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EMMA SHERIDAN, MD
MD
Internal Medicine Physician
NPI: 1720822083Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
9994(NE)
Research & Publications (20)
Delay in reporting meningococcal disease to public health departments.
PMID 15481208·Commun Dis Public Health·2004
8-other
Brucellosis in the UK: a risk to laboratory workers? Recommendations for prevention and management of laboratory exposure.
PMID 18495792·J Clin Pathol·2010
5-case
Replication of the recessive STBMS1 locus but with dominant inheritance.
PMID 19218600·Invest Ophthalmol Vis Sci·2009
8-other
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations.
PMID 19420365·N Engl J Med·2009
7-preclinical
Familial exudative vitreoretinopathy and DiGeorge syndrome: a new locus for familial exudative vitreoretinopathy on chromosome 22q11.2?
PMID 19501404·Ophthalmology·2009
5-case
Macular dystrophy associated with the Arg172Trp substitution in peripherin/RDS: genotype-phenotype correlation.
PMID 19262438·Retina·2009
4-observational
IBDfinder and SNPsetter: tools for pedigree-independent identification of autozygous regions in individuals with recessive inherited disease.
PMID 19405095·Hum Mutat·2009
8-other
Psychologists in academic health centers: reflections on traditions and innovations in education, science, and practice.
PMID 19104958·J Clin Psychol Med Settings·2008
8-other
Variable expression of neurological phenotype in autosomal recessive oculodentodigital dysplasia of two sibs and review of the literature.
PMID 17476528·Eur J Pediatr·2008
5-case
Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombination.
PMID 18824584·J Exp Med·2008
5-case
Clinical inquiries. Should you treat a symptomatic patient by phone when his child has confirmed strep throat?
PMID 17343817·J Fam Pract·2007
6-review
Evaluation of the Wayson stain for the rapid diagnosis of melioidosis.
PMID 17360835·J Clin Microbiol·2007
4-observational
X-linked retinoschisis in a female with a heterozygous RS1 missense mutation.
PMID 17304551·Am J Med Genet A·2007
5-case
Exudative retinopathy in a girl with Alström syndrome due to a novel mutation.
PMID 17576719·Br J Ophthalmol·2007
5-case
Extensive gene conversion at the PMS2 DNA mismatch repair locus.
PMID 17253626·Hum Mutat·2007
7-preclinical
Reduced bone mineral density and hyaloid vasculature remnants in a consanguineous recessive FEVR family with a mutation in LRP5.
PMID 16929062·Br J Ophthalmol·2006
5-case
Producing decisions in service-user groups for people with an intellectual disability: two contrasting facilitator styles.
PMID 16970516·Ment Retard·2006
8-other
Gene symbol: VHL. Disease: von Hippel-Lindau syndrome. Accession #Hd0512.
PMID 17297680·Hum Genet·2006
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
- 982005 NEBRASKA MEDICAL CENTER
OMAHA, NE 68198 - Phone
- (402) 559-0390
Quick Facts
- NPI
- 1720822083
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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