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NICOLA BRUNETTI-PIERRI, MD
MD
Pediatrics Physician
NPI: 1568609576Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) Physician
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
N1567(TX)
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
N1567(TX)
Research & Publications (20)
Efficient, long-term hepatic gene transfer using clinically relevant HDAd doses by balloon occlusion catheter delivery in nonhuman primates.
PMID 19050700·Mol Ther·2009
7-preclinical
Bioengineered factor IX molecules with increased catalytic activity improve the therapeutic index of gene therapy vectors for hemophilia B.
PMID 19196177·Hum Gene Ther·2009
4-observational
Rapidly progressive neurological deterioration in a child with Alpers syndrome exhibiting a previously unremarkable brain MRI.
PMID 18991199·Neuropediatrics·2008
5-case
Case report: pathological features of aberrant pancreatic development in congenital hyperinsulinism due to ABCC8 mutations.
PMID 18988933·Ann Clin Lab Sci·2008
5-case
Robinow syndrome: phenotypic variability in a family with a novel intragenic ROR2 mutation.
PMID 18831060·Am J Med Genet A·2008
5-case
Phenotypic correction of ornithine transcarbamylase deficiency using low dose helper-dependent adenoviral vectors.
PMID 18563850·J Gene Med·2008
7-preclinical
15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization.
PMID 18561338·Am J Med Genet A·2008
5-case
GM1 gangliosidosis: review of clinical, molecular, and therapeutic aspects.
PMID 18524657·Mol Genet Metab·2008
6-review
Spondylocarpotarsal synostosis: long-term follow-up of a case due to FLNB mutations.
PMID 18386804·Am J Med Genet A·2008
5-case
Generalized metabolic bone disease in Neurofibromatosis type I.
PMID 18289904·Mol Genet Metab·2008
8-other
Progress and prospects: gene therapy for genetic diseases with helper-dependent adenoviral vectors.
PMID 18288209·Gene Ther·2008
6-review
Brain proton magnetic resonance spectroscopy and neuromuscular pathology in a patient with GM1 gangliosidosis.
PMID 18184943·J Child Neurol·2008
5-case
Gene therapy for inborn errors of liver metabolism: progress towards clinical applications.
PMID 19490653·Ital J Pediatr·2008
8-other
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
PMID 19029900·Nat Genet·2008
8-other
Gray matter heterotopias and brachytelephalangic chondrodysplasia punctata: a complication of hyperemesis gravidarum induced vitamin K deficiency?
PMID 17163521·Am J Med Genet A·2007
5-case
Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization.
PMID 17916097·Clin Genet·2007
5-case
Parkes Weber syndrome occurring in a family with capillary malformations.
PMID 17551330·Clin Dysmorphol·2007
5-case
Pseudo-hydrodynamic delivery of helper-dependent adenoviral vectors into non-human primates for liver-directed gene therapy.
PMID 17285138·Mol Ther·2007
7-preclinical
Intrauterine growth retardation and placental vacuolization as presenting features in a case of GM1 gangliosidosis.
PMID 17712606·J Inherit Metab Dis·2007
5-case
Progress towards the clinical application of helper-dependent adenoviral vectors for liver and lung gene therapy.
PMID 17078387·Curr Opin Mol Ther·2006
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2 GREENWAY PLZ, SUITE 900
HOUSTON, TX 77046 - Phone
- (713) 798-1750
Quick Facts
- NPI
- 1568609576
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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