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WILLIAM HERRERA, M.D.
M.D.
Neurology Physician
NPI: 1730181645Individual
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
26506(CO)
Research & Publications (8)
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
PMID 19578027·Invest Ophthalmol Vis Sci·2009
8-other
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization.
PMID 19503738·Mol Vis·2009
8-other
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
PMID 18463160·Hum Mol Genet·2008
7-preclinical
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations.
PMID 18385078·Invest Ophthalmol Vis Sci·2008
4-observational
Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene.
PMID 18281613·Invest Ophthalmol Vis Sci·2008
8-other
EEG and behavioral changes following neurofeedback treatment in learning disabled children.
PMID 14521276·Clin Electroencephalogr·2003
3-trial
Detection of mercury and other undetermined materials in skin biopsies of endemic pemphigus foliaceus.
PMID 14501287·Am J Dermatopathol·2003
8-other
Sources of EEG activity in learning disabled children.
PMID 12449846·Clin Electroencephalogr·2002
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 175 S UNION BLVD, SUITE 310
COLORADO SPRINGS, CO 80910 - Phone
- (719) 473-3272
Quick Facts
- NPI
- 1730181645
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 8
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