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Differential
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advances in neurology
affect, flat
agitation
akathisia
akinetic mute
amyloid
amyloid angiopathy, cerebral
amyloid beta protein
amyloid plaques
angiitis, isolated of CNS
animal exposure
anorexia
anxiety
apraxia
apraxia, dressing
areflexia
arm weakness
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
autoantibodies
autoimmune disease
autonomic dysfunction
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
blood transfusion
bovine spongiform encephalopathy
bradykinesia
bradyphrenia
brain biopsy
burning paresthesia
CAT scan
CAT scan, emission, abnormal
CAT scan, false negative
caudate nucleus, lesion of, bilateral
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar plaques, amyloid
cerebral cortex
cerebral cortical atrophy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, enzymes in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, misdiagnosis
chewing movements
chorea
choreoathetosis
chromosomal abnormality
chromosome 20
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
coma
concentration, impaired
confabulation
confusion
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, diagnostic evaluation of
dementia, familial
dementia, presenile
dementia, prevention of
dementia, rapidly progressive
dementia, screening for
dementia, thalamic
dementia, transmissible
depression
dexterity, impaired
diagnostic criteria
diet
differential diagnosis
diplopia
disorientation
driving
dysarthria
dysdiadochokinesia
dysmetria
dyspraxia
echolalia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electron microscopy
electrophoretic pattern, CSF
encephalitis, viral
encephalopathy
encephalopathy, Hashimoto's
encephalopathy, metabolic
endoscopy
enolase
epidemic
epidemiology of neurology
eye movement, disorders of
falling
false negative
familial
fasciculation
fatal familial insomnia
fatal sporadic insomnia
fatigue
finger nose finger test
frontal lobe, anatomy and physiology
gait disorder
gait, apraxic
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
grasp reflex
grasping
gray matter
growth hormone
gyrus, abnormal
hallucination
handwriting
head turning
hemianopia, homonymous
heralding manifestation
hockey stick sign
hyperhidrosis
hypertension
hyperthermia
hypophonia
hyporeflexia
iatrogenic neurologic disorders
imbalance
immunohistochemistry
inattention
incidence
incoordination
incubation period
insight, loss
insomnia
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, multiple
intracerebral hemorrhage, recurrent
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, Heidenhain variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, unilateral
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
kuru
laminar necrosis, cortical
laughing, pathologic
life expectancy
linear lesion
masked facies
memory, defect of recent
memory, impairment of
mimics
Mini Mental Status Examination
misdiagnosis
molecular genetics
monoparesis
mortality
motor cortex
movement disorder
movement disorder, extrapyramidal
MRI
MRI pattern
MRI, abnormal
MRI, diffusion weighted
MRI, diffusion weighted, pattern
MRI, false negative
MRI, FLAIR
MRI, high signal intensity of basal ganglia
MRI, indications for
MRI, negative
MRI, serial
MRI, spinal cord
MRI, susceptibility weighted
multiple sclerosis
multiple system atrophy
mutism
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, stimulus sensitive
nasal brushings
neurofibrillary degeneration
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuron specific enolase
neuropathology
neuropathology, brain
next-generation sequencing
nystagmus
occipital cortex
occipital lobe, lesion of
occupational neurologic disorders
old age, neurology of
olfactory biopsy
olfactory bulb
olfactory cortex
olfactory mucosa
olfactory pathway
olfactory tract
pain
pain, leg
paresthesias
parietal lobe, lesion of
parietal lobe, syndromes of
Parkinson disease
Parkinsonism syndrome
pathognomonic
pathologic reflex
perseveration
personality change
pituitary, hormones of
polymerase chain reaction
preclinical
prevention of neurologic disorders
prion disease
prion protein gene
procainamide
prognosis
progressive neurologic disorder
progressive supranuclear palsy
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
protein 14-3-3, cerebrospinal fluid, false positive
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
pulvinar sign
pursuit eye movements, abnormal
pyramidal tract dysfunction
rapidly progressing neurologic illness
real-time quaking-induced conversion
release phenomena
remote effect of cancer on the nervous system
review article
risk factors
Romberg's sign
rooting reflex
roving eye movements
saccadic eye movements, abnormal
sarcoidosis, CNS
scrapie
seizure
senile plaques
sensory symptoms
single photon emission computed tomography
sleep pathology and physiology
snout reflex
somnolence
spinal cord
spinal cord, lesion of
spongy degeneration of brain
square wave jerks
startle myoclonus
startle reaction
striatum, lesion of
striatum, lesion of, bilateral
stuporous
symmetric brain lesions
tachycardia
tandem gait, ataxic
tau protein
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
tonsil biopsy
toxic encephalopathy
treatment of neurologic disorder
urinary incontinence
viral infection, CNS
virus, slow
vision, blurred
visual loss
visual loss, progressive
walking, difficulty with
weakness, acute
weakness, focal
weight loss
West Nile fever
Western immunoblot test
wheelchair
wide based gait
Showing articles 150 to 200 of 2705 << Previous Next >>

The Genetics of Alzheimer Disease, Current Status and Future Prospects
Arch Neurol 55:294-296, Blacker,D.&Tanzi,R.E., 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Exploring the Etiology of Alzheimer Disease Using Molecular Genetics
JAMA 277:825-831, Lendon,C.L.,et al, 1997

Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997

The 14-3-3 Brain Protein and Transmissible Spongiform Encephalopathy
NEJM 336:873-875, Moussavian,M.,et al, 1997

Detection of 14-3-3 Protein in the CSF of Genetic Creutzfeldt-Jakob Disease
Neurol 49:593-595, Rosemann,H.,et al, 1997

Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996

Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation
Stroke 27:1719-1720, Brey,R.L.&Coull,B.M., 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Risk Factors for Creutzfeldt-Jakob Disease:A Reanalysis of Case-Control Studies
Neurol 46:1287-1291, Wientjens,D.P.W.M.,et al, 1996

Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
JNNP 61:204-205, Kimber,T.,et al, 1996

Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation
Neurol 46:758-761, Chapman,J.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
Stroke 26:885-890, Simioni,P.,et al, 1995

Down's Syndrome and the Links with Alzheimer's Disease
JNNP 59:111-114, Holland,A.J.&Oliver,C., 1995

Familial Alzheimer's Disease
Ann Neurol 36:335-336, Bird,T.D., 1994

The Mutations at nt 8993 of Mitochondrial DNA is a Common Cause of Leigh's Syndrome
Ann Neurol 34:827-834, Santorelli,F.M.,et al, 1993

Choroido-Cerebral Calcification Syndrome with Retardation
Neurol 43:2387-2389, Singh,B.,et al, 1993

Genetic Susceptibility in Familial Multiple Sclerosis not Linked to the Myelin Basic Protein Gene
Lancet 341:1179-1181, Rose,J.,et al, 1993

Molecular Genetic Characterization of an X-Linked Form of Leigh's Syndrome
Ann Neurol 33:652-655, Matthews,P.M.,et al, 1993

Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
Lancet 340:987-991, Tienari,P.J.,et al, 1992

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
Brain 115:979-989, Harding,A.E.,et al, 1992

Use of CT, MRI, & Localized 1H MR Spectroscopy in Canavan's Disease:A Case Report
Ann Neurol 30:106-110, Marks,H.G.,et al, 1991

Genetic Predisposition to Iatrogenic Creutzfeldt-Jakob Disease
Lancet 337:1441-1442, Collinge,J.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Cesarean Section Before Onset of Labor & Motor Function in Infants with Meningomyelocele Diag Antenatally
NEJM 324:662-666, 6901991., Luthy,D.S.,et al, 1991

Familial Creutzfeldt-Jakob Disease without Periodic EEG Activity
Ann Neurol 28:585-588, Tietjen,G.E.&Drury,I., 1990

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Leigh Disease (Subacute Necrotizing Encephalomyelopathy) :CT & MR in Five Cases
J Comput Assist Tomogr 12:40-44, Geyer,C.A.,et al, 1988

Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
Neurol 38:938-942, Schapiro,M.B.,et al, 1988

Creutzfeldt-Jakob Disease Following Pituitary-Derived Human Growth Hormone Therapy:A New American Case
Neurol 38:1131-1133, Marzewski,D.J.,et al, 1988

Familial Alzheimer's Disease with Myoclonus and'Spongy Change'
Arch Neurol 45:1097-1100, Duffy,P.,et al, 1988

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

Abnormal Proteins in the Cerebrospinal Fluid of Patients with Creutzfeldt-Jakob Disease
NEJM 315:279-283, Harrington,M.G.,et al, 1986

Cerebrospinal Fluid Findings in Healthy Siblings of Multiple Sclerosis Patients
Neurol 36:727-729, Duquette,P.&Charest,L., 1986

Alzheimer's Disease
NEJM 314:964-973, Katzman,R., 1986

Cerebral Haemorrhagic Infarction in Young Patients with Hereditary Protein C Deficiency
BMJ 290:350-352, Wintzen,A.R.,et al, 1985

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983



Showing articles 150 to 200 of 2705 << Previous Next >>