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GRADY HOLDER, MD
MD
Family Medicine Physician
NPI: 1366543902Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
DR.0028219(CO)
Research & Publications (20)
Clinicopathological case series of four patients with inherited macular disease.
PMID 19279306·Invest Ophthalmol Vis Sci·2009
5-case
Medical therapy in patients with acromegaly: predictors of response and comparison of efficacy of dopamine agonists and somatostatin analogues.
PMID 19158203·J Clin Endocrinol Metab·2009
8-other
ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing.
PMID 18611979·J Med Genet·2009
8-other
Blue cone monochromacy: causative mutations and associated phenotypes.
PMID 19421413·Mol Vis·2009
8-other
Monitoring disease activity using GH and IGF-I in the follow-up of 501 patients with acromegaly.
PMID 19178529·Clin Endocrinol (Oxf)·2009
8-other
ISCEV Standard for full-field clinical electroretinography (2008 update).
PMID 19030905·Doc Ophthalmol·2009
6-review
Haemorrhagic pituitary tumour presenting with unilateral paracentral visual disturbance.
PMID 18806763·Eye (Lond)·2009
5-case
Macular and retinal dysfunction of unknown origin in adults with normal fundi: evidence for an autoimmune pathophysiology.
PMID 18255057·Exp Mol Pathol·2008
7-preclinical
Differential changes in color and motion-onset visual evoked potentials from both eyes in early- and late-onset strabismic amblyopia.
PMID 18539945·Invest Ophthalmol Vis Sci·2008
8-other
Effect of gene therapy on visual function in Leber's congenital amaurosis.
PMID 18441371·N Engl J Med·2008
3-trial
Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy.
PMID 17962389·Br J Ophthalmol·2008
8-other
Phenotypic variation in enhanced S-cone syndrome.
PMID 18436841·Invest Ophthalmol Vis Sci·2008
8-other
Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways.
PMID 18252212·Am J Hum Genet·2008
8-other
Biallelic mutation of BEST1 causes a distinct retinopathy in humans.
PMID 18179881·Am J Hum Genet·2008
8-other
Thyrotoxicosis factitia masquerading as recurrent Graves' disease: endogenous antibody immunoassay interference, a pitfall for the unwary.
PMID 18482926·Ann Clin Biochem·2008
5-case
Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance.
PMID 18227217·Br J Ophthalmol·2008
5-case
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update.
PMID 17985165·Doc Ophthalmol·2008
6-review
The loss of the PDE6 deactivating enzyme, RGS9, results in precocious light adaptation at low light levels.
PMID 18318613·J Vis·2008
4-observational
Electrophysiological monitoring in a patient with an optic nerve glioma.
PMID 18301934·Doc Ophthalmol·2008
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 11005 RALSTON RD, SUITE 100 - G
ARVADA, CO 80004 - Phone
- (303) 431-0844
Quick Facts
- NPI
- 1366543902
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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