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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 200 to 250 of 1608 << Previous Next >>

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

Management of Acute Retinal Ischemia
Ophthalmol 125:1597-1607, Viousse, V.,et al, 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

The Laser Shoes
Neurol 90:e164-e171, Barthel, C.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

White Matter Lesion Related to Decompression Sickness Following Extreme Breath-Hold Diving
Neurol 91:847-848, Guerreiro, C.,et al, 2018

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Neuro-Sweet Disease Presenting as Ischemic Stroke and Aseptic Meningitis
Neurol 91:e2197-e2199, Das, A.S.,et al, 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Rapid Progression of Reversible Cognitive Impairment in an 80-year-old Man
Neurol 91:1109-1113, Bouthour, W.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

A 23-year-old woman with fever and vertical diplopia
Neurol 90:e2006-e2010, Lin, D.J.,et al, 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Risk of Ischemic and Hemorrhagic Strokes in Occult and Manifest Cancers
Stroke 49:1585-1592, Andersen, K.K. & Olsen, T.S., 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018

Isolated Gait Dysfunction Due to Intracranial Hypotension
Neurol 91:271-272, Sasikumar,S.,et al, 2018

Coxa Saltans Misdiagnosed as Functional Gait Disorder
Neurol 91:276-277, Gilbert,D.L.,et al, 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Ophthalmic Manifestations of Giant Cell Arteritis
Rheumatology 57:ii63-1172, Vodopivec, I. & Rizzo, J.F. III, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Acute Bilateral Isolated Foot Drop: Changing the Paradigm in Management of Degenerative Spine Surgery with Percutaneous Endoscopy
World Neurosurg 110:319-322, Adsul, N.,et al, 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

The Tadpole Pupil
JAMA Neurol 74:481, Aggarwal, K. & Hildebrand, G.D., 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017



Showing articles 200 to 250 of 1608 << Previous Next >>