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MARIA CARMELA TARTAGLIA, M.D.
M.D.
Neurology Physician
NPI: 1508195165Individual
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
A105485(CA)
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
Mental fatigue alters the pattern and increases the volume of cerebral activation required for a motor task in multiple sclerosis patients with fatigue.
PMID 18353127·Eur J Neurol·2008
8-other
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
The relationship between diffuse axonal damage and fatigue in multiple sclerosis.
PMID 14967766·Arch Neurol·2004
8-other
Choline is increased in pre-lesional normal appearing white matter in multiple sclerosis.
PMID 12382153·J Neurol·2002
8-other
A competitive PCR-based method to measure human fibroblast growth factor receptor 1-4 (FGFR1-4) gene expression.
PMID 11445008·DNA Cell Biol·2001
8-other
Muscle phosphorus magnetic resonance spectroscopy oxidative indices correlate with physical activity.
PMID 10639607·Muscle Nerve·2000
3-trial
Fatigue in post-poliomyelitis syndrome: association with disease-related, behavioral, and psychosocial factors.
PMID 19627931·PM R·2009
8-other
RAS signaling dysregulation in human embryonal Rhabdomyosarcoma.
PMID 19681119·Genes Chromosomes Cancer·2009
8-other
Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutations.
PMID 19396835·Am J Med Genet A·2009
5-case
Acute lymphoblastic leukemia-associated JAK1 mutants activate the Janus kinase/STAT pathway via interleukin-9 receptor alpha homodimers.
PMID 19139102·J Biol Chem·2009
7-preclinical
Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype-phenotype correlations.
PMID 19156172·Eur J Hum Genet·2009
8-other
Second-trimester genetic sonogram for detection of fetal chromosomal abnormalities in a community-based antenatal testing unit.
PMID 19173242·Ultrasound Obstet Gynecol·2009
4-observational
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.
PMID 19206169·Hum Mutat·2009
8-other
Cognitive profile of disorders associated with dysregulation of the RAS/MAPK signaling cascade.
PMID 19133693·Am J Med Genet A·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
- 350 PARNASSUS, STE 905
SAN FRANCISCO, CA 94143 - Phone
- (415) 502-0551
Quick Facts
- NPI
- 1508195165
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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