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Differential
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acetylcholine receptor antibody
alopecia
alternating hemiplegia
alternating hemiplegia of childhood
areflexia
ataxia
ataxia telangiectasia
ataxia, cerebellar
ATP1A3 gene
autoantibodies
autoimmune disease
autonomic dysfunction
biologic markers
cataplexy
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar atrophy, primary
children
chorea
choreoathetosis
Clinical Pathologic Conference(C.P.C.)
conversion reaction
developmental retardation
diabetes mellitus
diagnostic criteria
dysarthria
dysdiadochokinesia
dysmetria
dyspnea
dystonia
eczema
electromyogram
encephalopathy
eye movement, disorders of
falling
Friedreich's ataxia
gait disorder
gammaglobulin therapy, intravenous
gene
gene mutation
genetic neurologic disorders
genetic testing
glutamic acid decarboxylase, antibody
hearing loss
hemiplegia
hyperreflexia
hypersomnia
hypotonia
imbalance
incoordination
infantile hemiplegia
intellectual deficit
leukoencephalopathy
low back pain
meningitis, carcinomatous
mental retardation
microcephaly
misdiagnosis
molecular genetics
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movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, negative
muscle stiffness
myasthenia gravis
myasthenia gravis, neonatal
myelomalacia
narcolepsy
nerve conduction studies
neurologic disease, diagnoses of
nystagmus
nystagmus, monocular
nystagmus, periodic
ocular motility, disorders of
old age, neurology of
optic atrophy
pain
pain, back
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
polysomnogram
precipitating factors
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
review article
saccadic eye movements, abnormal
seizure
sensorineural hearing loss
sleep pathology and physiology
staggering
startle reaction
status epilepticus
stiff legs
stiff man syndrome
strabismus
tandem gait, ataxic
thrombocytopenia
thyrotoxicosis
tone, muscle
transient loss of muscle tone
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
valium
vitamin E deficiency
vitiligo
walking, difficulty with
white matter disease
wide based gait
workup
Showing articles 300 to 350 of 8558 << Previous Next >>

Mild Encephalitis/Encephalopathy with a Reversible Splenial Lesion Associated with Systemic Mycoplasma Pneumoniae Infection in North America: A Case Report
J Med Case Reports doi:10.1186/s13256-022-03299-6, Talukder,N.T.,et al, 2022

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

Recurrent Amaurosis Fugax Secondary to Tolosa-Hunt Syndrome: A Case Report and Review of Phenotypes and Pathology
Cureus doi.10.7759/Cureus.15281, Kesserwani,H. & Heersink,M., 2021

Giant Cell Arteritis:Its Ophthalmic Manifestations
Indian J Ophthalmol 69:227-235, Hayreh, S.S., 2021

Clinicopathologic Conference, Cerebral Amyloid Angiopatny-Related Inflammation
NEJM 385:358-368, Case 22-2021, 2021

A 68-Year-Old Man with Proximal Weakness and Seizures
Neurol 97:e423-e428, Chen, T., 2021

Clinicopathologic Conference, Acute human immunodeficiency virus type 1
NEJM 385:641-648, Case 24-2021, 2021

Progressive Ataxia and Doenbeat Nystagmus in an Adult
JAMA Neurol 78:1018-10019, Fernandez, A.C.,et al, 2021

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

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

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Nitromethane-Induced Acute Reversible Encephalopathy
Neurol 97:e1361-e1362, Palumbo, G.,et al, 2021

An Unusual Case of Acute Psychosis and Tetraparesis in a Young Zambian Man
Neurol 97:1002-1005, Zimba, S.,et al, 2021

Spontaneous Intracranial Hypotension
NEJM 385:2173-2178, Schievink, W.I., 2021

Sudden Loss of Vision at the Gym
BMJ 375:e067964, Ng, J.K.Y.,et al, 2021

Clinicopathologic Conference, Fat Embolism Syndrome
NEJM 385:2464-2474, Case 39-2021, 2021

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

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

Clinicopathologic Conference, Disseminated Mycobacterium Bovis Infection
NEJM 384:651-662, Case 5-2021, 2021

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

A 71-Year-Old Man Presenting with Acute Onset Dysarthria and Dysphagia
Neurol 96:180-184, Spagni, G.,et al, 2021

Factors Associated with Risk of Recurrent Transient Global Amnesia
JAMA Neurol 77:1551-1558, Morris, K.A.,et al, 2020

Clinicopathologic conference, Vitamin D deficiency
NEJM 383:2462-2470, Case 39-2020, 2020

"Cortical" Wrist Drop due to a Cerebral Peduncle Infarct
Case Rep Neurol 12:207-211, Venketasubramanian, N.,et al, 2020

Covd-19-Associated Myopathy Caused by Type 1 Interferonopathy
NEJM 383:2389-2390, Manzano, A.C.,et al, 2020

A 62-year-old man with history of catheter ablation presenting with recurrent strokes
Neurol 95:e3065-e3069, Jeanneret, V.,et al, 2020

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
Neurol 95:e1285-e1289, Seese, R.R.,et al, 2020

Diffusion-Weighted MRI in Transient Global Amnesia and its Diagnositc Implications
Neurol 95:e206-e212, Szabo, K.,et al, 2020

A 10-Year-Old Girl with Muscle Stiffness
Neurol 95:e773-e778, Prior, D.E. & Ghosh, P.S., 2020

Immunoglobulin G4-Related Orbital Disease with Bilateral Optic Perineuritis and Maxillary Nerves Involvement:A Case Report
Ophthalmol Ther 9:1089-1099, Hung,C-H., 2020

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

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 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

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

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

A Rare Presentation of Whipple Disease
Neurol 94:e758-e761, Koek, A.T.,et al, 2020

Epilepsy in Older People
Lancet 395:735-748, Sen, A.,et al, 2020

Functional Neurological Disorder
Stroke 51:1629-1635, Popkirov, 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

COVID-19: A Global Threat to the Nervous System
Ann Neurol 88:1-11, Koralnik, I.J. & Tyler, K.L., 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Neuropathological Features of Covid-19
NEJM doi:10.1056/NEJMc2019373, Solomon, I.H.,et al, 2020

A 59-year-old Woman with Multiple Myeloma and Lower Extremity Weakness and Numbness
Neurol 94:794-800, Gadot, R.,et al, 2020

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

A Young Health Woman with Difficult-to-Wean Acute Ventilator Dependence
Neurol 94:e1340-e1343, Chandrashekhar, S.,et al, 2020



Showing articles 300 to 350 of 8558 << Previous Next >>