Jan Wollack , MD, PhD

MultiPlan

Oxford Health Plans

QualCare

Tricare

United Healthcare (UHC)

UnitedHealthcare (UHC) Community Plan

US Family Health Plan

WellPoint

anencephaly

arnold chiari malformation type 1

arnold chiari malformation type 2

arnold chiari malformation type 3

arnold chiari malformation type 4

arterial dissection

asperger syndrome

asymmetrical crying facies

auditory processing disorder (apd)

autism

autonomic nervous system disorders

becker muscular dystrophy

behcet syndrome

benign focal amyotrophy

benign paroxysmal torticollis of infancy

bethlem myopathy

brachycephaly

carotid stenosis

central core disease

cephalocele

cerebellar disease

cerebral aneurysm

cerebral anomalies

cerebral degeneration in childhood

cerebral dysgenesis

cerebral heterotopia

cerebrovascular accident (cva)

cervical dystonia

charcot marie tooth disease

childhood epilepsy

chronic infantile neurologic cutaneous and articular syndrome

cloves syndrome

cns vasculitis

concussive seizure

congenital anomalies of the central nervous system

congenital ataxia

congenital brain malformations

congenital cerebral hemiatrophy

congenital cerebral hemorrhage

congenital cerebral hypoplasia

congenital deformity of nervous system

congenital hydrocephalus

congenital lesions of the nervous system

congenital macrocephaly

congenital muscular dystrophy

congenital myasthenic syndromes

congenital myopathies

congenital paralysis

cornelia de lange syndrome

costello syndrome

cranial nerve injury

dejerine sottas disease

demyelinating disease

development coordination disorder

developmental disabilities

diabetic neuropathy

diffuse cerebral sclerosis

distal motor neuropathy

distal muscular dystrophy

distal myopathy

dopamine responsive dystonia

down syndrome

duchenne muscular dystrophy

dup15q syndrome

dysarthria

dysautonomia

dysembryoplastic neuroepithelial tumor

dyslexia

dystonia

emery dreifuss muscular dystrophy

encephalopathies

epilepsy

erb palsy

fabry disease

facial nerve paralysis

facial paresis

facioscapulohumeral muscular dystrophy

familial ataxia

familial spinal muscle atrophy

femoral neuropathy

flaccid hemiplegia

focal dystonia

focal seizures

friedreich ataxia

fukuyama congenital muscular dystrophy

generalized seizures

genetic dystonia

glycogen storage disease

guillain barre syndrome (gbs)

head trauma

hemicrania continua

hemidystonia

hemifacial microsomia

hemineglect

hemiparesis

hemiplegia

hemorrhagic stroke

hereditary sensory and autonomic neuropathy

hereditary spastic paraplegia

hydrocephalus

hydromyelia

hypertonia

hypoglossal nerve disease

hypoglossal nerve injury

hypotonia

inclusion body myopathy

increased intracranial pressure

infantile hemiplegia

infantile spasms

intracranial hypertension

juvenile myoclonic epilepsy

juvenile spinal muscular atrophy

kinetic tremor

landau kleffner syndrome

leigh's disease

lennox gastaut syndrome

leukodystrophy

limb girdle muscular dystrophy

lissencephaly

lobar atrophy of brain

macrocephaly

marcus gunn phenomenon

meningocele

merosin deficient congenital muscular dystrophy

metabolic brain disorders

metabolic myopathy

microcephaly

mitochondrial disorders

moebius syndrome

movement diseases and disorders

moyamoya

multifocal motor neuropathy

multiple sclerosis

muscle atrophy

muscle eye brain disease

muscular disorder

muscular dystrophy

myasthenia gravis

myelitis

myoclonus

myositis

myotonia

myotonia congenita

myotonic dystrophy

nerve root disorder

nervous system disorders

neural tube defects

neuralgia

neuralgic amyotrophy

neuro complications of pellagra

neurocutaneous syndromes

neurofibromatosis

neuroinflammatory disorders

neurologic complications of meningitis

neurometabolic disorder

neuromuscular diseases

neurovascular disease

niemann pick disease

non ruptured cerebral aneurysm

oculopharyngeal muscular dystrophy

pachygyria

paramyotonia congenita

paraplegia

parkinson's disease (pd)

paroxysmal hemicrania

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections

pediatric epilepsy

peripheral nerve disease

peripheral neuropathy

periventricular leukomalacia

petit mal seizure

pierre robin sequence

plagiocephaly

plantar nerve lesions

poliodystrophia cerebri

polymicrogyria

post concussion syndrome

post traumatic amnesia

primary cerebellar degeneration

primary exercise headache

primary progressive aphasia

primary stabbing headache

primary thunderclap headache

progressive muscular atrophy

progressive supranuclear palsy

quadriplegia

rasmussen syndrome

rett syndrome

reye syndrome

schizencephaly

schwannomatosis

sensory impairment

sensory neuronopathy

small fiber neuropathy

spasmus nutans

spastic infantile paralysis

speech disorder

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar degeneration

spinocerebellar diseases

sturge weber syndrome

subarachnoid hemorrhage

tay sachs disease

temporal lobe epilepsy

tetraplegia

tibial neuropathy

tonic clonic seizure

torsion dystonia

tourette syndrome

transient limb paralysis

traumatic brain injury

vagal nerve disorders

vagus nerve disease

vascular malformations of the brain

vascular malformations of the spine

vasomotor symptoms

vein of galen malformation

ventriculomegaly

volitional tremor

von hippel lindau disease

williams syndrome

abdominal migraine

arm weakness

arteriovenous malformation (avm)

Ataxia

attention deficit hyperactivity disorder

Autonomic Dysreflexia

Brain Injury

Cerebral Palsy

cognitive impairment

concussion

Dementia

encephalitis

facial nerve palsy

facial nerve palsy and paresis

facial pain

fasciculations

febrile convulsions

learning disorders

Muscle Weakness

numbness

optic neuritis

paresthesia

Peripheral Autonomic Neuropathy

peripheral nerve injury

problems with smell and taste

pseudotumor cerebri

Radiculopathy

Spina Bifida

Syncope

tic disorders

Tinnitus

Torticollis

Tremor

Trigeminal Neuralgia

Vertigo