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CHRISTINA GURNETT, MD
MD
Epilepsy Physician
NPI: 1255359998Individual
Specialties, Licenses & Credentials
Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology
Code: 2084N0402X
2003001991(MO)
Psychiatry & Neurology — Clinical Neurophysiology
Code: 2084N0600X
2003001991(MO)
Research & Publications (20)
Congenital myasthenic syndrome: presentation, electrodiagnosis, and muscle biopsy.
PMID 15119478·J Child Neurol·2004
5-case
Skeletal muscle contractile gene (TNNT3, MYH3, TPM2) mutations not found in vertical talus or clubfoot.
PMID 19142688·Clin Orthop Relat Res·2009
8-other
Genetic linkage localizes an adolescent idiopathic scoliosis and pectus excavatum gene to chromosome 18 q.
PMID 19139660·Spine (Phila Pa 1976)·2009
8-other
Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation.
PMID 18950742·Am J Hum Genet·2008
8-other
Impact of congenital talipes equinovarus etiology on treatment outcomes.
PMID 18611198·Dev Med Child Neurol·2008
3-trial
Absence of HOXD10 mutations in idiopathic clubfoot and sporadic vertical talus.
PMID 17417092·Clin Orthop Relat Res·2007
8-other
New ideas in epilepsy genetics: novel epilepsy genes, copy number alterations, and gene regulation.
PMID 17353374·Arch Neurol·2007
6-review
Early results of the Ponseti method for the treatment of clubfoot associated with myelomeningocele.
PMID 19487512·J Bone Joint Surg Am·2009
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
- 1 CHILDRENS PL, DIV NEUROLOGY PEDIATRICS
SAINT LOUIS, MO 63110 - Phone
- (314) 362-1408
Quick Facts
- NPI
- 1255359998
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
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