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ANDREW SORENSON, M.D.
M.D.
Ophthalmology Physician
NPI: 1326139981IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
G66123(CA)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
UNIVERSITY OF CALIFORNIA, SAN DIEGO SCHOOL OF MEDICINE
Class of 1995
Research & Publications (20)
Ultrasonographic measurement of induced myopia associated with capsular bag distention syndrome.
PMID 10811082·Ophthalmology·2000
3-trial
Discordance for X-linked hypophosphataemic rickets in identical twin girls.
PMID 19258716·Horm Res·2009
4-observational
Ablation of the Galnt3 gene leads to low-circulating intact fibroblast growth factor 23 (Fgf23) concentrations and hyperphosphatemia despite increased Fgf23 expression.
PMID 19213845·Endocrinology·2009
7-preclinical
Vascular nitric oxide and superoxide anion contribute to sex-specific programmed cardiovascular physiology in mice.
PMID 19144750·Am J Physiol Regul Integr Comp Physiol·2009
7-preclinical
Myelinated, synapsing cultures of murine spinal cord--validation as an in vitro model of the central nervous system.
PMID 18793322·Eur J Neurosci·2008
4-observational
Corneal cupremia in multiple myeloma: a clinicopathologic correlation.
PMID 18625955·Arch Ophthalmol·2008
5-case
Mutational survey of the PHEX gene in patients with X-linked hypophosphatemic rickets.
PMID 18625346·Bone·2008
8-other
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis.
PMID 17710231·J Clin Invest·2007
5-case
Novel GALNT3 mutations causing hyperostosis-hyperphosphatemia syndrome result in low intact fibroblast growth factor 23 concentrations.
PMID 17311862·J Clin Endocrinol Metab·2007
5-case
Tumoral calcinosis presenting with eyelid calcifications due to novel missense mutations in the glycosyl transferase domain of the GALNT3 gene.
PMID 16940445·J Clin Endocrinol Metab·2006
5-case
Teenage mothers' anger over twelve years: partner conflict, partner transitions and children's anger.
PMID 16898991·J Child Psychol Psychiatry·2006
8-other
Intronic deletions in the SLC34A3 gene cause hereditary hypophosphatemic rickets with hypercalciuria.
PMID 16849419·J Clin Endocrinol Metab·2006
8-other
A novel method of generating individual communications for participants in large surveys.
PMID 15357532·Soz Praventivmed·2004
8-other
Impact of 'Mad Cow Disease' publicity on trends in meat and total vitamin A consumption in Geneva between 1993 and 2000.
PMID 12548314·Eur J Clin Nutr·2003
7-preclinical
A better understanding of health issues through population-based surveillance. Why surveys?
PMID 11851066·Soz Praventivmed·2001
8-other
Acute corneal endothelial changes after laser in situ keratomileusis.
PMID 11473159·Cornea·2001
8-other
Bone-related mineral content of water samples collected on the Navajo reservation.
PMID 10967411·Toxicology·2000
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
- 3010 COLBY ST, SUITE 114
BERKELEY, CA 94705 - Phone
- (510) 848-1413
Quick Facts
- NPI
- 1326139981
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 31
- Publications
- 20
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