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Differential
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acanthocytosis
acral sensory symptoms
Addison's disease
Adies pupil
adrenomyeloneuropathy
adult polyglucosan body disease
adverse drug reaction
allodynia
alternating rapid movement
alternating rapid movement, impaired
ammonia
amyotrophic lateral sclerosis, differential diagnosis
ANA
anemia
angiography, cerebral, beaded vessels
angiography, cerebral
ankle edema
ankle reflex, absent
anorexia
anorexia nervosa
anti citrullinated antibody
anti MAG antibodies
anticonvulsants
anticonvulsants, untoward effects of
areflexia
arrhythmia, cardiac
arsenic
arteritides
arthralgia
ascending paralysis
ascites
astereognosis
astrocytoma
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
athetosis
atrophy, muscle
auditory evoked brainstem potentials
autonomic dysfunction
axonal degeneration
axonopathy, distal
B 12 deficiency
Babinski sign
BAL
basal ganglia, lesion of
basophilic stippling of red blood cells
bedridden
beriberi
biologic markers
bladder dysfunction
blink reflex
bone marrow suppression
bradykinesia
brainstem, infarction of
bulbar palsy
burning paresthesia
cachexia
calf atrophy
carcinoma
cardiac arrest
cardiac arrest and resuscitation
cardiomegaly
cardiomyopathy
cast
CAT scan
CAT scan, abdomen
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cauda equina
cauda equina, enhancement
cauda equina, lesion of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar lesion
cerebellum, disease of
cerebrospinal fluid, abnormal
cerebrospinal fluid, drainage of
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, mimics
Charcot-Marie-Tooth
chest x-ray, abnormal
children
cholestanol
chorea
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
coma
compression neuropathy
conduction block
confusion
congenital myopathy
congestive heart failure
corneal reflex, abnormal
corneal reflex, absent
cough
cranial nerve enhancement
cranial neuropathy
cranial neuropathy, multiple
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
deep gray nuclei
dementia
demyelinating disease
denervation potentials
dermatitis
descending paralysis
dexterity, impaired
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diabetic mononeuropathy
diarrhea
differential diagnosis
difficulty climbing stairs
digital health, wearable technology
diplopia
dissociated sensory loss
distal muscle atrophy
distal muscle weakness
drowsiness
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
edema, pedal
edema, periorbital
efficacy
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, inflammatory disease
electromyogram
electromyogram, decremental response
electron microscopy
encephalopathy
entrapment neuropathy
enzyme, defect
enzyme, muscle disease
eosinophilia
erythrocyte
ethylene oxide
evoked potentials
exercise
exome sequencing
eye movement, disorders of
face, numbness of
facial pain
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failed medical management
fall prevention
fall risk
falling
familial
fasciculation
fatigue
fever
fibrillations
fine motor function, impaired
fingernails, abnormal
flaccid paralysis
foot deformity
foot drop
foot, swollen
Friedreich's ataxia
F-wave response
gadolinium
gait disorder
gait speed
gait, waddling
gammaglobulin therapy, intravenous
ganglionitis
gastroenteritis
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glioma
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, infantile and childhood form
Guillain Barre syndrome, sensory
hammertoes
hand deformity
hand numbness
hand swelling
hand weakness
headache
headache, severe
hearing loss
heavy metal intoxication
heel-knee-shin test
hemoglobinuria
hepatitis
hepatosplenomegaly
heralding manifestation
herpes simplex virus
herpes virus
herpes virus infection
herpes, genital
high arched feet
hip flexor weakness
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
hot cross bun sign
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, treatment of
hyperamylasemia
hyperkeratosis
hypersomnia
hypogonadism
hyponatremia
hypophosphatemia
hypopigmentation of skin
hyporeflexia
hypotonia
imbalance
imbalance, postural
immunoelectrophoresis, serum
immunohistochemistry
immunomodulation
immunosuppression
immunosuppressive agents
inappropriate antidiuretic(A.D.H.)hormone
inclusion bodies
incoordination
industrial neurologic disorders
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
Jakob-Creutzfeldt disease
jaw pain
Jewish
lactic dehydrogenase(LDH)
leg atrophy
leg numbness
leg weakness, bilateral
leg weakness, unilateral
lethargy
leukodystrophy
leukoencephalopathy
leukopenia
lid closure, weakness of
liver disease
liver function enzymes
long bone lesion
lumbosacral plexopathy
lymphadenopathy
lymphoma
McLeod syndrome
mediastinum, mass of
Mees lines
memory, impairment of
meningeal enhancement
meningismus
mental status, abnormal
midbrain, atrophy
midbrain, infarction of
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuritis multiplex
mononeuropathy
mononeuropathy chronic inflammatory demyelinating
mononeuropathy, children
mortality
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, lumbosacral plexus
MRI, muscle
MRI, negative
MRI, peripheral nerve
MRI, spinal cord
multiple myeloma
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, facioscapulohumeral
myasthenia gravis
myasthenia gravis, late-onset
myasthenia gravis, misdiagnosis of
myasthenia gravis, presenting manifestations
myelin protein zero gene
myeloma, osteosclerotic
myelomalacia
myeloneuropathy
myelopathy
myoclonic jerks
myopathy
myopathy, focal
myopathy, monomelic
nausea and vomiting
neoplasm, primary intracerebral
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
nerve conduction studies, sensory
nerve enlargement
nerve hypertrophy
nerve root biopsy
nerve root enhancement
nerve root hypertrophy
neuritis, heavy metals causing
neuroendocrinology
neurogenic bladder
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuronopathy
neuronopathy, sensory
neuronopathy, sensory and motor
neuropathology, brain
neuropathy
neuropathy, chronic
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, toxic
neuropathy, vasculitic, systemic
night blindness
numbness, extremity
numbness, generalized
nystagmus
occupational neuropathies
old age, neurology of
opportunistic infection
organomegaly
ornithine transcarbamylase deficiency
orthostatic hypotension
pain
pain, abdominal
pain, back
pain, calf
pain, foot
pain, leg
pain, thigh
pain, total body
pancreatitis
pancytopenia
papilledema
paraneoplastic ganglionopathy
paraparesis
paraparesis, spastic
paraproteinemia
parenteral alimentation
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
Parkinson disease, diagnosis
Parkinson disease, early symptoms
Parkinson disease, presymptomatic detection
periarteritis nodosa
pericardial effusion
pericarditis
perioral numbness
peripheral blood smear
peripheral blood smear, abnormal
peroneal nerve
peroneal nerve palsy
peroneal nerve palsy, bilateral
peroneal nerve, lesion of
pes cavus
plasmacytoma
pleocytosis of cerebrospinal fluid
pleural effusion
pneumonia
POEMS syndrome
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic inflammatory demyelinating, childhood
polyradiculoneuropathy
position sensation, abnormal
positional head-hanging test
posterior column disease
postoperative neurologic complications
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proprioception
proprioception, abnormal
pruritus
pseudohypertrophy
psychological testing
pulmonary infiltrates
pupil
pupil, dilated and fixed, bilateral
pyramidal
pyramidal tract dysfunction
quadriceps atrophy
quadriparesis
quadriplegia
reading disorder, acquired
real-time quaking-induced conversion
remote effect of cancer on the nervous system
renal cell carcinoma
repetitive nerve stimulation
respiratory failure
retroperitoneal mass
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rheumatoid arthritis, neurologic complications of
rheumatoid vasculitis
risk factors
rituximab
Romberg's sign
Sabin-Feldman dye test
saccadic eye movements, abnormal
scannig speech
sciatic neuropathy
sclerosis, bone
sedimentation rate
sedimentation rate, elevated
sensory ganglia
sensory ganglia, abnormal
sensory loss
sensory loss, asymmetric
sensory loss, band distribution
sensory polyneuropathy
serum glutamic oxaloacetic transaminase
shooting pain
shoulder-girdle wasting
shunt procedure, ventricular
Sjogren's syndrome
skin, lesions in neurologic disorders
slurred speech
sodium valproate
sodium valproate, toxicity
somatosensory evoked potentials
spasticity
speech disorder
speech disorder, non aphasic
splenomegaly
staggering
steppage gait
steroid
steroid therapy, CNS treatment and complications with
suspended sensory loss
sweating, abnormality of
synovitis
systemic illness
Tai chi
tandem gait, ataxic
tauopathy
telangiectases
temporalis muscle wasting
thiamine deficiency
thrombocytopenia
thrombocytosis
thrush
tongue, fasciculations of
toxoplasma complement fixation test
toxoplasmosis, acquired
toxoplasmosis, CNS
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremor, postural
trigeminal nerve, abnormality of
turning slowly
urea-cycle enzymopathies
uremia
urinary incontinence
urine test in toxic screen
uveitis
varicella zoster virus
vascular endothelial growth factor
vasculitides
vestibular migraine
vestibulopathy
vibratory sensation
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual impairment
vitamin deficiency
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weight loss
wheelchair
whistle, inability to
white matter disease
wide based gait
winging of scapula
workup
zoster sine herpete
Showing articles 50 to 100 of 2661 << Previous Next >>

A Woman with Parkinson Disease, Dyskinesia, Rhadomyolysis, Subcutaneous Emphysema, and Pneumomediastinum
Neurol 106:e218064, Iqbal,M.M.,et al, 2026

A 50-Year-Old Male Patient With Acute Severe Sensory Deafferentation and Bilateral Ptosis with Rapid Recovery
Neurol 106:e214435, Pseruk,F.,et al, 2025

Niemann-Pick Disease Type C
Gene Reviews www.genereview.org, Bremova-Ertl,T. & Patterson, M., 2025

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

A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
Neurol 105:e214429, Trentadue,T.,et al, 2025

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

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

Methamphetamine-Induced Basal Ganglia Toxicity Presenting as Parkinsonism
Neurol 104:e213365, Yi,M.Y.,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

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

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

Long-Term Consumption of Ultraprocessed Foods and Prodromal Features of Parkinson Disease
Neurol 104:e213562, Wang,P.,et al, 2025

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

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,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

Isolated Foot Drop, An Unusual Presentation of a Disabling NIHSS 0 Stroke
Neurologist 30:264-265, Couto,R.,et al, 2025

Clinicopathological Conference, Powasan Virus Encephalitis
NEJM 393:176-184, Case 19-2025, 2025

The Spectrum of Fragile X Disorders
NEJM 393:281-288, Hagerman,R.H. & Hagerman,P.J., 2025

A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
Neurol 105:e213993, Shen,F.,et al, 2025

A 73-Year-Old Man With Progressive Proximal Muscle Weakness and Binocular Diplopia
Neurol 105:e214173, Wold,K.J.,et al, 2025

Gait Analysis in Neurologic Disorders, Methodology, Applications and Clinical Considerations
Neurol 105:e214154, Ali,F.,et al, 2025

Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
Neurol 105:e214099, Mizutani,H.,et al, 2025

A 58-Year-Old Man With Resting tremor, Bradykinesia, and Distal Numbness
Neurol 105:e214183, Costa,R., et al, 2025

A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
Neurol 105:e214233, Bu,S.,et al, 2025

A 38-Year-Old Man With Involuntary Jerk-Like Movements and Ataxia
Neurol 105:e214381, Gomez,A.C.et al, 2025

A 24-Year-Old Man With Persistent Spontaneous Dizziness
Neurol 105:e214337, Isaza-Pierotti,D.F., et al, 2025

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 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

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

Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
Neurol 102:e208040, Alferes,A.R.,et al, 2024

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

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

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

Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
Neurol 102:e209259, Moehlman,M. & Kornbluh,A.B., 2024

Association of Coffee Consumption and Prediagnostic Caffeine Metabolites with Incident Parkinson Disease in a Population-Based Cohort
Neurol 102:e209201, Zhao,Y.,et al, 2024

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

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

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

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

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,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

SGLT2 Inhibitor Use and Risk of Dementia and Parkinson Disease Among Patients With Type 2 Diabetes
Neurol 103:e209805, Kim,H.K.,et al, 2024

Neurologic Manifestations of Hyperthyroidism and Graves Disease
www.UptoDate.com, Oct 28, Rubin,D.I., 2024

Skin Lesions, Foot Drop, and Hand Contractures
JAMA doi:10.1001/JAMA.2023.9915, Filley,A.R.,et al, 2023

Risk of Parkinson Disease Among Service Members at Marine Corps Base Camp Lejeune
JAMA Neurol 80:673-681, Goldman,S.M.,et al, 2023



Showing articles 50 to 100 of 2661 << Previous Next >>