Courtney Elizabeth Briamonte, APN

vein of galen malformation

reye syndrome

moebius syndrome

dysembryoplastic neuroepithelial tumor

cloves syndrome

arterial dissection

acute disseminated encephalomyelitis

infantile spasms

volitional tremor

vertigo

ventriculomegaly

vasomotor symptoms

vascular malformations of the spine

vascular malformations of the brain

vagus nerve disease

vagal nerve disorders

trigeminal neuralgia

tremor

traumatic brain injury

transient limb paralysis

tourette syndrome

torticollis

torsion dystonia

tibial neuropathy

tetraplegia

temporal lobe epilepsy

tay sachs disease

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 supranuclear palsy

progressive muscular atrophy

problems with smell and taste

primary progressive aphasia

post traumatic amnesia

post concussion syndrome

polymicrogyria

poliodystrophia cerebri

plantar nerve lesions

plagiocephaly

petit mal seizure

periventricular leukomalacia

peripheral neuropathy

peripheral autonomic neuropathy

paresthesia

paraplegia

pachygyria

optic neuritis

oculopharyngeal muscular dystrophy

numbness

niemann pick disease

neuromuscular diseases

neurometabolic disorder

neurologic complications of meningitis

neurofibromatosis

neurocutaneous syndromes

neuro complications of pellagra

neuralgic amyotrophy

neuralgia

neural tube defects

nervous system disorders

nerve root disorder

nerve conduction studies

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

movement diseases and disorders

mitochondrial disorders

microcephaly

metabolic myopathy

metabolic brain disorders

meningocele

marcus gunn phenomenon

macrocephaly

lobar atrophy of brain

lissencephaly

limb girdle muscular dystrophy

leukodystrophy

lennox gastaut syndrome

leigh's disease

learning disorders

landau kleffner syndrome

kinetic tremor

juvenile spinal muscular atrophy

juvenile myoclonic epilepsy

intracranial hypertension

brain injury

hypotonia

hypoglossal nerve injury

hypoglossal nerve disease

hypertonia

hydromyelia

hydrocephalus

hereditary spastic paraplegia

hereditary sensory and autonomic neuropathy

infantile hemiplegia

hemiplegia

hemiparesis

hemineglect

hemifacial microsomia

hemidystonia

hemicrania continua

head trauma

guillain barre syndrome (gbs)

glycogen storage disease

genetic dystonia

generalized seizures

friedreich ataxia

focal seizures

focal dystonia

flaccid hemiplegia

febrile convulsions

fasciculations

familial spinal muscle atrophy

familial ataxia

facioscapulohumeral muscular dystrophy

facial paresis

facial pain

facial nerve palsy

fabry disease

erb palsy

epilepsy

encephalopathies

encephalitis

emery dreifuss muscular dystrophy

dystonia

dyslexia

dysautonomia

dysarthria

duchenne muscular dystrophy

down syndrome

dopamine responsive dystonia

diffuse cerebral sclerosis

developmental disabilities

demyelinating disease

cranial nerve injury

cornelia de lange syndrome

congenital paralysis

congenital myopathies

congenital myasthenic syndromes

congenital muscular dystrophy

congenital macrocephaly

congenital lesions of the nervous system

congenital hydrocephalus

congenital deformity of nervous system

congenital cerebral hypoplasia

congenital cerebral hemorrhage

congenital cerebral hemiatrophy

congenital brain malformations

congenital ataxia

congenital anomalies of the central nervous system

concussive seizure

chronic infantile neurologic cutaneous and articular syndrome

childhood epilepsy

charcot marie tooth disease

cerebrovascular accident (cva)

cerebral palsy

cerebral heterotopia

cerebral dysgenesis

cerebral degeneration in childhood

cerebral anomalies

primary cerebellar degeneration

cerebellar disease

spinocerebellar ataxia

cephalocele

concussion

brachycephaly

behcet syndrome

becker muscular dystrophy

autonomic nervous system disorders

autonomic dysreflexia

autism

auditory processing disorder (apd)

attention deficit hyperactivity disorder

ataxia

asymmetrical crying facies

asperger syndrome

arnold chiari malformation type 4

arnold chiari malformation type 3

arnold chiari malformation type 2

arnold chiari malformation type 1

anencephaly

agenesis of brain

agenesis of the corpus callosum

brain injury rehabilitation

increased intracranial pressure

merosin deficient congenital muscular dystrophy

fukuyama congenital muscular dystrophy

benign focal amyotrophy

distal myopathy

paramyotonia congenita

distal muscular dystrophy

dejerine sottas disease

central core disease

bethlem myopathy

agnosia

small fiber neuropathy

acoustic neurofibromatosis

acute flaccid myelitis

pierre robin sequence

facial nerve paralysis

22q deletion

paroxysmal hemicrania

pediatric epilepsy

primary stabbing headache

primary thunderclap headache

primary exercise headache

aicardi syndrome

dup15q syndrome

williams syndrome

benign paroxysmal torticollis of infancy

abdominal migraine

absence epilepsy

abnormal eeg

development coordination disorder

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections

cns vasculitis

peripheral nerve injury

von hippel lindau disease

schizencephaly

costello syndrome