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Differential
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abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abscess, intracerebral

aceruloplasminemia

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, multiphasic

acute respiratory distress syndrome

addiction, heroin

adult polyglucosan body disease

adverse drug reaction

alcohol intolerance

altered states of consciousness

alternating rapid movement

Alzheimer's disease

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

anemia, megaloblastic

ankle reflex, absent

antecedent illness

anterior tibial muscle weakness

anti GQ1b IgG antibody

anticholinergic drugs

anticoagulant, complications of

anticoagulant, treatment

antiviral agents

Argyll Robertson pupil

arm swing, reduced

Arnold Chiari malformation

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

attention deficit disorder with hyperactivity

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

azidodeoxythymidine

B 12 deficiency

Babinski sign in new born

bacterial infection

bacterial infection, CNS

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior modification

behavioral disorder

Bell's phenomenon

Bickerstaff's brainstem encephalitis

bladder dysfunction

brain biopsy, false negative

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

Brudzinski's sign

bulbar palsy, progressive

burning paresthesia

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

central nervous system, infection of

cerebellar atrophy, primary

cerebellar lesion

cerebral cortical atrophy

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrovascular accident

ceruloplasmin, serum

Chaddock's sign

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

choreoathetosis

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

comprehension, impaired

compression fracture

concentration, impaired

congenital bilateral perisylvian syndrome

congenital malformation

convergence, impaired

conversion reaction

copper deficiency

corneomandibular reflex

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial neuropathy

C-reactive protein, elevated

critical care unit

crying, pathologic

cystatin C mutation

decompressive spinal cord surgery

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine's sign

Dejerine-Sottas syndrome

delay in diagnosis

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dropped head syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

dysdiadochokinesia

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, focal

dystonia, treatment of

ears of the Lynx MR sign

electrical sensation

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

emergencies, neurologic

emergencies, neurosurgical

emotional lability

Emperor's clothes syndrome

empyema, epidural-spinal

encephalitis, brainstem

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, progressive

enzyme, muscle disease

epidemiology of neurology

episodic disorders

episodic neurologic deficits

Erdheim-Chester disease

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

face, numbness of

facial weakness

facial weakness, bilateral

feeding disorder

ferritin, elevated

fine motor function, impaired

finger nose finger test

fingers, abnormal

Fisher's syndrome

flaccid paralysis

fragile-X syndrome

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric partitioning

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

giant axonal neuropathy

gliomatosis cerebri

globus pallidus

globus pallidus, lesion of

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

glycogen storage disease

granular osmiphilic material

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

headache, positional

headache, recurrent

headache, severe

heel-knee-shin test

hematoma, epidural-spinal

hemiplegia, progressive

hexosaminidase-A

high arched feet

hip flexor weakness

history of neurology

Hoffmann's sign

homocysteine, serum

human immunodeficiency virus type 1

hypereosinophilic syndrome(HES)

hyperhomocysteinemia

hyperparathyroidism

hyperpigmentation of skin

hypersegmented polys

hyperthyroidism

hypomyelination

hypotension, systemic

hypothalamus, disturbance of

imbalance, postural

immunosuppression

inborn errors of metabolism

inclusion bodies

incontinence, fecal

initiative, lack of

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

interobserver agreement

intrinsic hand muscles, wasting of

iron, serum, low

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jaw jerk, abnormal

Krabbe's disease

lactic acidemia

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

laughing, pathologic

left-right orientation

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

level of consciousness, decreased

Lhermitte's sign

lipid storage disorder of CNS

locked-in syndrome

loss of sympathy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lysosomal storage disease

malformation, CNS, congenital

manganese intoxication

meconium staining

mediastinum, lymph-node biopsy

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, bacterial

meningitis, neutrophilic

meningitis, pneumococcal

mental retardation

mental retardation, familial

mental status, abnormal

methylmalonic acid, serum

methylmalonic acidemia

midbrain, lesion of

middle cerebellar peduncle, lesion

molecular genetics

Montreal cognitive assessment

motor dysfunction

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, psychogenic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gradient-echo

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, linear enhancement

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle weakness

mycoplasma pneumoniae

myelitis, longitudinal

myelitis, post infectious

myelitis, transverse

myelogram, cervical

myeloneuropathy

myelopathy, chronic progressive

myelopathy, vacuolar

myeloradiculopathy

myoclonus, epilepsy

nausea and vomiting

neoplasm, primary of CNS

nerve conduction studies

nerve root hypertrophy

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, sensory

neuropsychiatry

next-generation sequencing

night blindness

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular motility, disorders of

old age, neurology of

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, total

optic chiasm, enlarged

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

oral contraceptives

orthostatic hypotension

osteomyelitis, spinal

pain, interscapular

palmomental response

palpebromandibular synkinesia

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, spastic

paraplegia, in flexion

paraplegia, progressive

parathyroid adenoma

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, hemiparesis in

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal neurologic disorder

PAS positive material in the brain

pathologic reflex

patient information and support

pediatric neurology

perivascular enhancement

pernicious anemia

Persistent postural-perceptual dizziness

personality change

pharyngeal sensation

photic sneeze reflex

pituitary stalk

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polyneuropathy, familial

pons, infarction of

pons, lesion of

position sensation, abnormal

posterior column disease

posterior leukoencephalopathy syndrome

postictal neurologic deficits

precipitating factors

precocious puberty

prenatal diagnosis by amniocentesis

primary lateral sclerosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pupil, light reflex, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

reflex, cutaneous

release phenomena

repetition, impaired

respiratory failure

respiratory tract infection

retinal degeneration

retinal exudates

retinitis pigmentosa

reversible neurologic disorder

saccadic eye movements, abnormal

saddle anesthesia

sarcoidosis, CNS

sea-blue histiocytes

seizure, children

seizure, familial

seizure, hysterical

selective serotonin reuptake inhibitors

sensory loss, cutaneous

serologic testing

serotonin norepinephrine reuptake inhibitors

severe acute respiratory syndrome

skin, lesions in neurologic disorders

sleep pathology and physiology

slow virus infection of CNS

spastic paraplegia, type 11

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal stenosis

spinal stenosis, familial

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spongy degeneration of brain

spontaneous remission

startle myoclonus

startle reaction

status epilepticus

steroid therapy, CNS treatment and complications with

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

substantia nigra

superior sagittal sinus thrombosis

symmetric brain lesions

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular enlargement

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, fasciculations of

tongue, impaired movements of

tonic foot response

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

unconsciousness

upgaze, paralysis of

urinary frequency

urinary incontinence

urinary retention

urinary urgency

vaccination, neurologic complications with

valsalva maneuver

ventricular enlargement

vertigo, episodic

vibratory sensation, abnormal

viral infection

viral infection, CNS

visual acuity, decreased

visual evoked response

visual fields, constricted

vitamin deficiency

vitamin E deficiency

walking, delayed

walking, difficulty with

watershed infarcts

weakness, generalized

weakness, progressive

weaning from respirator, failure to

white matter disease

wide based gait

x-linked mental retardation

x-ray, thoracic spine

Showing articles 200 to 250 of 733 << Previous Next >>

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Clinical Reasoning: A Middle-Aged Woman with Progressive Symmetric Weakness and a CSF Pleocytosis
Neurol 78:e88-e92, Marks,D.,et al, 2012

Acute Symptomatic Seizures
The Neurologist 18:109-119, Beleza,P., 2012

Guillain-Barre Syndrome
NEJM 366:2294-2304, Yuki, N. & Hartung, H.P., 2012

Clinicopathologic Conference, Acute Ischemic Stroke due to Basilar Artery Embolism. Patent Foramen Ovale
NEJM 367:1450-1460, Case 31-2012, 2012

Clinical Reasoning: A Case of Acute Onset Bilateral Ptosis in a Young Child
Neurol 79:e155-e160, Das, D.,et al, 2012

Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
AJNR 33:1945-1950, Lee,H.,et al, 2012

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Clinical Reasoning: A 34-year-old man with recurrent limb weakness
Neurol 77:e68-e72, Karam, C.,et al, 2011

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

Chronic Inflammatory Demyelinating Polyneuropathy: Etiology, Clinical Features, and Diagnosis
UpToDate, Sept, Lewis, R., 2010

Predictors of Neurologic Outcome in Hypothermia After Cardiac Arrest
Ann Neurol 68:907-914, Fugate,J.E.,et al, 2010

Clinical Reasoning: Seizures in a Child With Sensorineural Deafness and Agitation
Neurol 74:e61-e63, Auvin,S., et al, 2010

Hot Water Epilepsy: Seizure Type, Water Temperature, EEG Findings and Treatment
The Neurologist 16:109-112, Gokcil,Z.,et al, 2010

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Isolated Bilateral Trigeminal Neuropathy in Sarcoidosis Presenting with Neurotrophic Corneal Ulcers
Ophthalmology & Eye Diseases 2:69-73, Gupta, M.,et al, 2010

Trigeminal Sensory Neuropathy Associated with Systemic Sclerosis
Arq Neuropsiquiatr 67:494-495, Ribeiro, R.T.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Neurologic Prognosis After Cardiac Arrest
NEJM 361:605-611, Young,G.B., 2009

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

Clinicopath Conf, Neuro-Behcets Disease
NEJM 360:2341-2351, Case 17-2009, 2009

Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
NEJM 360:171-181, Case 1-2009, 2009

Update on Blepharospasm: Report from the BEBRF International Workshop
Neurol 71:1275-1282, Hallett,M.,et al, 2008

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Woke Up Paralysed--Without Injury or Stroke
Lancet 371:870, Bawaskar,H.S. &Bawaskar,P.H., 2008

Predicting Outcome After Traumatic Brain Injury: Practical Prognostic Models Based on Large Cohort of International Patients
BMJ 336:425-429,397, MRC Crash Trial Collaborators, 2008

Seizure Occurrence: Precipitants and Prediction
Neurol 69:1905-1910, Haut,S.R.,et al, 2007

Obstructive Sleep Apnea is Associated With Seizure Occurrence in Older Adults With Epilepsy
Neurol 69:1823-1827, Chihorek,A.M.,et al, 2007

10 Questions About the Clinical Determination of Brain Death
Neurologist 13:380-381, Wijdicks,E.F.M., 2007

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

Seizures on Hearing the Alarm Clock
Lancet 370:2172, Vollmar,C.,et al, 2007

A 63-Year-Old Man With Headaches and Behavioral Deterioration
Neurol 68:782-787, Greenberg,S.M.,et al, 2007

Narcolepsy With Cataplexy
Lancet 369:499-511, Dauvilliers,Y.,et al, 2007

A 46-Year-Old Woman With Severe Weakness Following Acute Respiratory Distress Syndrome
Neurol 68:1529-1535, Waclawik,A.J.,et al, 2007

Pyramidal Tract Degeneration in Sporadic Creutzfeldt-Jakob Disease
Neuropathology 27:434-441, Iwasaki,Y.,et al, 2007

Concomitant Chronic Inflammatory Demyelinating Polyneuropathy and Myasthenia Gravis Following Cytomegalovirus Infection
J Neurol Sci 240:103-106, Mori, M.,et al, 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Pathological Yawning as a Presenting Symptom of Brain Stem Ischaemia in Two Patients
JNNP 77:98-100,3, Cattaneo,L.,et al, 2006

The First Seizure and Its Management in Adults and Children
BMJ 332:339-342, Pohlmann-Eden,B.,et al, 2006

Spinal cord Stimulation for Chronic Reflex Sympathetic Dystrophy--Five-Year Follow-up
NEJM 354:2394-2396, Barendse,G.A.M.,et al, 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Early Clinical Signs and Imaging Findings in Gerstmann-Straussler-Scheinker Syndrome (Pro102Leu)
Neurol 66:1672-1678, Arata,H.,et al, 2006

Practice Parameter: Prediction of Outcome in Comatose Survivors After Cardiopulmonary Resuscitation (An Evidence-Based Review).
Neurol 67:203-210, Wijdicks,E.F.M.,et al, 2006

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Severe Botulism After Focal Injection of Botulinum Toxin
Neurol 67:1855-1856, Souayah,N.,et al, 2006

A Fatal Encephalitis
Lancet 365:358, Schankin, C.J., et al, 2005

Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005

Effect of Stress Related to the 9/11/2001 Terror Attack on Seizures in Patients with Epilepsy
Neurol 64:1815-1816, Klein,P. &van Passel,L., 2005

A Floppy Child with Failure to Thrive
Lancet 366:176, Loma-Sanner,I.,et al, 2005

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Showing articles 200 to 250 of 733 << Previous Next >>