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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 1050 to 1100 of 3794 << Previous Next >>

Miller Fisher Syndrome with Positivity of Anti-GAD Antibodies
Clin Neurol Neurosurg 115:1479-1481, Pietrini, V.,et al, 2013

Bilateral Cerebellar Peduncle Lesions in JC Virus Encephalitis
IJID 17:e1086-e1087, , 2013

Cerebral Amyloid Angiopathy and Transient Focal Neurological Episodes
Cerebrovasc Dis 36:245-246, Charidimou, A.,et al, 2013

Mystery Case: A Young Boy with Myoclonic Jerks
Neurol 81:e130-e134, Musleh, C.,et al, 2013

A Pilot Study of Focused Ultrasound Thalamotomy for Essential Tremor
NEJM 369:640-648, Elias, W.J.,et al, 2013

Tolosa-Hunt Syndrome - a Rare Cause of Headache and Ophthalmoplegia
Lancet 382:912, Zurawski, J. & Akhondi, H., 2013

Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
NEJM 369:1253-1261, Case 30-2013, 2013

Chiasmal Enlargement and Enhancement in Leber Hereditary Optic Neuropathy
Neurol 81:e126-e127, Ong, E.,et al, 2013

Central Nervous System Involvement in Whipple Disease
Medicine 92:324-330, Compain, C.,et al, 2013

Recurrent Meningitis
www.MedLink.com, Aug, Greenlee, J.E.,et al, 2013

Tumefactive MS Lesions under Fingolimod
Neurol 81:1654-1658, Pilz, G.,et al, 2013

Extending the KCNQ2 encephalopathy Spectrum
Neurol 81:1697-1703, Weckhuysen, S.,et al, 2013

Clinical Reasoning: A Woman with Recurrent Aphasia and Visual Field Defects
Neurol 81:e141-e144, Nourbakhsh, B.,et al, 2013

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

Faxtor Xa Inhibitors Versus Vitamin K Antagonists for Preventing Cerebral or Systemic Embolism in Patients with Atrial Fibrillation
Stroke 44:e165-e167, Bruins, K.M.H., & Berge, E., 2013

Spectrum of Transient Visual Symptoms in a Transient Ischemic Attack Cohort
Stroke 44:3312-3317, Lavallee, P.C.,et al, 2013

Evaluation of Patients for Paroxysmal Atrial Fibrillation after Ischemic Stroke
Stroke 44:e168-e170, Sundararajan, K.,et al, 2013

Edoxaban Versus Warfarin in Patients with Atrial Fibrillation
NEJM 369:2093-2104, Giugliano, R.P.,et al, 2013

Clinical Features of MS Associated with Leber Hereditary Optic Neuropathy mtDNA Mutations
Neurol 81:2073-2081, Pfeffer, G.,et al, 2013

Parkin Disease
JAMA Neurol 70:571-579, Doherty, K.,et al, 2013

Newly Diagnosed Atrial Fibrillation Linked to Wake-Up Stroke and TIA
Neurol 80:1834-1840, Riccio, P.,et al, 2013

Aquaporin-4 Antibody-Positive Cases Beyond Current Diagnosis Criteria for NMO Spectrum Disorders
Neurol 80:2210-2216, Sato, D.,et al, 2013

Summary of Evidence-Based Guideline Update: Evaluation and Management of Concussion in Sports
Neurol 80:2250-2257, Giza, C.,et al, 2013

Insertable Cardiac Event Recorder in Detection of Atrial Fibrillation After Cryptogenic Stroke
Stroke 44:2007-2009, Etgen, T.,et al, 2013

Clinicopathologic Conference, Oligoastrocytoma, Grade II with Temporal-Lobe Seizure and Ictal Asystole (Arrhythmogenic Epilepsy)
NEJM 368:2304-2312, Case 18-2013, 2013

Clinicopathologic Conference, Blind and Confused, Neuromyelitis Optica Spectrum Disorder
JAMA Neurol 70:932-936, Sharma, V.,et al, 2013

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Carotid Plaque Hemorrhage on Magnetic Resonance Imaging Strongly Predicts Recurrent Ischemia and Stroke
Ann Neurol 73:774-784, Hosseini, A.,et al, 2013

Stroke Patients with Suspected Atrial Fibrillation Should be Started on Anticoagulation Pending the Results of Long-Term Cardiac Monitoring
Stroke 44:298-299,302, Diener, H., 2013

Stroke Patients with Suspected Atrial Fibrillation Should NOT be Started on Anticoagulation WHILE AWAITING the Results of Long-Term Cardiac Monitoring
Stroke 44:300-301,302, Katsnelson, M. & Sacco, R., 2013

Symptomatic Recurrence of Intracranial Arterial Dissections Follow-Up Study of 143 Consecutive Cases and Pathological Investigation
Stroke 44:126-131, Ono,H.,et al, 2013

Efficacy and Safety of Everolimus for Subependymal Giant Cell Astrocytomas Associated with Tuberous Sclerosis Complex (EXIST-1): A Multicenter, Randomized, Placebo-Controlled Phase 3 Trial
Lancet 381:125-132, Franz, D.,et al, 2013

Pilot Randomized Trial of Outpatient Cardiac Monitoring After Cryptogenic Stroke
Stroke 44:528-530, Kamel, H.,et al, 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Diffusion-Weighted Magnetic Resonance Imaging May Underestimate Acute Ischemic Lesions
Stroke 44:1056-1061, Kawana, H.,et al, 2013

Hospital-Onset Seizures
JAMA Neurol 70:360-364, Fields, M.C.,et al, 2013

Teaching NeuroImages: Acute Cerebellitis Caused by Salmonella Typhimurium
Neurol 80: e118, Rizek, P.,et al, 2013

A Man with Tingling Fingers
BMJ 346:f1443, Larkman, M.,et al, 2013

Transglutaminase 6 Antibodies in the Diagnosis of Gluten Ataxia
Neurol 80:1740-1745, Hadjivassilou, M.,et al, 2013

Longitudinally Extensive Transverse Myelitis in Neuro-Beh�et Disease
Neurol 80:e189-e190, Graham, D.,et al, 2013

Occult Atrial Fibrillation in Cryptogenic Stroke
Stroke 44:1449-1452, Ritter, M.,et al, 2013

Limbic Encephalitis as the Presenting Feature of Sj�gren Syndrome
Neurol Clin Pract 3:165-167, Finelli, P. & Inoa, V., 2013

Incidence of Atrial Fibrillation Detected by Implantable Loop Recorders in Unexplained Stroke
Neurol 80:1546-1550, Corter, P.,et al, 2013

Association Between Childhood Migraine and History of Infantile Colic
JAMA 309:1607-1612,1636, Romanello, S.,et al, 2013

Cost-Effectiveness of Apixaban, Dabigatran, Rivaroxaban, and Warfarin for Stroke Prevention in Atrial Fibrillation
Stroke 44:1676-1681, Harringotn, A.,et al, 2013

Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
NEJM 368:1992-2003, Margolin, D.,et al, 2013

Summary of Evidence-Based Guideline: Periprocedural Management of Antithrombic Medications in Patients with Ischemic Cerebrovascular Disease
Neurol 80:2065-2069, Armstrong, M.,et al, 2013

Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
NEJM 368:1971-1979, Shirley, M.,et al, 2013

Management of Anticoagulation Before and After Elective Surgery
www.uptodate.com Dec. 2012, Lip, G. & Douketis, J., 2012

Stroke and Bleeding in Atrial Fibrillation with Chronic Kidney Disease
NEJM 367:625-635, Olesen, J.B.,et al, 2012



Showing articles 1050 to 1100 of 3794 << Previous Next >>