Back to Search

MARTHA GARZON, MD

MD

Obstetrics & Gynecology Physician

NPI: 1881673960IndividualAccepts Medicare

Specialties, Licenses & Credentials

Obstetrics & Gynecology PhysicianPrimary

Obstetrics & Gynecology

Code: 207V00000X

ME73125(FL)

CMS Specialties

PrimaryOBSTETRICS/GYNECOLOGY

Education

UNIVERSITY OF ILLINOIS COLLEGE OF MED (CHI/PEOR/ROCK/CHM-URB)

Class of 1991

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
1150 N 35TH AVE, SUITE 400
HOLLYWOOD, FL 33021

Location

Practice Location

1150 N 35TH AVE, HOLLYWOOD, FL
(954) 963-6363

Quick Facts

NPI
1881673960
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
35
Publications
20

Are you this provider?

Claim Your Profile