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HOANG TRANG, DO
DO
Diagnostic Radiology Physician
NPI: 1376735902IndividualAccepts Medicare
Specialties, Licenses & Credentials
Diagnostic Radiology PhysicianPrimary
Radiology — Diagnostic Radiology
Code: 2085R0202X
OS014385(PA)
CMS Specialties
PrimaryDIAGNOSTIC RADIOLOGY
Education
LAKE ERIE COL OF OSTEO MED AT SETON HILL UNIV
Class of 2004
Research & Publications (20)
[Ondine syndrome or central congenital hypoventilation syndrome].
PMID 16584036·Rev Prat·2006
6-review
The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype.
PMID 15653965·Chest·2005
8-other
Short-term blood pressure and heart rate variability in congenital central hypoventilation syndrome (Ondine's curse).
PMID 15544572·Clin Sci (Lond)·2005
8-other
PHOX2B gene mutation in a patient with late-onset central hypoventilation.
PMID 15334515·Pediatr Pulmonol·2004
5-case
24-hour BP in children with congenital central hypoventilation syndrome.
PMID 14555571·Chest·2003
8-other
Use of nasal cannula for detecting sleep apneas and hypopneas in infants and children.
PMID 12186821·Am J Respir Crit Care Med·2002
4-observational
Chiari type I malformation causing central apnoeas in a 4-month-old boy.
PMID 18783970·Eur J Paediatr Neurol·2009
5-case
Second trimester abortion in Viet Nam: changing to recommended methods and improving service delivery.
PMID 18772095·Reprod Health Matters·2008
8-other
Delineation of late onset hypoventilation associated with hypothalamic dysfunction syndrome.
PMID 18670370·Pediatr Res·2008
7-preclinical
PHOX2B germline and somatic mutations in late-onset central hypoventilation syndrome.
PMID 18079495·Am J Respir Crit Care Med·2008
8-other
Pediatric disorders with autonomic dysfunction: what role for PHOX2B?
PMID 15901893·Pediatr Res·2005
6-review
PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome.
PMID 15657873·Am J Hum Genet·2005
7-preclinical
Relevance of a portable spirometer for detection of small airways obstruction.
PMID 15573392·Pediatr Pulmonol·2005
3-trial
Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse).
PMID 14532329·Hum Mol Genet·2003
7-preclinical
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.
PMID 12640453·Nat Genet·2003
8-other
Exclusion of RNX as a major gene in congenital central hypoventilation syndrome (CCHS, Ondine's curse).
PMID 12548735·Am J Med Genet A·2003
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
- 1400 LOCUST ST
PITTSBURGH, PA 15219 - Phone
- (412) 232-7910
Quick Facts
- NPI
- 1376735902
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 22
- Publications
- 20
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