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ANDREW TONELLI, DMD 5/18/2014
DMD 5/18/2014
General Practice Dentistry
NPI: 1831515535Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
DN1856917(MA)
Research & Publications (20)
Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin.
PMID 19593598·Neurogenetics·2010
5-case
Bronchiectasis, a long-term sequela of ammonia inhalation: a case report and review of the literature.
PMID 18538935·Burns·2009
5-case
Erythromycin improves gastric emptying half-time in adult cystic fibrosis patients with gastroparesis.
PMID 19269261·J Cyst Fibros·2009
8-other
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function.
PMID 19431184·Hum Mutat·2009
5-case
Aberrant splicing due to a silent nucleotide change in CCM2 gene in a family with cerebral cavernous malformation.
PMID 19475721·Clin Genet·2009
8-other
Assessment of the genotoxic and carcinogenic risks of p-nitrophenol when it is present as an impurity in a drug product.
PMID 19500632·Regul Toxicol Pharmacol·2009
4-observational
Decreased diversity of the fecal Microbiome in recurrent Clostridium difficile-associated diarrhea.
PMID 18199029·J Infect Dis·2008
8-other
NMR studies of the inclusion complex of cloprostenol sodium salt with beta-cyclodextrin in aqueous solution.
PMID 18064541·Pharm Res·2008
8-other
A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.
PMID 18644608·J Neurol Sci·2008
5-case
Treatment of a ruptured saphenous vein graft pseudoaneurysm using a vascular plug.
PMID 18360846·Catheter Cardiovasc Interv·2008
5-case
A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia.
PMID 18200586·Hum Mutat·2008
8-other
Biomarkers, metabonomics, and drug development: can inborn errors of metabolism help in understanding drug toxicity?
PMID 17915830·AAPS J·2007
6-review
Seizures as the first manifestation of chromosome 22q11.2 deletion syndrome in a 40-year old man: a case report.
PMID 18053182·J Med Case Rep·2007
8-other
Peaked T--waves and sinus arrhythmia before prolonged sinus pauses and atrioventricular block in guillain-barre syndrome.
PMID 17957274·Indian Pacing Electrophysiol J·2007
8-other
Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine.
PMID 17877748·Clin Genet·2007
8-other
Effect of guest hydrophobicity on water sorption behavior of oligomer/alpha-cyclodextrin inclusion complexes.
PMID 17391022·J Phys Chem B·2007
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
- 205 MAIN ST
NORTH READING, MA 01864 - Phone
- (508) 265-9644
Quick Facts
- NPI
- 1831515535
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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