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MARCELA GARZON, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1407646359Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Ultrapotent topical corticosteroid treatment of hemangiomas of infancy.
PMID 15692474·J Am Acad Dermatol·2005
5-case
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 2.
PMID 19659975·Australas J Dermatol·2009
6-review
Conditions masquerading as infantile haemangioma: Part 1.
PMID 19397559·Australas J Dermatol·2009
6-review
Comparison of infantile hemangiomas in preterm and term infants: a prospective study.
PMID 18794478·Arch Dermatol·2008
4-observational
Postauricular cerebriform sebaceous nevus: case report and literature review.
PMID 19034079·Ann Plast Surg·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
Rapidly involuting congenital haemangioma associated with transient thrombocytopenia and coagulopathy: a case series.
PMID 18410425·Br J Dermatol·2008
5-case
Growth characteristics of infantile hemangiomas: implications for management.
PMID 18676554·Pediatrics·2008
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 18383593·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383596·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 18383591·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
- 1108 ROSS CLARK CIR STE 210
DOTHAN, AL 36301 - Phone
- (334) 712-3329
Quick Facts
- NPI
- 1407646359
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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