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Differential
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acquired immunodeficiency syndrome

adolescent medicine

adverse drug reaction

akinesia of eyelid function

alcohol, neurologic complications with

alien hand syndrome

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

anticardiolipin antibodies

anticonvulsants, untoward effects of

antiphospholipid antibody syndrome

aphasia, progressive, primary

apraxia of eye movements

apraxia of eyelid opening

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

B 12 deficiency

bacterial infection

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

bent spine syndrome

bilirubin encephalopathy

biologic markers

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bladder dysfunction

blinking, reduced

bone marrow transplantation

botulinum toxin

botulinum toxin, complications of

bradykinesia, facial

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

carcinoembryonic antigen

carcinoma of breast

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, muscle

caudate nucleus, atrophy

celiac disease, adult

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellitis, autoimmune

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral hypoperfusion

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, three territory involvement

chewing movements

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

collagen vascular disease

congenital infection, CNS

contractures, joint

controversies in neurology

conversion reaction

corpus callosum, thinning

cortical-basal ganglionic degeneration

cost effectiveness

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, treatment of

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

disease modifying agents

distal muscle atrophy

dopa responsive dystonia

DPPX, antibodies, encephalitis

drug abuse, neurologic complications of

dysdiadochokinesia

dyskinesia, buccal lingual facial

dystonia, cervical

dystonia, children

dystonia, drug induced

dystonia, focal

dystonia, painful

dystonia, treatment of

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalopathy, neonatal

encephalopathy, progressive

endarterectomy, carotid

epidemiology of neurology

episodic neurologic deficits

evidence-based research

exercise intolerance

exome sequencing

extralimbic encephalitis

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial movement disorder

facial nerve palsy

fatal familial insomnia

fluorescent treponema antibody absorption/false positive

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

frontal behavioral spatial syndrome

frontal lobe, anatomy and physiology

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

granulomatous disease

growth retardation

Guillain Barre syndrome

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

hemifacial spasm

hepatic failure

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

hippocampus, hyperintense

Horner's syndrome

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

hyperammonemic encephalopathy

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hypocomplementemia

hypometric saccades

hypothalamus, disturbance of

hypoxic encephalopathy

imbalance, postural

immunocompetent

immunodeficiency

immunomodulation

immunosuppression

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

intellectual deficit

intellectual deterioration

internal capsule

intracranial hypertension, benign

Isaacs syndrome

Jakob-Creutzfeldt disease

jaw jerk, abnormal

leg spasms, painful

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

Lewy body disease, diffuse

lid abnormalities

limbic encephalitis

lipid storage disorder of CNS

lymphadenopathy, hilar

lysosomal storage disease

manganese intoxication

marche a petits pas

McLeod syndrome

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, carcinomatous

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

methylmalonic acidemia

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Mini Mental Status Examination

mitochondrial disease

mitochondrial disease, pathogenesis

molecular genetics

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gradient-echo

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple sclerosis

multiple system atrophy

muscle stiffness

muscle weakness

muscle weakness, proximal

muscular dystrophy

myasthenia gravis

myelopathy, hepatic

myoclonic ataxia

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myopathy, metabolic

nausea and vomiting

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic signs

neuron specific enolase

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

next-generation sequencing

Niemann-Pick disease

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, monocular

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculomasticatory myorhythmia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

orthostatic hypotension

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

parenteral alimentation

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

peripheral blood smear

peripheral nerve, lesion of

personality change

pigmentary retinopathy

pituitary, lesion of

pleocytosis of cerebrospinal fluid

polymerase chain reaction

portal caval shunt

posterior inferior cerebellar artery syndrome

postural abnormality

precipitating factors

premature infant

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

reading problem, causes of

remote effect of cancer on the nervous system

retinitis pigmentosa

rigidity, axial

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis, CNS

sea-blue histiocytes

seizure, laughing as manifestation

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

spastic dysphonia

speech disorder

speech disorder, childhood

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 2

spongy degeneration of brain

standing difficulty

startle reaction

status epilepticus

status epilepticus, intractable

steroid therapy, CNS treatment and complications with

stiff limb syndrome

stiff man syndrome

stimulant drugs

stooped posture

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

subthalamic nucleus

symmetric brain lesions

synucleinopathy

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

Three territory sign

thrombophlebitis

tonic foot response

transient ischemic attack

transient ischemic attack, limb shaking

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

tremor, postural

tremor, writing

trigeminal neuropathy

trinucleotide repeats

tyrosine hydroxylase deficiency

unconsciousness

unconsciousness, transient

urinary frequency

urinary incontinence

vestibular migraine

viral infection

viral infection, CNS

visual evoked response

visual impairment

vitamin deficiency

walking, difficulty with

weakness, generalized

weakness, progressive

Whipple's disease

white matter disease

wide based gait

Showing articles 750 to 800 of 18245 << Previous Next >>

Neurologic Complications of Heroin Addiction
Bull NY Acad Sci 49:4, Ritcher,R.W.,et al, 1973

Tardive Dyskinesia Associated with Antipsychotic Drugs
FDA Drug Bulletin, May 1973., , 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Clinical Diagnosis of the Dyskinesias
Med Clin of North Am 56:1321, Duvoisin,R., 1972

Thromboangiitis Obliterans Cerebri
Edited by, Vinken, E. , Handbook Clinical Neurol 12:3842., Bernsmeier,A.&Held,K., 1972

Neuropsychiatric Problems in SLE
BMJ 4:342, Bennett,R.,et al, 1972

Benign Essential Tremor
Lancet 471, 1972 Sept., , 1972

Implications of Amphetamine-Induced Stereotyped Behavior as a Model for Tardive Dyskinesias
Arch Gen Psychiat 27:502-507, Rubovits,R.,et al, 1972

Enlargement of the Sylvian Aqueduct:A Sequel of Head Injuries
JNNP 35:463-467, Boller,F.C.,et al, 1972

Drug-Induced Movement Disorders
Postgrad Med 180, 1971, Sept., North,R., 1971

Diseases of the Extrapyramidal System
Disease-a-month-Jan 1970., Klawans,H.,et al, 1970

Dopamine & Disease
C M A Journ 103:824, Barbeau,A., 1970

Supranuclear Abnorm. of the Vert. Ocular Motor Syst
Trans Ophth United King 90:433, Sanders,M.D.,et al, 1970

Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
Am J Ophthalmol 67:561, Johnson,R.V.,et al, 1969

Function of the Basal Ganglia
Handbook of Clinical Neurology 6:90-115, Ward,A., 1968

Neuropathological Findings in Three Cases of Persistent Dyskinesia following Phenothiazine Medication
J Neurol Sci 7:263, Hunter,R.,et al, 1968

Senile Chorea-Handbook of Clinical Neurology
6:437, Vinken & Bruyn68., , 1968

Complicated Migraine
In Handbook of Clinical Neuro. , Ed. Vinken & Bruyn-5:Chap 6 N. Holland Pub. Co., Bruyn,G.W., 1968

Neurological Manifestations of SLE
Medicine 47:337, Johnson,R.,et al, 1968

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

Some Neuro-ophthalmological Observations
JNNP 30:383, Fisher,C.M., 1967

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

Neurologic Complications of Polycythemia
Ann Int Med 57:909, Silverstein,A.,et al, 1962

Neuro CPC of MGH
Jacob-Creutzfeldt Disease, NEJM 264:1359-13641961., , 1961

Diseases of the Basal Ganglia-Their Relation to Disorders of Movement
Lancet 1099, 1960, Nov., Denny-Brown,D., 1960

A Note on the Pathology of Senile Chorea (Non-Hereditary)
Brain 59:376, Alcock,N.S., 1936

"Athetosis" & Post-hemiplegic Disorders of Movement
Medico-Chirurgical Transactions, 219, May 9876., Gowers,Wm., 1876

An 81-Year-Old Man with Imbalance and Memory Impairment
, Golbe,L.I.,et al,

Mucormycosis
NEJM 394:684-698, Kontoyiannia,D.P. & Walsh, T.J., 2026

Clinicopathologic Conference, Disseminated Infection with Hypervirulent Klebsiella Pneumoniae
NEJM 394:282-294, Case 202026, 2026

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
Neurol 106:e214622, German,A.,et al, 2026

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

Association of Changes in Activity Patterns with Brain Atrophy and Disability Progression in People with Multiple Sclerosis
Neurol 106:e214678, e214742, Fitzgerald,K.C.,et al, 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

A 67-Year-Old Man with Exercise Intolerance nd Progressive Weakness
Neurol 106:e214830, Gosset,A.,et al, 2026

A 41-Year-Old Man Presenting with Right Foot Tingling
Neurol 106:214781, Lu,V.,et al, 2026

Deep Venous Dural Arteriovenous Fistula Mimicking Progressive Dementia
Stroke 57:e180-181, Langlois-Therien,T.,et al, 2026

Autoimmune Encephalitis as Treatment-Responsive Cause of Rapidly Progressive Dementia
Neurol 106:e214933, van Steenhoven,R.W.,et al, 2026

A 32-Year-Old Woman with Progressive Vision Loss and Confusion
Neurol 106:e214988, Kumar,A.B.,et al, 2026

A 55-Year-Old Man with Rapidly Progressive Weakness and Numbness
Neurol 106:e218063, Li,X.,et al, 2026

An 81-Year-Old Woman with Chronic Isolated Neck Extensor Weakness
Neurol 106:e218060, Chen,J.,et al, 2026

Creutzfeldt-Jakob-Like Presentation in Anti-AMPAR Encephalitis
Ann Neurol 99:1466-1467, Durbano,K.et al, 2026

A 28-Year-Old Man with Seizures and Thalamic Lesions
Neurol 106:e218065, Santos-Rojo,A.B.,et al, 2026

A 35-Year-Old Patient with Rapidly Progressive Ascending Weakness Leading to Loss of Brainstem Reflexes
Neurol 106:e218059, Lyons,H.J.,et al, 2026

Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2243-2253, 2264, Johnson,M.D.,& Williams, M.A., 2025

A 50-Year-Old Male Patient With Acute Severe Sensory Deafferentation and Bilateral Ptosis with Rapid Recovery
Neurol 106:e214435, Pseruk,F.,et al, 2025

A 5-Year-Old Boy with Subacute and Refractory Myoclonus
Neurol 106:e214457, Park,P.S.,et al, 2025

Recurrent Ischemic Strokes Due to Os Odontoideum
Ann Neurol 98:1315-1317, Wang,J.,et al, 2025

Showing articles 750 to 800 of 18245 << Previous Next >>