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CHRISTINA GURNETT, MD

MD

Epilepsy Physician

NPI: 1255359998Individual

Specialties, Licenses & Credentials

Neurology with Special Qualifications in Child Neurology Physician

Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology

Code: 2084N0402X

2003001991(MO)
Clinical Neurophysiology Physician

Psychiatry & Neurology — Clinical Neurophysiology

Code: 2084N0600X

2003001991(MO)
Epilepsy PhysicianPrimary

Psychiatry & Neurology — Epilepsy

Code: 2084E0001X

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
Pilocytic astrocytoma in a child with Noonan syndrome.
PMID 19621452·Pediatr Blood Cancer·2009
5-case
DICER1 mutations in familial pleuropulmonary blastoma.
PMID 19556464·Science·2009
8-other
Early results of the Ponseti method for the treatment of clubfoot associated with myelomeningocele.
PMID 19487512·J Bone Joint Surg Am·2009
4-observational
Update on clubfoot: etiology and treatment.
PMID 19224303·Clin Orthop Relat Res·2009
6-review
Magnetic resonance angiography in clubfoot and vertical talus: a feasibility study.
PMID 19127394·Clin Orthop Relat Res·2009
5-case
Polygenic threshold model with sex dimorphism in clubfoot inheritance: the Carter effect.
PMID 19047715·J Bone Joint Surg Am·2008
8-other
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.
PMID 18976727·Am J Hum Genet·2008
8-other
Disruption of sodium bicarbonate transporter SLC4A10 in a patient with complex partial epilepsy and mental retardation.
PMID 18413482·Arch Neurol·2008
5-case
Case report: Congenital knee dislocation in a patient with larsen syndrome and a novel filamin B mutation.
PMID 18322662·Clin Orthop Relat Res·2008
5-case
Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly.
PMID 17152067·Am J Med Genet A·2007
8-other
Additional evidence of a locus for complex febrile and afebrile seizures on chromosome 12q22-23.3.
PMID 16972079·Neurogenetics·2007
5-case
Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy.
PMID 16839746·Epilepsy Res·2006
8-other
Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11-q22.3.
PMID 16838310·Am J Med Genet A·2006
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
1 CHILDRENS PL, DIV NEUROLOGY PEDIATRICS
SAINT LOUIS, MO 63110

Location

Practice Location

1 CHILDRENS PL, SAINT LOUIS, MO
(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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