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SUSAN KOHL, MD

MD

Internal Medicine Physician

NPI: 1528098811IndividualAccepts Medicare

Specialties, Licenses & Credentials

Hospitalist Physician

Hospitalist

Code: 208M00000X

J5599(TX)
Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

J5599(TX)

CMS Specialties

PrimaryINTERNAL MEDICINE

Education

UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL SCHOOL AT DALLAS

Class of 1991

Research & Publications (20)

[Genetic causes of hereditary cone and cone-rod dystrophies].
PMID 19184602·Ophthalmologe·2009
6-review
Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase.
PMID 19459154·Hum Mutat·2009
8-other
Chondroid metaplasia mimicking recurrent squamous cell carcinoma of the head and neck.
PMID 19172559·Ear Nose Throat J·2009
5-case
An aluminium mold for intraoperative production of antibiotic-loaded PMMA knee prostheses.
PMID 19424917·Acta Orthop·2009
8-other
Genotyping microarray for CSNB-associated genes.
PMID 19578023·Invest Ophthalmol Vis Sci·2009
8-other
Consecutive thermal H2 and light-induced O2 evolution from water promoted by a metal complex.
PMID 19342584·Science·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
Transposition of a bacterial insertion sequence in chloroplasts.
PMID 19144000·Plant J·2009
8-other
GPR98 mutations cause Usher syndrome type 2 in males.
PMID 19357117·J Med Genet·2009
8-other
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
Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsia.
PMID 18521937·Hum Mutat·2008
8-other
CNGA3 mutations in two United Arab Emirates families with achromatopsia.
PMID 18636117·Mol Vis·2008
8-other
Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.
PMID 18487367·Invest Ophthalmol Vis Sci·2008
4-observational
CYLD mutations in familial skin appendage tumours.
PMID 18234730·J Med Genet·2008
8-other
Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
PMID 18235024·Invest Ophthalmol Vis Sci·2008
8-other
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies.
PMID 18285826·Eur J Hum Genet·2008
8-other
Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C).
PMID 18445228·Eur J Neurosci·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
Cutaneous malakoplakia.
PMID 18181662·Arch Pathol Lab Med·2008
6-review

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
3600 GASTON AVE, 550
DALLAS, TX 75246

Location

Practice Location

3600 GASTON AVE, DALLAS, TX
(214) 821-1177

Quick Facts

NPI
1528098811
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
2
Locations
1
Years in Practice
35
Publications
20

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