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Differential
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abdominal x-ray
adverse drug reaction
affect, flat
agitation
akathisia
akinetic mute
aluminum
Alzheimer's disease
Alzheimer's disease, early onset
Alzheimer's disease, familial
ammonia
amyloid angiopathy, cerebral
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
anorexia
anti IgLON5
antibiotics
antibodies to measles
anticonvulsants
anticonvulsants, selection of
antithyroid antibodies
aphasia
aphasia, progressive
apnea
apraxia
arm swing, reduced
arm weakness
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
bismuth
Borrelia miyamotoi infection
bradykinesia
brain atrophy
brain biopsy
brain biopsy, false negative
brainstem, atrophy
brainstem, lesion of
bulbar palsy
cachexia
CAG repeats
calcification, intracranial
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
cataracts
central nervous system, infection of
cerebellar atrophy, primary
cerebellar degeneration
cerebellar plaques, amyloid
cerebral cortex
cerebral cortical atrophy
cerebral glucose metabolism
cerebral vasculature
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
cherry red spot-myoclonus syndrome
chewing movements
children
chorea
chorea, familial
choreoathetosis
chromosomal abnormality
chronic progressive external ophthalmoplegia
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10 deficiency
cognition
color vision, impaired
coma
coma, episodic
coma, sudden onset
confabulation
confusion
congenital infection, CNS
congenital paresis
cortical blindness
cranial nerve palsies
Creutzfeldt-Jakob disease, genetic
crying, pathologic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
delusion
dementia
dementia, differential diagnosis of
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
dementia, treatment of
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
developmental milestones, loss of
diabetes mellitus
diagnostic criteria
dialysis
dialysis dementia
differential diagnosis
diplopia
doll's head maneuver
downward deviation of eyes
Dravet syndrome
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphasia
dyssynergia cerebellaris myoclonica
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, triphasic delta waves
electroencephalogram, video monitoring with
electromyogram
electron microscopy
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalomyelitis, autoimmune
encephalopathy
encephalopathy, Hashimoto's
encephalopathy, metabolic
encephalopathy, progressive
enterovirus
enterovirus infection of CNS
epidemic
episodic disorders
episodic neurologic deficits
episodic unconsciousness
extralimbic encephalitis
eye movement, disorders of
eye movement, painful
eye, pain in
faciobrachial dystonic seizure
failure to thrive
falling
familial
fasciculation
fatal familial insomnia
fatigue
fever
fine motor function, impaired
finger nose finger test
flaccid paralysis
floaters
gait disorder
gamma amino butyric acid receptor antibody
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
glutamic acid decarboxylase, antibody
glycine receptor antibodies
granular osmiphilic material
gray matter
growth retardation
hallucination
hallucination, visual
hand-foot-mouth disease
handwriting
headache
hearing loss
heart block
hemimyoclonic jerks
hemiparesis
hepatosplenomegaly
heralding manifestation
hoarseness
hyperammonemic encephalopathy
hyperreflexia
hypersomnia
hyperthyroidism
hypoglycorrhachia
hyponatremia
hypophonia
hypothermia
hypothyroidism
hypotonia
imbalance
imbalance, postural
immunohistochemistry
immunosuppression
immunotherapy
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intracytopasmic
incoordination
infection
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracranial pressure, increased
intrauterine infection
intrauterine infection, viral of CNS
introverted
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
juvenile paresis
Kearns-Sayre syndrome
lactic acidemia
Lafora body
Lafora's disease
lateropulsion
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
lethargy
leucine rich glioma inactivated 1 antibodies
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
life expectancy
limbic encephalitis
linear lesion
maculopathy
mediastinum, mass of
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, neutrophilic
meningitis, treatment of
meningoencephalitis
mental retardation
mental status, abnormal
MERRF syndrome
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoparesis
mortality
motor cortex
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, negative
MRI, pelvis
MRI, spinal cord
MRI, sulcal hyperintensity
MRI, susceptibility weighted
multinucleated giant cell
muscle biopsy
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelination of nervous system
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, segmental
myoclonus, stimulus sensitive
myopathy
myopathy, mitochondrial
nausea and vomiting
neck stiffness
negative
neuroendocrinology
neurologic complications
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neurotoxic
neurotoxin
neutropenia
New England
next-generation sequencing
nicotine
NMDA antagonists
normal
ophthalmoplegia
ophthalmoplegia, progressive external
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
optic atrophy, hereditary
optic neuropathy
oral ulcerations
ornithine transcarbamylase deficiency
ovarian tumor
palatal myoclonus
pancytopenia
papilledema
paralysis, acute
paralysis, acute areflexic
paraparesis, spastic
parasomnia
paratonia
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
persistent vegetative state
personality change
phonophobia
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
pontocerebellar atrophy
potassium channel antibodies
prion disease
prognosis
progressive encephalomyelitis with rigidity syndrome
progressive infantile poliodystrophy
progressive myoclonic epilepsy
progressive neurologic disorder
progressive pallidum atrophy
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
pursuit eye movements, abnormal
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
Ramsay Hunt syndrome
rapidly progressing neurologic illness
real-time quaking-induced conversion
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
respiratory failure
retinopathy
retro-orbital pain
reversible neurologic disorder
review article
rigidity
Romberg's sign
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
saccadic eye movements, abnormal
seizure
seizure, children
seizure, drug resistance
seizure, focal
seizure, intractable
seizure, paradoxical
seizure, teenager
seizure, treatment of
sensorineural hearing loss
serologic testing
serologic testing of cerebrospinal fluid
short stature
skin, biopsy
sleep pathology and physiology
slow virus infection of CNS
slurred speech
somnolence
sonophobia
speech disorder
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
spirochete infection
spongy degeneration of brain
square wave jerks
stare
staring spells
startle myoclonus
startle reaction
status epilepticus
status epilepticus, intractable
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
strokelike episodes
stuporous
stuttering
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
sudden death
symmetric brain lesions
systemic illness
tandem gait, ataxic
tau protein
temporal lobe, lesion, bilateral
temporalis muscle wasting
teratoma, ovarian
thalamus, lesion of-bilateral
thymoma
thyroiditis
toxins, nervous system
transient neurologic deficit
transplacental virus infections
treatment of neurologic disorder
tremor
tremor, postural
tremulousness
trichopoliodystrophy
uncal herniation
unconsciousness
unconsciousness, episodic
unconsciousness, transient
Unverricht-Lundborg disease
upgaze, paralysis of
urea-cycle enzymopathies
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
vision, blurred
vision, blurred, monocular
visual loss
visuospatial disturbance
vocalizations
walking, difficulty with
weakness
weakness, acute
weakness, focal
weakness, generalized
weight loss
wheelchair
white matter disease
white matter disease, subcortical
wide based gait
word-finding difficulty
Showing articles 0 to 50 of 5415 Next >>

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

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

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

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

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

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

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016

A 27-Year Old Man with Rapidly Progressive Coma
Neurol 85:e74-e78, Wong,J.M.,et al, 2015

Lafora Periodic Acid-Schiff Inclusion Bodies
Neurol 85:e130-e131, de Assis Franco, I.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, Dialysis Encephalopathy (Dialysis Dementia)
Adams & Victors Principles of Neurology Chp 40, pg 1146, Ropper, A.H.,et al, 2014

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
Adams & Victors Principles of Neurology, Chp 33, pg 769, Ropper, A.H.,et al, 2014

Mystery Case: A Young Boy with Myoclonic Jerks
Neurol 81:e130-e134, Musleh, C.,et al, 2013

Progressive Gait Deterioration in Adolescents with Dravet Syndrome
Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012

Progressive Encephalomyelitis with Rigidity and Myoclonus Gycine and NMDA Receptor Antibodies
Neurol 77:439-443,414, Turner, M.R.,et al, 2011

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Voltage-Gated Potassium Channel Autoimmunity Mimicking Creutzfeldt-Jakob Disease
Arch Neurol 65:1341-1346, Geschwind,M.D.,et al, 2008

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
Arch Neurol 62:737-742, Barragan-Campos,H.M.,et al, 2005

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Nicotine-Sensitive Paresis
Neurol 42:382-388, Yokota,T.,et al, 1992

Aluminium Intoxication in Undialysed Adults with Chronic Renal Failure
JNNP 55:697-700, Russo,L.S.,et al, 1992

Clinicopath Conf
Cerebral Amyloid Angiopathy, Case 27-1991, NEJM 325:42-54991., , 1991

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Mitochondrial Myopathies
Ann Neurol 17:521-538, DiMauro,S.,et al, 1985

Dialysis Encephalopathy, Clinical, Electroencephalographic & Interventional Aspects
Medicine 62:129-141, O'Hare,J.A., 1983

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981



Showing articles 0 to 50 of 5415 Next >>