Back to Search
HOA TRANG, PHARMD
PHARMD
Pharmacist
NPI: 1427451640Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
PH60224721(WA)
Research & Publications (20)
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
[Ondine syndrome or central congenital hypoventilation syndrome].
PMID 16584036·Rev Prat·2006
6-review
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
The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype.
PMID 15653965·Chest·2005
8-other
Relevance of a portable spirometer for detection of small airways obstruction.
PMID 15573392·Pediatr Pulmonol·2005
3-trial
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
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
Long-term noninvasive mechanical ventilation for children at home: a national survey.
PMID 12526073·Pediatr Pulmonol·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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1965 S UNION AVE
TACOMA, WA 98405 - Phone
- (253) 414-9533
Quick Facts
- NPI
- 1427451640
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile