New England Neurological Associates, PC - Lawrence, Massachusetts

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New England Neurological Associates, PC is a clinic in Lawrence, MA offering Concierge Neurology, with 1 physician on staff.

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About New England Neurological Associates, PC

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Riverwalk Dental, 354 Merrimack Street Lawrence,
MA 01843

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Card | Cash

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Bruce Cook, MD

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Concierge Neurology

Riverwalk Dental, 354 Merrimack Street, Lawrence, MA 01843

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Holistic/Lifestyle Med - Pending

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Bruce Cook, MD

New England Neurological Associates, PC

Concierge Neurology

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Fee N/A

Max no. of Patients: N/A

Accepting New Patients: NA

Riverwalk Dental, 354 Merrimack Street, Lawrence, MA 01843

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Conditions Treated

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

more..

Treatments & Procedures

Eeg
Neuromodulation
Emg
Lumbar puncture
Electromyogram
Electroencephalogram
Diagnostic medial branch block
Peripheral nerve stimulation
Brain aneurysm repair
Tms transcranial magnetic stimulation
Concussion management
Occupational therapy evaluation
Neuroma

Frequently Asked Questions

Where is New England Neurological Associates, PC located?

New England Neurological Associates, PC is located in Riverwalk Dental, 354 Merrimack Street Lawrence, MA 01843.

What are the various modes of payment does New England Neurological Associates, PC Accept?

New England Neurological Associates, PC accepts Card | Cash.

What are the doctors who practice in New England Neurological Associates, PC specialize in?

Currently there are around 1 providers practice in New England Neurological Associates, PC who specialise in Concierge Neurology, etc

How can I make appointments with doctors in New England Neurological Associates, PC?

You can take appointments for doctors who practice in New England Neurological Associates, PC online on their website or by calling them.

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