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JOHN HECKENLIVELY, MD
MD
Ophthalmology Physician
NPI: 1801818901Individual
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
G27232(CA)4301082763(MI)
Research & Publications (20)
Management of autoimmune retinopathies with immunosuppression.
PMID 19365013·Arch Ophthalmol·2009
8-other
Antioxidant or neurotrophic factor treatment preserves function in a mouse model of neovascularization-associated oxidative stress.
PMID 19188685·J Clin Invest·2009
7-preclinical
Detection of retinal metabolic stress resulting from central serous retinopathy.
PMID 19491721·Retina·2009
8-other
Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase.
PMID 19459154·Hum Mutat·2009
8-other
Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa.
PMID 19520207·Am J Hum Genet·2009
8-other
New mutation, P575L, in the GUCY2D gene in a family with autosomal dominant progressive cone degeneration.
PMID 18332321·Arch Ophthalmol·2008
5-case
Frequency of anti-retinal antibodies in normal human serum.
PMID 18347451·J Neuroophthalmol·2008
8-other
Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa.
PMID 18509552·Mol Vis·2008
5-case
Progress toward personalized medicine for age-related macular degeneration.
PMID 18519068·Ophthalmology·2008
8-other
Rapid, noninvasive detection of diabetes-induced retinal metabolic stress.
PMID 18625939·Arch Ophthalmol·2008
8-other
Retinal flavoprotein autofluorescence as a measure of retinal health.
PMID 19277237·Trans Am Ophthalmol Soc·2008
8-other
The need for standardization of antiretinal antibody detection and measurement.
PMID 18672221·Am J Ophthalmol·2008
6-review
Mutations in known genes account for 58% of autosomal dominant retinitis pigmentosa (adRP).
PMID 18188946·Adv Exp Med Biol·2008
8-other
Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene.
PMID 18805803·Hum Mol Genet·2008
4-observational
The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa.
PMID 17982421·Mol Vis·2007
5-case
Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.
PMID 17267005·Vision Res·2007
7-preclinical
Molecular testing for hereditary retinal disease as part of clinical care.
PMID 17296903·Arch Ophthalmol·2007
5-case
Genetic factors modifying clinical expression of autosomal dominant RP.
PMID 17249547·Adv Exp Med Biol·2006
6-review
Senile panretinal cone dysfunction in age-related macular degeneration (AMD): a report of 52 amd patients compared to age-matched controls.
PMID 17471344·Trans Am Ophthalmol Soc·2006
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1000 WALL ST
ANN ARBOR, MI 48105 - Phone
- (734) 764-4190
Quick Facts
- NPI
- 1801818901
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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