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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
celiac disease, adult
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
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
cingulate gyrus
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
diet
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, acute
encephalopathy, Hashimoto's
encephalopathy, metabolic
encephalopathy, progressive
enterovirus
enterovirus infection of CNS
epidemic
episodic disorders
episodic neurologic deficits
episodic unconsciousness
exome sequencing
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
gluten ataxia
gluten sensitivity
gluten-free diet
glycine receptor antibodies
granular osmiphilic material
gray matter
growth retardation
hallucination
hallucination, visual
hand-foot-mouth disease
handwriting
headache
hearing loss
heart block
hemianopia, homonymous
hemimyoclonic jerks
hemiparesis
hepatosplenomegaly
heralding manifestation
HHH syndrome
hoarseness
hyperammonemic encephalopathy
hyperreflexia
hypersomnia
hyperthyroidism
hypoglycorrhachia
hypometric saccades
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
insular cortex
insular cortex, lesion
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 ataxia
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, multifocal
myoclonus, segmental
myoclonus, stimulus sensitive
myoclonus, treatment of
myoclonus-ataxia syndrome
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
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 150 to 200 of 5574 << Previous Next >>

The Acquired Metabolic Disorders of the Nervous System, Hashimoto Encephalopathy (Steroid Responsive Encephalopathy Syndrome)
Adams & Victors Principles of Neurology Chp 40, pg 1155, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Cocaine
Adams & Victors Principles of Neurology Chp 43, pg 1213, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Encephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 748, Ropper, A.H.,et al, 2014

Limbic Encephalitis Associated with Anti-Voltage-Gated Potassium Channel Complex Antibodies Mimicking Creutzfeldt-Jakob Disease
JAMA Neurol 71:79-82, Yoo,J.Y. & Hirsch, L.J., 2014

Clinical Reasoning: A 30-year-old Woman with Recurrent Seizures and a Cerebral Lesion Progressing over 2 Decades
Neurol 82:e56-e58, Tonder, M.,et al, 2014

Hyperintense Cortical Signal on Magnetic Resonance Imaging Reflects Focal Leukocortical Encephalitis and Seizure Risk in Progressive Multifocal Leukoencephalopathy
Ann Neurol 75:659-669, Khoury, M.N.,et al, 2014

Effect of Rituximab in Patients with Leucine-Rich, Glioma-Inactivated 1 Antibody-Associated Encephalopathy
JAMA Neurol 71:896-900, Irani, S.R.,et al, 2014

Clinicopathologic Conference, Chronic Meningoencephalitis Consistent with Rasmussens Encephalitis
NEJM 371:1737-1746, Case 34-2014, 2014

A Case of Early-Onset Rapidly Progressive Dementia
JAMA Neurol 71:1445-1449, Cachia, D.,et al, 2014

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

Psychosis in an Adolescent Girl: A Common Manifestation in Niemann-Pick Type C Disease
Child Adolesc Pych Ment Health 8:20, Wouters,S.,et al, 2014

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Misdiagnosis of Treatable Stroke Mimic: The Case for HIV Screening in Practice Guidelines
Neurohosp 3:125-130, Finelli, P.F., 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

A 62-Yeal-Old Man with Fluctuating Neurological Deficits and Skin Lesions
JAMA Neurol 70:120-124, Konikkara, J.,et al, 2013

Aspergillus Meningitis: A Rare Clinical Manifestation of Central Nervous System Aspergillosis
J Infect 66:218-238, Antinori, S.,et al, 2013

Comorbidity of Migraine in Children Presenting with Epilepsy to a Tertiary Care Center
Neurol 79:468-473, Kelly, S.A.,et al, 2012

Hashimoto Encephalopathy
Neurol 78:e134, Afshari, M.,et al, 2012

Clinical Reasoning: Encephalopathy in a 10-year-old boy
Neurol 79:e12-e18, Rodan, L. & Tein, I., 2012

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

Rapidly Progressive Alzheimer Disease
Arch Neurol 68:1124-1130, Schmidt, C.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

Clinicopathologic Conference, Limbic Encephaitis with Antibodies to Leucine - Rich Glioma - inactivated 1 (LGI 1).
NEJM 365:1825-1833, Case 34-2011, 2011

The Evaluation of Rapidly Progressive Dementia
The Neurologist 17:67-74, Rosenbloom,M.H. &Atri,A., 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK
JNNP 82:646-651, Heath, C.A.,et al, 2011

A Case of Hashimoto Encephalopathy Clinical Manifestation, Imaging, Pathology, Treatment, and Prognosis
The Neurologist 17:141-143, Zhao, W.,et al, 2011

Transition to Adult Care for Children with Chronic Neurological Disorders
Ann Neurol 69:437-444, Camfiled, P. & Camfield, C., 2011

Autoimmune Encephalopathy
Semin Neurol 31:144-157, Flanagan, E.,et al, 2011

Hashimotos Encephalopathy
Radiol Case Reports 6:445-449, Ramalho, J. & Castillo, M., 2011

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

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

Neurologic Manifestations of Localized Scleroderma: A Case Report and Literature Review
Neurol 71:1538-1545, Kister,I.,et al, 2008

Intravascular Large B-Cell Lymphoma
UptoDate, October, Freedman,A.S. &Aster,J.C., 2008

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
Brain 131:2553-2563, Saiz,A., et al, 2008

Acute Intermittent Porphyria Presenting as Acute Pancreatitis and Posterior Reversible Encephalopathy Syndrome
Acta Neurol Taiwan 17:177-183, Shen, F.,et al, 2008

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

Tiagabine-Induced Myoclonic Status Epilepticus in a Nonepileptic Patient
Neurol 68:310, Vollmar,C. &Noachtar,S., 2007

Rapidly Fatal Acanthamoeba Encephalitis and Treatment of Cryoglobulinemia
Emerg Infect Dis 13:469-471, Meersseman, W.,et al, 2007

Paraneoplastic Vasculitis of Central Nervous System Presenting as Recurrent Cryptogenic Stroke
Int J Clin Oncol 12:155-159, Taccone,F.S.,et al, 2007

Adult Onset Subacute Sclerosing Panencephalitis: Clinical Profile of 39 Patients From a Tertiary Care Centre
JNNP 77:630-633, Prashanth,L.K.,et al, 2006

Seizures and Their Outcome in Progressive Multifocal Leukoencephalopathy
Neurol 66:262-264, Lima,M.A.,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

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Clinicopath Conf., MELAS Syndrome
NEJM 353:2271-2280, Case 36-2005, 2005

Neurologic Manifestations in Welders with Pallidal MRI T1 Hyperintensity
Neurol 64:2033-2039,2001, Josephs,K.A.,et al, 2005

Angiography-Negative Primary Central Nervous System Vasculitis in Children
Arthritis Rheum 52:2159-2167, Benseler, S.M.,et al, 2005



Showing articles 150 to 200 of 5574 << Previous Next >>