Back to Search
PAUL SIEVING, MD
MD
Retina Specialist (Ophthalmology) Physician
NPI: 1275175788IndividualAccepts Medicare
Specialties, Licenses & Credentials
Retina Specialist (Ophthalmology) PhysicianPrimary
Ophthalmology — Retina Specialist
Code: 207WX0107X
G47797(CA)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
UNIVERSITY OF ILLINOIS COLLEGE OF MED (CHI/PEOR/ROCK/CHM-URB)
Class of 1978
Research & Publications (20)
Inhibition of the visual cycle in vivo by 13-cis retinoic acid protects from light damage and provides a mechanism for night blindness in isotretinoin therapy.
PMID 11172037·Proc Natl Acad Sci U S A·2001
7-preclinical
Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causing progressive and severe XLRS in a cross-sectional family study.
PMID 19474399·Invest Ophthalmol Vis Sci·2009
7-preclinical
Depleting Rac1 in mouse rod photoreceptors protects them from photo-oxidative stress without affecting their structure or function.
PMID 19470639·Proc Natl Acad Sci U S A·2009
7-preclinical
Photoreceptor protection by adeno-associated virus-mediated LEDGF expression in the RCS rat model of retinal degeneration: probing the mechanism.
PMID 19324854·Invest Ophthalmol Vis Sci·2009
7-preclinical
The effects of transient retinal detachment on cavity size and glial and neural remodeling in a mouse model of X-linked retinoschisis.
PMID 19387072·Invest Ophthalmol Vis Sci·2009
7-preclinical
Intravitreal delivery of AAV8 retinoschisin results in cell type-specific gene expression and retinal rescue in the Rs1-KO mouse.
PMID 19458650·Gene Ther·2009
7-preclinical
Organization and molecular interactions of retinoschisin in photoreceptors.
PMID 18188957·Adv Exp Med Biol·2008
6-review
Photopic ERG negative response from amacrine cell signaling in RCS rat retinal degeneration.
PMID 18172124·Invest Ophthalmol Vis Sci·2008
7-preclinical
Night blindness and the mechanism of constitutive signaling of mutant G90D rhodopsin.
PMID 18987202·J Neurosci·2008
7-preclinical
Genomics in the era of molecular ophthalmology: reflections on the National Ophthalmic Disease Genotyping Network (eyeGENE).
PMID 18332328·Arch Ophthalmol·2008
8-other
Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration.
PMID 19057657·Mol Vis·2008
7-preclinical
Synaptic pathology in retinoschisis knockout (Rs1-/y) mouse retina and modification by rAAV-Rs1 gene delivery.
PMID 18660429·Invest Ophthalmol Vis Sci·2008
7-preclinical
Preventing blindness in retinal disease: ciliary neurotrophic factor intraocular implants.
PMID 17508034·Can J Ophthalmol·2007
6-review
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene.
PMID 17605048·Hum Genet·2007
8-other
Constitutive excitation by Gly90Asp rhodopsin rescues rods from degeneration caused by elevated production of cGMP in the dark.
PMID 17699662·J Neurosci·2007
7-preclinical
CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function.
PMID 17652762·Invest Ophthalmol Vis Sci·2007
8-other
Retinoschisin gene therapy and natural history in the Rs1h-KO mouse: long-term rescue from retinal degeneration.
PMID 17652759·Invest Ophthalmol Vis Sci·2007
7-preclinical
A meta-analysis of N-acetylcysteine in contrast-induced nephrotoxicity: unsupervised clustering to resolve heterogeneity.
PMID 18001477·BMC Med·2007
1-meta
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4860 Y ST STE 2400
SACRAMENTO, CA 95817 - Phone
- (916) 734-6602
Quick Facts
- NPI
- 1275175788
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 48
- Publications
- 20
Are you this provider?
Claim Your Profile