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MARTHA GARZON, DMD, MS

DMD, MS

Pediatric Dentistry

NPI: 1376691709Individual

Specialties, Licenses & Credentials

Pediatric DentistryPrimary

Dentist — Pediatric Dentistry

Code: 1223P0221X

5504(OK)

Research & Publications (20)

Conditions masquerading as infantile haemangioma: Part 2.
PMID 19659975·Australas J Dermatol·2009
6-review
Conditions masquerading as infantile haemangioma: Part 1.
PMID 19397559·Australas J Dermatol·2009
6-review
Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene.
PMID 18803659·Exp Dermatol·2009
5-case
Growth characteristics of infantile hemangiomas: implications for management.
PMID 18676554·Pediatrics·2008
8-other
An infant with a facial hemangioma and more.
PMID 19073318·Semin Pediatr Neurol·2008
5-case
Comparison of infantile hemangiomas in preterm and term infants: a prospective study.
PMID 18794478·Arch Dermatol·2008
4-observational
Rapidly involuting congenital haemangioma associated with transient thrombocytopenia and coagulopathy: a case series.
PMID 18410425·Br J Dermatol·2008
5-case
Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations.
PMID 18446851·Hum Mutat·2008
8-other
The cerebral vasculopathy of PHACES syndrome.
PMID 18174492·Stroke·2008
8-other
Postauricular cerebriform sebaceous nevus: case report and literature review.
PMID 19034079·Ann Plast Surg·2008
5-case
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383593·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383594·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383595·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383591·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18380023·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383587·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383588·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383589·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383590·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383596·Hum Genet·2007
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
870 S KELLY AVE
EDMOND, OK 73003

Location

Practice Location

870 S KELLY AVE, EDMOND, OK
(405) 348-5757

Quick Facts

NPI
1376691709
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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