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SARAH KOHL, M.D.
M.D.
Pediatrics Physician
NPI: 1497756001Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
MD061194L(PA)
Research & Publications (20)
Consecutive thermal H2 and light-induced O2 evolution from water promoted by a metal complex.
PMID 19342584·Science·2009
8-other
Chondroid metaplasia mimicking recurrent squamous cell carcinoma of the head and neck.
PMID 19172559·Ear Nose Throat J·2009
5-case
[Genetic causes of hereditary cone and cone-rod dystrophies].
PMID 19184602·Ophthalmologe·2009
6-review
Clinical significance of benign glands at surgical margins in robotic radical prostatectomy specimens.
PMID 17572197·Urology·2007
3-trial
Renal hilar mass in an 85-year-old woman. Solitary fibrous tumor.
PMID 16390227·Arch Pathol Lab Med·2006
5-case
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
PMID 15657609·Eur J Hum Genet·2005
7-preclinical
The diagnosis and treatment of neonatal herpes simplex virus infection.
PMID 12455481·Pediatr Ann·2002
6-review
Limited antibody-dependent cellular cytotoxicity antibody response induced by a herpes simplex virus type 2 subunit vaccine.
PMID 10608784·J Infect Dis·2000
8-other
An aluminium mold for intraoperative production of antibiotic-loaded PMMA knee prostheses.
PMID 19424917·Acta Orthop·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
The mean anatomical shape of the tibial plateau at the knee arthroplasty resection level: an investigation using MRI.
PMID 19467875·Knee·2009
4-observational
Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutations.
PMID 19038374·Am J Ophthalmol·2009
8-other
FDG uptake in giant cell tumor of the tendon sheath in a patient restaged for gastrointestinal stroma tumor (GIST).
PMID 19352292·Clin Nucl Med·2009
5-case
CNGA3 mutations in two United Arab Emirates families with achromatopsia.
PMID 18636117·Mol Vis·2008
8-other
Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation.
PMID 18653602·Br J Ophthalmol·2008
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
- 1370 WASHINGTON PIKE, SUITE 107
BRIDGEVILLE, PA 15017 - Phone
- (412) 221-0160
Quick Facts
- NPI
- 1497756001
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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