00 A61K 49/00 G06K 9/00
US Classification:
600476, 424 92, 600558, 382128, 382168
Abstract:
Disease may be detected, monitored, etc. by detecting metabolic dysfunction in a patient's eyes. In one embodiment of an apparatus, an excitation light is generated by an excitation light source to induce autofluorescence in an ocular tissue (e.g., retinal tissue), wherein the excitation light excites flavoprotein autofluorescence (FA) and minimizes the excitation of non-flavoprotein autofluorescence. At least a single image representing the induced ocular tissue autofluorescence is captured. The at least single image is intensified to increase the signal strength of the ocular tissue autofluorescence. The at least single image is analyzed to generate an indicator of whether a patient has one or more of eye damage, a disease that causes eye damage, or to generate an indicator of the progression of a disease, an indicator of the effectiveness of a treatment, a personalized treatment for a subject, etc.
Victor M. Elner - Ann Arbor MI, US Howard R. Petty - Livonia MI, US
Assignee:
THE REGENTS OF THE UNIVERSITY OF MICHIGAN - Ann Arbor MI
International Classification:
A61B 6/00
US Classification:
600477, 600476
Abstract:
A method and apparatus for measuring the retinal auto-fluorescence of a subject retina includes an excitation light source for providing an excitation light at a wavelength of at least 450 nm and an image capture device for recording an ocular auto-fluorescence signal generated in response to the excitation light. The image capture device includes a filter for reducing background non-signal wavelengths from the ocular auto-fluorescence signal and an image intensifier for increasing the ocular auto-fluorescence signal strength. The method and apparatus may further include a processor that analyzes the ocular auto-fluorescence signal to determine a contrast change or pattern to thereby detect retinal disease or damage. The processor may compare the images with control images, past images of the same eye or other diagnostic modalities such as fundus photography, angiography, or visual field testing to detect the retinal disease or damage.
Method For Controlling Configuration Of Laser Induced Breakdown And Ablation
Gerard A. Mourou - Ann Arbor MI Detao Du - Ann Arbor MI Subrata K. Dutta - Ann Arbor MI Victor Elner - Ann Arbor MI Ron Kurtz - Ann Arbor MI Paul R. Lichter - Ann Arbor MI Xinbing Liu - Ann Arbor MI Peter P. Pronko - Dexter MI Jeffrey A. Squier - Ann Arbor MI
Assignee:
The Regents of the University of Michigan - Ann Arbor MI
International Classification:
B23K 2602
US Classification:
21912169
Abstract:
In one aspect the invention provides a method for laser induced breakdown of a material with a pulsed laser beam where the material is characterized by a relationship of fluence breakdown threshold (F. sub. th) versus laser beam pulse width (T) that exhibits an abrupt, rapid, and distinct change or at least a clearly detectable and distinct change in slope at a predetermined laser pulse width value. The method comprises generating a beam of laser pulses in which each pulse has a pulse width equal to or less than the predetermined laser pulse width value. The beam is focused to a point at or beneath the surface of a material where laser induced breakdown is desired. The beam may be used in combination with a mask in the beam path. The beam or mask may be moved in the x, y, and Z directions to produce desired features. The technique can produce features smaller than the spot size and Rayleigh range due to enhanced damage threshold accuracy in the short pulse regime.
Automated Measurement Of Changes In Retinal, Retinal Pigment Epithelial, Or Choroidal Disease
- Ann Arbor MI, US Christopher R. Ranella - Macomb MI, US Daniel L. Albertus - Ann Arbor MI, US Nathan T. Patel - Ann Arbor MI, US Victor M. Elner - Ann Arbor MI, US Matthew K. Johnson-Roberson - Chestnut Hill MA, US
International Classification:
A61B 3/12 G06T 7/00 A61B 3/00
US Classification:
351246
Abstract:
A method for for automatically measuring changes in retinal, retinal pigment epithelial, or choroidal disease includes retrieving a set of images of a fundus and selecting a plurality of images from the set of images. The plurality of images are co-registered and pre-processed such that the quality, contrast, and gain of each of the plurality of images is made similar. Then, a comparison is made between the plurality of images to determine a change in retinal, retinal pigment epithelial, or choroidal disease, wherein the change in retinal, retinal pigment epithelial, or choroidal disease is determined based on various disease metrics. Finally, an indication of the change in retinal, retinal pigment epithelial, or choroidal disease is generated for display to a user on a computing device.
Victor Elner 1972 graduate of Shaker Heights High School in Shaker heights, OH is on Classmates.com. See pictures, plan your class reunion and get caught up with Victor and other ...