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Differential
(Click to cross reference)
absence
acrocyanosis
agitation
Aicardi-Goutieres syndrome
akathisia
alcohol
alcohol intolerance
alcohol, neurologic complications with
Alexanders disease
Alexanders disease, adult onset
alternating rapid movement
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, early onset
Alzheimer's disease, familial
amyloid angiopathy, cerebral
animal exposure
anticonvulsants
anticonvulsants, discontinuation in seizure-free epileptics
anticonvulsants, effectiveness
anticonvulsants, selection of
anxiety
aphasia
aphasia, progressive
apolipoprotein E
APP gene
apraxia
areflexia
arm weakness
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autonomic dysfunction
axonal spheroid
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
beta adrenergic blocker
biologic markers
blindness
bone pain
bovine spongiform encephalopathy
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
CAG repeats
calcification, intracranial
CAT scan
CAT scan, abnormal
CAT scan, false negative
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar plaques, amyloid
cerebral cortex
cerebral cortical atrophy
cerebral vasculature
cerebrospinal fluid, abnormal
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
ceruloplasmin, serum
cherry red spot
cherry red spot-myoclonus syndrome
chewing movements
chilbran skin lesions
children
choking
chorea
chorea, familial
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 12
chromosome 2
chromosome 7
chromosome 8
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonazepam
clonus
cognition
cognition, slowed
cogwheel rigidty
color vision, impaired
coma
confabulation
consanguinity
copper metabolism, abnormal
Creutzfeldt-Jakob disease, genetic
crying, pathologic
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, differential diagnosis of
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, thalamic
dementia, transmissible
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
distal muscle atrophy
distal muscle weakness
dizziness
Dravet syndrome
drooling
dropped head syndrome
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyssynergia cerebellaris myoclonica
dystonia
dystonia, children
dystonia, face
dystonia, treatment of
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, video monitoring with
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
epileptic encephalopathy
epsilon sarcoglycan gene
eye movement, disorders of
failure to thrive
falling
familial
familial adult myoclonic epilepsy
fasciculation
fatal familial insomnia
fatigue
feeding disorder
fever
finger nose finger test
fingerprint bodies
fundus, abnormality of
gait disorder
gangliosidosis GM2
Gaucher's disease
Gaucher's disease, adult onset
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
granular osmiphilic material
growth hormone
growth retardation
Hallervorden Spatz disease
hallucination
hallucination, visual
handwriting
head lag
head nodding
headache
hearing loss
heel-knee-shin test
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
hexosaminidase-A
HLA
hyperekplexia
hyperhidrosis
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hyperthermia
hypertonia
hypertonia, congential
hypomyelination
hypothermia
hypotonia
iatrogenic neurologic disorders
imbalance
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
insight, loss
insomnia
intellectual deficit
intellectual deterioration
interferon alpha
intrauterine
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jewish
juvenile myoclonus epilepsy
Kayser-Fleischer ring
lactic acidemia
Lafora body
Lafora's disease
Leigh's disease
Leigh's disease, adult variety
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
life expectancy
linear lesion
lipid storage disorder of CNS
liver biopsy
liver disease
lysosomal storage disease
macular degeneration
MELAS syndrome
memory, defect of recent
memory, impairment of
mental retardation
MERRF syndrome
microcephaly
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoparesis
mortality
motor cortex
movement disorder
movement disorder, paroxysmal
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, FLAIR
MRI, hypointense signal foci on
MRI, punctate pattern
MRI, susceptibility weighted
multiple sclerosis, misdiagnosis
muscle biopsy
muscle spasm
muscle stiffness
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelination of nervous system
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, epilepsy
myoclonus, essential
myoclonus, sleep
myoclonus, stimulus sensitive
myopathy, mitochondrial
mysoline
negative
neuraminidase deficiency
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroendocrinology
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropsychiatry
next-generation sequencing
normal
nystagmus
nystagmus, rotary
ophthalmoplegia
optic atrophy
optic atrophy, hereditary
palatal myoclonus
paraparesis
paraparesis, spastic
paratonia
Parkinson disease
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pediatric neurology
penicillamine
pituitary, hormones of
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
pontocerebellar atrophy
prenatal
prion disease
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive pallidum atrophy
propranolol
protein 14-3-3, cerebrospinal fluid
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
Purkinje cell
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
rapidly progressing neurologic illness
real-time quaking-induced conversion
respiratory failure
retinal degeneration
review article
rigidity
Romberg's sign
Rosenthal fibers
SCN1A gene
screening
seizure
seizure, children
seizure, diagnosis of
seizure, drug resistance
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, prognosis in adults
seizure, stimulus sensitive
seizure, teenager
seizure, tonic-clonic
seizure, treatment of
sensorineural hearing loss
short stature
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
sodium channel dysfunction
sodium valproate
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
sphingolipodoses
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 16
spinocerebellar ataxia type 7
spinopontine atrophy, dominant
spongy degeneration of brain
startle myoclonus
startle reaction
status epilepticus
stereotypy
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
strokelike episodes
stuporous
stuttering
systemic illness
tachycardia
tandem gait, ataxic
Tay-Sachs disease
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
titubation
tone, muscle, increased
topiramate
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, leg
tremor, treatment of
trichopoliodystrophy
trinucleotide repeats
Unverricht-Lundborg disease
upgaze, paralysis of
visual acuity, decreased
visual loss
walking frame
walking, difficulty with
weakness
weakness, acute
weakness, focal
weight loss
wheelchair
white matter disease
wide based gait
Wolfram syndrome
workup
Showing articles 100 to 150 of 1975 << Previous Next >>

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

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

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

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

"Disappearing Infarct" Is Late-Onset MELAS
Ann Neurol 90:1001-1002, Landis,T.M.,et al, 2021

An Intramedullary Mass
BMJ 374:m1948, Yang, J.S.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

Clinical and Genetic Features in Patients with Reflex Bathing Epilepsy
Neurol 97:e577-e586, Accogli, A.,et al, 2021

Genetics of Cluster Headache Takes a Leap
Ann Neurol 90:191-192, Palotie, A., 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

Alzheimers Disease
Lancet 397:1577-1590, Scheltens, P.,et al, 2021

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Neurological Impairments in a Patient Returning from Cuba
JAMA Neurol 77:1570-1571, Serlin, Y.,et al, 2020

A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

Spasms and Myoclonus in a Young Woman with Hashimoto Thyroiditis
JAMA Neurol 77:650-651, Shen, D.,et al, 2020

A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
Neurol 94:994-999, Wildman, J.,et al, 2020

High Prevalence of Spinal Cord Cavernous Malformations in the Familial Cerebral Cavernous Malformations
AJNR 41:1126-1130, Mabray, M.C.,et al, 2020

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

MRI-EEG Correlation for Outcome Prediction in Postanoxic Myoclonus
Neurol 95:e335-e341, Beuchat, I.,et al, 2020

Generalized Myoclonus in COVID-19
Neurol 95:e767-e772, Rabano-Suarez, P.,et al, 2020

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

Tardive Diaphragmatic Tremor
Neurol 94:e656, Gupta, H.V., 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

Opsoclonus in Anti-Ma2 Brain-Stem Encephalitis
NEJM 383:e84, Sacks, C.A.,et al, 2020

Smoking Causes Fatal Subarachnoid Hemorrhage
Stroke 51:3018-3022, Rautalin, I.,et al, 2020

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

Recurrent Cerebral Ischemia During Pregnancies
Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020

Clinical Epidemiology of Familial Sarcoidosis
Respir Med 149:36-41, Terwiel, M. & Van Moorsel, C.H.M., 2019

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

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

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

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

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019



Showing articles 100 to 150 of 1975 << Previous Next >>