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MARCOS A UGARTE MD
MD
Surgery Physician
NPI: 1386661155IndividualAccepts Medicare
Specialties, Licenses & Credentials
Specialist
Specialist
Code: 174400000X
MD052860L(PA)
Surgery PhysicianPrimary
Surgery
Code: 208600000X
MD052860L(PA)
Education
UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE
Class of 1988
Research & Publications (20)
Hypertensive choroidopathy: recognizing clinically significant end-organ damage.
PMID 17888082·Acta Ophthalmol·2008
5-case
Spontaneous wound dehiscence after removal of single continuous penetrating keratoplasty suture: conservative management.
PMID 17172915·Cornea·2006
5-case
Horizontal and vertical micropsia following macula-off rhegmatogenous retinal-detachment surgical repair.
PMID 16544113·Graefes Arch Clin Exp Ophthalmol·2006
5-case
An experimental study of the elastic properties of the human Bruch's membrane-choroid complex: relevance to ageing.
PMID 16622094·Br J Ophthalmol·2006
8-other
A cohort study to estimate occupational mortality risks in Navarra.
PMID 15941748·Eur J Public Health·2005
8-other
Serpiginous choroidopathy: an unusual association with Crohn's disease.
PMID 12427238·Clin Exp Ophthalmol·2002
5-case
[Animal models of diabetic retinopathy: how are they helping us?].
PMID 19568986·Arch Soc Esp Oftalmol·2009
7-preclinical
The Missense p.S231F phenylalanine hydroxylase gene mutation causes complete loss of enzymatic activity in vitro.
PMID 19629656·Protein J·2009
8-other
Revisiting MSUD in Portuguese Gypsies: evidence for a founder mutation and for a mutational hotspot within the BCKDHA gene.
PMID 19456321·Ann Hum Genet·2009
8-other
High frequency of large genomic deletions in the PCCA gene causing propionic acidemia.
PMID 19157943·Mol Genet Metab·2009
8-other
Acute fatty liver of pregnancy and neonatal long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency.
PMID 18408953·Eur J Pediatr·2009
5-case
The activity of wild type and mutant phenylalanine hydroxylase with respect to the C-oxidation of phenylalanine and the S-oxidation of S-carboxymethyl-L-cysteine.
PMID 19036622·Mol Genet Metab·2009
8-other
Congenital disorder of glycosylation Ia: new differentially expressed proteins identified by 2-DE.
PMID 19101518·Biochem Biophys Res Commun·2009
4-observational
Functional analysis of three splicing mutations identified in the PMM2 gene: toward a new therapy for congenital disorder of glycosylation type Ia.
PMID 19235233·Hum Mutat·2009
8-other
Ten novel HMGCL mutations in 24 patients of different origin with 3-hydroxy-3-methyl-glutaric aciduria.
PMID 19177531·Hum Mutat·2009
8-other
Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group.
PMID 17957493·J Inherit Metab Dis·2008
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
- 401 ALLEGHENY AVE
HANOVER, PA 17331 - Phone
- (717) 630-2844
Quick Facts
- NPI
- 1386661155
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 38
- Publications
- 20
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