Back to Search
AMY HUEBNER, PHARMD
PHARMD
Pharmacist
NPI: 1356624365Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
14991-40(WI)
Research & Publications (20)
Autosomal dominant neurohypophyseal diabetes insipidus in two families. Molecular analysis of the vasopressin-neurophysin II gene and functional studies of three missense mutations.
PMID 19129716·Horm Res·2009
7-preclinical
Skin care in the NICU patient: effects of wipes versus cloth and water on stratum corneum integrity.
PMID 19407468·Neonatology·2009
2-rct
Intragenic deletion of TRIM32 in compound heterozygotes with sarcotubular myopathy/LGMD2H.
PMID 19492423·Hum Mutat·2009
8-other
Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome.
PMID 18551317·Eur J Pediatr·2009
5-case
Impaired gastric acidification negatively affects calcium homeostasis and bone mass.
PMID 19448635·Nat Med·2009
7-preclinical
CBP/p300-interacting transactivator, with Glu/Asp-rich C-terminal domain, 2, and pre-B-cell leukemia transcription factor 1 in human adrenal development and disease.
PMID 18984668·J Clin Endocrinol Metab·2009
8-other
Static microdroplet arrays: a microfluidic device for droplet trapping, incubation and release for enzymatic and cell-based assays.
PMID 19224019·Lab Chip·2009
8-other
An integrated cell culture lab on a chip: modular microdevices for cultivation of mammalian cells and delivery into microfluidic microdroplets.
PMID 19458865·Lab Chip·2009
7-preclinical
Familial glucocorticoid deficiency type 1 due to a novel compound heterozygous MC2R mutation.
PMID 18504396·Horm Res·2008
5-case
Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe.
PMID 18628786·Eur J Hum Genet·2008
5-case
Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and management.
PMID 18953174·Horm Res·2008
5-case
Development of quantitative cell-based enzyme assays in microdroplets.
PMID 18399662·Anal Chem·2008
8-other
The role of calcitonin and alpha-calcitonin gene-related peptide in bone formation.
PMID 18307972·Arch Biochem Biophys·2008
6-review
Three siblings with triple A syndrome with a novel frameshift mutation in the AAAS gene and a review of 17 independent patients with the frequent p.Ser263Pro mutation.
PMID 18172684·Eur J Pediatr·2008
5-case
Progressive muscle atrophy with hypokalemic periodic paralysis and calcium channel mutation.
PMID 17587224·Muscle Nerve·2008
5-case
Dysphagia due to triple A syndrome: successful treatment of achalasia by balloon dilatation.
PMID 17853339·Exp Clin Endocrinol Diabetes·2007
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2625 W NATIONAL AVE
MILWAUKEE, WI 53204 - Phone
- (414) 383-4021
Quick Facts
- NPI
- 1356624365
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile