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GENINE SICILIANO, MD
MD
Emergency Medicine Physician
NPI: 1649537424IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
P9256(TX)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
STATE UNIVERSITY OF NEW YORK AT STONY BROOK, SCHOOL OF MEDICINE
Class of 2012
Research & Publications (20)
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort.
PMID 19632744·Neurobiol Aging·2011
8-other
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype.
PMID 19488901·Amyotroph Lateral Scler·2010
8-other
Lack of association between the APEX1 Asp148Glu polymorphism and sporadic amyotrophic lateral sclerosis.
PMID 18482781·Neurobiol Aging·2010
8-other
Neuroprotective effects of tetracyclines: molecular targets, animal models and human disease.
PMID 19601819·CNS Neurol Disord Drug Targets·2009
6-review
Pleiotropic effects of spastin on neurite growth depending on expression levels.
PMID 19141076·J Neurochem·2009
7-preclinical
Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?
PMID 17888545·Neurobiol Aging·2009
8-other
The role of vascular factors in late-onset sporadic Alzheimer's disease. Genetic and molecular aspects.
PMID 19519304·Curr Alzheimer Res·2009
6-review
Risk of arrhythmia in type I myotonic dystrophy: the role of clinical and genetic variables.
PMID 19237383·J Neurol Neurosurg Psychiatry·2009
8-other
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
PMID 19193627·Hum Mol Genet·2009
8-other
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring.
PMID 18983896·Neurosci Lett·2009
8-other
The translational repressor Cup associates with the adaptor protein Miranda and the mRNA carrier Staufen at multiple time-points during Drosophila oogenesis.
PMID 18930123·Gene·2009
7-preclinical
Cardiac magnetic resonance imaging and management of dilated cardiomyopathy in a Duchenne muscular dystrophy manifesting carrier.
PMID 19253058·J Neurol·2009
5-case
Electron transfer mediators and other metabolites and cofactors in the treatment of mitochondrial dysfunction.
PMID 19674340·Nutr Rev·2009
6-review
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.
PMID 19236453·Eur J Neurol·2009
8-other
Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature.
PMID 19597763·Neurol Sci·2009
5-case
Mitochondrial DNA single deletion in a patient with postural tremor.
PMID 18709667·Mov Disord·2008
5-case
DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patients.
PMID 18708572·J Neurol Neurosurg Psychiatry·2008
8-other
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.
PMID 19049553·Eur J Neurol·2008
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
- 5201 HARRY HINES BLVD, HOUSE STAFF & GME
DALLAS, TX 75235 - Phone
- (214) 590-8058
Quick Facts
- NPI
- 1649537424
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 14
- Publications
- 20
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