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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 1650 to 1700 of 3794 << Previous Next >>

Clinical Relevance of Atrial Fibrillation/Flutter, Stroke, Pacemaker Implant, and Heart Failure in Emery-Dreifuss Muscular Dystrophy
Stroke 34:901-908, Boriani,G.,et al, 2003

Alzheimer's Disease and Parkinson's Disease
NEJM 348:1356-1364, Nussbaum,R.L. &Ellis,C.E., 2003

Long-term Outcome of Benign Paroxysmal Positional Vertigo
Neurol 60:1532-1534, Sakaida,M.,et al, 2003

Diffusion MR Imaging Changes Associated with Wilson Disease
AJNR 24:965-967, Sener,R.N., 2003

Early Asymptomatic Recurrence of Cervical Artery Dissection
Neurol 61:572-574, Touze,E.,et al, 2003

A Risk Score for Predicting Stroke or Death in Individuals with New-Onset Atrial Fibrillation in the Community
JAMA 290:1049-1056,1093, Wang,T.J.,et al, 2003

Stroke Prevention in Atrial Fibrillation
JAMA 290:1093-1095, Waldo,A.L., 2003

Learning Disability
Lancet 362:811-821, Gillberg,C.&Soderstrom,H., 2003

Autoantibodies to Glutamic Acid Decarboxylase in Downbeat Nystagmus
JNNP 74:998-999, Antonini,G.,et al, 2003

Alternate-Sided Homonymous Hemianopia as the Solitary Presentation of Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes Syndrome
Chang Gung Med J 26:199-203, Su,WY.,et al, 2003

Spontaneous Regression of Cerebral Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia
AJNR 23:1049-1050, Cloft,H.J., 2002

Nanging
Lancet 360:384, Ng, J. &Frith, R., 2002

Occurrence of Hemispheric and Retinal Ischemia in Atrial Fibrillation Compared with Carotid Stenosis
Stroke 33:1963-1968, Anderson,D.C.,et al, 2002

Jaw Drop in Kennedy's Disease
Neurol 59:1471-1472, Sumner,C.J. &Fischbeck,K.H., 2002

Prevalence of Atrial Fibrillation and Antithrombotic Prophylaxis in Emergency Department Patients
Stroke 33:2664-2669, Scott,P.A.,et al, 2002

Atrial Fibrillation, Stroke, and Acute Antithrombotic Therapy
Stroke 33;2722-2727, Hart,R.G.,et al, 2002

Clinicopath Conf., Acute Disseminated Encephalomyelitis
NEJM 347:1433-1440, Case 34-2002, 2002

Oral Anticoagulants vs Aspirin in Nonvalvular Atrial Fibrillation
JAMA 288:2441-2448, van Walraven,C.,et al, 2002

Stimulation of the Subthalamic Nucleus Increases Heart Rate in Patients with Parkinson Disease
Neurol 59:1657-1658, Kaufmann,H.,et al, 2002

Abnormality of Gait as a Predictor of Non-Alzheimer's Dementia
NEJM 347:1761-1768, Verghese,J.,et al, 2002

New Players in the Genetics of Stroke
NEJM 347:1711-1712, Tournier-Lasserve,E., 2002

Long-term Prognosis in Patients with Vasculopathic Sixth Nerve Palsy
Am J Ophthalmol 134:81-84, Sanders,S.K.,et al, 2002

A Double-blind Placebo-controlled Trial of Topiramate Treatment for Essential Tremor
Neurol 59:132-134, Connor,G.S., 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

Familial Dementia With Lewy Bodies
Arch Neurol 59:1622-1630, Tsuang,D.W.,et al, 2002

Indications and Usefulness of Nerve Biopsy
Arch Neurol 59:1532-1535, Said,G., 2002

Familial Infantile Bilateral Striatal Necrosis
Neurol 59:983-989, Straussberg,R.,et al, 2002

New Evidence for Stroke Prevention
JAMA 288:1388-1395, Straus,S.E.,et al, 2002

Recent Developments in Neurology
BMJ 324:656-660, Wiebe,S.,&Nicolle,M.W., 2002

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Subarachnoid Hemorrhage
Stroke 33:1321-1326, Kissela,B.M.,et al, 2002

Therapies for Movement Disorders
Arch Neurol 59:699-702, Goetz,C.G &Hinson,V.K., 2002

Friedreich Ataxia
Arch Neurol 59:743-747, Lynch,D.R.,et al, 2002

Familial Temporal Lobe Epilepsy with Febrile Seizures
Neurol 58:1429-1433, Depondt,C.,et al, 2002

Gluten Sensitivity as a Neurological Illness
JNNP 72:560-563, Hadjivassiliou,M.,et al, 2002

Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
Lancet 359:1461-1465,1450, Marrosu,M.G.,et al, 2002

Mitochondrial Optic Neuropathies
JNNP 72:423-425, Sadun,A.A., 2002

Opsoclonus-myoclonus Syndrome Following Epstein-Barr Virus Infection
Neurol 58:1131-1132, Verma,A. &Brozman,B., 2002

Reversible Metronidazole-Induced Lesions of the Cerebellar Dentate Nuclei
NEJM 346:68-69, Woodruff,B.K.,et al, 2002

Benefit of Atrial Pacing in Sleep Apnea Syndrome
NEJM 346:404-412,390,444, Garrigue,S., et al, 2002

Tranexamic Acid in Hereditary Hemorrhagic Telangiectasia
NEJM 346:457, Sabra,C.,et al, 2002

Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
Ann Neurol 51:264-270, van der Knaap,M.S.,et al, 2002

Ictal Heart Rate Differentiates Epileptic from Non-epileptic Seizures
Neurol 58:636-638, Opherk,C. &Hirsch,L.J., 2002

Familial Amyotrophic Lateral Sclerosis
Muscle Nerve 25:135-159, Hand,C.K. &Rouleau,G.A., 2002

Positional Down Beating Nystagmus in 50 Patients: Cerebellar Disorders and Possible Anterior Semicircular Canalithiasis
JNNP 72:366-372, Bertholon,P.,et al, 2002

Hearing Loss is a Common Feature of Symptomatic Children with Profound Biotinidase Deficiency
J Pediatr 140:242-246, Wolf,B.,et al, 2002

Legionella Infection
emedicine.com, Mobeen,R., 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Cerebrovascular Complication Associated with Pulmonary Vein Ablation
J Cardiovasc Electrophysiol 13:764-767, Kok,L.C.,et al, 2002



Showing articles 1650 to 1700 of 3794 << Previous Next >>