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ALISA MONTICELLI, M.D.
M.D.
Pediatrics Physician
NPI: 1376864934Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
A124777(CA)
Research & Publications (20)
New clues on the origin of the Friedreich ataxia expanded alleles from the analysis of new polymorphisms closely linked to the mutation.
PMID 14767759·Hum Genet·2004
4-observational
PPAR-gamma agonist Azelaoyl PAF increases frataxin protein and mRNA expression: new implications for the Friedreich's ataxia therapy.
PMID 19104905·Cerebellum·2009
8-other
DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients.
PMID 18697824·J Med Genet·2008
8-other
Recombinant human erythropoietin increases frataxin protein expression without increasing mRNA expression.
PMID 18581197·Cerebellum·2008
8-other
Triplet repeat instability correlates with dinucleotide instability in primary breast cancer.
PMID 17143498·Oncol Rep·2007
8-other
Somatic instability of the expanded GAA triplet-repeat sequence in Friedreich ataxia progresses throughout life.
PMID 17498922·Genomics·2007
8-other
Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients.
PMID 17262846·Ann Neurol·2007
8-other
Pro12Ala polymorphism of the PPARgamma2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients.
PMID 17259473·Diabetes Care·2007
8-other
Beta2-adrenergic receptor and UCP3 variants modulate the relationship between age and type 2 diabetes mellitus.
PMID 17150099·BMC Med Genet·2006
8-other
Extra-mitochondrial localisation of frataxin and its association with IscU1 during enterocyte-like differentiation of the human colon adenocarcinoma cell line Caco-2.
PMID 16091420·J Cell Sci·2005
8-other
Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia.
PMID 15534367·Nucleic Acids Res·2004
8-other
Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype.
PMID 15596775·Neurology·2004
5-case
Real time PCR quantification of frataxin mRNA in the peripheral blood leucocytes of Friedreich ataxia patients and carriers.
PMID 15201375·J Neurol Neurosurg Psychiatry·2004
8-other
Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype.
PMID 15060107·J Med Genet·2004
8-other
3-Nitropropionic acid increases frataxin expression in human lymphoblasts and in transgenic rat PC12 cells.
PMID 14550925·Neurosci Lett·2003
4-observational
Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells.
PMID 12393810·Hum Mol Genet·2002
4-observational
Identification of a novel transcript of X25, the human gene involved in Friedreich ataxia.
PMID 11852181·Neurosci Lett·2002
4-observational
Serum transferrin receptor levels in Friedreich's and other degenerative ataxias.
PMID 11445653·Neurology·2001
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
- 3200 KEARNEY ST
FREMONT, CA 94538 - Phone
- (510) 490-1222
Quick Facts
- NPI
- 1376864934
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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