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KIMBERLY HEDRICH, PHARM.D.
PHARM.D.
Psychiatric Pharmacist
NPI: 1669695987Individual
Specialties, Licenses & Credentials
Psychiatric PharmacistPrimary
Pharmacist — Psychiatric
Code: 1835P1300X
5302029610(MI)
Research & Publications (20)
Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles.
PMID 17934880·J Neurol·2007
8-other
Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia.
PMID 17724286·Neurology·2007
8-other
Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family.
PMID 17013904·Mov Disord·2007
8-other
Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification.
PMID 17674414·Mov Disord·2007
8-other
Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations.
PMID 17202228·J Neurol Neurosurg Psychiatry·2007
8-other
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene.
PMID 17415800·Mov Disord·2007
8-other
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.
PMID 16606941·Neurology·2006
8-other
Heterozygous PINK1 mutations: a susceptibility factor for Parkinson disease?
PMID 16755580·Mov Disord·2006
8-other
Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease.
PMID 16758483·Mov Disord·2006
8-other
Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?
PMID 16769864·Arch Neurol·2006
4-observational
Blink amplitude but not saccadic hypometria indicates carriers of Parkin mutations.
PMID 16786217·J Neurol·2006
8-other
Dominantly transmitted focal dystonia in families of patients with musician's cramp.
PMID 16924027·Neurology·2006
8-other
Co-occurrence of restless legs syndrome and Parkin mutations in two families.
PMID 16161156·Mov Disord·2006
8-other
Phenotype-genotype correlation in Dutch patients with myoclonus-dystonia.
PMID 16534121·Neurology·2006
8-other
Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency.
PMID 16361586·J Neurol Neurosurg Psychiatry·2006
8-other
Distal myoclonus and late onset in a large Dutch family with myoclonus-dystonia.
PMID 17101905·Neurology·2006
8-other
Distinguishing early-onset PD from dopa-responsive dystonia with transcranial sonography.
PMID 16801671·Neurology·2006
4-observational
PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism.
PMID 15970950·Eur J Hum Genet·2005
8-other
Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers.
PMID 16130111·Ann Neurol·2005
4-observational
Oculogyric dystonic states in early-onset parkinsonism with basal ganglia calcifications.
PMID 16157916·Neurology·2005
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
- 1200 N WEST AVE, SUITE 500
JACKSON, MI 49202 - Phone
- (517) 789-8579
Quick Facts
- NPI
- 1669695987
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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