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Differential
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abducens nerve paralysis

acute cerebellar ataxia

adverse drug reaction

alcohol, neurologic complications with

alcoholic withdrawal states, DT's, convulsions, etc.

Alexanders disease

Alexanders disease, adult onset

alternating hemiplegia

alternating hemiplegia of childhood

amaurosis fugax

aminoacidopathies

amyloid angiopathy, cerebral

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

angiography, vertebral artery

anti MAG antibodies

antibodies to voltage-gated calcium channels

arrhythmia, cardiac

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

atrial fibrillation

autoimmune disease

autoimmune GFAP astrocytopathy

autonomic dysfunction

B 12 deficiency

basal ganglia, lesion, bilateral

behavior modification

behavior, combative

behavioral disorder

Behcet's syndrome

benign positional vertigo

bladder dysfunction

brain biopsy, stereotaxic

brainstem, infarction of

brainstem, lesion of

brucellosis, nervous system involvement with

calcium antagonist

calcium channel dysfunction

CAT scan, abnormal

CAT scan, angiography

celiac disease, adult

central core disease

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebral cortex

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chloride channel dysfunction

chromosomal abnormality

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

collagen vascular disease

concentration, impaired

congestive heart failure

conversion reaction

cranial nerve palsies

cryopyrin-associated periodic syndrome

deafness, sudden

deafness, unilateral

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dentate nuclei, lesion of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

digital subtraction angiography

disability, neurological

diurnal variation

down-beat nystagmus

down-beat nystagmus, primary position of gaze

drug induced neurologic disorders

drug withdrawal

dystonia, psychogenic

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, viral

encephalopathy, acute

episodic disorders

episodic neurologic deficits

episodic unconsciousness

Epstein-Barr virus

exercise intolerance

exome sequencing

eye movement, disorders of

face, numbness of

facial nerve palsy

facial weakness

faciobrachial dystonic seizure

failure to thrive

familial hemiplegic migraine

familial periodic ataxia

fatal familial insomnia

fever, recurrent

fine motor function, impaired

Fisher's syndrome

fistula, perilymphatic

Friedreich's ataxia

frontal bossing

fundus, abnormality of

genetic neurologic disorders

genetic testing

gliadin antibodies

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

Guillain Barre syndrome

hallucination, visual

head circumference

head turning, neurologic complications with

headache, bifrontal

headache, episodic

headache, occipital

headache, recurrent

headache, severe

hemianopia, homonymous

hemimyoclonic jerks

hemosiderosis of CNS, superficial

hepatosplenomegaly

hypersegmented polys

hyperthyroidism

hypertrophic intracranial pachymeningitis

hypoglycorrhachia

hypokalemic periodic paralysis

hypotension, systemic

hypotonia, infants

iatrogenic neurologic disorders

imbalance, postural

immunomodulation

inborn errors of metabolism

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

kyphoscoliosis, neurologic causes of

lactic acidemia

lacunar infarction, differential diagnosis of

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

limbic encephalitis

lysosomal storage disease

malignant hyperpyrexia

maple syrup urine disease

memory, defect of recent

memory, impairment of

Meniere's disease

meningeal enhancement

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, fungal

meningitis, Mollaret's

meningitis, recurrent

meningoencephalitis

meningoencephalomyelitis

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

mitochondrial disease

molecular genetics

mononeuropathy multiplex

motor dysfunction

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, hyperkinetic

movement disorder, psychogenic

MRI, angiography

MRI, contrast enhanced

MRI, curvilinear peppering enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, nodular enhancement

multimodal neuroimaging

multiple sclerosis

multiple sclerosis, pain in

multiple sclerosis, paroxysmal symptoms in

muscle atrophy, progressive

muscle weakness

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, Duchenne

myasthenic syndrome

myoclonic jerks

myotonia congenita

myotonia dystrophica

nasal septum, perforation of

nausea and vomiting

neoplasm, primary of CNS

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology, brain

neuropathy, amyloid

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, vasculitic, systemic

neurotoxicity, acute

night blindness

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, intermittent

nystagmus, monocular

nystagmus, periodic

nystagmus, vertical

ophthalmoplegia

ophthalmoplegia, recurrent

optic atrophy, bilateral

otitis, neurologic complications with

pain, abdominal

pain, testicular

palatal myoclonus

paralysis, acute areflexic

paramyotonia congenita

paraparesis, spastic

paresthesias, feet

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal tonic upgaze

pathologic reflex

patient information and support

periarteritis nodosa

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

perivascular enhancement

perivascular inflammation

pernicious anemia

peroxisomal disease

Persistent postural-perceptual dizziness

personality disorder

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy, chronic relapsing

pons, lesion of

posterior leukoencephalopathy syndrome

potassium channel antibodies

potassium channel dysfunction

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

primary episodic ataxia

progressive neurologic disorder

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, acute

pulmonary infiltrates

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriplegia, transient

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Refsum's disease

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory tract infection

retinal artery occlusion

retinal detachment

retinitis pigmentosa

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

sedimentation rate, elevated

seizure, differential diagnosis of

seizure, withdrawal

selective serotonin reuptake inhibitors

sensorineural hearing loss

serologic testing

serotonin norepinephrine reuptake inhibitors

skin, lesions in neurologic disorders

skull bone, thickening

sleep pathology and physiology

sodium channel dysfunction

spinocerebellar ataxia

spinocerebellar ataxia type 6

spinocerebellar degeneration

spongy degeneration of brain

status epilepticus

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stress, emotional

strokelike episodes

subarachnoid hemorrhage, cerebral convexity

subcortical U fibers

superior cerebellar artery infarction

superior cerebellar artery syndrome

superior cerebellar peduncle

supratentorial lymphocytic inflam parenchy perivasc enhanc responsive to steroids

symmetric brain lesions

tandem gait, ataxic

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular biopsy

thalamus, lesion of

third nerve palsy

toxic encephalopathy

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, postural

tremor, psychogenic

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, sustained

urea-cycle enzymopathies

urinary frequency

urinary incontinence

vaccination, neurologic complications with

valsalva maneuver

vasospasm, cerebral

vertebral artery

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vertigo, episodic

vertigo, treatment of

violent behavior

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

vision, blurred

visual field defect

visual fields, constricted

vitamin E deficiency

Vogt-Koyanagi-Harada syndrome

walking, difficulty with

weakness, acute

weakness, episodic

weakness, generalized

white matter disease

wide based gait

Showing articles 1400 to 1450 of 2314 << Previous Next >>

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

Simultaneous, Multiple Cranial Neuropathies in Diabetes Mellitus
J Neuro-Ophthalmol 15:219-224, Eshbaugh,C.G.,et al, 1995

Benign Episodic Unilateral Mydriasis
Ophthalmol 102:1623-1627, Jacobson,D.M., 1995

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

Neurotoxicity in Liver Transplant Recipients with Cyclosporine Immunosuppression
Neurol 45:1962-1964, Wijdicks,E.F.M.,et al, 1995

Anticholinergic Poisoning Associated with Herbal Tea
Arch Int Med 155:2245-2248, Hsu,C.K.,et al, 1995

Accuracy of Transesophageal Echocardiography for Ident Left Atrial Thrombi:Prospective, Intraop Study
Ann Int Med 123:817-822, 8821995., Manning,W.J.,et al, 1995

Paroxysmal Dyskinesias:Clinical Features and Classification
Ann Neurol 38:571-579, Demirkiran,M.&Jankovic,J., 1995

Clinicopath Conf
Acute Disseminated Encephalomyelitis, (postviral encephalomyelitis) Case 37-1995, NEJM 333:1485-1493, 199, 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

Cost-Effectiveness of Warfarin and Aspirin for Prophylaxis of Stroke in Patients with Nonvalvular Atrial Fibrillation
JAMA 274:1839-1845, Gage,B.F.,et al, 1995

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

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Management of Acoustic Neuroma
BMJ 311:1141-1144, Wright,A.&Bradford,R., 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

Electrocardiographic Changes in Patients with Brain Tumors
Arch Neurol 52:152-155, Koepp,M.,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

Clinicopath Conf
Neurolymphomatosis, Case 8-1995, NEJM 332:730-737995., , 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

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

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy & Systemic Lupus Erythematosus, Case 20-1995, NEJM 332:17, 3-17995., 1995

Clinicopath Conf
Qunidine-Induced Thrombocytopenia, Cerebral Hemorrhage, Case 15-1995, NEJM 332:1363-137095., , 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

Newly Diagnosed Atrial Fibrillation and Acute Stroke, The Framingham Study
Stroke 26:1527-1530, Lin,H.J.,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

Optimal Oral Anticoag Therapy in Pts with Nonrheumatic Atrial Fib & Recent Cerebral Ischemia
European Atrial Fib Study Group, NEJM 333:5-10, 54995., , 1995

Cephalosporin-Induced Recurrent Aseptic Meningitis
Ann Neurol 37:815-817, Creel,G.B.&Hurtt,M., 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

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

Showing articles 1400 to 1450 of 2314 << Previous Next >>