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MARIA GARZON, M.D.
M.D.
Pediatric Dermatology Physician
NPI: 1487754784Individual
Specialties, Licenses & Credentials
Dermatology Physician
Dermatology
Code: 207N00000X
180502-1(NY)
Pediatric Dermatology PhysicianPrimary
Dermatology — Pediatric Dermatology
Code: 207NP0225X
180502(NY)
Research & Publications (20)
Ultrapotent topical corticosteroid treatment of hemangiomas of infancy.
PMID 15692474·J Am Acad Dermatol·2005
5-case
Vascular tumors and vascular malformations: evidence for an association.
PMID 10642685·J Am Acad Dermatol·2000
8-other
Hemangiomas: update on classification, clinical presentation, and associated anomalies.
PMID 11107514·Cutis·2000
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
Conditions masquerading as infantile haemangioma: Part 1.
PMID 19397559·Australas J Dermatol·2009
6-review
Conditions masquerading as infantile haemangioma: Part 2.
PMID 19659975·Australas J Dermatol·2009
6-review
Growth characteristics of infantile hemangiomas: implications for management.
PMID 18676554·Pediatrics·2008
8-other
Comparison of infantile hemangiomas in preterm and term infants: a prospective study.
PMID 18794478·Arch Dermatol·2008
4-observational
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
Rapidly involuting congenital haemangioma associated with transient thrombocytopenia and coagulopathy: a case series.
PMID 18410425·Br J Dermatol·2008
5-case
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 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 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
- 161 FORT WASHINGTON AVE, 12TH FLOOR
NEW YORK, NY 10032 - Phone
- (212) 305-5293
Quick Facts
- NPI
- 1487754784
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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