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STEPHANIE BATTISTINI MD
MD
Developmental - Behavioral Pediatrics Physician
NPI: 1467831099Individual
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
ME135110(FL)52642(KY)
Developmental - Behavioral Pediatrics PhysicianPrimary
Pediatrics — Developmental - Behavioral Pediatrics
Code: 2080P0006X
52642(KY)
Research & Publications (14)
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype.
PMID 19488901·Amyotroph Lateral Scler·2010
8-other
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
PMID 19193627·Hum Mol Genet·2009
8-other
CACNA1A gene non-synonymous single nucleotide polymorphisms and common migraine in Italy: a case-control association study with a micro-array technology.
PMID 19527141·Clin Chem Lab Med·2009
8-other
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation.
PMID 19450904·Neurobiol Aging·2009
8-other
Effect of additives on the chemical vapour generation of bismuthane by tetrahydroborate(III) derivatization.
PMID 17252220·Anal Bioanal Chem·2007
8-other
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population.
PMID 17462671·J Neurol Sci·2007
8-other
Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.
PMID 17562932·Arch Neurol·2007
8-other
SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.
PMID 15789135·J Neurol·2005
4-observational
Mutational analysis of the inhibin alpha gene in preeclamptic women.
PMID 15816368·J Endocrinol Invest·2005
8-other
Activity of protein phosphatase calcineurin is decreased in sporadic and familial amyotrophic lateral sclerosispatients.
PMID 15312178·J Neurochem·2004
4-observational
Decreased lifespan in the absence of expression of the mitochondrial small heat shock protein Hsp22 in Drosophila.
PMID 15331597·J Biol Chem·2004
7-preclinical
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence?
PMID 15060811·Neurol Sci·2004
5-case
Posterior knee pain: primary symptom of a small non-occlusive venous clot.
PMID 12876176·Arch Dis Child·2003
5-case
Deep vein thrombosis during varicella in a child with factor V Leiden mutation and familial deficiency of protein S.
PMID 11246564·Thromb Haemost·2001
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 411 E CHESTNUT ST # 2
LOUISVILLE, KY 40202 - Phone
- (502) 588-0850
Quick Facts
- NPI
- 1467831099
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 3
- Publications
- 14
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