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GERALD TILLER, M.D.
M.D.
Ophthalmology Physician
NPI: 1881618502Individual
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
MD6038(SC)
Research & Publications (11)
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda.
PMID 11326333·Am J Hum Genet·2001
7-preclinical
Chondrodysplasia punctata associated with maternal autoimmune diseases: expanding the spectrum from systemic lupus erythematosus (SLE) to mixed connective tissue disease (MCTD) and scleroderma report of eight cases.
PMID 19006208·Am J Med Genet A·2008
5-case
Restrictive dermopathy: two- and three-dimensional sonographic features.
PMID 18844329·Ultrasound Obstet Gynecol·2008
5-case
Safety and efficacy of enzyme replacement therapy in combination with hematopoietic stem cell transplantation in Hurler syndrome.
PMID 15714083·Genet Med·2005
3-trial
Nephrotic syndrome complicating alpha-glucosidase replacement therapy for Pompe disease.
PMID 15466083·Pediatrics·2004
5-case
Possible activation of an intramyocardial inflammatory process ( Staphylococcus aureus)after treatment with infliximab in a boy with Crohn disease.
PMID 12012225·Eur J Pediatr·2002
5-case
The molecular basis of X-linked spondyloepiphyseal dysplasia tarda.
PMID 11349230·Am J Hum Genet·2001
8-other
Situs inversus with hypertrophic cardiomyopathy in identical twins.
PMID 10766992·Am J Med Genet·2000
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 200 S MEETING ST
GEORGETOWN, SC 29440 - Phone
- (843) 340-0561
Quick Facts
- NPI
- 1881618502
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 11
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