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NATHAN BRAVERMAN, D.M.D., M.D.
D.M.D., M.D.
Oral and Maxillofacial Surgery (Dentist)
NPI: 1205945425Individual
Specialties, Licenses & Credentials
Oral and Maxillofacial Surgery (Dentist)Primary
Dentist — Oral and Maxillofacial Surgery
Code: 1223S0112X
019023544(IL)
CMS Specialties
PrimaryMAXILLOFACIAL SURGERY
Additional
ORAL SURGERY
Education
OTHER
Class of 1996
Research & Publications (20)
Maternal mixed connective tissue disease and offspring with chondrodysplasia punctata.
PMID 19110299·Semin Arthritis Rheum·2010
5-case
A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts.
PMID 19127411·J Inherit Metab Dis·2009
5-case
Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development.
PMID 18661548·Am J Med Genet A·2008
5-case
Clinical and molecular analysis of arylsulfatase E in patients with brachytelephalangic chondrodysplasia punctata.
PMID 18348268·Am J Med Genet A·2008
8-other
A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency.
PMID 18155630·Mol Genet Metab·2008
6-review
Role of nurses in a university hospital during mass casualty events.
PMID 17724245·Am J Crit Care·2007
8-other
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation.
PMID 16816004·Pediatrics·2006
5-case
Proton MR spectroscopy in hyperhomocysteinemia with elevated blood methionine levels.
PMID 16463305·J Magn Reson Imaging·2006
5-case
Progressive cavitating leukoencephalopathy: a novel childhood disease.
PMID 16315274·Ann Neurol·2005
8-other
Mucolipidosis II presenting as severe neonatal hyperparathyroidism.
PMID 15580357·Eur J Pediatr·2005
5-case
The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.
PMID 15542397·Mol Genet Metab·2004
4-observational
Severe tracheobronchial stenosis in the X-linked recessive form of chondrodysplasia punctata.
PMID 15611404·Arch Otolaryngol Head Neck Surg·2004
5-case
Metabolites in ventricular cerebrospinal fluid detected by proton magnetic resonance spectroscopic imaging.
PMID 15332258·J Magn Reson Imaging·2004
5-case
Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux.
PMID 15146390·Am J Hum Genet·2004
8-other
Mutational and functional analysis of SLC4A4 in a patient with proximal renal tubular acidosis.
PMID 15085340·Pflugers Arch·2004
5-case
A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.
PMID 12913067·Hum Mol Genet·2003
8-other
The relationship of plasma glutamine to ammonium and of glycine to acid-base balance in propionic acidaemia.
PMID 12872849·J Inherit Metab Dis·2003
8-other
Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap.
PMID 12765841·Mol Genet Metab·2003
5-case
Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype.
PMID 12325024·Hum Mutat·2002
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
- 1770 FIRST STREET, SUITE 350
HIGHLAND PARK, IL 60035 - Phone
- (847) 433-1516
Quick Facts
- NPI
- 1205945425
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 30
- Publications
- 20
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