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MARK ZEIGLER, M.D.
M.D.
Family Medicine Physician
NPI: 1255376851Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
18877(SC)
Research & Publications (20)
Mucolipidosis type IV: the effect of increased lysosomal pH on the abnormal lysosomal storage.
PMID 19247216·Pediatr Res·2009
8-other
Measuring tissue perfusion during pressure relief maneuvers: insights into preventing pressure ulcers.
PMID 18092567·J Spinal Cord Med·2007
8-other
A novel mutation of the CLN8 gene: is there a Mediterranean phenotype?
PMID 17560505·Pediatr Neurol·2007
5-case
Angiokeratoma corporis diffusum in human beta-mannosidosis: Report of a new case and a novel mutation.
PMID 17420068·J Am Acad Dermatol·2007
5-case
Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect.
PMID 17391250·J Intellect Disabil Res·2007
8-other
Successful treatment of Wolman disease by unrelated umbilical cord blood transplantation.
PMID 17033804·Eur J Pediatr·2007
5-case
The role of the NADPH oxidase complex, p38 MAPK, and Akt in regulating human monocyte/macrophage survival.
PMID 16931806·Am J Respir Cell Mol Biol·2007
7-preclinical
TAT gene mutation analysis in three Palestinian kindreds with oculocutaneous tyrosinaemia type II; characterization of a silent exonic transversion that causes complete missplicing by exon 11 skipping.
PMID 16917729·J Inherit Metab Dis·2006
8-other
When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patients.
PMID 16630736·Mol Genet Metab·2006
8-other
Identification of loci affecting flavour volatile emissions in tomato fruits.
PMID 16473892·J Exp Bot·2006
8-other
The frequency of mucolipidosis type IV in the Ashkenazi Jewish population and the identification of 3 novel MCOLN1 mutations.
PMID 16287144·Hum Mutat·2005
8-other
The metabolism of glycosaminoglycans is impaired in prion diseases.
PMID 15951190·Neurobiol Dis·2005
7-preclinical
Phenotypic heterogeneity in patients with Gaucher disease and the N370S/V394L genotype.
PMID 15857183·Genet Test·2005
8-other
A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humans.
PMID 15773042·Mol Genet Metab·2005
5-case
Prenatal diagnosis for arginase deficiency by second-trimester fetal erythrocyte arginase assay and first-trimester ARG1 mutation analysis.
PMID 15565656·Prenat Diagn·2004
5-case
A novel mutation in the SLC17A5 gene causing both severe and mild phenotypes of free sialic acid storage disease in one inbred Bedouin kindred.
PMID 15172005·Mol Genet Metab·2004
5-case
Genomic organisation of the UDP-N-acetylglucosamine-1-phosphotransferase gamma subunit (GNPTAG) and its mutations in mucolipidosis III.
PMID 15060128·J Med Genet·2004
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
- 1107 W POINSETT ST
GREER, SC 29650 - Phone
- (864) 879-8886
Quick Facts
- NPI
- 1255376851
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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