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CHANTAL BARBOT DO
DO
Pediatric Otolaryngology Physician
NPI: 1801255674Individual
Specialties, Licenses & Credentials
Otolaryngology Physician
Otolaryngology
Code: 207Y00000X
34.015962(OH)
Pediatric Otolaryngology PhysicianPrimary
Otolaryngology — Pediatric Otolaryngology
Code: 207YP0228X
34.015962(OH)
Research & Publications (20)
Efficient purification of recombinant proteins fused to maltose-binding protein by mixed-mode chromatography.
PMID 19329121·J Chromatogr A·2009
8-other
Use of magnetic carboxyl beads to purify a cationic peptide in a batch system.
PMID 18977331·Anal Biochem·2009
8-other
LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients.
PMID 18700894·Clin Genet·2008
8-other
Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type.
PMID 18512755·Mov Disord·2008
4-observational
Infantile neuroaxonal dystrophy: what's most important for the diagnosis?
PMID 18359254·Eur J Paediatr Neurol·2008
8-other
Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type.
PMID 18164228·Mol Genet Metab·2008
4-observational
Outcome of three cases of untreated maternal glutaric aciduria type I.
PMID 17661081·Eur J Pediatr·2008
5-case
Uncoupling protein-2 controls proliferation by promoting fatty acid oxidation and limiting glycolysis-derived pyruvate utilization.
PMID 17855623·FASEB J·2008
7-preclinical
Neurodegeneration associated with genetic defects in phospholipase A(2).
PMID 18799783·Neurology·2008
8-other
Stereotypies in Rett syndrome: analysis of 83 patients with and without detected MECP2 mutations.
PMID 17420401·Neurology·2007
8-other
Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathy.
PMID 17266923·Biochem Biophys Res Commun·2007
8-other
Solubility and dissolution rate of progesterone-cyclodextrin-polymer systems.
PMID 17012117·Drug Dev Ind Pharm·2006
8-other
[Usefulness of analysis of cerebrospinal fluid for the diagnosis of neurotransmitters and pterin defects and glucose and folate transport deficiencies across blood brain barrier].
PMID 16827996·Med Clin (Barc)·2006
8-other
Novel L2HGDH mutations in 21 patients with L-2-hydroxyglutaric aciduria of Portuguese origin.
PMID 16134148·Hum Mutat·2005
7-preclinical
Distinguishing the four genetic causes of Jouberts syndrome-related disorders.
PMID 15786477·Ann Neurol·2005
8-other
Use of radiotracer techniques to study subcellular distribution of metals and radionuclides in bivalves from the Noumea lagoon, New Calendonia.
PMID 16228877·Bull Environ Contam Toxicol·2005
7-preclinical
Development of cyclodextrin microspheres for pulmonary drug delivery.
PMID 16401391·J Pharm Pharm Sci·2005
4-observational
Homozygosity mapping of a third Joubert syndrome locus to 6q23.
PMID 15060101·J Med Genet·2004
8-other
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.
PMID 14770181·Nat Genet·2004
8-other
Regulation of vascular L-type Ca2+ channels by phosphatidylinositol 3,4,5-trisphosphate.
PMID 15242973·Circ Res·2004
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via DAYTON CHILDREN'S SPECIALTY PHYSICIANS, INC. · 4 locations total
- Address
- 1 CHILDRENS PLZ
DAYTON, OH 45404 - Phone
- (937) 641-4000
Quick Facts
- NPI
- 1801255674
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 4
- Publications
- 20
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