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abdominal x-ray
adverse drug reaction
affect, flat
agitation
akathisia
alcohol intolerance
alternating rapid movement
aluminum
anorexia
anti IgLON5
anticonvulsants
anticonvulsants, selection of
antithyroid antibodies
apnea
apraxia
arm swing, reduced
arm weakness
asterixis
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
autoantibodies
autonomic dysfunction
axonal spheroid
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bismuth
bradykinesia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
bulbar palsy
CAG repeats
carbon monoxide poisoning
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
celiac disease, adult
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortex
cerebral glucose metabolism
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, young adult
cherry red spot-myoclonus syndrome
chewing movements
children
choking
chorea
chorea, familial
choreoathetosis
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonus
coenzyme Q10 deficiency
cognition
color vision, impaired
coma
coma, episodic
confabulation
confusion
congenital infection, CNS
congenital paresis
cranial nerve palsies
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, differential diagnosis of
dementia, rapidly progressive
dementia, transmissible
dementia, treatment of
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones, loss of
diabetes mellitus
dialysis
dialysis dementia
diet
differential diagnosis
diplopia
doll's head maneuver
Dravet syndrome
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphasia
dyssynergia cerebellaris myoclonica
dystonia
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalopathy
encephalopathy, delayed
encephalopathy, Hashimoto's
enterovirus
enterovirus infection of CNS
epidemic
episodic disorders
episodic neurologic deficits
episodic unconsciousness
eye movement, disorders of
faciobrachial dystonic seizure
falling
familial
fasciculation
fatal familial insomnia
fatigue
fever
fine motor function, impaired
finger nose finger test
flaccid paralysis
gait disorder
gait, apraxic
gaze palsy, vertical
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
granular osmiphilic material
grasp reflex
gray matter
gyrus, abnormal
hallucination
hand-foot-mouth disease
handwriting
headache
hearing loss
heart block
heel-knee-shin test
hemimyoclonic jerks
hepatosplenomegaly
heralding manifestation
hoarseness
hyperreflexia
hypersomnia
hyperthyroidism
hypometric saccades
hyponatremia
hypophonia
hypothyroidism
hypotonia
imbalance
imbalance, postural
immunohistochemistry
immunotherapy
inattention
incontinence, fecal
incoordination
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
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
Lafora's disease
lateropulsion
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
leucine rich glioma inactivated 1 antibodies
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
limbic encephalitis
linear lesion
maculopathy
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningoencephalitis
mental retardation
MERRF syndrome
micrographia
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, diffusion weighted
MRI, false negative
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, pelvis
MRI, spinal cord
MRI, susceptibility weighted
mutism
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic ataxia
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, stimulus sensitive
myoclonus, treatment of
myoclonus-ataxia syndrome
myopathy
myopathy, mitochondrial
nausea and vomiting
neuroaxonal leukodystrophy
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neurotoxic
neurotoxin
next-generation sequencing
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, progressive external
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
optic atrophy, hereditary
optic neuropathy
oral ulcerations
ovarian tumor
palatal myoclonus
pancytopenia
paralysis, acute
paralysis, acute areflexic
paraparesis, spastic
parasomnia
Parkinsonism syndrome
paroxysmal neurologic deficits
pathologic reflex
personality change
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polyneuropathy
pontocerebellar atrophy
potassium channel antibodies
prion disease
prognosis
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
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
respiratory failure
retinopathy
review article
rigidity
Romberg's sign
rooting reflex
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
saccadic eye movements, abnormal
seizure
seizure, children
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
serologic testing
serologic testing of cerebrospinal fluid
short stature
sleep pathology and physiology
slow virus infection of CNS
slurred speech
snout reflex
sodium valproate
somnolence
spasticity
speech disorder
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 7
spongy degeneration of brain
square wave jerks
startle myoclonus
startle reaction
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
suicide
symmetric brain lesions
tandem gait, ataxic
tau protein
temporal lobe, lesion, bilateral
teratoma, ovarian
thalamus, lesion of-bilateral
thyroiditis
toxins, nervous system
transplacental virus infections
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
trinucleotide repeats
unconsciousness
unconsciousness, episodic
unconsciousness, transient
Unverricht-Lundborg disease
upgaze, paralysis of
urinary incontinence
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
vision, blurred
visual acuity, decreased
visual impairment
vocalizations
walking, difficulty with
weakness, acute
weakness, focal
weight loss
wheelchair
white matter disease
wide based gait
writing
Showing articles 1350 to 1400 of 3352 << Previous Next >>

Occurrence of Amyotrophic Lateral Sclerosis Among Gulf War Veterans
Neurol 61:742-749, Horner,R.D.,et al, 2003

Excess Incidence of ALS in Young Gulf War Veterans
Neurol 61:750-756, Haleyl,R.W., 2003

Multiple Sclerosis Presenting as Lower Motor Neuron Wasting and Weakness of the Distal Upper Extremity
Neurol 61:1303-1304, Chong,P.S.T.,et al, 2003

Primary Progressive Aphasia--A Language-Based Dementia
NEJM 349:1535-1542, Mesulam,M.-M., 2003

Paraneoplastic Syndromes Involving the Nervous System
NEJM 349:1543-1554, Darnell,R.B. &Posner,J.B., 2003

Neuropathological Findings in West Nile Virus Encephalitis: A Case Report
Ann Neurol 54:547-551, Agamanolis,D.P.,et al, 2003

Intrathecal Baclofen for Stiff-Person Syndrome: Life-Threatening Intermittent Catheter Leakage
Neurol 60:1976-1978, Bardutzky,J.,et al, 2003

A Longitudinal Study of Gait and Balance Dysfunction in Normal Older People
Arch Neurol 60:835-839, Baloh,R.W.,et al, 2003

Kennedy Disease
Arch Neurol 60:893-894, Paparounas,K.,et al, 2003

Challenging the Clinical Utility of the 14-3-3 Protein for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease
Arch Neurol 60:813-816,803, Geschwind,M.D.,et al, 2003

Clinicopath Conf., Giant-Cell Arteritis
NEJM 349:170-180, Case 21-2003, 2003

ALS Patients on TPPV
Neurol 61:135-137, Hayashi,H. &Oppenheimer,E.A., 2003

West Nile Virus Infection
Neurol 61:55-59, Jeha,L.E.,et al, 2003

Polymyositis Masquerading as Motor Neuron Disease
Arch Neurol 60:1001-1003, Ryan,A.,et al, 2003

Clinical Manifestations of Sarin Nerve Gas Exposure
JAMA 290:659-662, Lee,E.C., 2003

Neurologic Manifestations and Outcome of West Nile Virus Infection
JAMA 290:511-515,524,558, Sejvar,J.J.,et al, 2003

Biochemical And Clinical Aspects of Methotrexate Neurotoxicity
Chemotherapy 49:92-104, Vezmar,S.,et al, 2003

14-3-3 Protein in the CSF of Patients with Rapidly Progressive Dementia
Neurol 61:354-357, Huang,N.,et al, 2003

Prevalence and Clinical Features of HTLV Neurologic Disease in the HTLV Outcomes Study
Neurol 61:1588-1594, Orland,J.R.,et al, 2003

The Use of Mitoxantrone (Novantrone) for the Treatment of Multiple Sclerosis
Neurol 61:1332-1338, Goodin,D.S.,et al, 2003

Does This Patient Have Parkinson Disease?
JAMA 289:347-353, Rao,G.,et al, 2003

An Unconsious Girl with Sickle-Cell Disease
Lancet 361:136, van Mierlo,T.D.,et al, 2003

Detection of Pathologic Prion Protein in the Olfactory Epithelium in Sporadic Creutzfeldt-Jakob Disease
NEJM 348:711-719,681, Zanusso,G.,et al, 2003

Clinicopath Conf., Chronic Inflammatory Demyelinating Polyneuropathy
NEJM 348:735-743, Case 6-2003, 2003

Prognosis in Amyotrophic Lateral Sclerosis
Neurol 60:813-819, del Aguila,M.A.,et al, 2003

Cortical Myoclonus During Lithium Exposure
Arch Neurol 60:401-404, Caviness,J.N.,&Evidente,V.G.H., 2003

Clinical Features and Natural Histry of Progressive Supranuclear Palsy, A Clinical Cohort Study
Neurol 60:910-916, Nath,W.,et al, 2003

Diffusion-Weighted Imaging Discriminates Progressive Supranuclear Palsy from PD, But Not From the Parkinson Variant of Multiple System Atrophy
Neurol 60:922-927, Seppi,K.,et al, 2003

Early or Late Appearance of "Dropped Head Syndrome" in Amyotropic Lateral Sclerosis
JNNP 74:683-686, Gourie-Devi,M.,et al, 2003

The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
Neurol 60:1246-1251,1230, Poppe,M.,et al, 2003

Cerebellar Ataxia and Coenzyme Q10 Deficiency
Neurol 60:1206-1208, Lamperti,C.,et al, 2003

Clinical Relevance of Atrial Fibrillation/Flutter, Stroke, Pacemaker Implant, and Heart Failure in Emery-Dreifuss Muscular Dystrophy
Stroke 34:901-908, Boriani,G.,et al, 2003

Clinicopath Conf., Brain Abscess Due to Infection with Streptococcus milleri and Haemophilus aphrophilus
NEJM 348:2125-2132, Case 16:2003, 2003

Prevalence of Antigliadin Antibodies in Ataxia Patients
Neurol 60:1674-1675,1566, Abele,M.,et al, 2003

Asymmetric Flaccid Paralysis: A Neuromuscular Presentation of West Nile Virus Infection
Ann Neurol 53:703-710,691, Li,J.,et al, 2003

Neurologic Manifestations of Vitamin B12 Deficiency
NEJM 348:2208, Scherer,K., 2003

Pernicious Anemia with Neuropsychiatric Dysfunction in a Patient with Sickle Cell Anemia Treated with Folate Supplementation
NEJM 348:2204-2207, Dhar,M.,et al, 2003

Progressive Multifocal Leukoencephalopathy: Analysis of Lesion Development With Diffusion-Weighted MRI
Neuroradiol 45:717-721, Mader,I.,et al, 2003

Spinal Cord Biopsy: A Review of 38 Cases
Neurosurgery 52:806-816, Cohen-Gadol,A.A.,et al, 2003

Mitoxantrone in Progressive Multiple Sclerosis: A Placebo-Controlled, Double-Blind, Randomised, Multicentre Trial
Lancet 360:2018-2025, Hartung,H.,et al, 2002

Jaw Drop in Kennedy's Disease
Neurol 59:1471-1472, Sumner,C.J. &Fischbeck,K.H., 2002

Clinicopath Conf., Acute Disseminated Encephalomyelitis
NEJM 347:1433-1440, Case 34-2002, 2002

A Reversible Paralysis
Lancet 360:1160, Maury,E.,et al, 2002

Abnormality of Gait as a Predictor of Non-Alzheimer's Dementia
NEJM 347:1761-1768, Verghese,J.,et al, 2002

Difference in Distribution of Muscle Weakness Between Myasthenia Gravis and the Lambert-Eaton Myasthenic Syndrome
JNNP 73:766-768, Wirtz,P.W.,et al, 2002

Paresis Acquired in the Intensive Care Unit
JAMA 288:2859-2867, De Jonghe,B.,et al, 2002

Lacunar Stroke Is the Major Cause of Progressive Motor Deficits
Stroke 33:1510-1516,1443, Steinke,W. &Ley,S.C., 2002

Mimic Syndromes in Sporadic Cases of Progressive Spinal Muscular Atrophy
Neurol 58:1593-1596, Visser,J.,et al, 2002

Progressive Multifocal Leukoencephalopathy
Neurol 58:1825, Henderson,R.D.,et al, 2002

Nanging
Lancet 360:384, Ng, J. &Frith, R., 2002



Showing articles 1350 to 1400 of 3352 << Previous Next >>