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ALEXANDRA DURR, PHARMD
PHARMD
Pharmacist
NPI: 1528356011Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
MN123175(MN)
Research & Publications (20)
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.
PMID 19105190·Hum Mutat·2009
8-other
Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.
PMID 18853458·Hum Mutat·2009
8-other
Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA).
PMID 19153153·Brain·2009
4-observational
CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
PMID 19439420·Brain·2009
4-observational
Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data.
PMID 19646924·Lancet Neurol·2009
3-trial
Infantile hypokinetic-hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene.
PMID 19224593·Mov Disord·2009
8-other
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.
PMID 19491146·Brain·2009
8-other
Long-term outcome of presymptomatic testing in Huntington disease.
PMID 18716614·Eur J Hum Genet·2009
8-other
[Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature].
PMID 18439928·Rev Neurol (Paris)·2008
5-case
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.
PMID 18539534·Lancet Neurol·2008
4-observational
Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome.
PMID 18394578·Am J Hum Genet·2008
7-preclinical
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
PMID 18079167·Brain·2008
4-observational
Are parkin patients particularly suited for deep-brain stimulation?
PMID 18228569·Mov Disord·2008
8-other
Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment.
PMID 18378516·Brain·2008
4-observational
Mental deficiency in three families with SPG4 spastic paraplegia.
PMID 17957230·Eur J Hum Genet·2008
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
- 2900 AMES CROSSING RD
EAGAN, MN 55121 - Phone
- (000) 000-0000
Quick Facts
- NPI
- 1528356011
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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