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Differential
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alcohol
alcohol, neurologic complications with
altered states of consciousness
amnesic stroke
angiography, cerebral
angiography, cerebral, false negative
angiography, cerebral, negative
anorexia
antibodies to measles
apraxia
areflexia
aspirin
astasia abasia
astrocytoma
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic hemiparesis
audiogram
automobile accidents
autonomic dysfunction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
brain biopsy
brain biopsy, stereotaxic
CAT scan
CAT scan, abnormal
central artery of Percheron
cerebellar atrophy, secondary
cerebellar infarction
cerebral venous thrombosis, deep
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, women
children
chorea
choreoathetosis
chorioretinitis
Clinical Pathologic Conference(C.P.C.)
complications
confusion
confusional state, acute
corpus callosum
corpus callosum, lesion of
deafness
deafness, bilateral
deafness, sudden
deep gray nuclei
dementia
dementia, rapidly progressive
dementia, thalamic
dementia, treatment of
demyelinating disease
dentate nuclei
depression
differential diagnosis
diplopia
drowsiness
dysarthria
dysdiadochokinesia
dysmetria
efficacy
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
encephalitis
encephalopathy
epidemiology of neurology
eye movement, disorders of
facial pain
familial
fatal familial insomnia
fatigue
finger nose finger test
fistula, arterio-venous
fistula, arterio-venous, dural
fundus, abnormality of
funduscopic exam
gadolinium
gait disorder
gait, apraxic
gastrectomy, neurologic complications following
gastritis
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
genetic neurologic disorders
genetic testing
glioma
gliomatosis cerebri
gray matter
hammertoes
handwriting
headache
hearing loss
hearing loss, bilateral
hearing loss, sudden, bilateral
hemiataxia
hemiballismus
hemiparesis
hemisensory loss
hemorrhage, thalamic
hydrocephalus
hyperhidrosis
hyperphagia
hypersomnia
hypertension
hyperthermia
imbalance
immunohistochemistry
immunosuppressive agents
inattention
incidence
inclusion bodies
inclusion bodies, eosinophilic intranuclear
incoordination
insomnia
intellectual deterioration
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
lacunar infarction
L-dopa
lenticular nucleus, lesion of, bilateral
level of consciousness, decreased
malformation, vascular
malformation, vascular, dural
mammillary bodies
memory, defect of recent
memory, impairment of
mental status, abnormal
microangiopathy, brain
microangiopathy, retina
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
mortality
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, high signal foci on
multiple sclerosis
multiple sclerosis, misdiagnosis
muscle biopsy
myoclonic jerks
myoclonus
neoplasm, primary intracranial
neoplasm, primary of CNS
neurologic disease, diagnoses of
neurologic signs
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathology, brain
next-generation sequencing
non-dominant hemisphere
nutritional deficiency
nystagmus
nystagmus, gaze-evoked
ocular motility, disorders of
ophthalmoplegia
pain
pain, hemibody
paresthesias
Parkinson disease
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
periaqueductal lesion
personality change
pleocytosis of cerebrospinal fluid
POLG1 gene
position sensation
position sensation, abnormal
postural abnormality
pregnancy, neurologic complications in
prion disease
prognosis
progressive neurologic disorder
pseudochorea
psychiatric disorder
psychiatric problems in neurologic disorders
ptosis
ptosis, bilateral
pursuit eye movements, abnormal
pyramidal tract dysfunction
rapidly progressing neurologic illness
real-time quaking-induced conversion
retinal artery occlusion
retinal branch artery occlusion
retinal infarction
retinopathy
retropulsion
review article
Romberg's sign
rubeola virus
saccadic eye movements, abnormal
seizure
sensorineural hearing loss
sensory loss
skew deviation
sleep pathology and physiology
square wave jerks
steroid therapy, CNS treatment and complications with
stimulation, deep brain
straight sinus
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subthalamic nucleus
subthalamic nucleus deep brain stimulation
superior colliculus
Susac's syndrome
symmetric brain lesions
syncope
tachycardia
tau protein
thalamic ataxia syndrome
thalamic syndrome
thalamic tumors
thalamic tumors, bilateral
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve palsy, bilateral
third ventricle, wall
tinnitus
treatment of neurologic disorder
tremor
tremor, thalamic
tremor, thalamic stimulation for suppression of
tremor, treatment of
unconsciousness
urinary incontinence
vasculopathy
vertigo
viral infection
viral infection, CNS
vision, blurred
visual field defect
visual loss
visuospatial disturbance
walking, difficulty with
weight loss
Wernicke's encephalopathy
wheelchair
white matter disease
wide based gait
Showing articles 950 to 1000 of 1688 << Previous Next >>

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

Ipsilat Hemiplegia Caused by Right Inter Capsule & Thalamic Hemorr:Ipsilat Inner of Motor/Sensory Sys by MRI, MEP, & SEP
Neurol 46:1146-1149, Hosokawa,S.,et al, 1996

The Syndrome of Posterior Choroidal Artery Territory Infarction
Ann Neurol 39:779-788, Neau,J.&Bogousslavsky,J., 1996

Delayed-Onset Cerebellar Syndrome
Arch Neurol 53:450-454, Louis,E.D.,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

Thalamic Haemorrhage
Brain 119:1873-1886, Chung,C-S.,et al, 1996

Deep Brain Stimulation for Essential Tremor
Neurol 46:1150-1153, Hubble,J.P.,et al, 1996

An 85-Year-Old Woman with a History of Falls
JAMA 276:59-66, Lipsitz,L.A., 1996

A Woman with a Relapsing Psychosis Who Got Better with Prednisone
Lancet 347:1288, Cohen,L.,et al, 1996

BSE Linked to New Variant of CJD in Humans
BMJ 312:795, 791, 843, 85496., , 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

MR Findings in Listerial Rhombencephalitis
AJNR 17:593-596, Alper,G.,et al, 1996

Lyme Neuroborreliosis Disguised as Normal Pressure Hydrocephalus
Neurol 46:1743-1745, Danek,A.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 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

Falls and Urinary Incontinence in a 66-Year Old Woman
Lancet 347:1738, Yusuf,S.W.,et al, 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

MR Findings in Tay-Sachs Disease
J Comput Assist Tomogr 20:551-555, Mugikura,S.,et al, 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

Clinical Correlates of White Matter Findings on Cranial Magnetic Resonance Imaging of 3301 Elderly People
Stroke 27:1274-1282, 12691996., Longstreth,W.T.,et al, 1996

Treatment of Advanced Parkinson's Disease by Posterior GPi Pallidotomy:1-Year Results of a Pilot Study
Ann Neurol 40:355-366, 3411996., Baron,M.S.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Ataxic Hemiparesis and Hemiageusia from an Isolated Post-Traumatic Midbrain Lesion
Neurol 47:1348-1349, Johnson,T.M., 1996

Thalamic Tremor:Case Reports and Implications of the Tremor-Generating Mechanism
Neurol 46:75-79, Miwa,H.,et al, 1996

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

A Man with Weight Loss, Ataxia, and Confusion for 3 Months
Lancet 347:448, Beversdorf,D.,et al, 1996

Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
Ann Neurol 39:100-106, Elliott,M.A.,et al, 1996

Mycoplasma Pneumoniae Infection Associated with an Acute Brainstem Syndrome
Acta Neurol Scand 93:203-206, OBrien, P.M.,et al, 1996

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Neurological and Functional Outcome in Patients with Supratentorial Hemorrhages:A Prospective Study
Stroke 26:2249-2253, Lampl,Y.,et al, 1995

Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
Ann Neurol 48:684-687, Tuite,P.J.,et al, 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Leukoencephalopathy with Swelling & A Discrepantly Mild Clinical Course in Eight Children
Ann Neurol 37:324-334, van der Knaap,M.S.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Magnetic Resonance Angiography in the Diagnosis of Deep Cerebral Venous Thrombosis
J Stroke Cerebrovasc Dis 5:29-32, Finelli,P.F.,et al, 1995

Cranial MRI in Ataxia-Telangiectasia
Neuroradiology 37:77-82, Sardanelli,F.,et al, 1995

Gadolinium-Enhanced MR Findings in a Pediatric Case of Wernicke Encephalopathy
AJNR 16:700-702, Harter,S.B.&Nokes,S.R., 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Effect on Parkinsonian Signs and Symptoms of Bilateral Subthalamic Nucleus Stimulation
Lancet 345:91-95, Limousin,P.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Improvement of Paraneoplastic Opsoclonus-Myoclonus After Protein A Column Therapy
NEJM 332:192, Nitschke,M.,et al, 1995



Showing articles 950 to 1000 of 1688 << Previous Next >>