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JOSEPH GLEESON, M.D.
M.D.
Neurology with Special Qualifications in Child Neurology Physician
NPI: 1689745440Individual
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
G85292(CA)
Neurology with Special Qualifications in Child Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology
Code: 2084N0402X
G85292(CA)
Research & Publications (20)
Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes.
PMID 14981712·Am J Med Genet A·2004
5-case
Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes.
PMID 10915612·Am J Hum Genet·2000
8-other
Neuronal migration disorders: from genetic diseases to developmental mechanisms.
PMID 10906798·Trends Neurosci·2000
6-review
Classical lissencephaly and double cortex (subcortical band heterotopia): LIS1 and doublecortin.
PMID 10987567·Curr Opin Neurol·2000
6-review
Genetic and neuroradiological heterogeneity of double cortex syndrome.
PMID 10665503·Ann Neurol·2000
8-other
Differential predictors of critical comments and emotional over-involvement in first-episode psychosis.
PMID 19079825·Psychol Med·2010
4-observational
The primary cilium as a cellular signaling center: lessons from disease.
PMID 19477114·Curr Opin Genet Dev·2009
6-review
Mice lacking doublecortin and doublecortin-like kinase 2 display altered hippocampal neuronal maturation and spontaneous seizures.
PMID 19342486·Proc Natl Acad Sci U S A·2009
7-preclinical
A randomized controlled trial of relapse prevention therapy for first-episode psychosis patients.
PMID 19323964·J Clin Psychiatry·2009
2-rct
Development of a biomimetic collagen-hydroxyapatite scaffold for bone tissue engineering using a SBF immersion technique.
PMID 19180526·J Biomed Mater Res B Appl Biomater·2009
7-preclinical
The reliability and validity of the Alcohol, Smoking and Substance Involvement Screening Test (ASSIST) in first-episode psychosis.
PMID 19324499·Addict Behav·2009
8-other
Familial congenital unilateral cerebral ventriculomegaly: Delineation of a distinct genetic disorder.
PMID 19610102·Am J Med Genet A·2009
5-case
Diagnosis of spatiotemporal chaos in wave envelopes of a nematic electroconvection pattern.
PMID 19518320·Phys Rev E Stat Nonlin Soft Matter Phys·2009
8-other
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies.
PMID 19668216·Nat Genet·2009
7-preclinical
MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement.
PMID 19058225·Hum Mutat·2009
8-other
Accuracy of whole-body low-dose multidetector CT (WBLDCT) versus skeletal survey in the detection of myelomatous lesions, and correlation of disease distribution with whole-body MRI (WBMRI).
PMID 19009290·Skeletal Radiol·2009
4-observational
Magnetic-field induced isotropic to nematic liquid crystal phase transition.
PMID 19113668·Phys Rev Lett·2008
8-other
Enhancing treatment fidelity in psychotherapy research: novel approach to measure the components of cognitive behavioural therapy for relapse prevention in first-episode psychosis.
PMID 19016089·Aust N Z J Psychiatry·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
- 8010 FROST ST, SUITE 510
SAN DIEGO, CA 92123 - Phone
- (858) 966-5819
Quick Facts
- NPI
- 1689745440
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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