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MICHELLE TARTAGLIA, DMD
DMD
Dentist
NPI: 1851675193Individual
Specialties, Licenses & Credentials
DentistPrimary
Dentist
Code: 122300000X
DS038725(PA)8517(SC)
Research & Publications (20)
Acute stroke with hyperdense middle cerebral artery sign benefits from IV rtPA.
PMID 19235441·Can J Neurol Sci·2008
4-observational
Delusions and hallucinations in frontotemporal dementia: a clinicopathologic case report.
PMID 18541988·Cogn Behav Neurol·2008
8-other
Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.
PMID 17143282·Nat Genet·2007
4-observational
Differentiation between primary lateral sclerosis and amyotrophic lateral sclerosis: examination of symptoms and signs at disease onset and during follow-up.
PMID 17296839·Arch Neurol·2007
4-observational
Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease.
PMID 16358218·Am J Hum Genet·2006
8-other
Somatic PTPN11 mutations in childhood acute myeloid leukaemia.
PMID 15842656·Br J Haematol·2005
4-observational
Noonan syndrome and related disorders: genetics and pathogenesis.
PMID 16124853·Annu Rev Genomics Hum Genet·2005
6-review
Paternal germline origin and sex-ratio distortion in transmission of PTPN11 mutations in Noonan syndrome.
PMID 15248152·Am J Hum Genet·2004
8-other
Genetic evidence for lineage-related and differentiation stage-related contribution of somatic PTPN11 mutations to leukemogenesis in childhood acute leukemia.
PMID 14982869·Blood·2004
8-other
Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia.
PMID 12717436·Nat Genet·2003
7-preclinical
Exclusion of PTPN11 mutations in Costello syndrome: further evidence for distinct genetic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes.
PMID 12752577·Clin Genet·2003
8-other
Choline is increased in pre-lesional normal appearing white matter in multiple sclerosis.
PMID 12382153·J Neurol·2002
8-other
PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity.
PMID 11992261·Am J Hum Genet·2002
8-other
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome.
PMID 11704759·Nat Genet·2001
8-other
Muscle phosphorus magnetic resonance spectroscopy oxidative indices correlate with physical activity.
PMID 10639607·Muscle Nerve·2000
3-trial
RAS signaling dysregulation in human embryonal Rhabdomyosarcoma.
PMID 19681119·Genes Chromosomes Cancer·2009
8-other
Fatigue in post-poliomyelitis syndrome: association with disease-related, behavioral, and psychosocial factors.
PMID 19627931·PM R·2009
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
- 2039 MEDICAL PARK DR
NEWBERRY, SC 29108 - Phone
- (803) 276-3371
Quick Facts
- NPI
- 1851675193
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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