Neudle.com: "dystonia primary"

Differential
(Click to cross reference)

abscess, intracerebral

abscess, intracranial

abscess, retropharyngeal

abscess, sphenoid sinus

acanthocytosis

acetazolamide

aciduria

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

advances in neurology

adverse drug reaction

aggression

agitation

agnosia, color

Aicardi-Goutieres syndrome

airway obstruction

akathisia

akinesia of eyelid function

alcohol

alcohol, neurologic complications with

alcoholic withdrawal states, DT's, convulsions, etc.

alexia without agraphia

algorithm

alien hand syndrome

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

AMPA receptor antibodies

amphetamines, dyskinesia associated with

amphiphysin antibodies

amyloidosis

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

aneurysm, intracranial

angiography, cerebral

angiography, posterior fossa

ankle edema

anoxia

anterocollis

anti basal ganglia antibodies

anti GQ1b IgG antibody

anti IgLON5

anticholinergic drugs

anticholinesterase

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, untoward effects of

antidepressant

anti-dopamine 2 receptor antibody

antiemetic

antihistamines

antistreptolysin titer

anxiety

anxiolytic agents

aortic valve, lesion of

aphasia

aphasia, progressive, primary

aphonia

applause sign

apraxia

apraxia of eye movements

apraxia of eyelid opening

apraxia, constructional

arteriovenous malformation

arteriovenous malformation, cerebral

arthralgia

arthritis

arthrogryposis multiplex

ataxia telangiectasia

ataxic-dystonia syndromes

athetosis

athetosis, causes of

atlanto-axial subluxation

ATP1A3 gene

attention deficit disorder with hyperactivity

attention span

atypical

auditory evoked brainstem potentials

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

automobile accidents

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

behavioral disorder

benign essential tremor

bent spine syndrome

benzodiazepine

beta adrenergic blocker

bilirubin encephalopathy

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

botulinum toxin, complications of

brainstem, dysfunction

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, lesion of

brainstem, vascular malformation of

calcification, intracranial

calcium antagonist

calcium antagonist, side effects of

camptocormia

carbamazepine

carbamazepine, toxicity

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma

cardiac arrest

cardiac arrest and resuscitation

cardiomyopathy

cardiopulmonary bypass

carotid artery occlusion, neck

carpal tunnel syndrome

CAT scan

CAT scan, abnormal

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, isodense lesion with acute hemorrhage

caudate nucleus, atrophy

caudate nucleus, lesion of

cavernous hemangioma

cavernous sinus

cavernous sinus, metastasis to

cavernous sinus, syndrome

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar hemorrhage

cerebellar lesion

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellum

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral ischemia

cerebral palsy

cerebral palsy, adults

cerebral palsy, associated problems with

cerebral peduncle

cerebral vasculature, calcification

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, cell count, normal

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, infancy and childhood

cerebrovascular accident, prevention of

cerebrovascular accident, young adult

ceruloplasmin, serum

cervical spine

cervical spine injury

chilbran skin lesions

children

China

chiropractic manipulation

chiropractic manipulation, neurologic complications with

choreoathetosis, paroxysmal

chromosomal abnormality

chronic progressive external ophthalmoplegia

cinnarizine

cirrhosis

cirrhosis, causes of childhood

cisterna magna

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

colloid cyst of third ventricle

coma

coma, causes of

coma, episodic

coma, unknown etiology

comorbidities

complications

compression fracture

compression neuropathy

computers, neurologic diagnosis and

confusion

conjugate gaze, forced

copper metabolism, abnormal

cornea, opacity of

Cornelia de Lange syndrome

cortical blindness

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

crying, pathologic

cultured skin fibroblasts

degenerative diseases of CNS

dementia, treatment of

dental procedure, neurologic complications with

dentate nuclei, lesion of

depression

dermatomyositis

developmental milestones, loss of

developmental retardation

differential diagnosis

disability, neurological

discectomy

discectomy, cervical

distal muscle atrophy

dopa responsive dystonia

dopamine

dopamine agonist

dopamine antagonist

dopamine depleting agents

dopamine receptor, D2

dorsal column stimulator

DPPX, antibodies, encephalitis

drooling

droperidol

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

drug overdose

drug overdose, accidental

drug withdrawal

dural sinus thrombosis

dying

dysarthria

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia musculorum deformens, carrier

dystonia, axial

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, focal lesion causing

dystonia, focal task specific

dystonia, post traumatic

dystonia, prevalence of

dystonia, psychogenic

dystonia, segmental

dystonia, symptomatic

dystonia, tongue

dystonia, treatment of

dystonia, truncal

dystonic lipidosis

dystonic reaction, acute

ectatic basilar artery

ectopic pinealoma

edema, pedal

efficacy

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

ELISA

emergencies, neurologic

emotional lability

employment

empyema, epidural

empyema, epidural-spinal

empyema, subdural

encephalitis

encephalitis lethargica

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, clinical picture and treatment of

encephalitis, etiology

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post anoxic

encephalopathy, progressive

endocarditis

entrapment neuropathy

enuresis

enzyme, defect

ependymoma

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

epsilon sarcoglycan gene

exercise-induced neurologic dysfunction

exome sequencing

extralimbic encephalitis

extrapyramidal movement disorder, progressive

eye color

eye movement, disorders of

face, contractions

facial expression abnormality

facial nerve palsy

faciobrachial dystonic seizure

fine motor function, impaired

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

frontal behavioral spatial syndrome

frontal lobe, pathologic signs of

fungal infection, CNS

gait disorder

gait, apraxic

galactorrhea

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis, generalized

gaze deviation

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

gests antagoniste

Gilles de la Tourette syndrome

glabellar sign

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, stimulation

GLUT1

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glutaric acidemia

glutaric aciduria

glycine receptor antibodies

Guillain Barre syndrome

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

head injury, pediatric

hemianopia, homonymous

hemiparesis, transient

hemiplegia

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc, cervical

human immunodeficiency virus type 1

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's disease, children

hydrocephalus

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperekplexia

hyperhidrosis

hyperpyrexia, CNS disorder causing

hypoparathyroidism, idiopathic

hypotension, systemic

hypoxic encephalopathy

iatrogenic neurologic disorders

immunosuppressive agents

immunotherapy

inappropriate antidiuretic(A.D.H.)hormone

inattention

inborn errors of metabolism

incontinence, fecal

incoordination

infantile bilateral striatal necrosis

intellectual deterioration

interferon alpha

internal capsule

internal cerebral vein

internet

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracranial hemorrhage

intracranial pressure, increased

intrathecal antispasticity drugs

Jakob-Creutzfeldt disease

jaundice

jaw jerk, abnormal

jugular foramen syndrome

karyotyping

Kayser-Fleischer ring

Kearns-Sayre syndrome

kernicterus

ketoacidosis

ketogenic diet

Klinefelter's syndrome

klippel feil syndrome

laryngismus stridulus

laterocollis

laughing, pathologic

L-dopa

L-dopa, drug interactions with and side effects of

L-dopa, enteral infusion, continuous

Leber's hereditary optic neuropathy

left handedness

leg spasms

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

level of consciousness, decreased

levitation

Lewy body disease, diffuse

lipid storage disorder of CNS

liver function enzymes

liver transplantation

lysosomal storage disease

malformation, vascular

malformation, vascular, cerebral

manganese intoxication

masked facies

mastoiditis

mediastinum, mass of

medical-legal aspects of neurology

MELAS syndrome

memory

memory, defect of recent

memory, impairment of

meningismus

meningitis

mental retardation

mental retardation, etiology of

mental status, abnormal

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylmalonic acidemia

midbrain, infarction of

migraine, treatment of

mimics

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

mongolism

monoamines

monoclonal antibodies

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, paroxysmal

movement disorder, psychogenic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, FLAIR

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, mouse ears

MRI, negative

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, paroxysmal symptoms in

multiple system atrophy

Munchausen syndrome

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis, drug induced

myasthenia gravis, unmasked

myasthenic crisis

mycoplasma

mycoplasma pneumoniae

mycotoxin

myelogram

myelopathy

myelopathy, chronic progressive

myopathy, carcinomatous

myopathy, metabolic

myopathy, mitochondrial

myopathy, thyroid disease causing

neoplasm, intracranial

neoplasm, intracranial with metastasis extracranially

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-infants

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

neuritis, causes of

neurochemistry

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neuroleptic

neuroleptic malignant syndrome

neuroleptic, atypical

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neuropathology, brain

neuropathy

neuropathy, diabetic

neuropathy, peripheral

next-generation sequencing

nonsteroidal anti-inflammatory drug

norepinephrine

numb clumsy hands syndrome

nystagmus

nystagmus, congenital

obsessive-compulsive disorder

occipital lobe, lesion of

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

Oculinum

oculogyric crisis

old age, neurology of

opened mouth

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

optokinetic nystagmus, abnormal

oral contraceptives

oral contraceptives, choreiform movements with

orthostatic hypotension

osteomyelitis

osteomyelitis, skull

osteomyelitis, spinal

otitis, neurologic complications with

paraspinal muscle weakness

parkin gene

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, mode of onset

Parkinson disease, on-off phenomena in

Parkinson disease, postencephalitic

Parkinson disease, prognosis of

Parkinson disease, progression

Parkinson disease, psychogenic

Parkinson disease, rapid onset

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal exertion-induced dyskinesia

paroxysmal hypnogenic dyskinesia

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

paroxysmal neurologic disorder

paroxysmal nonkinesigenic dyskinesia

parsidol

pathognomonic

pathology

patient information and support

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

pediatric opioid use associated neurotoxicity

penguin silhouette sign

penicillamine

perineural invasion

peripheral nerve, lesion of

peroxisomal disease

personality change

personality disorder

phencyclidine poisoning

phenothiazine

phenothiazine, dyskinesia associated with

phenylketonuria

photophobia

pigmentary retinopathy

Pisa syndrome

pitfalls

pituitary, adenoma

pituitary, microadenoma

pleocytosis of cerebrospinal fluid

pleural effusion

poison, neurologic problems with

POLG1 gene

poliomyelitis

polycythemia, primary

polycythemia, secondary

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

posterior fossa, arteriovenous malformation

posterior fossa, lesion of

postoperative neurologic complications

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal

pretectal syndrome

prevention of neurologic disorders

primary episodic ataxia

primary familial brain calcification

procyclidine

progeria

prognosis

progressive neurologic disorder

progressive supranuclear palsy

proprioception, abnormal

pseudoathetosis

pseudobulbar palsy

pseudochorea

pseudohypoparathyroidism

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

psychosis, acute

psychosomatic disease

pupil, abnormality in neurologic disorders

pupil, tonic

pure sensory stroke

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radial nerve, palsy of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rectal biopsy

Red flags

reflex sympathetic dystrophy

release phenomena

remote effect of cancer on the nervous system

renal failure

renal stones

repetition strain injury

reserpine treatment in movement disorder

respirator

respiratory failure

respiratory tract infection

restless leg syndrome

reversible neurologic disorder

saccadic eye movements, abnormal

safety

salivation, excessive

sedimentation rate, elevated

seizure

seizure, adult onset

seizure, children

seizure, differential diagnosis of

seizure, dystonic

seizure, neonatal

seizure, psychomotor-temporal lobe

seizure, stimulus sensitive

seizure, unknown origin

selective serotonin reuptake inhibitors

self harm

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss

sensory loss, cortical

sensory tricks

sequencing difficulty

serologic testing

serologic testing, false negative

seronegative

sexual behavior, disorder of

single photon emission computed tomography

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

spasticity, treatment of

speech disorder

speech disorder, childhood

speech disorder, non aphasic

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, infants and children

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 16

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

splenomegaly

spondylosis

spongy degeneration of brain

sports medicine, neurology of

status epilepticus, intractable

stem cell transplantation

stereotaxic surgery

stereotypy

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

stimulation, deep brain, bilateral

stimulation, thalamic

stooped posture

strabismus

streptococcal infection

streptococcus pyogens

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

stridor

striopallidodentate calcifications, familial idiopathic

subarachnoid hemorrhage

symmetric brain lesions

tardive dyskinesia, treatment of

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

thoracic outlet syndromes

tongue, protrusion of

tonic foot response

tonic spasms

torticollis

torticollis, acute infectious

torticollis, benign paroxysmal

torticollis, familial

torticollis, infants and children

torticollis, natural history

torticollis, ocular

torticollis, post traumatic

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

transcutaneous electrical nerve stimulation

transient ischemic attack

transient neurologic deficit

transient paroxysmal dystonia in infancy

trauma

treatment failure

treatment of neurologic disorder

tremor, post traumatic

tricyclic antidepressant

trientine dihydrochloride

trigeminal neuralgia

trinucleotide repeats

tripping

typing

typist cramp

tyrosine hydroxylase deficiency

urea-cycle enzymopathies

uric acid, low

urinary incontinence

urinary sulfatidase excretion

urine test for metabolic disorders

urine test in toxic screen

valium

valvulopathy

vasospasm, cerebral

vertebral-basilar insufficiency

visual evoked response

visual field defect

visual impairment

visual symptoms

visuospatial disturbance

vitamin E deficiency

walking

walking frame

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weight loss

Werdnig-Hoffman disease

X-linked dystonia-parkinsonism syndrome

x-linked mental retardation

yips

zinc

Showing articles 0 to 50 of 4918 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Torticollis in a Child with Otalgia
BMJ 378:e070608, Sarathi, C.I.P.,et al, 2022

Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
Neurol 99:e1957-e1967, Corp, D.T.,et al, 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Clinicopathologic Conference, LGI1 autoimmune encephalitis
NEJM 382:1943-1950, Case 15-2020, 2020

A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
Ann Neurol 88:637-638, Wu, H.,et al, 2020

Clinical and Radiologic Features of Pedicatric Opioid Use-Associated Neurotoxicity with Cerebellar Edema (POUNCE) Syndrome
Neurol 94:710-712, Kim, D.D. & Prasad, A.N., 2020

Functional Gait Disorders
Neurol 94:1093-1099, Nonnekes, J.,et al, 2020

MR Imaging of the Brain in Neurologic Wilson Disease
AJNR 40:178-183, Yu, X.-E.,et al, 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
JAMA Neurol 76:728-729, Kim, D.D.,et al, 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
Neurol 91:98-101, Marques-Matos, C.,et al, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Lithium-Induced Reversible Pisa Syndrome
Neurol 88:e184, Kumar, N.,et al, 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

Thalamic Deep Brain Stimulation for Tremor in Parkinson Disease, Essential Tremor, and Dystonia
Neurol 89:1416-1423, Cury, R.G.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Facial Grimacing and Sensorineural Hearing Loss in a Woman with Cirrhosis of the Liver
Neurol 87:e239, Sgobbi de Souza, P.V.,et al, 2016

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016

Practice Guideline Update Summary: Botulinum Neurotoxin for the Treatment of Blepharospasm, Cervical Dystonia, Adult Spasticity, and Headache
Neurol 86:1818-1826, Simpson, D.M.,et al, 2016

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
JAMA Neurol 73:888-890, Kawarai, T.,et al, 2016

Myasthenia Gravis after Botulinum Toxin Type A Injection
Turk J Neurol 22:143-144, Tekce, H.D.,et al, 2016

Paroxysmal Dystonia as a Manifestation of Multiple Sclerosis
Neurologist 19:132-134, Machado, C.,et al, 2015

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

Autopsy Case of Severe Generalized Dystonia and Static Ataxia with Marked Cerebellar Atrophy
Neurol 85:1522-1524, Miyamoto, R.,et al, 2015

Paroxysmal Kinesigenic Dyskinesia
Neurol 85:1546-1553, Huang, X.J.,et al, 2015

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Antipsychosis Drugs
Adams & Victors Principles of Neurology Chp 43, pg 1208, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Encephalitis Lethargica (non Economo Disease, sleeping sickness)
Adams & Victors Principles of Neurology, Chp 33, pg 768, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
Adams & Victors Principles of Neurology, Chp 37, pg 968, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1096, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Dystonia Musculorum Deformans
Adams & Victors Principles of Neurology, Chp 39, pg 1099, Ropper, A.H.,et al, 2014

Alleviating Manoeuvres (Sensory Tricks) in Cervical Dystonia
JNNP 85:882-884, Patel, N.,et al, 2014

Deep-Brain Stimulation - Entering the Era of Human Neural-Network Modulation
NEJM 371:1369-1373, Okun, M.S., 2014

Showing articles 0 to 50 of 4918 Next >>