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CORA BRUNO, PHARMD
PHARMD
Pharmacist
NPI: 1629791827Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
106813-01(NY)
Research & Publications (20)
HyperCKemia as the only sign of McArdle's disease in a child.
PMID 10695902·J Child Neurol·2000
5-case
Synthesis and in vitro sodium channel blocking activity evaluation of novel homochiral mexiletine analogs.
PMID 19544349·Chirality·2010
7-preclinical
Caveolinopathies: from the biology of caveolin-3 to human diseases.
PMID 19584897·Eur J Hum Genet·2010
6-review
SMN transcript levels in leukocytes of SMA patients determined by absolute real-time PCR.
PMID 19603064·Eur J Hum Genet·2010
8-other
Congenital subglottic cyst in a term neonate.
PMID 19542316·Arch Dis Child Fetal Neonatal Ed·2009
5-case
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.
PMID 19105190·Hum Mutat·2009
8-other
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study.
PMID 19299310·Neurology·2009
4-observational
The association between maternal body mass index and severity of neonatal illness in very low birth weight infants.
PMID 19488942·J Matern Fetal Neonatal Med·2009
8-other
Electrochemical and theoretical investigation of corannulene reduction processes.
PMID 19173564·J Phys Chem B·2009
8-other
Health surveillance for subjects with past exposure to asbestos: from international experience and Italian regional practices to a proposed operational model.
PMID 19636166·Ann Ist Super Sanita·2009
6-review
Reliability of the North Star Ambulatory Assessment in a multicentric setting.
PMID 19553120·Neuromuscul Disord·2009
3-trial
Synthesis, photophysical, electrochemical, and electrochemiluminescent properties of 5,15-bis(9-anthracenyl)porphyrin derivatives.
PMID 19462051·Org Biomol Chem·2009
8-other
Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies.
PMID 18641458·Cell Cycle·2008
8-other
Novel mutations in the adipose triglyceride lipase gene causing neutral lipid storage disease with myopathy.
PMID 18952067·Biochem Biophys Res Commun·2008
5-case
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian study.
PMID 18513969·Neuromuscul Disord·2008
4-observational
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.
PMID 19049553·Eur J Neurol·2008
8-other
Non-parametric smoothing of multivariate genetic distances in the analysis of spatial population structure at fine scale.
PMID 18592207·Theor Appl Genet·2008
7-preclinical
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease.
PMID 18487559·J Neurol Neurosurg Psychiatry·2008
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 42084 NY-28
MARGARETVILLE, NY 12455 - Phone
- (845) 586-1344
Quick Facts
- NPI
- 1629791827
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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