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MATEO GARZON, MD
Student in an Organized Health Care Education/Training Program
NPI: 1124815329Individual
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)
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
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
Comparison of infantile hemangiomas in preterm and term infants: a prospective study.
PMID 18794478·Arch Dermatol·2008
4-observational
Growth characteristics of infantile hemangiomas: implications for management.
PMID 18676554·Pediatrics·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 18383590·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 18383588·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 18383596·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18380023·Hum Genet·2007
8-other
Subcutaneous nodule and diffuse lymphadenopathy in a 6-month-old boy from Africa.
PMID 17938353·Arch Dermatol·2007
5-case
Verrucous papules and plaques in a pediatric patient: cutaneous papillomas associated with Costello syndrome.
PMID 17875889·Arch Dermatol·2007
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 7727 LAKE UNDERHILL RD
ORLANDO, FL 32822 - Phone
- (407) 303-8110
Quick Facts
- NPI
- 1124815329
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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