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ROBERT CROOK, D.O.
D.O.
Physical Medicine & Rehabilitation Physician
NPI: 1275660060Individual
Specialties, Licenses & Credentials
Physical Medicine & Rehabilitation PhysicianPrimary
Physical Medicine & Rehabilitation
Code: 208100000X
DO814(TN)
Research & Publications (20)
Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP.
PMID 18667258·Neurobiol Aging·2010
8-other
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members.
PMID 19158106·Brain·2009
8-other
A biphasic memory curve in the chambered nautilus, Nautilus pompilius L. (Cephalopoda: Nautiloidea).
PMID 18515730·J Exp Biol·2008
4-observational
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.
PMID 18802454·PLoS Genet·2008
8-other
Cardiopulmonary bypass for surgical correction of congenital heart disease in children with sickle cell disease: a case series.
PMID 18312603·Anaesthesia·2008
5-case
Practical solvent system selection for counter-current separation of pharmaceutical compounds.
PMID 18801491·J Chromatogr A·2008
8-other
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia.
PMID 18723524·Hum Mol Genet·2008
8-other
A presenilin 1 mutation (L420R) in a family with early onset Alzheimer disease, seizures and cotton wool plaques, but not spastic paraparesis.
PMID 17645236·Neuropathology·2007
5-case
Whole-genome analysis of sporadic amyotrophic lateral sclerosis.
PMID 17671248·N Engl J Med·2007
8-other
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
PMID 17357082·Am J Hum Genet·2007
8-other
Conductance quantization at a half-integer plateau in a symmetric GaAs quantum wire.
PMID 16741116·Science·2006
8-other
Organic solvent nanofiltration in asymmetric hydrogenation: enhancement of enantioselectivity and catalyst stability by ionic liquids.
PMID 16767276·Chem Commun (Camb)·2006
8-other
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
PMID 16862116·Nature·2006
8-other
Use of an abbreviated form of the Edmonton staging system in a hospice setting.
PMID 16563310·J Pain Symptom Manage·2006
8-other
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
PMID 16950801·Hum Mol Genet·2006
8-other
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
PMID 16195395·Hum Mol Genet·2005
4-observational
Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease.
PMID 15729734·Am J Med Genet B Neuropsychiatr Genet·2005
8-other
Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic stroke.
PMID 16130105·Ann Neurol·2005
4-observational
Clinical, genetic, and neuropathologic characteristics of posterior cortical atrophy.
PMID 15477533·Neurology·2004
8-other
Genome-wide analysis of the parkinsonism-dementia complex of Guam.
PMID 15596609·Arch Neurol·2004
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2339 MCCALLIE AVE, PLAZA II, SUITE 407
CHATTANOOGA, TN 37404 - Phone
- (423) 698-8701
Quick Facts
- NPI
- 1275660060
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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