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abducens nerve paralysis
acetazolamide
acromegaly
adverse drug reaction
alcohol
Alexanders disease
Alexanders disease, adult onset
algorithm
alternating hemiplegia
alternating hemiplegia of childhood
amaurosis fugax
aminoacidopathies
aminoacidurias
amyloid angiopathy, cerebral
anemia
aneurysm
angiography, cerebral, beaded vessels
angiography, cerebral
angiography, cerebral, negative
angiography, vertebral artery
anorexia
anti IgLON5
antibodies to voltage-gated calcium channels
anxiety
aphasia
apnea
areflexia
arteritides
arteritis, temporal
arthralgia
astrogliopathy
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, truncal
ataxic gait
ATP1A3 gene
autoantibodies
autoimmune disease
autonomic dysfunction
behavioral disorder
blindness
brain biopsy
brainstem, infarction of
brainstem, lesion of
bulbar palsy
calcium antagonist
calcium channel dysfunction
carbamazepine
CAT scan
CAT scan, abnormal
CAT scan, angiography
cataracts
central core disease
central retinal artery occlusion
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral infarction
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, young adult
channelopathy
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chills
chloride channel dysfunction
chorea
chromosomal abnormality
chromosome 19
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
collagen vascular disease
coma
coma, episodic
complications
confusion
conversion reaction
cornea, abnormal
cough
deafness
deafness, unilateral
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, rapidly progressive
dentate nuclei, lesion of
depression
developmental retardation
diabetes insipidus
diagnostic criteria
differential diagnosis
digital subtraction angiography
diplopia
diurnal variation
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drug induced neurologic disorders
dysarthria
dysphagia
dystonia
dystonia, psychogenic
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, acute
episodic disorders
episodic neurologic deficits
episodic unconsciousness
epistaxis
exercise
exercise intolerance
eye movement, disorders of
face, numbness of
facial nerve palsy
facial weakness
faciobrachial dystonic seizure
failure to thrive
falling
familial
familial hemiplegic migraine
familial periodic ataxia
fasciculation
fatigue
fever
fine motor function, impaired
Friedreich's ataxia
fundus, abnormality of
gait disorder
gene
gene mutation
genetic neurologic disorders
genetic testing
GFAP gene
glaucoma
globus pallidus, lesion of, bilateral
Guillain Barre syndrome
gynecomastia
hallucination
hallucination, visual
head turning
head turning, neurologic complications with
headache
headache, bifrontal
headache, elderly
headache, occipital
headache, recurrent
headache, severe
hearing loss
hemianopia
hemianopia, homonymous
hemimyoclonic jerks
hemiparesis
hemiplegia
hepatomegaly
hoarseness
hypercalcemia
hyperparathyroidism
hyperreflexia
hypersomnia
hypertension
hyperthyroidism
hypokalemia
hypokalemic periodic paralysis
hyponatremia
hypophonia
hypotonia
iatrogenic neurologic disorders
imbalance
immunotherapy
inborn errors of metabolism
incoordination
infection
intellectual deficit
intracerebral hemorrhage
iritis
jaw claudication
lactic acidemia
lateropulsion
leg numbness
leg weakness, bilateral
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia
leukodystrophy
leukoencephalopathy
limbic encephalitis
lysosomal storage disease
macrocephaly
malignant hyperpyrexia
maple syrup urine disease
mastoiditis
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, elderly
mental status, abnormal
metabolic disorder, primary
methotrexate
microcephaly
microhemorrhage, intracerebral
migraine
migraine, hemiplegic
misdiagnosis
molecular genetics
mononeuropathy
mononeuropathy multiplex
monoparesis
mortality
motor dysfunction
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, hyperkinetic
movement disorder, psychogenic
MRI
MRI, abnormal
MRI, angiography
MRI, diffusion weighted
MRI, negative
MRI, spine
multimodal neuroimaging
multiple sclerosis
multiple sclerosis, pain in
multiple sclerosis, paroxysmal symptoms in
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
myasthenic syndrome
myoclonic jerks
myoclonus
myokymia
myotonia
myotonia congenita
nasal septum, perforation of
nausea and vomiting
negative
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination, focal
neurologic signs
neurologic symptoms
neurologic symptoms, unexplained
neurologic testing
neuromyotonia
neuroophthalmology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, vasculitic, systemic
neurotoxic
neurotoxicity, acute
night sweats
nystagmus
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, intermittent
nystagmus, monocular
nystagmus, periodic
nystagmus, vertical
old age, neurology of
ophthalmoplegia
optic ataxia
optic atrophy
optic neuritis
optic neuropathy, ischemic
oscillopsia
otitis, neurologic complications with
pain
pain, abdominal
pain, leg
pain, testicular
palatal myoclonus
palinopsia
papilledema
paralysis
paralysis, acute areflexic
paramyotonia congenita
paraparesis
paresthesias
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
paroxysmal tonic upgaze
pathology
periarteritis nodosa
periodic paralysis
periodic paralysis, thyrotoxic
peroxisomal disease
personality disorder
pleocytosis of cerebrospinal fluid
polyneuropathy
polyuria
posterior leukoencephalopathy syndrome
potassium
potassium channel antibodies
potassium channel dysfunction
precipitating factors
pregnancy, neurologic complications in
primary episodic ataxia
prognosis
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
psychosis, acute
ptosis
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, tonic
quadriplegia
quadriplegia, transient
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
REM sleep behavior disorder
retinal artery occlusion
retinopathy
reversible cerebral vasoconstrictive syndromes
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
scleritis
scotoma
sedimentation rate, elevated
seizure
seizure, differential diagnosis of
seizure, focal
sensorineural hearing loss
sinusitis
skin, lesions in neurologic disorders
sleep pathology and physiology
sodium channel dysfunction
sore throat
spinal cord, compression of
spinal stenosis
spinal stenosis, cervical canal
spinocerebellar ataxia
spinocerebellar ataxia type 6
status epilepticus
steroid therapy, CNS treatment and complications with
stress, emotional
strokelike episodes
subarachnoid hemorrhage, cerebral convexity
symmetric brain lesions
syncope
tachycardia
tandem gait, ataxic
temporal lobe, lesion, bilateral
testicular biopsy
third nerve palsy
thirst
thyrotoxicosis
tinnitus
tonic spasms
toxic encephalopathy
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, psychogenic
trigeminal neuralgia
trigeminal neuropathy
trigeminal neuropathy, sensory
trinucleotide repeats
unconsciousness
unconsciousness, episodic
unconsciousness, transient
upgaze
upgaze, sustained
urea-cycle enzymopathies
uremia
vaccination, neurologic complications with
vasculopathy
vasospasm, cerebral
vertebral artery
vertebral artery disease
vertebral artery occlusion
vertebral artery stenosis
vertebral-basilar insufficiency
vertigo
vertigo, episodic
Virchow-Robin spaces, dilated
vision, blurred
visual field defect
visual loss
vitamin E deficiency
vocalizations
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weight loss
white matter disease
wide based gait
Showing articles 850 to 900 of 1608 << Previous Next >>

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

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

Risk of Recurrent Stroke in Patients with Sickle Cell Disease Treated with Erythrocyte Transfusions
J Pediatr 126:896-899, Pegelow,C.H.,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

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 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

The Management of Thrombosis in the Antiphospholipid-Antibody Syndrome
NEJM 332:993-997, 10251995., Khamashta,M.A.,et al, 1995

Clinical Relevance and Frequency of Transient Stenoses of the Middle and Anterior Cerebral Arteries in Bacterial Meningitis
Stroke 26:1399-1403, Muller,M.,et al, 1995

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

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Pamidronate Treatment of the Neurologic Sequelae of Pagetic Spinal Stenosis
Arch Int Med 155:1813-1815, Wallace,E.,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

Clinicopath Conf
Ganglioneuroblastoma of Adrenal Gland, Opsoclonus-Myoclonus-Ataxia Syndrome, Paraneoplastic, Case 27, 199EJM 333:579-586,1995., 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

Assessment of the Narrow Cervical Spinal Canal:A Prospective Comparison of MRI, Myelography and CT-Myelography
Neuroradiology 37:187-191, Reul,J.,et al, 1995

Gabapentin Treatment of Seizures in Acute Intermittent Porphyria
Neurol 45:1216-1217, Tatum,W.O.&Zachariah,S.B., 1995

Transient Ictal Cortical Blindness During Middle Age:A Case Report and Review of the Literature
J Neuro-Ophthalmol 15:39-42, Joseph,J.M.&Louis,S., 1995

Ictal Amaurosis:MRI, EEG, and Clinical Features
Neurol 45:1619-1621, Gilliam,F.&Wyllie,E., 1995

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

The Transient Syndrome of Headache with Neurologic Deficits and CSF Lymphocytosis
Neurol 45:1648-1654, Berg,M.J.&Williams,L.S., 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

Paroxysmal Dyskinesias:Clinical Features and Classification
Ann Neurol 38:571-579, Demirkiran,M.&Jankovic,J., 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

Neuroradiologic Aspects of Chester-Erdheim Disease
AJNR 16:735-740, Caparros-Lefebvre,D.,et al, 1995

Erdheim-Chester Disease and Slowly Progressive Cerebellar Dysfunction
JNNP 58:238-240, Fukazawa,T.,et al, 1995

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

Treatable Gait Disorder & Polyneuropathy Assoc with High Titer Serum IgM Binding to Atg that Copurify with MAG
Muscle & Nerve 17:1293-1300994., Pestronk,A.,et al, 1994

Intermittent Diplopia in Chordoma
Ann Ophthalmol 26:20-22, Aydin,P.,et al, 1994

Acute Lumbosacral Polyradiculopathy in Acquired Immunodeficiency Syndrome:Experience in 23 Patients
Ann Neurol 35:53-58, So,Y.T.&Olney,R.K., 1994

Clinicopath Conf
Primary Malignant Lymphoma of CNS, Diffuse, Large-Cell]B-Cell Type, Case 36-1994, NEJM 331:861-8684., , 1994

Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease
Ann Neurol 36:630-635, Illarioshkin,S.N.,et al, 1994



Showing articles 850 to 900 of 1608 << Previous Next >>