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Differential
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abdominal cramps
abdominal reflex, absent
acute disseminated encephalomyelitis
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
ageusia
akinetic mute
alcohol
Alexanders disease
Alexanders disease, adult onset
aminoacidopathies
aminoacidurias
amnestic syndrome
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, prognosis
anatomy of
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angina pectoris
anhidrosis
anosmia
anti MAG antibodies
antispasticity drugs
aphasia
arteriopathy
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
attention deficit disorder with hyperactivity
autonomic dysfunction
Babinski sign
baclofen
basal ganglia, infarction
basal ganglia, lesion of
behavioral disorder
benign essential tremor
beta adrenergic blocker
bladder dysfunction
blink reflex
bone marrow transplantation
brain biopsy
brainstem
brainstem, infarction of
brainstem, lesion of
burning paresthesia
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
CAT scan, demyelinating disease
CAT scan, serial
catecholamine
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, immunoglobulins of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
Charcot-Marie-Tooth
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
cognition
congenital malformation
congestive heart failure
corneal dystrophy
cortical blindness
cortical blindness, transient
crying, pathologic
cyst, porencephalic
cystinuria
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, cerebrovascular disease causing
dementia, presenile
dementia, subcortical
dementia, thalamic
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
depression
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
dilantin
diplopia
disability, neurological
dopamine
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysphagia
dystonia
dystonia musculorum deformens
echocardiogram
echolalia
electrical sensation
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
ELISA
emotional lability
encephalitis
encephalitis, viral
encephalomalacia
encephalopathy
encephalopathy, metabolic
enzyme, defect
evoked potentials
exercise intolerance
eye, pain in
Fabry's disease
facial nerve palsy
facial weakness
facial weakness, bilateral
Fahr disease
familial
fatigue
fever
flexor spasm
gadolinium
gait disorder
gamma amino butyric acid
gamma amino butyric acid-mimetic drug
gamma knife therapy
gangliosidosis GM2
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
glioma
glutaric acidemia
granular osmiphilic material
haloperidol
head injury
head nodding
headache
hearing loss
hearing loss, bilateral
heavy metal intoxication
hemianopia
hemianopia, transient
hemiparesis
hemiparesis, transient
hemiplegia
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatolenticular degeneration(Wilson's disease)
hiccoughs
HLA
holoprosencephaly
homovanillic acid
hormone replacement
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hydrocephalus
hyperreflexia
hypersomnia
hypertension
hyperthyroidism
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
incoordination
intellectual deficit
intellectual deterioration
interferon
interferon beta 1-a
interferon beta 1-b
intrathecal antispasticity drugs
iron, brain
Japan
Krabbe's disease
lactic acidemia
lacunar infarction
laughing, pathologic
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
Lhermitte's sign
lipid storage disorder of CNS
liver disease
Lorenzo's oil
low birth weight
magnetic susceptibility
malformation, CNS, congenital
maple syrup urine disease
MELAS syndrome
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
metronidazole
microhemorrhage, intracerebral
migraine
misdiagnosis
mitochondrial disease
monoamines
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, negative
MRI, paramagnetic effect
MRI, serial
MRI, spinal cord
MRI, T1 weighted high signal foci
MRI, volumetry
multiple sclerosis
multiple sclerosis, asymptomatic
multiple sclerosis, chronic progressive
multiple sclerosis, clinical patterns
multiple sclerosis, conjugal
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, etiology of
multiple sclerosis, familial
multiple sclerosis, linoleic acid in
multiple sclerosis, misdiagnosis
multiple sclerosis, parental transmission
multiple sclerosis, pathogenesis
multiple sclerosis, prognosis
multiple sclerosis, risk factors for
multiple sclerosis, spinal form
multiple sclerosis, treatment of
muscle biopsy
myelin basic protein gene
myelinolysis, extrapontine
myelitis
myelitis, longitudinal
myelitis, transverse
myelomalacia
myelopathy
myelopathy, chronic progressive
myocardial infarction
myoclonus
mysoline
nausea and vomiting
neurochemistry
neurogenic bladder
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuropathology
neuropathy
neuropathy, peripheral
neurotransmitter
norepinephrine
Notch3 gene
nystagmus
obsessive-compulsive disorder
occipital lobe, infarction
occipital lobe, lesion of
old age, neurology of
optic atrophy
optic atrophy, bilateral
optic atrophy, hereditary
optic nerve, hypoplasia of
optic neuritis
optic neuritis, bilateral
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
palatal myoclonus
palilalia
paraparesis
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
paratrigeminal syndrome
paresthesias
Parkinson disease
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
periventricular leukomalacia
phenylketonuria
phenylketonuria, adult onset
pimozide
pleocytosis of cerebrospinal fluid
poison, neurologic problems with
polymerase chain reaction
pons, lesion of
posterior cerebral artery territory infarction
posterior leukoencephalopathy syndrome
premature infant
prevention of neurologic disorders
primary lateral sclerosis
prognosis
propranolol
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
pyramidal tract dysfunction
quadriparesis
quadriplegia
quality of life
radiation therapy, stereotactic
ragged-red fibers
Red flags
regional enteritis
renal stones
retrovirus
reversible neurologic disorder
review article
rigidity
Riley-Day syndrome
risk factors
Rosenthal fibers
Sandhoff's disease
Schilder's disease
scotoma
scotoma, central
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
smell
spasticity
spasticity, treatment of
speech disorder
speech, loss of
spinal cord
spinal cord, injury of
spinal cord, injury, management of
spinal cord, lesion of
spontaneous remission
steroid therapy, CNS treatment and complications with
stimulation, deep brain
symmetric brain lesions
systemic lupus erythematosus
tardive dyskinesia
taste
Tay-Sachs disease
temporal lobe, lesion, bilateral
thalamic tumors
thalamic tumors, bilateral
thalamotomy
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
thyrotoxicosis
tic
tinnitus
tongue, impaired movements of
top of the basilar syndrome
torticollis
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, classification
tremor, differential diagnosis of
tremor, intention
tremor, jaw
tremor, leg
tremor, rubral
tremor, surgical treatment of
tremor, thalamic stimulation for suppression of
tremor, treatment of
twins
ulcerative colitis
uremia
urinary frequency
urinary incontinence
urinary urgency
vasculitides
vasculopathy
vasospasm, cerebral
vertigo
vertigo, episodic
very long chain fatty acids
viral infection
viral infection, CNS
vision loss, sequential
visual acuity, decreased
visual evoked response
visual loss
visual loss, progressive
visual loss, sudden
visual loss, transient
walking, difficulty with
water channel antibodies
weakness
Wernicke's encephalopathy
white matter disease
workup
Showing articles 2150 to 2200 of 5493 << Previous Next >>

Clinicopathologic Conference, Antiphospholipid Syndrome due to SLE with Hypocomplimentemia
NEJM 389: 2277-2285, Case 38-2023, 2023

A Woman With Multifocal Ischemic Strokes and Progressive Cognitive Impairment Due to Intravascular Lymphoma
Stroke 54:e488-e451, Stamm,B., et al, 2023

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

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

Drug Resistant Epilepsy in a 61-Year-Old Man with Abnormal MRI Brain Findings and Management with Vagal Nerve Stimulator
Neurol 100:1111-1116, Mankad,J.P. & Lavingia,J.R., 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

Woman With Acute Bilateral Ophthalmoplegia
Neurol 101:140-144, Giacobbe,Alket al, 2023

Intracerebral Haemorrhage Caused by Iatrogenic Cerebral Amyloid Angiopathy in a Patient with a History of Neurosurgery 35 Years Earlier
Lancet 402:11, Fandler-Hofler,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

Idiopathic Orbital Inflammation and Tolosa-Hunt Syndrome with Intracranial Extension
Neurol 101:371-374, Yu,S. & Chen,T., 2023

Progressive Hemiparesis and White Matter Abnormalities in an HIV-Negative Patient
Neurol 100:1156-1163, Jabbari,E.,et al, 2023

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Cavernous Sinus Thrombosis
StatPearls PMID:28846357, Plewa,M.C.,et al, 2023

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023

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

A 25-Year-Old Woman With Eye Swelling and HEadache
Neurol 100:879-883, Hehir,A.,et al, 2023

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

Cutaneous a-Synuclein Signatures in Patients with MultipleSystem Atrophy and Parkinson Disease
Neurol 100:e1529-e1539, Gibbons,C.,et al, 2023

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

Salt and Pepper Sign, PLNTY for Drug-Resistant Epilepsy
Neurol 100:791-795, Paredes-Aragon,E.M.,et al, 2023

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
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Iatrogenic Cerebral Amyloid Angiopaty Post Neurosurgery:Frequency, Clinical Profile, Radiological Features, and Outcome
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Brain Calcification in a Young Woman With Seizures, Explore the Rare Differentials
Neurol 100:397-398, Menon,B.,et al, 2023

Clinicopathologic Conference, Paraneoplastic Vasculitis of the Central Nervous System
NEJM 388:747-757, Case 6-2023, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,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

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

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

Recurrent Anti-NMDA Receptor Encephalitis After Mycoplasma Pnemonia Infection
Am J Psychiatry 180:880-883, Dickson,K.S.,et al, 2023

Stroke in Patients with Common Noncancerous Gynecologic Diseases
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Cerebral and Retinal Infarction in Bicuspid Aortic Valve
J Am Heart Assoc 12:e028789, Huntley,G.D.,et al, 2023

Adult-Onset Niemann-Pick Disease Type C Masquerading As Spinocerebellar Ataxias
Mol Genet Genomic Med 10:e1906, Vo,M.L.,et al, 2022

Autoimmune Nodopathies, An Emerging Dignostic Category
Curr Opin Neurol 35:579-585, Martin-Agullar, L.,et al, 2022

Natural History of Carotid Artery Free-Floating Thrombus-A Single Center, Consecutive Cohort Analysis
Front Neurol doi:10.3389/fneur.2022.993559;2022, Muller,M.D.,et al, 2022

Spontaneous Escherichia Coli Meningitis and Brain Abscess in an Immunocompetent Adult
Cureus doi.10.7759/CUREUS.208728, Jeter,K.et al, 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

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

Magnetic Resonance Imaging of the Cranial Nerves in Infectious, Neoplastic, and Demyelinating Diseases, as Well as Other Inflammatory Diseases:A Pictorial Essay
Radiol Bras 55:38-46, Dalaqua,M.,et al, 2022

Case of Cocaine Induced Coronary and Carotid Artery Dissection
J Invest Med High Imp Case Report 10:1-4, Gill,T.,et al, 2022

Babesiosis: Clinical Manifgestations and Diagnosis
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Bilateral Middle Cerebellar Peduncle Stroke in Giant Cell Arteritis
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Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
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Three Territory Sign in COVID-19
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Confused About Confusion
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A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022



Showing articles 2150 to 2200 of 5493 << Previous Next >>