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ELIZABETH BERRY-KRAVIS M.D.
M.D.
Neurology with Special Qualifications in Child Neurology Physician
NPI: 1932130325IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
036-075082(IL)
Neurology with Special Qualifications in Child Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology
Code: 2084N0402X
036-075082(IL)
Education
OTHER
Class of 1985
Research & Publications (20)
A pilot open label, single dose trial of fenobam in adults with fragile X syndrome.
PMID 19126569·J Med Genet·2009
3-trial
Characterization of potential outcome measures for future clinical trials in fragile X syndrome.
PMID 18369716·J Autism Dev Disord·2008
8-other
Open-label treatment trial of lithium to target the underlying defect in fragile X syndrome.
PMID 18698192·J Dev Behav Pediatr·2008
3-trial
Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelines.
PMID 17618523·Mov Disord·2007
6-review
Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype.
PMID 16888290·Am J Respir Crit Care Med·2006
8-other
Effect of CX516, an AMPA-modulating compound, on cognition and behavior in fragile X syndrome: a controlled trial.
PMID 17069542·J Child Adolesc Psychopharmacol·2006
3-trial
Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation.
PMID 15622531·Ann Neurol·2005
5-case
Psychopharmacology in fragile X syndrome--present and future.
PMID 14994287·Ment Retard Dev Disabil Res Rev·2004
6-review
Tremor and ataxia in fragile X premutation carriers: blinded videotape study.
PMID 12730995·Ann Neurol·2003
8-other
Bruising and the ketogenic diet: evidence for diet-induced changes in platelet function.
PMID 11198302·Ann Neurol·2001
8-other
Prenatal testing for late infantile neuronal ceroid lipofuscinosis.
PMID 10665500·Ann Neurol·2000
5-case
A comparative neuropsychological test battery differentiates cognitive signatures of Fragile X and Down syndrome.
PMID 19054268·J Intellect Disabil Res·2009
8-other
HTR2A variation and sudden infant death syndrome: a case-control analysis.
PMID 18771483·Acta Paediatr·2009
8-other
Prepulse inhibition in fragile X syndrome: feasibility, reliability, and implications for treatment.
PMID 18785205·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B gene.
PMID 18798833·Acta Paediatr·2009
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
- 1725 W HARRISON ST, SUITE 710
CHICAGO, IL 60612 - Phone
- (312) 942-3034
Quick Facts
- NPI
- 1932130325
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 41
- Publications
- 20
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