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Differential
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acetazolamide
adrenergic blocker
advances in neurology
adverse drug reaction
agoraphobia
airway obstruction
alcohol
alcohol, neurologic complications with
alcoholism
Alexanders disease
Alexanders disease, adult onset
algorithm
alpha adrenergic blocker
alprazolam
alternating rapid movement
Alzheimer's disease
amenorrhea
aminoacidurias
ammonia
amygdala
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
anatomy of
anemia
anemia, hemolytic
ankle edema
ankle reflex, absent
ankle, swelling of
anorexia
anterocollis
anticholinergic drugs
anticonvulsants
anticonvulsants, untoward effects of
aphonia
areflexia
arotinolol
artane
arylsulfatase A
ascites
asterixis
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic-dystonia syndromes
athetosis
athetosis, causes of
attention deficit disorder with hyperactivity
atypical
auditory evoked brainstem potentials
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Behcet's syndrome
benign essential tremor
benign essential tremor, refractory
beta adrenergic blocker
biologic markers
blepharospasm
blinking, reduced
botulinum toxin
botulinum toxin, complications of
bradykinesia
brain atrophy
brainstem, lesion of
Brueghel's syndrome
caffeine
CAG repeats
calcification, intracranial
calcium antagonist
camptocormia
carbon monoxide poisoning
carbonic anhydrase inhibitor
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
catecholamine
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum, disease of
cerebral blood flow
cerebral cortical atrophy
cerebral infarction
cerebral ischemia
cerebral palsy
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
ceruloplasmin, serum
Charcot-Marie-Tooth
children
chorea
chorea, causes of
choreoathetosis
chromosomal abnormality
chromosome 14
chromosome 3
cingulate island sign
cirrhosis
cirrhosis, causes of childhood
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
coat-hanger pain
cognition
cogwheel rigidty
Collier's sign
complicated migraine
complications
consanguinity
copper
copper metabolism, abnormal
corpus callosum, lesion of
corpus callosum, thinning
cough
cyst
cyst, parenchymal
deafness
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delayed dentition
dementia
dementia, childhood
dementia, familial
depression
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diarrhea
diet
differential diagnosis
dilantin
disability, neurological
distal muscle atrophy
distal muscle weakness
dizziness
dopa responsive dystonia
dopamine
dopamine agonist
drooling
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysmetria
dysphagia
dysphonia
dyspnea
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, laryngeal
dystonia, post traumatic
dystonia, prevalence of
dystonia, symptomatic
dystonia, treatment of
DYT1 mutation
edema, pedal
efficacy
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
emotional lability
encephalitis
encephalitis, Japanese
encephalitis, viral
epidemiology of neurology
equinovarus
erectile dysfunction
esophageal varices
evoked potentials
excitotoxin
exome sequencing
eye movement, disorders of
facial expression abnormality
Fahr disease
failed medical management
falling
familial
familial hemiplegic migraine
fasciculation
fatigue
fine motor function, impaired
finger nose finger test
fingerprint bodies
flavivirus
flunarizine
foot deformity
foot drop
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
Friedreich's ataxia
frontal lobe, pathologic signs of
gabapentin
gait disorder
gait, festinating
gamma amino butyric acid
gamma knife therapy
gaze palsy
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
gests antagoniste
Gilles de la Tourette syndrome
glabellar sign
globus pallidus
globus pallidus, lesion of
glucose tolerance test, abnormal
granular osmiphilic material
grimacing
gynecomastia
Hallervorden Spatz disease
hammertoes
handedness
handwriting
head injury
head nodding
heavy metal intoxication
heel-knee-shin test
hemochromatosis
hemochromatosis, primary
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
hepatosplenomegaly
heralding manifestation
homovanillic acid
Huntington's chorea
hyperglycemia
hyperreflexia
hyperthyroidism
hypoalbuminemia
hypodontia
hypoglycemia
hypometric saccades
hypomyelination
hyponatremia
hyporeflexia
hyposmia
hypotension, neurologic causes of
hypotonia
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
imbalance, postural
impulsivity
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
incoordination
insomnia
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
iron, brain
Jakob-Creutzfeldt disease
jaundice
Kayser-Fleischer ring
kinesia paradoxica
kyphoscoliosis, neurologic causes of
lactic acidemia
laminectomy
laminectomy, lumbar
laterocollis
L-dopa
L-dopa, drug interactions with and side effects of
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of, bilateral
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
leukopenia
Lewy body
Lewy body disease, diffuse
lightheaded
liver disease
liver function enzymes
liver transplantation
locus ceruleus, lesion of
marche a petits pas
masked facies
memory, impairment of
mental retardation
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
metoprolol
micrographia
midbrain, atrophy
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
mirror writing
misdiagnosis
mitochondrial disease
molecular genetics
monoamines
mood change
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, negative
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle cramp
muscle stiffness
myelomalacia
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoclonus, essential
myopia
mysoline
nadolol
neck pain
negative
nerve biopsy
nerve conduction studies
neuroendocrinology
neurofibromatosis 1
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuronopathy
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropathy, sensory
neurotoxin
neurotransmitter
nigrostriatal pathway
nimodipine
norepinephrine
nutritional deficiency
nystagmus
nystagmus, pendular
nystagmus, primary position of gaze
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
obsessive-compulsive disorder
ocular motility, disorders of
old age, neurology of
opened mouth
optic atrophy
orthostatic hypotension
osmotic demyelination syndrome
pain
pain, head
palatal myoclonus
palilalia
pallidotomy
pancytopenia
panic attacks
paraparesis
paraparesis, spastic
paresthesias
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, atypical
Parkinson disease, benign tremulous
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, familial
Parkinson disease, freezing phenomena in
Parkinson disease, L-dopa nonresponsive
Parkinson disease, misdiagnosis
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
past pointing
patient information and support
Pelizaeus Merzbacher
penicillamine
personality change
pes cavus
phenobarbital
phenylketonuria
phlebotomy
poison, neurologic problems with
POLR3B
pons, lesion of
positional head-hanging test
postoperative neurologic complications
postural abnormality
practice guidelines
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
progressive supranuclear palsy
propranolol
pruritus
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
psychosocial aspects
pulmonary function tests
Purkinje cell
pursuit eye movements, abnormal
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quality of life
radiation therapy, stereotactic
radiculopathy
raphe nuclei
reading disorder, acquired
reflex sympathetic dystrophy
renal stones
respirations in CNS disease
respiratory failure
retinitis pigmentosa
retrocollis
review article
RFLPs
rigidity
Riley-Day syndrome
Rosenthal fibers
saccadic eye movements, abnormal
safety
salivation, excessive
schizophrenia
scoliosis
sea-blue histiocytes
seizure
seizure, children
seizure, differential diagnosis of
seizure, psychomotor-temporal lobe
sensory tricks
shaking
short stature
shoulder, pain in
sinemet
single photon emission computed tomography
skin, biopsy
skin, darkening of
sleep pathology and physiology
slit lamp examination
smell
Smell Identification Test
SNCA duplication
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, loss of
speech, slowed
speech, soft
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 12
spinocerebellar ataxia type 28
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spinopontine atrophy, dominant
splenomegaly
stage-fright
staggering
stare
status epilepticus
steppage gait
stereotaxic surgery
stimulation, deep brain
stimulation, thalamic
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
stridor
striopallidodentate calcifications, familial idiopathic
stuttering
substantia nigra
subthalamic nucleus
subthalamic nucleus deep brain stimulation
sural nerve
symmetric brain lesions
syncope
tandem gait, ataxic
tardive dyskinesia
tardive dystonia
tauopathy
teeth, abnormal
teeth, number of in infants
tetrabenazine
thalamotomy
thalamotuberal artery
thalamus
thalamus, focused ultrasound ablation
thalamus, infarction of
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thyrotoxicosis
tic
titubation
toe walking
tongue, fasciculations of
tonic foot response
topiramate
torticollis
torticollis, post traumatic
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, classification
tremor, differential diagnosis of
tremor, intention
tremor, jaw
tremor, leg
tremor, orthostatic
tremor, physiologic
tremor, post traumatic
tremor, postural
tremor, psychogenic
tremor, resting
tremor, rubral
tremor, surgical treatment of
tremor, thalamic stimulation for suppression of
tremor, treatment of
tremor, voice
tremor, wing beating
tremor, writing
trientine dihydrochloride
trinucleotide repeats
twins
ultrasonography
ultrasonography, head
ultrasonography, high-intensity focused
uric acid, low
urine, dark
vasospasm, cerebral
vertigo
vertigo, migraine causing
vestibulopathy
vibratory sensation, abnormal
visual evoked response
vitamin deficiency
vitamin E
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weakness
weight loss
wheelchair
white matter disease
wide based gait
workup
writers cramp
X-linked bulbospinal neuronopathy
zinc
Showing articles 150 to 200 of 2385 << Previous Next >>

Benign Essential Tremor
Lancet 471, 1972 Sept., , 1972

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Cavernous Maliformations of the Central Nervous System
NEJM 390:1022-1028, Smith,E.R., 2024

Rabbit Syndrome
Neurol102:e209275, Huynh,T.U., & Beckley, E.H., 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

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

Vascular Malformations of the Central Nervous System
www.UptoDate.Com, March, Singer,R.J.,et al, 2024

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

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

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
NEJM 391:1015-1027, Al-Samkari,H.,et al, 2024

A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
Neurol 103:e209796, Bouchart,J.,et al, 2024

Neuroleptic Malignant Syndrome
NEJM 391:1130-1138, Wijdicks,E.F.M. & Ropper,A.H., 2024

Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
Lancet 401:e2, Kovalchuk,B. & Khoramnia,R., 2023

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

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

Trial of Globus Pallidus Focused Ultrasound Ablation in Parkinsons Disease
NEJM 388:683-693, 759, Krishna,V.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.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

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 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,Limb-Shaking Transient Ischemia Attacks
NEJM 389:1416-1423, Case 31-2023, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
Stroke 54:e512-e515, Silveira,L.,et al, 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era
JAMA Neurol 79:405-413, Morton, S.U.,et al, 2022



Showing articles 150 to 200 of 2385 << Previous Next >>