clinic

St. Louis Neurosurgery

0 Stars (0 Review)

St. Louis Neurosurgery is a clinic that specializes in Concierge Neurology. The clinic is located in St. Louis, Missouri. St. Louis Neurosurgery is known for housing expert physicians. St. Louis Neurosurgery offers all the services, treatments and procedures pertinent to the specialties mentioned above.

1 Doctor | Website
Overview
Providers
Reviews
Services
Location
About St. Louis Neurosurgery
Address

13621 Big Bend Rd St. Louis,
MO 63122

Modes of Payment

Card | Cash

Providers
Armond Levy - 13621 Big Bend Rd, St. Louis, MO 63122, USA, St. Louis, Missouri, 63122
Armond Levy, MD
St. Louis Neurosurgery
Concierge Neurology
(0)
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
13621 Big Bend Rd, St. Louis, MO 63122
Message
Call
Website
Reviews

No reviews found.

Conditions Treated
  • Trigeminal neuralgia
  • Angelman syndrome
  • Torticollis
  • Amyotrophic lateral sclerosis
  • Scoliosis
  • Tension headache
  • Hiv
  • Sleep paralysis
  • Lewy body dementia
  • Encephalitis
  • Paraplegia
  • Addiction (alcohol)
  • Huntington's disease
  • Meningitis
  • Hydrocephalus
  • Tardive dyskinesia
  • Cluster headache
  • Alzheimer's disease
  • Peripheral neuropathy
  • Sleep apnea
  • Carpal tunnel syndrome
  • Brain aneurysm
  • Insomnia
  • Whiplash
  • Ptosis
  • Atrial fibrillation
  • Headache
  • Heart attack
  • Multiple sclerosis
  • Myasthenia gravis
  • Spinal stenosis
  • Radiculopathy
  • Glioblastoma
  • Narcolepsy
  • Neck pain
  • Neuropathy
  • Tinnitus
  • Epilepsy
  • Restless legs syndrome
  • Migraine
  • Seizures
  • Dementia
  • Parkinson's disease
  • Concussion
  • Cerebral palsy
  • Stroke
  • Guillain-barre syndrome
  • Vertigo
  • Absence seizure
  • Acoustic neuroma
  • Agnosia
  • Alcoholic neuropathy
  • Amaurosis fugax
  • Anosmia
  • Aphantasia
  • Apraxia
  • Arachnoid cysts
  • Arachnoiditis
  • Arteriovenous malformation
  • Autonomic dysreflexia
  • Autonomic neuropathy
  • Bacterial meningitis
  • Blurry vision
  • Brown sequard syndrome
  • Cerebellar hypoplasia
  • Cerebrospinal fluid leak
  • Cerebrovascular disease
  • Cervical dysplasia
  • Cervical myelopathy
  • Cervical radiculopathy
  • Cervical spondylosis
  • Charcot marie tooth disease
  • Chiari malformation type 1
  • Chorea
  • Chronic headache
  • Complex regional pain syndrome
  • Creutzfeldt jakob disease
  • Crps
  • Cubital tunnel syndrome
  • Dandy walker syndrome
  • Decerebrate posture
  • Decorticate posture
  • Deep brain stimulation
  • Delirium
  • Delirium tremens
  • Diabetic neuropathy
  • Diplopia
  • Dravet syndrome
  • Drowsiness
  • Duchenne muscular dystrophy
  • Dysarthria
  • Dysgraphia
  • Epidural hematoma
  • Erb's palsy
  • Erythromelalgia
  • Essential tremor
  • Eyestrain
  • Fainting
  • Fatal familial insomnia
  • Foot drop
  • Fragile x syndrome
  • Friedreich ataxia
  • Frontotemporal dementia
  • Glioma
  • Hemiplegia
  • Hemorrhagic stroke
  • Holoprosencephaly
  • Horner syndrome
  • Hydranencephaly
  • Hyperhidrosis
  • Hypopituitarism
  • Hypotonia
  • Inclusion body myositis
  • Ischemic stroke
  • Labyrinthitis
  • Lennox gastaut syndrome
  • Lissencephaly
  • Medulloblastoma
  • Memory loss
  • Meningioma
  • Microcephaly
  • Moebius syndrome
  • Moyamoya disease
  • Multiple system atrophy
  • Muscle atrophy
  • Myelitis
  • Myelomeningocele
  • Myositis
  • Myotonic dystrophy
  • Myotonic dystrophy type 2
  • Neuralgia
  • Neurofibromatosis
  • Neurofibromatosis type 1
  • Neurogenic bladder
  • Neurosyphilis
  • New daily persistent headache
  • Normal pressure hydrocephalus
  • Notalgia paresthetica
  • Obsessive compulsive disorder
  • Optic neuritis
  • Orthostatic hypotension
  • Papilledema
  • Periodic limb movement disorder
  • Pinched nerves
  • Pituitary tumor
  • Poliomyelitis
  • Polymyositis
  • Pompe disease
  • Postural orthostatic tachycardia syndrome
  • Progressive supranuclear palsy
  • Prolactinoma
  • Pseudobulbar affect
  • Rett syndrome
  • Schwannoma
  • Sleep disorders
  • Spasticity
  • Spinal cord injury
  • Spinal muscular atrophy
  • Status epilepticus
  • Stiff person syndrome
  • Sturge weber syndrome
  • Subarachnoid hemorrhage
  • Syringomyelia
  • Tarlov cysts
  • Tarsal tunnel syndrome
  • Tethered cord syndrome
  • Thoracic outlet syndrome
  • Transient global amnesia
  • Transient ischemic attack
  • Transverse myelitis
  • Traumatic brain injury
  • Tuberous sclerosis
  • Vascular dementia
  • Viral meningitis
  • Wernicke korsakoff syndrome
  • Acute flaccid myelitis
  • Adrenoleukodystrophy
  • Aicardi goutieres syndrome
  • Aicardi syndrome
  • Alexander disease
  • Alien hand syndrome
  • Alstrom syndrome
  • Anti nmda receptor encephalitis
  • Anton syndrome
  • Ataxia telangiectasia
  • Athetosis
  • Auditory neuropathy spectrum disorder
  • Becker muscular dystrophy
  • Benign essential blepharospasm
  • Benign rolandic epilepsy
  • Bilateral perisylvian polymicrogyria
  • Brachial plexopathy
  • Brain abscess
  • Brain herniation
  • Bulging fontanelles
  • Canavan disease
  • Carotid stenosis
  • Carpenter syndrome
  • Cavernous sinus thrombosis
  • Central pain syndrome
  • Cerebellar degeneration
  • Cerebral amyloid angiopathy
  • Cerebral cavernous malformation
  • Cerebral hypoxia
  • Chiari malformation type 2
  • Childhood disintegrative disorder
  • Choroid plexus cyst
  • Choroid plexus papilloma
  • Chronic subdural hematoma
  • Coffin lowry syndrome
  • Coloboma of optic nerve
  • Congenital myasthenic syndrome
  • Corpus callosum agenesis
  • Cortical dysplasia
  • Corticobasal degeneration
  • Cramp fasciculation syndrome
  • Cysticercosis
  • Diabetic peripheral neuropathy
  • Emery dreifuss muscular dystrophy
  • Empty sella syndrome
  • Encephalitis lethargica
  • Ependymoma
  • Excessive daytime sleepiness
  • Facial paralysis
  • Facioscapulohumeral muscular dystrophy
  • Familial dysautonomia
  • Familial hemiplegic migraine
  • Fetal hydantoin syndrome
  • Focal dystonia
  • Foxg1 syndrome
  • Frey's syndrome
  • Fumarase deficiency
  • Ganglioglioma
  • Generalized tonic clonic seizure
  • Gerstmann syndrome
  • Gliosarcoma
  • Glossodynia
  • Glossopharyngeal neuralgia
  • Glutaric acidemia type 1
  • Gm1 gangliosidosis
  • Hemimegalencephaly
  • Hereditary spastic paraparesis
  • Herpes simplex encephalitis
  • Herpes zoster oticus
  • Hyperkalemic periodic paralysis
  • Hypokalemic periodic paralysis
  • Hypothalamic hamartomas
  • Increased intracranial pressure
  • Infant botulism
  • Isaacs syndrome
  • Japanese encephalitis
  • Joubert syndrome
  • Juvenile myoclonic epilepsy
  • Kleine levin syndrome
  • Kluver bucy syndrome
  • Lafora disease
  • Lambert eaton syndrome
  • Landau kleffner syndrome
  • Leigh syndrome
  • Leukodystrophy
  • Limb girdle muscular dystrophy
  • Mal de debarquement syndrome
  • Meige syndrome
  • Melas syndrome
  • Melkersson rosenthal syndrome
  • Metachromatic leukodystrophy
  • Miller fisher syndrome
  • Mononeuritis multiplex
  • Multifocal motor neuropathy
  • Myoclonic epilepsy
  • Myoclonus dystonia
  • Myotonia congenita
  • Nemaline myopathy
  • Nerve compression
  • Nerve injury
  • Neurofibromatosis type 2
  • Neurogenic bowel
  • Neuromyelitis optica
  • Neuronal ceroid lipofuscinoses
  • Neurosarcoidosis
  • Neurotrophic keratitis
  • Niemann pick disease
  • Oculopharyngeal muscular dystrophy
  • Opisthotonos
  • Optic glioma
  • Osmotic demyelination syndrome
  • Palatal myoclonus
  • Partial seizure
  • Pelizaeus merzbacher disease
  • Periventricular leukomalacia
  • Photosensitive epilepsy
  • Pneumococcal meningitis
  • Poems syndrome
  • Polymicrogyria
  • Pontocerebellar hypoplasia
  • Porencephaly
  • Post polio syndrome
  • Primary lateral sclerosis
  • Primary progressive aphasia
  • Progressive multifocal leukoencephalopathy
  • Pudendal neuralgia
  • Rasmussen encephalitis
  • Refsum disease
  • Sandhoff disease
  • Schizencephaly
  • Schwannomatosis
  • Septo optic dysplasia
  • Spasmodic dysphonia
  • Spasmus nutans
  • Spastic paraparesis
  • Spinal muscular atrophy type 1
  • Spinal shock
  • Spinal tumor
  • Spinocerebellar ataxia
  • Subacute combined degeneration
  • Subacute sclerosing panencephalitis
  • Subependymoma
  • Susac syndrome
  • Tabes dorsalis
  • Tick paralysis
  • Tolosa hunt syndrome
  • Transient cerebral ischemia
  • Tuberculous meningitis
  • Tuberous sclerosis complex
  • Vertebral artery dissection
  • Vocal cord paralysis
  • Walker warburg syndrome
  • Wallerian degeneration
  • West syndrome
  • Acrocallosal syndrome
  • Acute cerebellar ataxia
  • Adenylosuccinate lyase deficiency
  • Adie syndrome
  • Adult polyglucosan body disease
  • Aids dementia complex
  • Allan herndon dudley syndrome
  • Alpers huttenlocher syndrome
  • Andermann syndrome
  • Andersen tawil syndrome
  • Angiostrongyliasis
  • Autosomal dominant nocturnal frontal lobe epilepsy
  • Behr syndrome
  • Bilirubin encephalopathy
  • Brain and nerves
  • Cdkl5 deficiency disorder
  • Central core disease
  • Centronuclear myopathy
  • Cerebellar agenesis
  • Cerebral arteriovenous malformation
  • Cerebrotendinous xanthomatosis
  • Chorea acanthocytosis
  • Cln2 disease
  • Coach syndrome
  • Common peroneal nerve dysfunction
  • Congenital insensitivity to pain with anhidrosis
  • Congenital mirror movement disorder
  • Cytochrome c oxidase deficiency
  • Dentatorubral pallidoluysian atrophy
  • Diencephalic syndrome
  • Diffuse midline glioma h3 k27m mutant
  • Dihydrolipoamide dehydrogenase deficiency
  • Door syndrome
  • Dopa responsive dystonia
  • Drug induced dyskinesia
  • Dysferlinopathy
  • Dystrophinopathy
  • Early infantile epileptic encephalopathy
  • Familial periodic paralysis
  • Femoral nerve dysfunction
  • Fourth cranial nerve palsy
  • Gaba transaminase deficiency
  • Gerstmann straussler scheinker syndrome
  • Giant axonal neuropathy
  • Gliomatosis cerebri
  • Glycine encephalopathy
  • Gomez lopez hernandez syndrome
  • Hallervorden spatz disease
  • Hepatocerebral degeneration
  • Hereditary ataxia
  • Hereditary neuralgic amyotrophy
  • Hyperprolinemia
  • Hypothalamic tumor
  • Intracranial injury
  • Intraventricular hemorrhage of the newborn
  • Jumping frenchmen of maine
  • L1 syndrome
  • Laryngeal nerve damage
  • Lhermitte duclos disease
  • Limb girdle muscular dystrophy type 2a
  • Marchiafava bignami disease
  • Marcus gunn phenomenon
  • Marden walker syndrome
  • Marinesco sjogren syndrome
  • Meige disease
  • Meningoencephalocele
  • Migraine and headache
  • Migraine with brainstem aura
  • Mitochondrial complex 1 deficiency
  • Miyoshi myopathy
  • Monomelic amyotrophy
  • Multiple mononeuropathy
  • Multiple sulfatase deficiency
  • Myofibrillar myopathy
  • Neural crest tumor
  • Neurocutaneous melanosis
  • Neuroretinitis
  • Olivopontocerebellar atrophy
  • Opsoclonus myoclonus syndrome
  • Pantothenate kinase associated neurodegeneration
  • Paramyotonia congenita
  • Paraneoplastic cerebellar degeneration
  • Peho syndrome
  • Peripheral nerve disorders
  • Periventricular heterotopia
  • Perrault syndrome
  • Petrositis
  • Pineocytoma
  • Post traumatic epilepsy
  • Posterior fossa tumor
  • Primary amebic meningoencephalitis
  • Primary lymphoma of the brain
  • Primary orthostatic tremor
  • Progressive external ophthalmoplegia
  • Progressive hemifacial atrophy
  • Progressive myoclonic epilepsy
  • Pseudotumor cerebri syndrome
  • Pyridoxine deficiency
  • Pyruvate carboxylase deficiency
  • Pyruvate dehydrogenase deficiency
  • Radial nerve dysfunction
  • Relapsing multiple sclerosis
  • Renpenning syndrome
  • Satoyoshi syndrome
  • Schindler disease
  • Secondary parkinsonism
  • Sensorimotor polyneuropathy
  • Shapiro syndrome
  • Sialidosis
  • Smith kingsmore syndrome
  • Snyder robinson syndrome
  • Spinal and bulbar muscular atrophy
  • Spinal cord abscess
  • Spinal muscular atrophy type 2
  • Spinal muscular atrophy type 3
  • Spinal trauma
  • Spinocerebellar ataxia type 1
  • Spinocerebellar ataxia type 2
  • Spinocerebellar ataxia type 3
  • Spinocerebellar ataxia type 6
  • Spinocerebellar ataxia type 7
  • Sporadic hemiplegic migraine
  • Staphylococcal meningitis
  • Stormorken syndrome
  • Subcortical band heterotopia
  • Subdural effusion
  • Succinic semialdehyde dehydrogenase deficiency
  • Sulfite oxidase deficiency
  • Supranuclear ophthalmoplegia
  • Syringobulbia
  • Thyrotoxic periodic paralysis
  • Troyer syndrome
  • Tubular aggregate myopathy
  • Tumefactive multiple sclerosis
  • Western equine encephalitis
  • Wieacker wolff syndrome
  • Wildervanck syndrome
  • Wyburn mason syndrome
  • X linked myotubular myopathy
  • Accessory deep peroneal nerve
  • Adenosine monophosphate deaminase deficiency
  • Alg1 cdg
  • Alg3 cdg
  • Alg6 cdg
  • Amyotonia congenita
  • Aromatic l amino acid decarboxylase deficiency
  • Ataxia pancytopenia syndrome
  • Autosomal dominant partial epilepsy with auditory features
  • Autosomal recessive primary microcephaly
  • Axillary nerve dysfunction
  • Benign familial neonatal seizures
  • Beta propeller protein associated neurodegeneration
  • Boucher neuhauser syndrome
  • Cach syndrome
  • Capos syndrome
  • Cerebellar multiple system atrophy
  • Cln1 disease
  • Cln3 disease
  • Cln5 disease
  • Collagen vi related myopathy
  • Congenital fiber type disproportion
  • Congenital muscular dystrophy type 1a
  • Contracture deformity
  • Cytoplasmic body myopathy
  • Dihydropteridine reductase deficiency
  • Distal 18q deletion syndrome
  • Distal median nerve dysfunction
  • Dizziness and falls
  • Epilepsy with myoclonic atonic seizures
  • Familial paroxysmal nonkinesigenic dyskinesia
  • Familial porencephaly
  • Familial transthyretin amyloidosis
  • Fragile xe syndrome
  • Genetic epilepsy with febrile seizures plus
  • Glucose transporter deficiency
  • Glutamate decarboxylase deficiency
  • Granulomatous hypophysitis
  • Guanidinoacetate methyltransferase deficiency
  • Harding ataxia
  • Hereditary cerebral amyloid angiopathy
  • Hereditary hyperekplexia
  • Hereditary sensory and autonomic neuropathy type 2
  • Hereditary sensory neuropathy type 1
  • Horizontal gaze palsy with progressive scoliosis
  • Htlv 1 associated myelopathy
  • Hydrocephalus due to congenital stenosis of aqueduct of sylvius
  • Inclusion body myopathy 2
  • Infantile axonal neuropathy
  • Infantile onset spinocerebellar ataxia
  • Infantile refsum disease
  • Internal carotid agenesis
  • Irregular sleep wake syndrome
  • L 2 hydroxyglutaric aciduria
  • Lateral meningocele syndrome
  • Limb girdle muscular dystrophy type 1a
  • Limb girdle muscular dystrophy type 1b
  • Limb girdle muscular dystrophy type 2b
  • Limb girdle muscular dystrophy type 2c
  • Limb girdle muscular dystrophy type 2i
  • Maternally inherited leigh syndrome
  • Mcleod neuroacanthocytosis syndrome
  • Megalencephalic leukoencephalopathy with subcortical cysts
  • Mitochondrial complex 2 deficiency
  • Mitochondrial complex 3 deficiency
  • Mitochondrial complex v deficiency
  • Mitochondrial neurogastrointestinal encephalopathy disease
  • Mitochondrial trifunctional protein deficiency
  • Myelin oligodendrocyte glycoprotein antibody associated disease
  • Nerve laceration
  • Neuroepithelioma
  • Neurohypophyseal diabetes insipidus
  • Neuronal intranuclear inclusion disease
  • Neurotoxicity syndromes
  • Oculocerebrocutaneous syndrome
  • Oppenheim dystonia
  • Optic atrophy type 1
  • Pena shokeir syndrome type 2
  • Phosphoglycerate mutase deficiency
  • Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
  • Potassium aggravated myotonia
  • Primary familial brain calcification
  • Pyruvate decarboxylase deficiency
  • Radiation induced meningioma
  • Retinal vasculopathy with cerebral leukodystrophy
  • Riboflavin transporter deficiency neuronopathy
  • Rigid spine syndrome
  • Sengers syndrome
  • Sialic acid storage disease
  • Sialuria
  • Spastic ataxia charlevoix saguenay type
  • Spastic paraplegia type 11
  • Spastic paraplegia type 2
  • Spastic paraplegia type 4
  • Spastic paraplegia type 7
  • Spinocerebellar ataxia type 10
  • Spinocerebellar ataxia type 11
  • Spinocerebellar ataxia type 12
  • Spinocerebellar ataxia type 13
  • Spinocerebellar ataxia type 14
  • Spinocerebellar ataxia type 15
  • Spinocerebellar ataxia type 17
  • Spinocerebellar ataxia type 27
  • Spinocerebellar ataxia type 28
  • Spinocerebellar ataxia type 29
  • Spinocerebellar ataxia type 4
  • Spinocerebellar ataxia type 5
  • Spinocerebellar ataxia type 8
  • Subacute cerebellar degeneration
  • Subependymal nodular heterotopia
  • Supranuclear ocular palsy
  • Syphilitic aseptic meningitis
  • Tomaculous neuropathy
  • Ulnar nerve dysfunction
  • Unverricht lundborg syndrome
  • Vldlr associated cerebellar hypoplasia
  • Woodhouse sakati syndrome
  • X linked creatine deficiency
  • X linked dystonia parkinsonism
  • X linked infantile spinal muscular atrophy
more..
Treatments & Procedures
  • Eeg
  • Neuromodulation
  • Emg
  • Neurology
  • Electromyogram
  • Electroencephalogram
  • Lumbar puncture
  • Neuroma
  • Peripheral nerve stimulation
  • Tms transcranial magnetic stimulation
  • Brain aneurysm repair
  • Concussion management
  • Diagnostic medial branch block
  • Occupational therapy evaluation

Frequently Asked Questions

Where is St. Louis Neurosurgery located?

St. Louis Neurosurgery is located in 13621 Big Bend Rd St. Louis, MO 63122.

What are the various modes of payment does St. Louis Neurosurgery Accept?

St. Louis Neurosurgery accepts Card | Cash.

What are the doctors who practice in St. Louis Neurosurgery specialize in?

Currently there are around 1 providers practice in St. Louis Neurosurgery who specialise in Concierge Neurology, etc

How can I make appointments with doctors in St. Louis Neurosurgery?

You can take appointments for doctors who practice in St. Louis Neurosurgery online on their website or by calling them.

Location