Jessica Demarest Wharton, MD

Description

Keywords brain injury, headache, developmental delay, cerebellar ataxia, agenesis of brain, merosin deficient congenital muscular dystrophy, paramyotonia congenita, small fiber neuropathy, weakness, paroxysmal hemicrania, pediatric epilepsy, primary stabbing headache, primary thunderclap headache, primary exercise headache, aicardi syndrome, dup15q syndrome, developmental regression, benign paroxysmal torticollis of infancy, absence epilepsy, abnormal reflexes, abnormal eeg, cns vasculitis, peripheral nerve injury, schizencephaly, moebius syndrome, acute disseminated encephalomyelitis, botox for migraines, infantile spasms, volitional tremor, vertigo, ventriculomegaly, vasomotor symptoms, vascular malformations of the spine, vascular malformations of the brain, vagal nerve stimulator, trigeminal neuralgia, tremor, transient limb paralysis, tourette syndrome, torticollis, torsion dystonia, tic disorders, tibial neuropathy, tetraplegia, temporal lobe epilepsy, sturge weber syndrome, spinocerebellar diseases, spinocerebellar degeneration, spinal muscular atrophy, spina bifida, speech disorder, spastic infantile paralysis, spasmus nutans, sensory impairment, schwannomatosis, rett syndrome, rasmussen syndrome, radiculopathy, quadriplegia, pseudotumor cerebri, progressive muscular atrophy, primary progressive aphasia, polymicrogyria, petit mal seizure, periventricular leukomalacia, peripheral neuropathy, paresthesia, paraplegia, papilledema, pachygyria, optic neuritis, oculopharyngeal muscular dystrophy, numbness, neuropathy, neuromuscular diseases, neurometabolic disorder, neurologic complications of meningitis, neurofibromatosis, neurocutaneous syndromes, neuralgic amyotrophy, neuralgia, nervous system disorders, myotonic dystrophy, myotonia congenita, myotonia, myositis, myoclonus, tonic clonic seizure, myelitis, myasthenia gravis, muscular dystrophy, muscular disorder, muscle eye brain disease, muscle weakness, multiple sclerosis, moyamoya, movement diseases and disorders, mitochondrial disorders, microcephaly, metabolic myopathy.