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abdominal distention
abdominal x-ray
adverse drug reaction
affect, flat
agitation
akathisia
alcohol intolerance
alien hand syndrome
altered states of consciousness
alternating rapid movement
aluminum
AMPA receptor antibodies
anemia
angiokeratoma
anorexia
anti IgLON5
anti Ri antibody
antibiotics
antibiotics, neurologic complications with
antibodies to measles
anticonvulsants
anticonvulsants, effectiveness
anticonvulsants, selection of
antidepressant
antioxidant
antithyroid antibodies
aphasia
apnea
apraxia
arm swing, reduced
arm weakness
arthralgia
arthritis
Asia
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxia, truncal, associated with ocular oscillations
ataxic gait
athetosis
autoantibodies
autoimmune disease
autonomic dysfunction
axonal spheroid
Babinski sign
bacterial infection
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bismuth
blindness
boomerang sign
bovine spongiform encephalopathy
bradykinesia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
bruxism
bulbar palsy
CAG repeats
carbon monoxide poisoning
carcinoma
carcinoma of breast
carcinoma of lung
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
celiac disease, adult
central nervous system, infection of
cephalosporins
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellum
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral glucose metabolism
cerebrospinal fluid
cerebrospinal fluid, abnormal
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
cherry red spot-myoclonus syndrome
chewing movements
children
choking
chorea
chorea, familial
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 12
chromosome 2
chromosome 21
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonazepam
clonus
coenzyme Q10 deficiency
cognition
cogwheel rigidty
cold intolerance
color vision, impaired
coma
coma, episodic
complications
confabulation
confusion
congenital infection, CNS
congenital paresis
conjugate gaze, forced
contactin associated protein like 2 antibodies
cortical-basal ganglionic degeneration
cranial nerve palsies
Creutzfeldt-Jakob disease, genetic
crying
deafness
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, differential diagnosis of
dementia, rapidly progressive
dementia, reversible
dementia, transmissible
dementia, treatment of
demyelinating disease
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
dialysis
dialysis dementia
diarrhea
diet
differential diagnosis
diplopia
disability, neurological
dizziness
doll's head maneuver
downward gaze, paralysis of
Dravet syndrome
drooling
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphasia
dyspraxia
dyssynergia cerebellaris myoclonica
dystonia
dystonia, focal
Ekbom's Syndrome
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, triphasic delta waves
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, diagnosis of
encephalitis, etiology
encephalitis, paraneoplastic
encephalitis, viral
encephalitis, viral-causes of
encephalomyelitis
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
encephalopathy, Hashimoto's
encephalopathy, parainfectious
enterovirus
enterovirus infection of CNS
enzyme, defect
epidemic
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
eye movement, disorders of
facial movement disorder
faciobrachial dystonic seizure
falling
familial
fasciculation
fatal familial insomnia
fatigue
fever
fine motor function, impaired
finger nose finger test
fingerprint bodies
flaccid paralysis
gait disorder
gait, apraxic
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
gliadin antibodies
globus pallidus, lesion of
GluD2
glutamic acid decarboxylase, antibody
gram positive rod
granular osmiphilic material
grasp reflex
gray matter
gyrus, abnormal
Hallervorden Spatz disease
hallucination
hand-foot-mouth disease
handwriting
head lag
headache
hearing loss
heart block
heavy metal intoxication
heel-knee-shin test
hemimyoclonic jerks
hemiparesis
hemiplegia
hepatomegaly
hepatosplenomegaly
heralding manifestation
hoarseness
human immunodeficiency virus type 1
hydrocephalus
hyperhidrosis
hyperpigmentation of skin
hyperreflexia
hypersomnia
hypertension
hyperthermia
hyperthyroidism
hyponatremia
hypophonia
hypothalamus, disturbance of
hypothyroidism
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
idiopathic
imbalance
imbalance, postural
immune reconstitution inflammatory syndrome
immunohistochemistry
immunosuppressive agents
immunotherapy
impotence
inattention
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
incontinence, fecal
incoordination
infection
influenza
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intestinal biopsy
intestinal pseudoobstruction
intrauterine infection
intrauterine infection, viral of CNS
introverted
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
juvenile paresis
Kearns-Sayre syndrome
kuru plaques
lactic acidemia
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
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
level of consciousness, decreased
limbic encephalitis
linear lesion
lipid storage disorder of CNS
lithium
liver function enzymes
lymphadenopathy
macular degeneration
maculopathy
malabsorption
malabsorption syndrome
malaise
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningoencephalitis
mental retardation
mental status, abnormal
MERRF syndrome
metronidazole
micrographia
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoparesis
mortality
motor cortex
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, false negative
MRI, FLAIR
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, orthostatic
myoclonus, segmental
myoclonus, stimulus sensitive
myoclonus, treatment of
myopathy
myopathy, mitochondrial
myorhythmia
N-acetylcysteine
nausea and vomiting
negative
neuraminidase deficiency
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroaxonal leukodystrophy
neuroblastoma
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neurosyphilis
neurotoxic
neurotoxin
next-generation sequencing
night sweats
nystagmus
nystagmus, rotary
nystagmus, vertical
ocular flutter
ocular motility, disorders of
oculomasticatory myorhythmia
old age, neurology of
olivary degeneration, hypertrophic
ophthalmoplegia
ophthalmoplegia, progressive external
opsoclonus
opsoclonus, differential diagnosis of
opsoclonus-myoclonus syndrome
optic atrophy
optic atrophy, hereditary
optic neuropathy
oral ulcerations
organ transplantation
orthostatic hypotension
ovarian tumor
pain, abdominal
palatal myoclonus
pancytopenia
papilledema
paralysis, acute
paralysis, acute areflexic
paraparesis, spastic
parasomnia
Parkinson disease
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pathologic reflex
penicillin
pericarditis
personality change
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pleurisy
pneumonia
polymerase chain reaction
polyneuropathy
pons, lesion of
pontocerebellar atrophy
potassium channel antibodies
pregnancy, neurologic complications in
prevention of neurologic disorders
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 disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
pulmonary edema
Purkinje cell
Purkinje cell surface antibody
pursuit eye movements, abnormal
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
Ramsay Hunt syndrome
rapidly progressing neurologic illness
rash
rash, hand
real-time quaking-induced conversion
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
respiratory failure
respiratory tract infection
retinal degeneration
retinopathy
Rett's syndrome
review article
rigidity
risk factors
Romberg's sign
rooting reflex
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
saccadic eye movements, abnormal
salivation, excessive
SCN1A gene
sedimentation rate, elevated
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, tonic-clonic
seizure, treatment of
senile plaques
sensorineural hearing loss
sensory loss, cortical
seroconversion
serologic testing
serologic testing of cerebrospinal fluid
short stature
sleep apnea, obstructive
sleep pathology and physiology
slow virus infection of CNS
slurred speech
snout reflex
sodium channel dysfunction
sodium valproate
somnolence
spasticity
speech disorder
speech, loss of
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 16
spinocerebellar ataxia type 7
splenium of corpus callosum
spongy degeneration of brain
square wave jerks
standing difficulty
startle myoclonus
startle reaction
status epilepticus
steatorrhea
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
stuporous
stuttering
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
suck, poor
suicide
symmetric brain lesions
syphilis, diagnosis and treatment
syphilis, neurologic complications with
systemic illness
tachycardia
tandem gait, ataxic
tau protein
temporal lobe, lesion, bilateral
teratoma, ovarian
term infant
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
thyrotropin
titubation
tonic spasms
topiramate
toxins, nervous system
transplacental virus infections
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
triangle of Guillain and Mollaret
trinucleotide repeats
ultrasonography
unconsciousness
unconsciousness, episodic
unconsciousness, transient
Unverricht-Lundborg disease
upgaze
upgaze, paralysis of
urinary incontinence
uveitis
vaccine
vasculitides
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
vision, blurred
visual acuity, decreased
visual impairment
visual loss
visuospatial disturbance
vitreous opacities
vocalizations
walking, difficulty with
weakness, acute
weakness, focal
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
Wolfram syndrome
writing
Showing articles 750 to 800 of 1450 << Previous Next >>

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

Neurotoxicity Related to the Use of Topical Tretinoin (Retin-A)
Ann Int Med 124:227-228, Bernstein,A.L.&Leventhal-Rochon,J.L., 1996

Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
Neurol 46:19-25, Cramer,S.C.,et al, 1996

Prevalence of Parkinsonian Signs and Associated Mortality in a Community Population of Older People
NEJM 334:71-76, Bennett,D.A.,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

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

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

An Emotional 13-Year Old Girl
Lancet 348:1000, Kanabar,D.J.,et al, 1996

Gait Disorders in Older Adults
J Am Geriatr Soc 44:434-452, Alexander,N.B., 1996

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

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,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

Neuroblastoma-Associated Opsoclonus-Myoclonus Treated with IVIgG
J Pediatr 127:328-329, Petruzzi,M.J.&deAlarcon,P.A., 1995

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
Neuroradiology 37:238-243, Tortori-Donati,P.,et al, 1995

'Anesthesia Paresthetica':Nitrous Oxide-Induced Cobalamin Deficiency
Neurol 45:1608-1610, 14351995., Kinsella,L.J.&Green,R., 1995

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,et al, 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

Midcervical Central Cord Syndrome:Numb & Clumsy Hands Due to Midline Cervical Disc Protrusion at C3-4 Intervert Level
JNNP 58:607-613, Nakajima,M.&Hirayama,K., 1995

Reversible Downbeat Nystagmus and Ataxia in Felbamate Intoxication
Neurol 45:845, Hwang,T.L.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Neurotox of Antimicrob & Antimalarial Agents
In Intox of Nervous System, Part II, Handbk Clin Neurol, Elsevier Science 21 (65) :471., Moorhouse,D.F.,et al, 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

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

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

Serotonin Syndrome
Neurol 45:219-223, Bodner,R.A.,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

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

Syndromes of Pontine Base Infarction:A Clinical-Radiological Correlation Study
Stroke 26:950-955, Kim,J.S.,et al, 1995

Clinical and Topographical Range of Callosal Infarction:A Clinical and Radiological Correlation Study
JNNP 59:238-242, Giroud,M.&Duman,R., 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995



Showing articles 750 to 800 of 1450 << Previous Next >>