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HAILEE DAHL, PHARMD
PHARMD
Pharmacist
NPI: 1952177925Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
17944(NE)
Research & Publications (20)
The contribution of GJB2 mutations to slight or mild hearing loss in Australian elementary school children.
PMID 16840571·J Med Genet·2006
8-other
Prevalence and nature of connexin 26 mutations in children with non-syndromic deafness.
PMID 11587277·Med J Aust·2001
8-other
Towards reliable prenatal diagnosis of mtDNA point mutations: studies of nt8993 mutations in oocytes, fetal tissues, children and adults.
PMID 11041530·Hum Reprod·2000
6-review
Drug treatment or alleviating the negative consequences of imprisonment? A critical view of prison-based drug treatment in Denmark.
PMID 19427186·Int J Drug Policy·2010
4-observational
Effect of training with different mechanical loadings on MyHC and GLUT4 changes.
PMID 19092697·Med Sci Sports Exerc·2009
8-other
Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease.
PMID 18940309·Am J Hum Genet·2008
5-case
An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss.
PMID 17918732·Hum Mutat·2008
7-preclinical
A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes.
PMID 18223651·Nat Genet·2008
7-preclinical
Effect of training with different intensities and volumes on muscle fibre enzyme activity and cross sectional area in the m. triceps brachii.
PMID 18351376·Eur J Appl Physiol·2008
8-other
Central nervous system signs in X-linked Charcot-Marie-Tooth disease after hyperventilation.
PMID 18358413·Pediatr Neurol·2008
5-case
Rehabilitative ultrasound imaging: understanding the technology and its applications.
PMID 17877280·J Orthop Sports Phys Ther·2007
8-other
Levodopa response in Parkinsonism with multiple mitochondrial DNA deletions.
PMID 17357142·Mov Disord·2007
5-case
A novel splice site mutation in EYA4 causes DFNA10 hearing loss.
PMID 17568404·Am J Med Genet A·2007
8-other
Postcollection synthesis of ethyl glucuronide by bacteria in urine may cause false identification of alcohol consumption.
PMID 17717128·Clin Chem·2007
8-other
Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28.
PMID 17726694·Am J Med Genet A·2007
8-other
Molecular characterization of a novel X-linked syndrome involving developmental delay and deafness.
PMID 17935254·Am J Med Genet A·2007
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
- 4101 WOOLWORTH AVE
OMAHA, NE 68105 - Phone
- (402) 366-9841
Quick Facts
- NPI
- 1952177925
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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