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HAROLD SLATER, PH.D.
PH.D.
Clinical Psychologist
NPI: 1376573758Individual
Specialties, Licenses & Credentials
Clinical PsychologistPrimary
Psychologist — Clinical
Code: 103TC0700X
PSY11033(CA)
Research & Publications (20)
A GntR family transcriptional regulator (PigT) controls gluconate-mediated repression and defines a new, independent pathway for regulation of the tripyrrole antibiotic, prodigiosin, in Serratia.
PMID 16339930·Microbiology (Reading)·2005
8-other
The Serratia gene cluster encoding biosynthesis of the red antibiotic, prodigiosin, shows species- and strain-dependent genome context variation.
PMID 15528645·Microbiology (Reading)·2004
8-other
Phosphate availability regulates biosynthesis of two antibiotics, prodigiosin and carbapenem, in Serratia via both quorum-sensing-dependent and -independent pathways.
PMID 12519208·Mol Microbiol·2003
8-other
Exercise-induced mechanical hypoalgesia in musculotendinous tissues of the lateral elbow.
PMID 19679505·Man Ther·2010
4-observational
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.
PMID 19015223·J Med Genet·2009
8-other
Newborn adiposity measured by plethysmography is not predicted by late gestation two-dimensional ultrasound measures of fetal growth.
PMID 19640967·J Nutr·2009
4-observational
Tibial geometry in individuals with neurofibromatosis type 1 without anterolateral bowing of the lower leg using peripheral quantitative computed tomography.
PMID 19118659·Bone·2009
8-other
Analysis of radiographic characteristics of anterolateral bowing of the leg before fracture in neurofibromatosis type 1.
PMID 19461382·J Pediatr Orthop·2009
5-case
Improved methodology for assessment of mRNA levels in blood of patients with FMR1 related disorders.
PMID 19505339·BMC Clin Pathol·2009
8-other
Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15.
PMID 19423733·Clin Chem·2009
8-other
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion.
PMID 19073947·Neurology·2009
5-case
A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study.
PMID 18580686·Genet Med·2008
8-other
Prenatal detection of deletion-duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversion.
PMID 18438967·Prenat Diagn·2008
5-case
IGF-1 and IGF-binding proteins and bone mass, geometry, and strength: relation to metabolic control in adolescent girls with type 1 diabetes.
PMID 18665784·J Bone Miner Res·2008
8-other
An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1).
PMID 18471319·Mol Cytogenet·2008
8-other
A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes.
PMID 18057083·J Med Genet·2008
5-case
Impact of practice size on delivery of diabetes care before and after the Quality and Outcomes Framework implementation.
PMID 18682020·Br J Gen Pract·2008
4-observational
A three-decade review of thermal injuries among the elderly at a regional burn centre.
PMID 17913372·Burns·2008
8-other
Effectiveness of ultrasound-guided corticosteroid injection in the treatment of Morton's neuroma.
PMID 18510900·Foot Ankle Int·2008
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2400 CHISLEHURST DR
LOS ANGELES, CA 90027 - Phone
- (323) 660-2829
Quick Facts
- NPI
- 1376573758
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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