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acetazolamide
alcohol
Alexanders disease
Alexanders disease, adult onset
alternating hemiplegia
alternating hemiplegia of childhood
aminoacidopathies
aminoacidurias
antibodies to voltage-gated calcium channels
areflexia
arrhythmia, cardiac
arthralgia
astrogliopathy
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
ATP1A3 gene
autonomic dysfunction
Babinski sign
bladder dysfunction
bulbar palsy
calcium channel dysfunction
cardiomyopathy
CAT scan
CAT scan, abnormal
cataracts
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
channelopathy
Charcot-Marie-Tooth
children
chloride channel dysfunction
chorea
chromosomal abnormality
chromosome 19
ciguatera poisoning
clubfoot as related to neurologic disease
coma
coma, episodic
congestive heart failure
conjunctivitis
cryopyrin-associated periodic syndrome
deafness
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, subcortical
dentate nuclei, lesion of
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
down-beat nystagmus
down-beat nystagmus, primary position of gaze
dysarthria
dysmetria
dystonia
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
encephalopathy
episodic disorders
episodic neurologic deficits
exercise
exercise intolerance
exome sequencing
eye movement, disorders of
failure to thrive
familial
familial hemiplegic migraine
familial periodic ataxia
fatal familial insomnia
fever
fever, recurrent
foot deformity
Friedreich's ataxia
frontal bossing
gait disorder
gait, spastic
gene
gene mutation
genetic neurologic disorders
genetic testing
GFAP gene
globus pallidus, lesion of, bilateral
Guillain Barre syndrome
hammertoes
head circumference
headache
hearing loss
heart block
hyperhidrosis
hyperreflexia
hypertension
hyperthermia
hyperthyroidism
hypertrophic intracranial pachymeningitis
hypokalemic periodic paralysis
hypotonia
imbalance
inborn errors of metabolism
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
incoordination
insomnia
intellectual deficit
intellectual deterioration
kyphoscoliosis, neurologic causes of
lactic acidemia
leukodystrophy
leukoencephalopathy
lysosomal storage disease
macrocephaly
malignant hyperpyrexia
maple syrup urine disease
meningitis, aseptic
meningitis, carcinomatous
metabolic acidosis
metabolic disorder, primary
microcephaly
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, diffusion weighted
muscle atrophy, progressive
muscle weakness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
myasthenic syndrome
myoclonus
myokymia
myopathy
myotonia
myotonia congenita
myotonia dystrophica
nausea and vomiting
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neurologic testing
neuromyotonia
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
night blindness
NOTCH2NLC
nystagmus
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, monocular
nystagmus, periodic
nystagmus, vertical
optic atrophy
optic atrophy, bilateral
oscillopsia
palatal myoclonus
paralysis
paramyotonia congenita
paraparesis
paraparesis, spastic
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
periodic paralysis
peroxisomal disease
pes cavus
phytanic acid
pleocytosis of cerebrospinal fluid
polyneuropathy
pons, lesion of
potassium channel antibodies
potassium channel dysfunction
precipitating factors
pregnancy, neurologic complications in
primary episodic ataxia
prion disease
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
red eye
Refsum's disease
respiratory tract infection
retinitis pigmentosa
review article
Romberg's sign
scoliosis
seizure
sensorineural hearing loss
sensory loss
short stature
skin, biopsy
skin, lesions in neurologic disorders
skull bone, thickening
sleep pathology and physiology
slurred speech
sodium channel dysfunction
spinocerebellar ataxia
spinocerebellar ataxia type 6
spinocerebellar degeneration
status epilepticus
stress, emotional
strokelike episodes
subcortical U fibers
sudden death
symmetric brain lesions
tachycardia
thalamus, lesion of
tinnitus
transient neurologic deficit
treatment of neurologic disorder
trinucleotide repeats
urea-cycle enzymopathies
urinary frequency
urinary incontinence
vertigo
vertigo, episodic
vertigo, treatment of
visual fields, constricted
vitamin E deficiency
weakness
weight loss
white matter disease
Showing articles 1350 to 1400 of 3794 << Previous Next >>

Familiality in Brain Tumors
Neurol 71:1015-1020, Blumenthal,D.T.&Cannon-Albright,L.A., 2008

Two Sets of Identical Twins with Cervical Artery Dissection Concordant for Temporal Artery Pathology
Neurol 71:1035-1037, V�lker,W.,et al, 2008

Neurologic Manifestations of von Hippel-Lindau Disease
JAMA 300:1334-1342, Butman,J.A.,et al, 2008

Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
Neurol 71:925-929, Van Gerpen,J.A.,et al, 2008

Curable Cause of Paraplegia: Spinal Dural Arteriovenous Fistulae
Stroke 39:2756-2759, Aghakhani,N.,et al, 2008

Overview of Phenylketonuria
UptoDate (May), Bodamer,O.A., 2008

Practice Parameter: Assessing Patients in a Neurology Practice for Risk of Falls (An Evidence-Based Review)
Neurol 70:473-479, Thurman,D.J.,et al, 2008

Serial Electrocardiographic Assessments Significantly Improve Detection of Atrial Fibrillation 2.6-Fold in Patients With Acute Stroke
Stroke 39:480-482, Douen,A.G.,et al, 2008

Atherosclerotic Plaque Composition and Occurrence of Restenosis After Carotid Endarterectomy
JAMA 299:547-554, Hellings,W.E.,et al, 2008

Barriers to the Use of Anticoagulation for Nonvalvular Atrial Fibrillation: A Representative Survey of Australian Family Physicians
Stroke 39:227-230,7, Gattellari,M.,et al, 2008

Psychogenic Tremor Occurring After Deep Brain Stimulation Surgery for Essential Tremor
Neurol 70:1498-1499, McKeon,A.,et al, 2008

Extension of the Clinical Spectrum of Danon Disease
Neurol 70:1358-1359, van der Kooi,A.J.,et al, 2008

Intracranial Stenting of Severe Symptomatic Intracranial Stenosis: Results of 100 Consecutive Patients
AJNR 29:781-785, Suh,D.C.,et al, 2008

Opsoclonus-Myoclonus Syndrome Asssociated with Benign Ovarian Teratoma
Neurol 70:1292-1293, Fitzpatrick,A.S.,et al, 2008

Oral Anticoagulants Versus Antiplatelet Therapy for Preventing Stroke in Patients With Nonvalvular Atrial Fibrillation and No History of Stroke or Transient Ischemic Attacks
Stroke 39:1399-1400, Aguilar,M.I. &Hart,R., 2008

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Association of Gait and Balance Disorders With Age-Related White Matter Changes: The LADIS Study
Neurol 70:935-942, Baezner,H.,et al, 2008

Tuberous Sclerosis Complex: A Tale of Two Genes
Neurol 70:904-905, Nass,R. &Crino,P.B., 2008

Nearly Completely Reversible Brain Abnormalities in a Patient With Incontinentia Pigmenti
AJNR 29:431-433, Lou,H.,et al, 2008

Woke Up Paralysed--Without Injury or Stroke
Lancet 371:870, Bawaskar,H.S. &Bawaskar,P.H., 2008

A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
NEJM 358:1009-1017, Stepens,A.,et al, 2008

Risks and Benefits of Oral Anticoagulation Compared With Clopidogrel Plus Aspirin in Patients With Atrial Fibrillation According to Stroke Risk: The Atrial Fibrillation Clopidogrel Trial With Irbesartan for Prevention of Vascular Events (ACTIVE-W)
Stroke 39:1482-1486,1406, Healey,J.S.,et al, 2008

Cerebral Impairment in Chronic Solvent-Induced Encephalopathy
Ann Neurol 63:572-580, Visser,I.,et al, 2008

Sudden Falls Due to Seizure-Induced Cardiac Asystole in Drug-Resistant Focal Epilepsy
Neurol 70:1933-1935, Rubboli,G.,et al, 2008

Klein-Levin Syndrome: A Systematic Study of 108 Patients
Ann Neurol 63:482-492, Arnulf,I.,et al, 2008

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

a-Synuclein Gene Duplication Is Present in Sporadic Parkinson Disease
Neurol 70:43-49,7, Ahn,T.-B.,et al, 2008

Diffusion-Weighted MR Imaging: Diagnosing Atypical or Malignant Meningiomas and Detecting Tumor Dedifferentiation
AJNR 29:1147-1152, Nagar,V.A., et al, 2008

JC Viral Infection-Related Cerebellar Degeneration as the First Manifestation of AIDS
Eur Neurol 59:205-207, Shin,H.-W.,et al, 2008

Managing the Anticoagulated Patient with Atrial Fibrillation at High Risk of Stroke Who Needs Coronary Intervention
BMJ 337:1110-1111, Lip,G.Y.H., 2008

Anticoagulation Prior to and After Restoration of Sinus
UpToDate, December, Manning,W.J. &Arnsdorf,W.F., 2008

Anti-NMDA-Receptor Encephalitis: Case Series and Analysis of the Effects of Antibodies
Lancet Neurol 7:1091-1098, Dalmau,J.,et al, 2008

Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
Brain 131:2553-2563, Saiz,A., et al, 2008

Bilateral Basal Ganglia Lesions in Patients with End-Stage Diabetic Nephropathy
Nephrology 13:68-72, Li, J.,et al, 2008

Acute Intermittent Porphyria Presenting as Acute Pancreatitis and Posterior Reversible Encephalopathy Syndrome
Acta Neurol Taiwan 17:177-183, Shen, F.,et al, 2008

Auto-Immune Cerebellar Ataxia with Anti-GAD Antibodies Accompanied by De Novo Late-Onset Type 1 Diabetes Mellitus
Diabetes Metab 34:386-388, Bayreuther,C.,et al, 2008

Opsoclonus-Myoclonus-Ataxia Syndrome with Autoantibodies to Glutamic Acid Decarboxylase
Clin Neurol Neurosurg 110:619-621, Markakis,I.,et al, 2008

Pontine Warning Syndrome
Arch Neurol 65:1375-1377, Saposnik, G.,et al, 2008

Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
J Neuro-Ophthalmol 28:58-68, Ko,M.W.,et al, 2008

Classical Disease Revisited: Transient Global Amnesia
Postgrad Med 83:236-239, Owen, D.,et al, 2007

Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
J Neurol 254:1609-1611, Collison,K. and Rees,J., 2007

"Salt and Pepper" in the Eye and Face: A Prelude to Brainstem Ischemia
Am J Ophthalmol 144:322-325, Conforto, A.B.,et al, 2007

The Syndrome of Bilateral Basal Ganglia Lesions in Diabetic Uremic Patients Presenting with a Relapsing and Remitting Course: A Case Report
Acta Neurol Taiwan 16:226-230, Sheu, Y.,et al, 2007

Cerebral Amyloid Angiopathy With Symptomatic or Occult Subarachnoid Haemorrhage
Eur Neurol 57:103-105, Karabatsou,K.,et al, 2007

Incidence and Prognosis of Transient Neurological Attacks
JAMA 298:2877-2885,2912,2978, Bos,M.J.,et al, 2007

Parkinson Disease, 10 Years After Its Genetic Revolution: Multiple Clues to a Complex Disorder
Neurol 69:2093-2104, Klein,C. &Schlossmacher,M.G., 2007

Variability of Age at Onset in Siblings With Familial Alzheimer Disease
Arch Neurol 64:1743-1748, G�mez-Tortosa,E.,et al, 2007

Chronic Pain in Machado-Joseph Disease: A Frequent and Disabling Symptom
Arch Neurol 64:1767-1770, Fran�a,M.C. Jr., et al, 2007

Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007

Can Patients at Elevated Risk of Stroke Treated With Anticoagulants Be Further Risk Stratified?
Stroke 38:2459-2463,2409, Baruch,L.,et al, 2007



Showing articles 1350 to 1400 of 3794 << Previous Next >>