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MEGAN ADAMOWICZ, PHARMD
PHARMD
Pharmacist
NPI: 1366106155Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
S025533(AZ)
Research & Publications (20)
Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival.
PMID 19321599·Hum Mol Genet·2009
8-other
CDG type Ia and congenital cytomegalovirus infection: two coexisting conditions.
PMID 19168813·J Child Neurol·2009
5-case
Ophthalmological abnormalities in children with congenital disorders of glycosylation type I.
PMID 19019927·Br J Ophthalmol·2009
8-other
Multiplexed glycoproteomic analysis of glycosylation disorders by sequential yolk immunoglobulins immunoseparation and MALDI-TOF MS.
PMID 18712764·Proteomics·2008
8-other
Pericardial and abdominal fluid accumulation in congenital disorder of glycosylation type Ia.
PMID 18571450·Mol Genet Metab·2008
5-case
Congenital disorder of glycosylation type Ix: review of clinical spectrum and diagnostic steps.
PMID 18500572·J Inherit Metab Dis·2008
8-other
Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
PMID 17971833·Eur J Hum Genet·2008
5-case
Elevated carbohydrate-deficient transferrin (CDT) and its normalization on dietary treatment as a useful biochemical test for hereditary fructose intolerance and galactosemia.
PMID 17515832·Pediatr Res·2007
8-other
Transferrin hypoglycosylation in hereditary fructose intolerance: using the clues and avoiding the pitfalls.
PMID 17457694·J Inherit Metab Dis·2007
8-other
Characterization of two unusual truncating PMM2 mutations in two CDG-Ia patients.
PMID 17307006·Mol Genet Metab·2007
8-other
Graduated Embryo Score and soluble human leukocyte antigen-G expression improve assisted reproductive technology outcomes and suggest a basis for elective single-embryo transfer.
PMID 17224145·Fertil Steril·2007
8-other
Frequent amplifications and abundant expression of TRIO, NKD2, and IRX2 in soft tissue sarcomas.
PMID 16752383·Genes Chromosomes Cancer·2006
8-other
Validation of male-specific, 12-locus fluorescent short tandem repeat (STR) multiplex.
PMID 16156007·Forensic Sci Int·2005
4-observational
Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups.
PMID 16037491·Glycobiology·2005
8-other
Twelve short tandem repeat loci Y chromosome haplotypes: genetic analysis on populations residing in North America.
PMID 15837004·Forensic Sci Int·2005
8-other
Validation of a male-specific, 12-locus fluorescent short tandem repeat (STR) multiplex.
PMID 15607584·Forensic Sci Int·2005
4-observational
The graduated embryo score predicts the outcome of assisted reproductive technologies better than a single day 3 evaluation and achieves results associated with blastocyst transfer from day 3 embryo transfer.
PMID 14667868·Fertil Steril·2003
4-observational
Clinical heterogeneity and molecular findings in five Polish patients with glycerol kinase deficiency: investigation of two splice site mutations with computerized splice junction analysis and Xp21 gene-specific mRNA analysis.
PMID 12855219·Mol Genet Metab·2003
8-other
Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2.
PMID 12478664·Int J Cancer·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
- 14696 N FRANK LLOYD WRIGHT BLVD
SCOTTSDALE, AZ 85260 - Phone
- (480) 391-1186
Quick Facts
- NPI
- 1366106155
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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