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Differential
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acetazolamide
adverse drug reaction
agnosia, color
akathisia
akinesia of eyelid function
alexia without agraphia
algorithm
alien hand syndrome
alpha-fetoprotein
Alzheimer's disease
amnesic stroke
anatomy of
anemia
ankle edema
anti IgLON5
anticholinergic drugs
anticholinesterase
anxiety
aphasia
aphasia, progressive, primary
aphonia
applause sign
apraxia
apraxia of eye movements
apraxia of eyelid opening
arm swing, reduced
arylsulfatase A
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
athetosis
autoantibodies
Babinski sign
basal ganglia
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bent spine syndrome
biologic markers
biopterin deficiency
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
blepharospasm
botulinum toxin
bradykinesia
brain biopsy
brain damage
brainstem, dysfunction
brainstem, lesion of
bruxism
bulbar dysfunction
bulbar palsy
CAG repeats
calcification, intracranial
camptocormia
carbamazepine
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, false negative
CAT scan, muscle
cataracts
caudate nucleus, atrophy
central hypoventilation
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar pontine angle
cerebellar pontine angle tumor
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral palsy
cerebral palsy, associated problems with
cerebral peduncle
cerebrovascular accident
ceruloplasmin, serum
channelopathy
Charcot's sign
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 20
cirrhosis
cisterna magna
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
cold intolerance
coma
coma, episodic
comorbidities
complications
conjugate gaze, forced
consanguinity
conversion reaction
cortical-basal ganglionic degeneration
cranial nerve palsies
creatine phosphokinase(CPK)elevated
crying, pathologic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
depression
dexterity, impaired
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
diplopia
diurnal variation
donepezil
dopa responsive dystonia
down-beat nystagmus
downward gaze
drooling
drug induced neurologic disorders
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, facial
dysmetria
dysphagia
dysphasia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, classification
dystonia, drug induced
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, painful
dystonia, post traumatic
dystonia, treatment of
dystonia, truncal
dystonic reaction, acute
DYT1 mutation
edema, pedal
electromyogram
emotional lability
employment
encephalitis, autoimmune
enzyme, defect
ependymoma
episodic disorders
episodic neurologic deficits
equinovarus
esophageal varices
ethics in neurology
exercise
exercise-induced neurologic dysfunction
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial expression abnormality
falling
familial
fever
fine motor function, impaired
fluctuate
foot deformity
fourth ventricle, enlargement of
fourth ventricle, neoplasm of
frontal behavioral spatial syndrome
gait disorder
gait, apraxic
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
gests antagoniste
glabellar sign
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
globus pallidus, stimulation
grasp reflex
grimacing
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hand weakness
hands, fisted
head nodding
headache
health insurance
hearing loss
hemiakathisia
hemianopia
hemianopia, homonymous
hemichorea
hemidystonia
hemifacial spasm
hemiplegia
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
HLA
hoarseness
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's disease, children
hyperreflexia
hypoalbuminemia
hypometric saccades
hypophonia
hypotonia
iatrogenic neurologic disorders
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
immunotherapy
inattention
incontinence, fecal
incoordination
insomnia
intellectual deficit
intellectual deterioration
internet
intracranial pressure, increased
iron, brain
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Kayser-Fleischer ring
kyphosis
laughing, pathologic
L-dopa
leg spasms
leg spasms, painful
leg weakness, bilateral
lenticular nucleus, lesion of, bilateral
leukemia
leukodystrophy
leukopenia
levitation
lithium
liver disease
liver function enzymes
low back pain
lymphoma
lysosomal storage disease
manganese intoxication
masked facies
memory, defect of recent
memory, impairment of
meningismus
meningitis
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
midbrain
midbrain, atrophy
midbrain, infarction of
migraine
misdiagnosis
molecular genetics
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, extrapyramidal-treatment of
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, mouse ears
MRI, negative
MRI, paramagnetic effect
MRI, spine
MRI, T1 weighted high signal foci
MRS
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle hypertrophy
muscle spasm, face
muscle weakness
muscular dystrophy
myasthenia gravis
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myokymia
myopathy
myopathy, metabolic
myorhythmia
neoplasm, posterior fossa
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neurocutaneous disease
neuroendocrinology
neuroleptic
neuroleptic, atypical
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neuromyotonia
neuroophthalmology
neuropathology
neuropathy
numb clumsy hands syndrome
nystagmus
nystagmus, vertical
obsessive-compulsive disorder
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
old age, neurology of
opened mouth
ophthalmoplegia
optic atrophy
pain
palilalia
palinopsia
PANK2 mutation
paraparesis
parasomnia
paraspinal muscle
paraspinal muscle weakness
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
pathology
penguin silhouette sign
penicillamine
personality change
pigmentary retinopathy
Pisa syndrome
pitfalls
pleocytosis of cerebrospinal fluid
polycythemia, secondary
posterior cerebral artery
posterior cerebral artery embolism
posterior cerebral artery territory infarction
postural abnormality
precipitating factors
pregnancy, neurologic complications in
primary episodic ataxia
procyclidine
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
pull test
pure sensory stroke
pyramidal tract
pyramidal tract dysfunction
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
Red flags
release phenomena
renal stones
respirations in CNS disease
retinal degeneration
retinitis pigmentosa
retinopathy
retrocollis
retropulsion
Rett's syndrome
reversible neurologic disorder
review article
rigidity
rigidity, axial
risk factors
running
saccadic eye movements, abnormal
salivation, excessive
Saudi Arabia
screening
sea-blue histiocytes
seizure
sensorineural hearing loss
sensory loss
sensory loss, cortical
sensory tricks
sequencing difficulty
short stature
shoulder, elevation
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
somnolence
spasticity
speech disorder
speech disorder, childhood
spinal cord
spinal cord, lesion of
spinal muscular atrophy
splenomegaly
stare
stem cell transplantation
stimulation, deep brain
stimulation, deep brain, bilateral
stooped posture
striatum, lesion of
striatum, lesion of, bilateral
substantia nigra
suck reflex
suicide
swallow evaluation
symmetric brain lesions
tardive dystonia
tau protein
tauopathy
telangiectases
tetrahydrobiopterin
thalamus, infarction of
thrombocytopenia
toe walking
tonic foot response
torticollis
trauma
treatment of neurologic disorder
treatment, empirical
tremor
tremor, intention
tremor, jaw
tremor, postural
tricyclic antidepressant
trientine dihydrochloride
trinucleotide repeats
tripping
upgaze
upgaze, paralysis of
urinary incontinence
urinary sulfatidase excretion
vision, blurred
visual evoked response
visual field defect
visual symptoms
vocal cord paralysis
walking
walking frame
walking, difficulty with
weakness, progressive
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
zinc
Showing articles 50 to 100 of 1183 << Previous Next >>

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Risk Assessment and Prevention of Falls In Older Community-Dwelling Adults
JAMA doi.10.1001/JAMA.2024.1416, Colon-Emeric,C.S.,et al, 2024

Posttransplant Anti-GABAA Receptor Antibody-Associated Autoimmune Encephalitis
Neurol 102:e209245, Togni,C.L.,et al, 2024

Diffusely Enhancing Lesions on MRI in DPPX Antibody-Associated Encephalitis
JAMA Neurol 8:418-419, Liu,M.,et al, 2024

Bilateral Hemifacial Spasm and Left Glossopharyngeal Neuralgia Caused by Bilateral Vertebral Artery Displacement
Neurol 102:e209422, Han,Z.,et al, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
Neurologist 29:166-169, Eaton,J.E.,et al, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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Congenital and Acquired Chiari Syndrome
NEJM 390:2191-2198, Friedlander,R.M., 2024

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Wernekinck Commissure Syndrome
Radiopaedia doi.org/10.53347/rlD-85274, Aug, Deng,F.,et al, 2023

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

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

A 47-Year-Old Man With an Upper Respiratory Infection, Acute Confusion, Dysarthria, and Ataxia
Neurol 100:978-983, Kubicki,K.,et al, 2023

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

Neurologic Complications of Babesiosis, United States, 2011-2021
Emerg Inf Dis 29:1127-1135, Locke,S.,et al, 2023

Clinicopathologic Conference, Noncirrhotic hyperammonemia after Roux-en-Y Gastric Bypass
NEJM 389:1221-1230, Case 30-2023, 2023

Manganese Accumulation in the Brain
NEJM 389:1320, Sherman,S.V., 2023

Clinicopathologic Conference,Limb-Shaking Transient Ischemia Attacks
NEJM 389:1416-1423, Case 31-2023, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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Pachymeningitis and Aortitis as the Initial Presentation of Granulomatosis with Polyangiitis
Neurol 101:979-980, Li,X.,et al, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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Occult Breast Cancer with Anti-Ri Antibody Positivity and Pontine Hot Cross Bun Sign
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A 57-Year-Old Man with Stepwise Progressive Paraparesis, Sensory Loss, Urinary Retention, and Constipation
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A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
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Clinicopathologic Conference, Neurosyphilis
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A Dizzy Architect
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A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
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More Than a Little Unsteady
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Progressive Vertebrobasilar Vasculopathy and Stroke Secondary to Giant Cell Arteritis
Stroke 53:e435-e438, Mahjoub, Y.,et al, 2022

A 68-Year-Old Man with Palmar Rash, Leg Pain, and Inability to Walk
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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

Torticollis in a Child with Otalgia
BMJ 378:e070608, Sarathi, C.I.P.,et al, 2022

Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
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Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
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Showing articles 50 to 100 of 1183 << Previous Next >>