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acoustic nerve
advances in neurology
alien hand syndrome
alpha-fetoprotein
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anti IgLON5
anticholinergic drugs
anxiety
aphasia
aphasia, progressive, primary
aphonia
applause sign
apraxia
apraxia of eye movements
arm swing, reduced
aspiration
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic-dystonia syndromes
athetosis
attention span
autoantibodies
autoimmune basal ganglia encephalitis
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basilar impression
behavioral disorder
biologic markers
biopterin deficiency
bladder dysfunction
blepharospasm
bradykinesia
brainstem, atrophy
brainstem, lesion of
bruxism
bulbar palsy
calcitonin
carbamazepine
carcinoembryonic antigen
carcinoma
cardiomyopathy
cataplexy
cataracts
central hypoventilation
cerebellar ataxia, children
cerebellar ataxia, hereditary
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cerebellar degeneration
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebrovascular accident
cerebrovascular accident, young adult
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 20
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
comorbidities
compression fracture
conjugate gaze, forced
conversion reaction
cortical-basal ganglionic degeneration
cranial neuropathy, multiple
crying, pathologic
cultured skin fibroblasts
degenerative diseases of CNS
delay in diagnosis
dementia
developmental milestones, loss of
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
diurnal variation
dopa responsive dystonia
downward gaze
drooling
dysarthria
dysarthria-clumsy hand syndrome
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, face
dystonia, focal
dystonia, psychogenic
dystonia, treatment of
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
enzyme, defect
equinovarus
exercise
exercise-induced neurologic dysfunction
exome sequencing
exophthalmus
eye movement, disorders of
facial nerve palsy
falling
familial
fine motor function, impaired
foam cells
foot deformity
frontal behavioral spatial syndrome
gait disorder
gait, apraxic
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gangliosidosis GM1
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamic acid decarboxylase, antibody
grasp reflex
grimacing
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hand weakness
hands, fisted
head circumference
headache
hearing loss
heart block
hemidystonia
hemifacial spasm
hemiplegia
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
HLA
hoarseness
Hodgkin's disease
hydrocephalus
hyperreflexia
hypometric saccades
hypophonia
hyposmia
hypotonia
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
immunotherapy
inattention
incontinence, fecal
incoordination
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
iron, brain
Jakob-Creutzfeldt disease
jaundice
Kayser-Fleischer ring
Kearns-Sayre syndrome
laughing, pathologic
L-dopa
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
leucine rich glioma inactivated 1 antibodies
leukemia
limbic encephalitis
lipid storage disorder of CNS
liver disease
low back pain
lymphoma
macular degeneration
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
mental retardation
mental status, abnormal
MERRF syndrome
midbrain
midbrain, atrophy
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoclonal antibodies
mortality
motor dysfunction
movement disorder
movement disorder, extrapyramidal
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, mouse ears
MRI, negative
MRI, paramagnetic effect
MRI, spine
multiple system atrophy
muscle spasm, face
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neurologic symptoms, unexplained
neuroophthalmology
neuropathology
neuropathy
Niemann-Pick disease
NMDA antagonists
numb clumsy hands syndrome
nystagmus
ocular motility, disorders of
opened mouth
ophelia syndrome
ophthalmoplegia
optic atrophy
optic atrophy, unilateral
optic neuropathy
optokinetic nystagmus, abnormal
Paget's disease
Paget's disease, psychosis in
Paget's disease, spinal cord problem in
pain
palilalia
pancytopenia
PANK2 mutation
paraparesis
parasomnia
parkin gene
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, differential diagnosis of
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
paroxysmal neurologic deficits
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penguin silhouette sign
personality change
personality disorder
pigmentary retinopathy
pitfalls
pleocytosis of cerebrospinal fluid
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
procyclidine
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
pull test
radiation hypersensitivity
radiculopathy
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
Red flags
release phenomena
respirations in CNS disease
retinal artery occlusion
retinal hemorrhages
retinopathy
retrocollis
Rett's syndrome
reversible neurologic disorder
review article
rigidity
rigidity, axial
risk factors
rituximab
root lesion, nerve
running
saccadic eye movements, abnormal
salivation, excessive
screening
seizure
sensorineural hearing loss
sensory loss, cortical
sequencing difficulty
serologic testing
serologic testing, false negative
seronegative
short stature
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
speech disorder
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
stare
steroid
steroid therapy, CNS treatment and complications with
striatal encephalitis
suck reflex
superior orbital fissure syndrome
swallow evaluation
tau protein
tauopathy
telangiectases
tetrahydrobiopterin
toe walking
tonic foot response
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, postural
tremor, psychogenic
trigeminal neuralgia
tripping
upgaze
upgaze, paralysis of
urinary incontinence
vertebral-basilar insufficiency
vision, blurred
visual symptoms
vocal cord paralysis
walking
walking frame
walking, difficulty with
weight loss
wheelchair
wide based gait
Wolfram syndrome
Showing articles 50 to 100 of 8601 << Previous Next >>

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

A 57-Year-Old Man with Stepwise Progressive Paraparesis, Sensory Loss, Urinary Retention, and Constipation
Neurol 98:e555-e560, Alkabie, S.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
Neurol 98:251-255, Decker, J. & Singh, M., 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

A 68-Year-Old Man with Palmar Rash, Leg Pain, and Inability to Walk
Neurol 99:347-353, YoungHun, J.,et al, 2022

Functional Neurological Disorders
Neurologist 27:276-289, Mishra, A. & Pandey, S., 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Nonalcoholic Wernicke Encephalopathy
Neurol 97:e1541-e1542, Hansen, G.,et al, 2021

Shoulder-Tap Test for Functional Gait Disorders
Neurol 97:1070-1071, Coebergh, J.,et al, 2021

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

Paraneoplastic Myeloneuropathies
Neurol 96:e632-e639, Shah, S.,et al, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Bithalamic Lesions
Stroke 51:e355-e358, Chen, P.M.,et al, 2020

Clinicopathologic Conference, LGI1 autoimmune encephalitis
NEJM 382:1943-1950, Case 15-2020, 2020

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

Opsoclonus in Anti-Ma2 Brain-Stem Encephalitis
NEJM 383:e84, Sacks, C.A.,et al, 2020

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

Clinical and Radiologic Features of Pedicatric Opioid Use-Associated Neurotoxicity with Cerebellar Edema (POUNCE) Syndrome
Neurol 94:710-712, Kim, D.D. & Prasad, A.N., 2020

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke
Neurologist 25:82-84, Uzawa, A.,et al, 2020

Psychogenic Paroxysmal Hemifacial Spasm
Ann Neurol 88:14-15, Park, J.E., 2020

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

Cyclic Vomiting Syndrome in Children
AJGH 2:doi:10.33552/AJGH.2020, Al-Ansari, N., 2020

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

Neurosyphilis
NEJM 381:1358-1363, Ropper, A.H.,et al, 2019



Showing articles 50 to 100 of 8601 << Previous Next >>