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ANDRIEL BRICE, PHD
PHD
Professional Counselor
NPI: 1598509945Individual
Specialties, Licenses & Credentials
Professional CounselorPrimary
Counselor — Professional
Code: 101YP2500X
94774(TX)
Research & Publications (20)
Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study.
PMID 19475631·Am J Med Genet B Neuropsychiatr Genet·2010
1-meta
CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
PMID 19439420·Brain·2009
4-observational
Infantile hypokinetic-hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene.
PMID 19224593·Mov Disord·2009
8-other
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration.
PMID 19350673·Ann Neurol·2009
8-other
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy.
PMID 19451530·Neurology·2009
8-other
Atlastin-1, the dynamin-like GTPase responsible for spastic paraplegia SPG3A, remodels lipid membranes and may form tubules and vesicles in the endoplasmic reticulum.
PMID 19573020·J Neurochem·2009
4-observational
Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity.
PMID 19438933·Clin Genet·2009
8-other
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
PMID 19433740·Neurology·2009
8-other
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease.
PMID 19357115·J Med Genet·2009
8-other
A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutations.
PMID 19617340·J Nucl Med·2009
8-other
Parkinson's disease: from monogenic forms to genetic susceptibility factors.
PMID 19297401·Hum Mol Genet·2009
6-review
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
PMID 19278672·Biol Psychiatry·2009
8-other
The p.Asp216His TOR1A allele effect is not found in the French population.
PMID 19260107·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
A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson's disease.
PMID 19214605·Neurogenetics·2009
8-other
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.
PMID 19214208·PLoS Genet·2009
8-other
Parkin deficiency delays motor decline and disease manifestation in a mouse model of synucleinopathy.
PMID 19680561·PLoS One·2009
7-preclinical
Parkin protects dopaminergic neurons from excessive Wnt/beta-catenin signaling.
PMID 19591802·Biochem Biophys Res Commun·2009
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 7322 Southwest Fwy
Houston, TX 77074 - Phone
- (346) 279-8175
Quick Facts
- NPI
- 1598509945
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 20
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